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It's funny. I'm reading a book by Ann Louise Gittlemen " Why am I always so

tired? " About copper overload, because it's in everything we consume, leading

to zinc deficiency. Carbohydrates especially grains have a lot of copper. She

seems to feel we have way too much copper in our systems today.

Suzanne

Ohio

Autism and LOW copper

DC NutritionI have been researching copper deficiency the last few days as my

father has an aneurysm. Itseems the aortic wall is inflamed and lacks elastin

both have a common denominator..low copper.

So trolling through the net I came across this list of low copper symptoms

and darn I thought..very strong resemblance to autism... Copper also is needed

for the brown pigment in hair. Aren't the majority of our children blonde with

many parents even reporting their child's hair turning white!

I am wondering if copper toxicity isn't really copper deficiency. I just

read an interesting paper on Alzheimers where the author found low brian copper

in his subjects. If the body is low on copper, I believe the response is the

liver releasing it's copper reserve..hence high copper in blood!

Note the high iron storage..Aren't most opf our children exceptionally high

in ferritin?

Note also low neutrophils!

Nosebleeds common in autism would indicate low copper as the vein integrity

is compromised due to lack of Elastin ( Copper is needed in the cross-linking

process)

Look how low copper correlates highly with inflammation ( inflamed guts!!)

Look how copper si necessary fopr lipid mertabolism . Don't our children

have grave problems with this.

Not mentioned below but copper is important functioning of the

Metallothionein protein!!

Also copper integral to functioning of the MAO enzyme which breaks down

neurotransmittors! Children with autism often have difficulty with high levels!

I wonder if we are overlooking the Bleeding Obvious! (Pardon my French!)

It would be interesting to document the copper staus in the Mums. I assume

the fetus absorbed what little reserves the mother had, used it in high amounts

in the first years and then reserves tumbled.

I am talking to a British research scientist who has found a relationship

between low brain copper and high managnese in fertilizers!

This same scientist has found that widely used pesticides chelate copper.

These pesticides became increasingly common in America and the UK in the 1980s

and 90s which would correspond with the increase in autism rates!!

The above should be considered not just in cases of autism but also anaemia

problems.

Lastly, my interest was piqued when I read an article in the German press

about copper being protective for Alzheimers. Alzheimers mice which were copper

deficient were found to have lowered Amyloid deposits after copper

supplementation. Amyloid deposits I have discovered on another list could be

what's behind " Glue Ear " phenomena.

Best,

in Germany

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About

This Site Copper (Cu) - General Discussion a.. Copper (Cu)

References

a.. Minerals list

a.. Minerals introduction

Cu - Copper is found in igneous rocks at 55 ppm; shale at 45

ppm; sandstone at 5 ppm; limestone 4 ppm; fresh water at 0.01 ppm; sea water at

0.003 ppm; soils at 2 to 100 ppm (copper is strongly absorbed by humus; there

are known areas of the world with extreme copper deficiency); marine plants 11

ppm; land plants 14 ppm; marine animals 4 to 50 ppm; accumulates in the blood of

annelids (worms), crustaceans and mollusks, especially cephalopods; land animals

at 2 to 4 ppm with highest levels in the liver.

Symptoms Associated with Copper Deficiency

- White hair

- Gray hair

- Dry brittle hair ( " steely wool " in sheep)

- Ptosis (sagging tissue - eye lids, skin etc.)

- Hernias (Congenital and acquired)

- Varicose veins

- Aneurysms (large artery blowouts, cerebral artery blowouts)

- Kawasaki Disease (congenital aneurysms with Streptococcal

infection)

- Anemia (especially in vegan and high milk diets)

- Hypo and hyper thyroid

- Arthritis (especially where growth plate is involved)

- Ruptured vertebral disc

- Liver cirrhosis

- Violent behavior, blind rage, explosive outbursts, criminal

behavior

- Learning disabilities

- Cerebral palsy and hypoplasia of the cerebellum (congenital

ataxia)

- High blood cholesterol

- Iron storage disease (abnormal iron accumulation in liver)

- Reduced glucose tolerance (low blood sugar)

- Neutropenia (low neutrophils)

Copper is essential to all living organisms and is a universally

important cofactor for many hundreds of metalloenzynes. Copper deficiency is

widespread and appears in many forms . Copper is required in many physiological

functions (RNA, DNA, lysil oxidase cofactor, melanin production (hair and skin

pigment), electron transfer of oxygen subcellular respiration, tensile strength

of elastic fibers in blood vessels, skin, vertebral discs, etc.).

Neonatal enzootic ataxia (sway back, lamkruis) was recognized as

a clinical entity in 1937 as a copper deficiency in pregnant sheep. Copper

supplements prevented the syndrome which was characterized by demyelination of

the cerebellum and spinal cord. Cavitation or gelatinous lesions of the cerebral

white matter, chromatolysis, nerve cell death and myelin aplasia (failure to

form). These are all changes identical with human cerebral palsy.

Four to six of every 100 Americans autopsied have died of a

ruptured aneurysm, an additional 40 percent have aneurysms that had not yet

ruptured.

The average well-nourished adult human body contains between 80

and 120 mg of copper. Concentrations are higher in the

brain, liver, heart and kidneys. Bone and muscle have lower

percentages of copper but contain 50 percent of the body total copper reserves

because of their mass. It is of interest that the greatest concentration of

copper is found in the newborn and their daily requirement is 0.08 mg/kg,

toddlers require 0.04 mg/kg and adults only 0.03 mg/ kg.

The average plasma copper for women ranges from 87 to 153 mg/dl

and for men it ranges from 89 to 137 mg/dl; about 90 percent of the plasma

copper is found in ceruloplasmin.

Copper functions as a co-factor and activator of numerous

cuproenzymes that are involved in the development (deficiency of Cu in the

pregnant female results in congenital defects of the heart, i. e. - Kawasaki

Disease and brain cerebral palsy and hypoplasia of the cerebellum) and

maintenance of the cardiovascular system (deficiency results in reduced lysyl

oxidase activity causing a reduction in conversion of pro elastin to elastin

causing a decrease in tinsel strength of arterial walls and ruptured aneurysms

and skeletal integrity (deficiency results in a specific type of arthritis of

the young in the form of spurs in the bones growth plate); deficiency can result

in myelin defects; deficiency results in anemia; and poor hair keratinization

and loss of hair color. Neutropenia (reduced numbers of neutophillic WBC) and

leukopenia (reduced total WBC) are the earliest indicators of copper deficiency

in infants; infants whose diets are primarily cows milk frequently develop

anemia; iron storage disease can result from chronic copper deficiency.

Menkes' Kinky Hair Syndrome is thought to be a sex-linked

recessive defect of copper absorption. The affected infants exhibit retarded

growth, defective keratin formation and loss of hair pigment, low body

temperature, degeneration and fracture of aortic elastin (aneurysms), arthritis

in the growth plate of long bones, and a progressive mental deterioration (brain

tissue is totally free of the essential enzyme Cytochrome c oxidase). Because of

absorption problems of metallic copper, injections of copper are useful.

Serum and plasma copper increase 100 % in pregnant women and

women using oral contraceptives. Serum copper levels are also elevated during

acute infections, liver disease and pellagra (niacin deficiency).

Accumulations of copper in the cornea form - Kayser Fleischer

rings.

Copper deficiency and thyroid function

Rats were fed diets containing adequate, marginal or deficient

amounts of copper for 35 days. Copper deficiency resulted in a significant

increase in serum cholesterol levels and a significant decline in plasma

thyroxine concentrations and body temperatures. Compared with rats fed the

adequate diet, those fed the marginal and deficient diets had significantly

lower plasma concentrations of triiodothyronine (T3) and significantly higher

TSH levels. The activity of thyroxine 5'-monodeiodinase (the enzyme that

converts T4 to T3) was reduced in the liver and brown adipose tissue of copper

deficient rats.

COMMENT: This study suggests that copper deficiency interferes

with thyroid hormone metabolism and can promote hypothyroidism, as indicated by

a reduction in T3 levels and body temperatures and an increase in TSH. Copper,

zinc and selenium all have been shown to play a role in the metabolism of

thyroid hormones, and a deficiency of any one of these trace minerals might be a

contributing factor in patients who exhibit hypothyrold symptoms.

Dr. Carl Pfeiffer has pointed out that an excessive body burden

of copper can result in various neuropsychiatric symptoms. Because of Pfeiffer's

work, many clinicians view copper primarily as a toxic mineral (because copper

supplements are not as water-soluble as they should be). Indeed, a number of

popular multivitamin/mineral formulas are advertised as being " copper free. "

However, copper is also an essential nutrient, and the average American diet

provides only about half the RDA (about 1 mg/day). Therefore, mild copper

deficiency may be a more common problem than copper excess.

Lukaski H C et al. Body temperature and thyroid hormone

metabolism of copper deficient rats. Nutr Biochem 1995;6:445-451.

------------------------------------------------------------------

Copper is an essential trace mineral. The body of an adult

contains 100 mg to 150 mg of copper. Though copper is present in all tissues,

including red cells, the liver is the main site of copper storage. Most of serum

copper is bound to ceruloplasmin, the copper transport protein synthesized by

the liver. Ceruloplasmin also aids in iron transportation and storage. Like most

trace minerals, copper functions as an enzyme cofactor by activating certain key

enzymes required to strengthen the structural protein collagen, which in turn

strengthens cartilage, tendons, bones, and blood vessels. Copper also serves as

a cofactor of a protein in the blood that helps maintain lung tissue and prevent

emphysema; and it is essential for insulating (mylination) nerve cells. As a

cofactor for the enzyme superoxide dismutase, copper helps prevent oxidative

damage by a highly reactive form of oxygen and thus is classified as an

antioxidant. Copper functions as a cofactor for cytochrome oxidase of

mitochondria, the enzyme complex that ultimately transfers electrons from the

oxidation of fat, carbohydrate and protein to oxygen for energy production.

Copper also serves as a cofactor in the synthesis of norepinephrine, an

important neurotransmitter and adrenal hormone.

The estimated safe and adequate daily intake of copper for

normal adults is 2 to 3 mg. About 30% of dietary copper is assimilated. Good

sources of copper include liver, kidneys, shellfish, nuts, seeds, fruit and

dried legumes. Cow's milk is low in copper. The standard American diet is copper

deficient and between 66 and 75% of the U.S. population do not consume enough

copper. Dieters, elderly persons and chronic alcoholics are especially

vulnerable. The following factors increase the need for copper: excessive

dietary fiber, high zinc supplements (50 mg or more daily), cadmium, excessive

vitamin C and excessive sugar (fructose) intake (at least in rats).

Low copper consumption increases the risk of high blood

cholesterol and coronary heart disease, lowered immunity, gout, diabetes, high

blood pressure, anemia, nervous disorders, decreased pigmentation of skin,

fragile bones and erratic heartbeat. Low dietary copper is linked with an

increased risk of heart attack. Evidence also links copper deficiency with

increased oxidative damage to cell membranes. Levels of norepinephrine in the

brain are decreased with copper deficiency but may be restored by supplemental

copper. There are certain precautions to keep in mind for copper supplements.

Consumption of 10 to 15 mg of copper daily can cause side effects. Patients with

a rare copper accumulation disease ('s disease) should not use copper

supplements. An excessive copper overload has been linked to various psychiatric

syndromes. A green stain in the sink from a faucet drip, or in a teakettle,

suggests excessive copper in drinking water, leached from copper plumbing.

Prohaska, ph R. and Failla, Mark L., " Copper and Immunity, "

in Human Nutrition--A Comprehensive Treatise, vol. 8 of Nutrition and

Immunology, Klurfeld, M., ed. New York: Plenum Press, 1993.

Also, included from: Minerals in Animal and Human Nutrition

By Lee McDowell

Copper Physiology

Copper is required for cellular respiration, bone formation,

proper cardiac function, connective tissue development, myelination of the

spinal cord, keratinization, and tissue pigmentation. Copper is an essential

component of several physiologically important metalloenzymes including

cytochrome oxidase, lysyl oxidase, superoxide dismutase,

dopamine-beta-hydroxylase, and tyrosinase.

1. IRON METABOLISM AND CELLULAR RESPIRATION

Along with Fe, Cu is necessary for hemoglobin synthesis. Copper

is not contained in hemoglobin, but a trace of it is necessary to serve as a

catalyst before the body can utilize Fe for hemoglobin formation. Anemia can

develop with either a Fe or Cu deficiency. With Cu deficiency there is an

apparent delay in maturation and shortened life span of red blood cells (Baxter

and Van Wyk, 1953).

Copper plays a key role in Fe absorption and mobilization. Serum

Fe levels tend to be low in Cu deficiency, and hypochromic anemia develops while

intestinal mucosa and liver Fe levels are higher than normal. Ceruloplasmin

(ferroxidase), which is synthesized in the liver and contains Cu, is necessary

for the oxidation of Fe, permitting it to bind with the Fe-transport protein,

transferrin. Ceruloplasmin (, 1978) is a multifunctional enzyme involved in

Fe metabolism, transport of Cu, and regulation of certain amines.

Iron must be converted to the ferrous form to be mobilized from

stored ferritin and/or to be incorporated into hemoglobin or myoglobin. For

storage as ferritin or for transport as transferrin, Fe must be converted to the

ferric form (Curzon, 1961), a reaction performed by ceruloplasmin.

Copper is a constituent of the important metalloenzyme,

cytochrome oxidase. This enzyme is the terminal oxidase in the respiratory

chain; it catalyzes the reduction of 0, to water, an essential step in cellular

respiration.

2. CROSS-LINKING OF CONNECTIVE TISSUE

With a Cu deficiency, there is failure of collagen to undergo

cross-linking and maturation ( and O'Dell, 1974). The key Cu-containing

enzyme in the formation of the cross-links in collagen and elastin is lysyl

oxidase, which is necessary to add a hydroxyl group to lysine residues in

collagen, allowing crosslinking between collagen fibers. These cross-links give

the proteins structural rigidity and elasticity. Aortic aneurysms and ruptures

result from failure to convert lysine to desmosine, the cross-linking residue in

elastin.

3. PIGMENTATION AND KERATINIZATION OF HAIR AND WOOL

Achromotrichia (lack of pigmentation) is a principal

manifestation of Cu deficiency in many species. It is commonly observed in the

hair and wool of mammals, and is usually attributed to lack of tyrosinase

(polyphenyl oxidase) activity. A breakdown in the conversion of tyrosine to

melanin is the probable explanation.

Impaired keratinization of hair and wool are noted in

Cu.-deficient animals. The characteristic physical properties of wool, including

crimp, are dependent on disulfide groups that provide cross-linkages or bonding

of keratin and on alignment or orientation of long-chain keratin fibrillae in

the fiber. Straight steely wool has more sulfhydryl groups and fewer disulfide

groups than normal (Marston, 1946). Copper is required for formation or

incorporation of disulfide groups in keratin synthesis.

4. CENTRAL NERVOUS SYSTEM

The link between Cu deficiency and the integrity of the central

nervous system, i.e., swayback (enzootic ataxia) of lambs, results from a

reduction in cytochrome oxidase activity and thus incomplete myelin formation

(Howell and son, 1959). Myelin is composed largely of phospholipid. Loss of

cytochrome oxidase in Cu deficiency leads to depressed phospholipid synthesis by

liver mitochondria. The inhibition of myelin synthesis results in the ensuing

neurological disturbances. Other central nervous system effects of Cu deficiency

are reduction of at least two neurotransmitters, dopamine and norepinephrine

(O'Dell, 1984).

5. REPRODUCTION

Reproductive failure is commonly observed in mammals fed

Cu-deficient diets (Underwood, 1977). For rats and guinea pigs, Cu deficiency

has resulted in fetal death and resorption. Embryos from Cu-deficient hens

exhibited anemia, retarded development, and a high incidence of hemorrhage after

72 to 96 hours of incubation, and a reduction in monoamine oxidase activity. The

anemia, hemorrhages, and mortality are probably caused by defects in red blood

cell and connective tissue formation during early embryonic development.

6. IMMUNE SYSTEM

Copper metabolism affects T and B cells, neutrophils, and

macrophages. An impaired humoral immune response (i.e., decreased numbers of

antibody-producing cells) was observed in mice with hypocuprosis (Prohaska et

al., 1983). The magnitude of this impairment was highly correlated with the

degree of its functional deficiency. In a literature review, et al (1979)

concluded that the relationship of Cu to the immune system is through superoxide

dismutase, a Zn-, Cu-, and Mn-dependent enzyme, and its role in the microbial

systems of phagocytes.

In cattle affected by Cu deficiency induced by Mo, neutrophils

were impaired in their ability to kill ingested Candida albicans (Boyne and

Arthur, 1986). The ability of polymorphonuclear leukocytes to phagocytose C.

albicans in sheep with low Cu status is comparatively lower than that of sheep

on a normal Cu diet (Olkowski et al 1990). A decreased resistance to infection

has been observed in sheep affected by Cu deficiency (Wooliams et A, 1986).

7. LIPID MATABOLISM

A number of studies have demonstrated the effect of Cu

deficiency on lipid metabolism. ing et al (1977) reported that Cu

deficiency results in elevated levels of serum triglyceride, phospholipids, and

cholesterol in the rat. Altered heart function of rats fed low Cu is associated

with alterations in lipid and long-chain fatty acid metabolism (Cunnane et al.,

1987), which may be attributable to the predominant role of Cu in the superoxide

dismutase enzyme system.ool r Physiology

COPPER: The Missing Link in Your Diet

By Sherry A. , M.D.

When we think of copper, we often think of toxic or high levels

from copper tubing and water pipes. In reality, the majority of Americans are

deficient in copper. The National Institutes of Health did a study showing that

81 percent of people have less than two-thirds of the recommended daily

allowance of copper. Another study revealed that hospital meals provide only

0.76 mg of copper per day, whereas people need 2-4 mg for health, and even more

for healing.

A study by the Food and Drug Administration showed that, in an

analysis, 234 foods that constitute the core of the American diet provided less

than 80 percent of the RDA of copper. A study of 270 United States Navy SEAL

trainees, all of them highly selected healthy young men, revealed that 37

percent had low plasma copper levels, and plasma copper, as you will see, is a

very insensitive indicator of copper status.

One study showed that 80 percent of Americans get 1 mg of copper

per day, and another study, which analyzed 20 different types of U.S. diets,

showed that only 25 percent of the people got 2 mg of copper a day and the

majority of the diets provided 0.78 mg of copper per day.

So all copper studies seem to point to the majority of people

being deficient.

When we studied 228 of our patients, 165 (or 72 percent) were

deficient in copper. So, no matter whose studies you look at over the last 20

years, there is a wealth of data showing that copper deficiency is rampant in

the United States. But the best test for copper deficiency is intracellular, or

red blood cell (RBC), while serum or plasma copper tests are too insensitive,

and hence not worth obtaining.

Why Copper Is Needed

So why do we need copper? Copper is present in about 21

different enzymes, and its importance has been known since 1928. For example,

one important enzyme is histaminase, which breaks down histamine. So all

allergic people, who overproduce histamine, certainly need to ensure that they

have normal copper levels. Another copper-dependent enzyme is cytochrome

oxidase, which is necessary for energy metabolism. Indeed, some people with

weakness and chronic fatigue have marked copper deficiencies.

Copper is also present in superoxide dismutase, an enzyme which

is useful in protecting us from developing chemical sensitivity. For example, a

33-year-old lab technician for years could not tolerate shopping malls, auto

exhaust fumes and many businesses because of chemical sensitivity. She felt

confused, suffered from headaches, and became weak and tired when she breathed

the higher levels of chemicals commonly encountered in these environments. When

we found that she had a copper deficiency and corrected it, within one month she

was no longer as chemically sensitive, and could tolerate these exposures

without symptoms.

Remember that chemical sensitivity requires multiple factors,

one of which is that the person must be deficient in certain nutrients that are

necessary for the detoxification pathways to operate normally. Once the

deficiencies in these pathways are corrected many times, the chemical

sensitivity is corrected.

As well, the enzyme superoxide dismutase (SOD) plays a role in

the retarding of aging, arthritis and general body deterioration. In fact, in

nearly all diseases, lower than normal levels of SOD are found. For example,

people with colitis were found to have much lower levels of superoxide dismutase

in the bowel, and people with Alzheimer's disease were found to have much lower

levels of superoxide dismutase in the brain. In other studies, chemically

induced tumors were analyzed and found to be low in copper-containing protective

superoxide dismutase.

Detoxification

There are many other enzyme pathways where copper is used for

the detoxification of chemicals besides superoxide dismutase. For example, it is

in polyphenol oxidase, which is necessary for the breakdown of phenols that emit

gas from common household cleaning products. Also copper is necessary for the

action of glutathione peroxidase and catalase pathways, even though it is not

directly used in those enzymes. Studies on rats show that those which were

deficient in copper developed severe liver necroses (tissue death) when exposed

to carbon tetrachloride. But when the copper deficiency was corrected, they did

not develop the expected chemical toxicity and suffer death.

Just as important, copper has a very important role in mood

chemistry. For example, the enzyme dopamine beta-hydroxyl is responsible for the

metabolism of norepinephrine, which affects depression and fatigue. It is also

important in the synthesis of other mood hormones, like dopamine and serotonin

(the one that many antidepressants -like Prozac -work on), and in the major

stress (adrenal) hormone, epinephrine. And copper has an even' greater influence

on our moods, for it is necessary for the action of aminoxidases, which

influence the metabolism of many neurotransmitter proteins in the brain that are

responsible for moods and thoughts.

The Heart Protector

With all of these benefits, copper is still essential for many

more enzymes. It is very important in protecting against arteriolosclerosis and

hypercholesterolemia; aneurysms (weakened blood vessels that burst and can cause

sudden death); EKG abnormalities; hypercoagulable states which lead to heart

attacks and strokes; and sugar metabolism. As an example, many people with high

cholesterol lack minerals like copper to properly metabolize their cholesterol.

It is an error to prescribe cholesterol-lowering drugs without checking the RBC

copper status.

For example, copper is important in an enzyme deta-9-desaturase.

This has to do with the propermetabolism of essential fatty acids that make up

the structural integrity of cell membranes. Remember that the most important

membranes are the cell walls, from which allergic reactions, degenerative

diseases and autoimmune diseases emanate.

Calcium channel blockers are commonly prescribed expensive drugs

to control blood pressure and heart arrhythmias, but the reason the membrane

calcium channels must be blocked has to do with minerals and essential fatty

acid deficiencies in the membranes. A headache isn't an aspirin deficiency, so

we should be less inclined to " drug " every symptom and more inclined to find the

nutrient deficiency behind the symptom. For example, if the mitochondrial

membrane wall, where energy is created, is deficient, we can get chronic

fatigue.

Furthermore, another very important membrane is the nuclear

membrane, which protects our genetic DNA material from damage from chemicals.

When the nuclear membrane is weak, chemicals can penetrate the nucleus and

damage DNA; this is one of the mechanisms for instigating cancers as well as

other degenerative diseases. Another Very important membrane complex is the

endoplasmic reticulum, where detoxification of everyday home, office and outdoor

chemicals must, be done.

At this point, you might be eager to run out and comer the

market on copper and consume it, but this can be dangerous without knowing the

proper level of copper, or the proper level of complementary, but antagonistic,

minerals such as (RBC) zinc, (RBC) molybdenum and iron. By taking copper, one

can lower the values of these important minerals and create secondary

deficiencies.

Foods that are high in copper include nuts, legumes (peas and

beans), seeds, organ meats and shellfish, in particular. Foods especially low in

copper are processed foods in general, especially white flour, white sugar and

fructose (fruit sugars).

Man is still trying to figure out why there are such folk

remedies as copper bracelets for the care of arthritis. Some researchers presume

that the copper is actually absorbed and incorporated into the anti-inflammatory

enzyme superoxide dismutase, which tends to turn off inflammatory conditions

like arthritis or Lupus.

Bob, a 54-year-old engineer, had 10 years of headaches. Allergy

injections, dietary changes, and correction of nutrient deficiencies documented

on blood tests corrected other symptoms, but they did not relieve his headaches.

However, when a RBC copper deficiency was found and corrected, within one month

his headaches disappeared. Certainly, people like this teach us that copper is

the " missing link. "

About the author: Sherry A. , M.D., has a private practice

in environmental and nutritional medicine.

COPPER DEFICIENCY AND MULTIPLE SCLEROSIS

A nervous disorder in sheep characterized by uncoordination of

gait has been recognized for many years. This disorder is most common in sheep

but it has also been reported in goat kids and more rarely in calves and

piglets. Various local names have been given to this condition but swayback is

the most common. Voisin prefers the term enzootic ataxia. In Trail, British

Columbia, young dogs and cats could not be raised without encountering similar

disabilities until more effective pollution controls were introduced in the

early 1930s. More recently young foals brought into the Trail area suffered

similar problems whereas older horses survived.

These problems seemingly were all associated with a copper

deficiency in the locality or with the presence of too much lead which element

nullifies the copper present in the fodder or in the atmosphere.

The enzootic ataxia in sheep parallels multiple sclerosis in

humans. Both diseases are characterized by demyelination, that is, destruction

of the myelin sheath.

In multiple sclerosis Plumb and Hansen found normal total copper

values both in serum and in cerebrospinal fluid but in the serum they found

reduced activity in copper oxidase. The same writers noted " this new finding

does not yet appear to have attracted comment and its confirmation and further

investigation will be awaited with interest, since vital clues to the role of

trace minerals in myelination are badly needed. "

Voisin wrote " Australian biochemists, able specialists in

deficiency diseases, set to work and found that one could prevent the disease by

administering copper salts orally to the ewes " . Ruth Allcroft obtained similar

results in England.

A few years ago Dr Haine, from Gloucester in England,

suggested that it might be worthwhile to add small copper supplements in some

appropriate form to those persons whose blood contained too little copper.

However this suggestion has apparently met with no support, at least in British

Columbia. This suggestion would seem to be worth investigating.

Copper Deficiency

A variety of symptoms have been associated with copper

deficiency in animals, many of which are seen also in humans; they include

hypochromic anemia, neutropenia (low neutrophils), hypopigmentation (graying) of

the hair and skin, abnormal bone formation with skeletal fragility and

osteoporosis, vascular abnormalities and uncrimped or steely hair. There is no

single specific indicator of copper deficiency. Measurements which, despite

major limitations, are currently considered to be of value in establishing a

range for normal copper status include serum copper (normal range 0.64-1.56

ug/ml), ceruloplasmin (0.18-0.40mg/ml), urinary copper (32-64pg/24h) and hair

copper (10-20 ug/g), all of which are depressed in frankly copper-deficient

subjects but are less sensitive to a marginal copper status. The possibility

that a decline in erythrocyte copper-zinc superoxide dismutase, normally 0.47 +

0.07 (SEM) mg/g of hemoglobin, may provide a more suitable and early indication

of deficiency is being investigated.

Neutropenia is nowadays regarded as a sufficiently constant

feature of copper deficiency in humans to be of diagnostic value, while evidence

of a rapid decline in plasma enkephalins warrants further investigation.

As late as the early to mid-1920s a new trace element, copper,

was suggested, on the basis of empirical evidence, to be of value in the diet of

rats (Bodansky, 192 1; McHargue, 1925, 1926). Copper deficiency was subsequently

shown to inhibit hematopoiesis in the rat (Hart et al., 1928) and in exclusively

milk-fed human infants (phs, 1931). However, it was later discovered that

copper is required for the formation of aortic elastin (O'Dell et al., 1961),

and thus is of crucial importance for heart functioning. Following these

findings, chronic copper deficiency, or a relative copper deficiency induced by

high zinc intakes, has been suggested to be a major etiological factor in human

ischemic heart disease (Klevay, 1975). Copper-deficient laboratory animals have

since been found to be hypercholesterolemic and hyperuricemic and to exhibit

glucose intolerance and abnormalities of cardiac function. They also show

abnormal connective tissues and lipid deposits in the arteries. Deficient

animals may die suddenly with a ruptured heart, caused by thinning of the aortic

wall. These findings have ominous significance in the light of recent copper

estimates in typical human diets in the United States; 75% of the diets examined

furnished less than 2 mg of copper per day, the amount thought to be required by

adults (Klevay, 1982).

Tissue distribution

Copper is widely distributed in biological tissues, where it

occurs largely in the form of organic complexes, many of which are

metalloproteins and function as enzymes. Copper enzymes are involved in a

variety of metabolic reactions, such as the utilization of oxygen during cell

respiration and energy utilization. They are also involved in the synthesis of

essential compounds, such as the complex proteins of connective tissues of the

skeleton and blood vessels, and in a range of neuroactive compounds concerned in

nervous tissue function. It has been estimated that the adult human body

contains 80 mg of copper, with a range of 50-120 mg. Tissue copper levels range

from < 1 ug/g (dry weight) in many organs to > 10 ug/g (dry weight) in the liver

and brain. Copper levels in the fetus and young infant differ from those in the

adult. Concentrations of copper may be 6-10-fold greater in the liver of infants

where, during the first 2 months of postnatal life, it presumably serves as a

store of copper to tide the infant over the period when intake from breast milk

is relatively small.

Copper in human blood is principally distributed between the

erythrocytes and the plasma. In erythrocytes, most copper (60%) occurs as the

copper-zinc metalloenzyme superoxide dismutase, the remaining 40% being loosely

bound to other proteins and amino acids. Total erythrocyte copper in normal

humans is around 0.9-1.0 ug/ml of packed red cells.

In plasma, about 93% of copper is firmly bound to the enzyme

ceruloplasmin, believed to be involved in iron mobilization by maintaining the

supply of oxidized iron transported after its incorporation into transferrin.

The remaining plasma copper (7%) is bound less firmly to albumin and amino

acids, and constitutes transport copper capable of reacting with receptor

proteins or of diffusing, probably in the form of charged complexes, across cell

membranes. Plasma or serum copper in normal humans is in the range 0.8-1.2 ug/ml

and is not significantly influenced by cyclical rhythms or by feeding. The mean

value for females is about 10% higher than that for males and is elevated by a

factor of up to 3 in late pregnancy and in women taking estrogen-based oral

contraceptives.

a.. References for Copper (Cu)

a.. Back to the Minerals introduction

a.. Back to the Minerals list

------------------------------------------------------------------------

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Guest guest

Very interesting! Thanks for posting this information...my child

tests low for copper and demonstrates many of the clinical symtoms

cited by the article...hmmm. Did you find any suggestions regarding

low dose, " bio-available " copper supplements?

I wonder if this is truly a deficiency or a metabolic derangement

related to competition/dysregulation associated with heavy metals?

> DC NutritionI have been researching copper deficiency the last few

days as my father has an aneurysm. Itseems the aortic wall is

inflamed and lacks elastin both have a common denominator..low copper.

>

> So trolling through the net I came across this list of low copper

symptoms and darn I thought..very strong resemblance to autism...

Copper also is needed for the brown pigment in hair. Aren't the

majority of our children blonde with many parents even reporting

their child's hair turning white!

>

> I am wondering if copper toxicity isn't really copper deficiency.

I just read an interesting paper on Alzheimers where the author found

low brian copper in his subjects. If the body is low on copper, I

believe the response is the liver releasing it's copper

reserve..hence high copper in blood!

>

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Guest guest

Seems like I remember reading about some connection between Organophosphate

pesticides, copper, and manganese.

I have often wondered about pesticides subtle effects in our bodies that may

be being overlooked including in children with autism and other neurological

disorders. Many pesticides work as neurotoxins, it makes sense to

investigate all neurotoxins in addition to mercury /lead /etc. Good website

for info on pesticides www.beyondpesticides.org in Washington DC. I am

interested in your theories- keep us posted.

Autism and LOW copper

DC NutritionI have been researching copper deficiency the last few days as

my father has an aneurysm. Itseems the aortic wall is inflamed and lacks

elastin both have a common denominator..low copper.

So trolling through the net I came across this list of low copper symptoms

and darn I thought..very strong resemblance to autism... Copper also is

needed for the brown pigment in hair. Aren't the majority of our children

blonde with many parents even reporting their child's hair turning white!

I am wondering if copper toxicity isn't really copper deficiency. I just

read an interesting paper on Alzheimers where the author found low brian

copper in his subjects. If the body is low on copper, I believe the response

is the liver releasing it's copper reserve..hence high copper in blood!

Note the high iron storage..Aren't most opf our children exceptionally

high in ferritin?

Note also low neutrophils!

Nosebleeds common in autism would indicate low copper as the vein

integrity is compromised due to lack of Elastin ( Copper is needed in the

cross-linking process)

Look how low copper correlates highly with inflammation ( inflamed guts!!)

Look how copper si necessary fopr lipid mertabolism . Don't our children

have grave problems with this.

Not mentioned below but copper is important functioning of the

Metallothionein protein!!

Also copper integral to functioning of the MAO enzyme which breaks down

neurotransmittors! Children with autism often have difficulty with high

levels!

I wonder if we are overlooking the Bleeding Obvious! (Pardon my French!)

It would be interesting to document the copper staus in the Mums. I assume

the fetus absorbed what little reserves the mother had, used it in high

amounts in the first years and then reserves tumbled.

I am talking to a British research scientist who has found a relationship

between low brain copper and high managnese in fertilizers!

This same scientist has found that widely used pesticides chelate copper.

These pesticides became increasingly common in America and the UK in the

1980s and 90s which would correspond with the increase in autism rates!!

The above should be considered not just in cases of autism but also

anaemia problems.

Lastly, my interest was piqued when I read an article in the German press

about copper being protective for Alzheimers. Alzheimers mice which were

copper deficient were found to have lowered Amyloid deposits after copper

supplementation. Amyloid deposits I have discovered on another list could be

what's behind " Glue Ear " phenomena.

Best,

in Germany

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About

This Site Copper (Cu) - General Discussion a.. Copper (Cu)

References

a.. Minerals list

a.. Minerals introduction

Cu - Copper is found in igneous rocks at 55 ppm; shale at 45

ppm; sandstone at 5 ppm; limestone 4 ppm; fresh water at 0.01 ppm; sea water

at 0.003 ppm; soils at 2 to 100 ppm (copper is strongly absorbed by humus;

there are known areas of the world with extreme copper deficiency); marine

plants 11 ppm; land plants 14 ppm; marine animals 4 to 50 ppm; accumulates

in the blood of annelids (worms), crustaceans and mollusks, especially

cephalopods; land animals at 2 to 4 ppm with highest levels in the liver.

Symptoms Associated with Copper Deficiency

- White hair

- Gray hair

- Dry brittle hair ( " steely wool " in sheep)

- Ptosis (sagging tissue - eye lids, skin etc.)

- Hernias (Congenital and acquired)

- Varicose veins

- Aneurysms (large artery blowouts, cerebral artery blowouts)

- Kawasaki Disease (congenital aneurysms with Streptococcal

infection)

- Anemia (especially in vegan and high milk diets)

- Hypo and hyper thyroid

- Arthritis (especially where growth plate is involved)

- Ruptured vertebral disc

- Liver cirrhosis

- Violent behavior, blind rage, explosive outbursts, criminal

behavior

- Learning disabilities

- Cerebral palsy and hypoplasia of the cerebellum (congenital

ataxia)

- High blood cholesterol

- Iron storage disease (abnormal iron accumulation in liver)

- Reduced glucose tolerance (low blood sugar)

- Neutropenia (low neutrophils)

Copper is essential to all living organisms and is a

universally important cofactor for many hundreds of metalloenzynes. Copper

deficiency is widespread and appears in many forms . Copper is required in

many physiological functions (RNA, DNA, lysil oxidase cofactor, melanin

production (hair and skin pigment), electron transfer of oxygen subcellular

respiration, tensile strength of elastic fibers in blood vessels, skin,

vertebral discs, etc.).

Neonatal enzootic ataxia (sway back, lamkruis) was recognized

as a clinical entity in 1937 as a copper deficiency in pregnant sheep.

Copper supplements prevented the syndrome which was characterized by

demyelination of the cerebellum and spinal cord. Cavitation or gelatinous

lesions of the cerebral white matter, chromatolysis, nerve cell death and

myelin aplasia (failure to form). These are all changes identical with human

cerebral palsy.

Four to six of every 100 Americans autopsied have died of a

ruptured aneurysm, an additional 40 percent have aneurysms that had not yet

ruptured.

The average well-nourished adult human body contains between

80 and 120 mg of copper. Concentrations are higher in the

brain, liver, heart and kidneys. Bone and muscle have lower

percentages of copper but contain 50 percent of the body total copper

reserves because of their mass. It is of interest that the greatest

concentration of copper is found in the newborn and their daily requirement

is 0.08 mg/kg, toddlers require 0.04 mg/kg and adults only 0.03 mg/ kg.

The average plasma copper for women ranges from 87 to 153

mg/dl and for men it ranges from 89 to 137 mg/dl; about 90 percent of the

plasma copper is found in ceruloplasmin.

Copper functions as a co-factor and activator of numerous

cuproenzymes that are involved in the development (deficiency of Cu in the

pregnant female results in congenital defects of the heart, i. e. - Kawasaki

Disease and brain cerebral palsy and hypoplasia of the cerebellum) and

maintenance of the cardiovascular system (deficiency results in reduced

lysyl oxidase activity causing a reduction in conversion of pro elastin to

elastin causing a decrease in tinsel strength of arterial walls and ruptured

aneurysms and skeletal integrity (deficiency results in a specific type of

arthritis of the young in the form of spurs in the bones growth plate);

deficiency can result in myelin defects; deficiency results in anemia; and

poor hair keratinization and loss of hair color. Neutropenia (reduced

numbers of neutophillic WBC) and leukopenia (reduced total WBC) are the

earliest indicators of copper deficiency in infants; infants whose diets are

primarily cows milk frequently develop anemia; iron storage disease can

result from chronic copper deficiency.

Menkes' Kinky Hair Syndrome is thought to be a sex-linked

recessive defect of copper absorption. The affected infants exhibit retarded

growth, defective keratin formation and loss of hair pigment, low body

temperature, degeneration and fracture of aortic elastin (aneurysms),

arthritis in the growth plate of long bones, and a progressive mental

deterioration (brain tissue is totally free of the essential enzyme

Cytochrome c oxidase). Because of absorption problems of metallic copper,

injections of copper are useful.

Serum and plasma copper increase 100 % in pregnant women and

women using oral contraceptives. Serum copper levels are also elevated

during acute infections, liver disease and pellagra (niacin deficiency).

Accumulations of copper in the cornea form - Kayser Fleischer

rings.

Copper deficiency and thyroid function

Rats were fed diets containing adequate, marginal or deficient

amounts of copper for 35 days. Copper deficiency resulted in a significant

increase in serum cholesterol levels and a significant decline in plasma

thyroxine concentrations and body temperatures. Compared with rats fed the

adequate diet, those fed the marginal and deficient diets had significantly

lower plasma concentrations of triiodothyronine (T3) and significantly

higher TSH levels. The activity of thyroxine 5'-monodeiodinase (the enzyme

that converts T4 to T3) was reduced in the liver and brown adipose tissue of

copper deficient rats.

COMMENT: This study suggests that copper deficiency interferes

with thyroid hormone metabolism and can promote hypothyroidism, as indicated

by a reduction in T3 levels and body temperatures and an increase in TSH.

Copper, zinc and selenium all have been shown to play a role in the

metabolism of thyroid hormones, and a deficiency of any one of these trace

minerals might be a contributing factor in patients who exhibit hypothyrold

symptoms.

Dr. Carl Pfeiffer has pointed out that an excessive body

burden of copper can result in various neuropsychiatric symptoms. Because of

Pfeiffer's work, many clinicians view copper primarily as a toxic mineral

(because copper supplements are not as water-soluble as they should be).

Indeed, a number of popular multivitamin/mineral formulas are advertised as

being " copper free. " However, copper is also an essential nutrient, and the

average American diet provides only about half the RDA (about 1 mg/day).

Therefore, mild copper deficiency may be a more common problem than copper

excess.

Lukaski H C et al. Body temperature and thyroid hormone

metabolism of copper deficient rats. Nutr Biochem 1995;6:445-451.

------------------------------------------------------------------

Copper is an essential trace mineral. The body of an adult

contains 100 mg to 150 mg of copper. Though copper is present in all

tissues, including red cells, the liver is the main site of copper storage.

Most of serum copper is bound to ceruloplasmin, the copper transport protein

synthesized by the liver. Ceruloplasmin also aids in iron transportation and

storage. Like most trace minerals, copper functions as an enzyme cofactor by

activating certain key enzymes required to strengthen the structural protein

collagen, which in turn strengthens cartilage, tendons, bones, and blood

vessels. Copper also serves as a cofactor of a protein in the blood that

helps maintain lung tissue and prevent emphysema; and it is essential for

insulating (mylination) nerve cells. As a cofactor for the enzyme superoxide

dismutase, copper helps prevent oxidative damage by a highly reactive form

of oxygen and thus is classified as an antioxidant. Copper functions as a

cofactor for cytochrome oxidase of mitochondria, the enzyme complex that

ultimately transfers electrons from the oxidation of fat, carbohydrate and

protein to oxygen for energy production. Copper also serves as a cofactor in

the synthesis of norepinephrine, an important neurotransmitter and adrenal

hormone.

The estimated safe and adequate daily intake of copper for

normal adults is 2 to 3 mg. About 30% of dietary copper is assimilated. Good

sources of copper include liver, kidneys, shellfish, nuts, seeds, fruit and

dried legumes. Cow's milk is low in copper. The standard American diet is

copper deficient and between 66 and 75% of the U.S. population do not

consume enough copper. Dieters, elderly persons and chronic alcoholics are

especially vulnerable. The following factors increase the need for copper:

excessive dietary fiber, high zinc supplements (50 mg or more daily),

cadmium, excessive vitamin C and excessive sugar (fructose) intake (at least

in rats).

Low copper consumption increases the risk of high blood

cholesterol and coronary heart disease, lowered immunity, gout, diabetes,

high blood pressure, anemia, nervous disorders, decreased pigmentation of

skin, fragile bones and erratic heartbeat. Low dietary copper is linked with

an increased risk of heart attack. Evidence also links copper deficiency

with increased oxidative damage to cell membranes. Levels of norepinephrine

in the brain are decreased with copper deficiency but may be restored by

supplemental copper. There are certain precautions to keep in mind for

copper supplements. Consumption of 10 to 15 mg of copper daily can cause

side effects. Patients with a rare copper accumulation disease ('s

disease) should not use copper supplements. An excessive copper overload has

been linked to various psychiatric syndromes. A green stain in the sink from

a faucet drip, or in a teakettle, suggests excessive copper in drinking

water, leached from copper plumbing.

Prohaska, ph R. and Failla, Mark L., " Copper and

Immunity, " in Human Nutrition--A Comprehensive Treatise, vol. 8 of Nutrition

and Immunology, Klurfeld, M., ed. New York: Plenum Press, 1993.

Also, included from: Minerals in Animal and Human Nutrition

By Lee McDowell

Copper Physiology

Copper is required for cellular respiration, bone formation,

proper cardiac function, connective tissue development, myelination of the

spinal cord, keratinization, and tissue pigmentation. Copper is an essential

component of several physiologically important metalloenzymes including

cytochrome oxidase, lysyl oxidase, superoxide dismutase,

dopamine-beta-hydroxylase, and tyrosinase.

1. IRON METABOLISM AND CELLULAR RESPIRATION

Along with Fe, Cu is necessary for hemoglobin synthesis.

Copper is not contained in hemoglobin, but a trace of it is necessary to

serve as a catalyst before the body can utilize Fe for hemoglobin formation.

Anemia can develop with either a Fe or Cu deficiency. With Cu deficiency

there is an apparent delay in maturation and shortened life span of red

blood cells (Baxter and Van Wyk, 1953).

Copper plays a key role in Fe absorption and mobilization.

Serum Fe levels tend to be low in Cu deficiency, and hypochromic anemia

develops while intestinal mucosa and liver Fe levels are higher than normal.

Ceruloplasmin (ferroxidase), which is synthesized in the liver and contains

Cu, is necessary for the oxidation of Fe, permitting it to bind with the

Fe-transport protein, transferrin. Ceruloplasmin (, 1978) is a

multifunctional enzyme involved in Fe metabolism, transport of Cu, and

regulation of certain amines.

Iron must be converted to the ferrous form to be mobilized

from stored ferritin and/or to be incorporated into hemoglobin or myoglobin.

For storage as ferritin or for transport as transferrin, Fe must be

converted to the ferric form (Curzon, 1961), a reaction performed by

ceruloplasmin.

Copper is a constituent of the important metalloenzyme,

cytochrome oxidase. This enzyme is the terminal oxidase in the respiratory

chain; it catalyzes the reduction of 0, to water, an essential step in

cellular respiration.

2. CROSS-LINKING OF CONNECTIVE TISSUE

With a Cu deficiency, there is failure of collagen to undergo

cross-linking and maturation ( and O'Dell, 1974). The key

Cu-containing enzyme in the formation of the cross-links in collagen and

elastin is lysyl oxidase, which is necessary to add a hydroxyl group to

lysine residues in collagen, allowing crosslinking between collagen fibers.

These cross-links give the proteins structural rigidity and elasticity.

Aortic aneurysms and ruptures result from failure to convert lysine to

desmosine, the cross-linking residue in elastin.

3. PIGMENTATION AND KERATINIZATION OF HAIR AND WOOL

Achromotrichia (lack of pigmentation) is a principal

manifestation of Cu deficiency in many species. It is commonly observed in

the hair and wool of mammals, and is usually attributed to lack of

tyrosinase (polyphenyl oxidase) activity. A breakdown in the conversion of

tyrosine to melanin is the probable explanation.

Impaired keratinization of hair and wool are noted in

Cu.-deficient animals. The characteristic physical properties of wool,

including crimp, are dependent on disulfide groups that provide

cross-linkages or bonding of keratin and on alignment or orientation of

long-chain keratin fibrillae in the fiber. Straight steely wool has more

sulfhydryl groups and fewer disulfide groups than normal (Marston, 1946).

Copper is required for formation or incorporation of disulfide groups in

keratin synthesis.

4. CENTRAL NERVOUS SYSTEM

The link between Cu deficiency and the integrity of the

central nervous system, i.e., swayback (enzootic ataxia) of lambs, results

from a reduction in cytochrome oxidase activity and thus incomplete myelin

formation (Howell and son, 1959). Myelin is composed largely of

phospholipid. Loss of cytochrome oxidase in Cu deficiency leads to depressed

phospholipid synthesis by liver mitochondria. The inhibition of myelin

synthesis results in the ensuing neurological disturbances. Other central

nervous system effects of Cu deficiency are reduction of at least two

neurotransmitters, dopamine and norepinephrine (O'Dell, 1984).

5. REPRODUCTION

Reproductive failure is commonly observed in mammals fed

Cu-deficient diets (Underwood, 1977). For rats and guinea pigs, Cu

deficiency has resulted in fetal death and resorption. Embryos from

Cu-deficient hens exhibited anemia, retarded development, and a high

incidence of hemorrhage after 72 to 96 hours of incubation, and a reduction

in monoamine oxidase activity. The anemia, hemorrhages, and mortality are

probably caused by defects in red blood cell and connective tissue formation

during early embryonic development.

6. IMMUNE SYSTEM

Copper metabolism affects T and B cells, neutrophils, and

macrophages. An impaired humoral immune response (i.e., decreased numbers of

antibody-producing cells) was observed in mice with hypocuprosis (Prohaska

et al., 1983). The magnitude of this impairment was highly correlated with

the degree of its functional deficiency. In a literature review, et

al (1979) concluded that the relationship of Cu to the immune system is

through superoxide dismutase, a Zn-, Cu-, and Mn-dependent enzyme, and its

role in the microbial systems of phagocytes.

In cattle affected by Cu deficiency induced by Mo, neutrophils

were impaired in their ability to kill ingested Candida albicans (Boyne and

Arthur, 1986). The ability of polymorphonuclear leukocytes to phagocytose C.

albicans in sheep with low Cu status is comparatively lower than that of

sheep on a normal Cu diet (Olkowski et al 1990). A decreased resistance to

infection has been observed in sheep affected by Cu deficiency (Wooliams et

A, 1986).

7. LIPID MATABOLISM

A number of studies have demonstrated the effect of Cu

deficiency on lipid metabolism. ing et al (1977) reported that Cu

deficiency results in elevated levels of serum triglyceride, phospholipids,

and cholesterol in the rat. Altered heart function of rats fed low Cu is

associated with alterations in lipid and long-chain fatty acid metabolism

(Cunnane et al., 1987), which may be attributable to the predominant role of

Cu in the superoxide dismutase enzyme system.ool r Physiology

COPPER: The Missing Link in Your Diet

By Sherry A. , M.D.

When we think of copper, we often think of toxic or high

levels from copper tubing and water pipes. In reality, the majority of

Americans are deficient in copper. The National Institutes of Health did a

study showing that 81 percent of people have less than two-thirds of the

recommended daily allowance of copper. Another study revealed that hospital

meals provide only 0.76 mg of copper per day, whereas people need 2-4 mg for

health, and even more for healing.

A study by the Food and Drug Administration showed that, in an

analysis, 234 foods that constitute the core of the American diet provided

less than 80 percent of the RDA of copper. A study of 270 United States Navy

SEAL trainees, all of them highly selected healthy young men, revealed that

37 percent had low plasma copper levels, and plasma copper, as you will see,

is a very insensitive indicator of copper status.

One study showed that 80 percent of Americans get 1 mg of

copper per day, and another study, which analyzed 20 different types of U.S.

diets, showed that only 25 percent of the people got 2 mg of copper a day

and the majority of the diets provided 0.78 mg of copper per day.

So all copper studies seem to point to the majority of people

being deficient.

When we studied 228 of our patients, 165 (or 72 percent) were

deficient in copper. So, no matter whose studies you look at over the last

20 years, there is a wealth of data showing that copper deficiency is

rampant in the United States. But the best test for copper deficiency is

intracellular, or red blood cell (RBC), while serum or plasma copper tests

are too insensitive, and hence not worth obtaining.

Why Copper Is Needed

So why do we need copper? Copper is present in about 21

different enzymes, and its importance has been known since 1928. For

example, one important enzyme is histaminase, which breaks down histamine.

So all allergic people, who overproduce histamine, certainly need to ensure

that they have normal copper levels. Another copper-dependent enzyme is

cytochrome oxidase, which is necessary for energy metabolism. Indeed, some

people with weakness and chronic fatigue have marked copper deficiencies.

Copper is also present in superoxide dismutase, an enzyme

which is useful in protecting us from developing chemical sensitivity. For

example, a 33-year-old lab technician for years could not tolerate shopping

malls, auto exhaust fumes and many businesses because of chemical

sensitivity. She felt confused, suffered from headaches, and became weak and

tired when she breathed the higher levels of chemicals commonly encountered

in these environments. When we found that she had a copper deficiency and

corrected it, within one month she was no longer as chemically sensitive,

and could tolerate these exposures without symptoms.

Remember that chemical sensitivity requires multiple factors,

one of which is that the person must be deficient in certain nutrients that

are necessary for the detoxification pathways to operate normally. Once the

deficiencies in these pathways are corrected many times, the chemical

sensitivity is corrected.

As well, the enzyme superoxide dismutase (SOD) plays a role in

the retarding of aging, arthritis and general body deterioration. In fact,

in nearly all diseases, lower than normal levels of SOD are found. For

example, people with colitis were found to have much lower levels of

superoxide dismutase in the bowel, and people with Alzheimer's disease were

found to have much lower levels of superoxide dismutase in the brain. In

other studies, chemically induced tumors were analyzed and found to be low

in copper-containing protective superoxide dismutase.

Detoxification

There are many other enzyme pathways where copper is used for

the detoxification of chemicals besides superoxide dismutase. For example,

it is in polyphenol oxidase, which is necessary for the breakdown of phenols

that emit gas from common household cleaning products. Also copper is

necessary for the action of glutathione peroxidase and catalase pathways,

even though it is not directly used in those enzymes. Studies on rats show

that those which were deficient in copper developed severe liver necroses

(tissue death) when exposed to carbon tetrachloride. But when the copper

deficiency was corrected, they did not develop the expected chemical

toxicity and suffer death.

Just as important, copper has a very important role in mood

chemistry. For example, the enzyme dopamine beta-hydroxyl is responsible for

the metabolism of norepinephrine, which affects depression and fatigue. It

is also important in the synthesis of other mood hormones, like dopamine and

serotonin (the one that many antidepressants -like Prozac -work on), and in

the major stress (adrenal) hormone, epinephrine. And copper has an even'

greater influence on our moods, for it is necessary for the action of

aminoxidases, which influence the metabolism of many neurotransmitter

proteins in the brain that are responsible for moods and thoughts.

The Heart Protector

With all of these benefits, copper is still essential for many

more enzymes. It is very important in protecting against arteriolosclerosis

and hypercholesterolemia; aneurysms (weakened blood vessels that burst and

can cause sudden death); EKG abnormalities; hypercoagulable states which

lead to heart attacks and strokes; and sugar metabolism. As an example, many

people with high cholesterol lack minerals like copper to properly

metabolize their cholesterol. It is an error to prescribe

cholesterol-lowering drugs without checking the RBC copper status.

For example, copper is important in an enzyme

deta-9-desaturase. This has to do with the propermetabolism of essential

fatty acids that make up the structural integrity of cell membranes.

Remember that the most important membranes are the cell walls, from which

allergic reactions, degenerative diseases and autoimmune diseases emanate.

Calcium channel blockers are commonly prescribed expensive

drugs to control blood pressure and heart arrhythmias, but the reason the

membrane calcium channels must be blocked has to do with minerals and

essential fatty acid deficiencies in the membranes. A headache isn't an

aspirin deficiency, so we should be less inclined to " drug " every symptom

and more inclined to find the nutrient deficiency behind the symptom. For

example, if the mitochondrial membrane wall, where energy is created, is

deficient, we can get chronic fatigue.

Furthermore, another very important membrane is the nuclear

membrane, which protects our genetic DNA material from damage from

chemicals. When the nuclear membrane is weak, chemicals can penetrate the

nucleus and damage DNA; this is one of the mechanisms for instigating

cancers as well as other degenerative diseases. Another Very important

membrane complex is the endoplasmic reticulum, where detoxification of

everyday home, office and outdoor chemicals must, be done.

At this point, you might be eager to run out and comer the

market on copper and consume it, but this can be dangerous without knowing

the proper level of copper, or the proper level of complementary, but

antagonistic, minerals such as (RBC) zinc, (RBC) molybdenum and iron. By

taking copper, one can lower the values of these important minerals and

create secondary deficiencies.

Foods that are high in copper include nuts, legumes (peas and

beans), seeds, organ meats and shellfish, in particular. Foods especially

low in copper are processed foods in general, especially white flour, white

sugar and fructose (fruit sugars).

Man is still trying to figure out why there are such folk

remedies as copper bracelets for the care of arthritis. Some researchers

presume that the copper is actually absorbed and incorporated into the

anti-inflammatory enzyme superoxide dismutase, which tends to turn off

inflammatory conditions like arthritis or Lupus.

Bob, a 54-year-old engineer, had 10 years of headaches.

Allergy injections, dietary changes, and correction of nutrient deficiencies

documented on blood tests corrected other symptoms, but they did not relieve

his headaches. However, when a RBC copper deficiency was found and

corrected, within one month his headaches disappeared. Certainly, people

like this teach us that copper is the " missing link. "

About the author: Sherry A. , M.D., has a private

practice in environmental and nutritional medicine.

COPPER DEFICIENCY AND MULTIPLE SCLEROSIS

A nervous disorder in sheep characterized by uncoordination of

gait has been recognized for many years. This disorder is most common in

sheep but it has also been reported in goat kids and more rarely in calves

and piglets. Various local names have been given to this condition but

swayback is the most common. Voisin prefers the term enzootic ataxia. In

Trail, British Columbia, young dogs and cats could not be raised without

encountering similar disabilities until more effective pollution controls

were introduced in the early 1930s. More recently young foals brought into

the Trail area suffered similar problems whereas older horses survived.

These problems seemingly were all associated with a copper

deficiency in the locality or with the presence of too much lead which

element nullifies the copper present in the fodder or in the atmosphere.

The enzootic ataxia in sheep parallels multiple sclerosis in

humans. Both diseases are characterized by demyelination, that is,

destruction of the myelin sheath.

In multiple sclerosis Plumb and Hansen found normal total

copper values both in serum and in cerebrospinal fluid but in the serum they

found reduced activity in copper oxidase. The same writers noted " this new

finding does not yet appear to have attracted comment and its confirmation

and further investigation will be awaited with interest, since vital clues

to the role of trace minerals in myelination are badly needed. "

Voisin wrote " Australian biochemists, able specialists in

deficiency diseases, set to work and found that one could prevent the

disease by administering copper salts orally to the ewes " . Ruth Allcroft

obtained similar results in England.

A few years ago Dr Haine, from Gloucester in England,

suggested that it might be worthwhile to add small copper supplements in

some appropriate form to those persons whose blood contained too little

copper. However this suggestion has apparently met with no support, at least

in British Columbia. This suggestion would seem to be worth investigating.

Copper Deficiency

A variety of symptoms have been associated with copper

deficiency in animals, many of which are seen also in humans; they include

hypochromic anemia, neutropenia (low neutrophils), hypopigmentation

(graying) of the hair and skin, abnormal bone formation with skeletal

fragility and osteoporosis, vascular abnormalities and uncrimped or steely

hair. There is no single specific indicator of copper deficiency.

Measurements which, despite major limitations, are currently considered to

be of value in establishing a range for normal copper status include serum

copper (normal range 0.64-1.56 ug/ml), ceruloplasmin (0.18-0.40mg/ml),

urinary copper (32-64pg/24h) and hair copper (10-20 ug/g), all of which are

depressed in frankly copper-deficient subjects but are less sensitive to a

marginal copper status. The possibility that a decline in erythrocyte

copper-zinc superoxide dismutase, normally 0.47 + 0.07 (SEM) mg/g of

hemoglobin, may provide a more suitable and early indication of deficiency

is being investigated.

Neutropenia is nowadays regarded as a sufficiently constant

feature of copper deficiency in humans to be of diagnostic value, while

evidence of a rapid decline in plasma enkephalins warrants further

investigation.

As late as the early to mid-1920s a new trace element, copper,

was suggested, on the basis of empirical evidence, to be of value in the

diet of rats (Bodansky, 192 1; McHargue, 1925, 1926). Copper deficiency was

subsequently shown to inhibit hematopoiesis in the rat (Hart et al., 1928)

and in exclusively milk-fed human infants (phs, 1931). However, it was

later discovered that copper is required for the formation of aortic elastin

(O'Dell et al., 1961), and thus is of crucial importance for heart

functioning. Following these findings, chronic copper deficiency, or a

relative copper deficiency induced by high zinc intakes, has been suggested

to be a major etiological factor in human ischemic heart disease (Klevay,

1975). Copper-deficient laboratory animals have since been found to be

hypercholesterolemic and hyperuricemic and to exhibit glucose intolerance

and abnormalities of cardiac function. They also show abnormal connective

tissues and lipid deposits in the arteries. Deficient animals may die

suddenly with a ruptured heart, caused by thinning of the aortic wall. These

findings have ominous significance in the light of recent copper estimates

in typical human diets in the United States; 75% of the diets examined

furnished less than 2 mg of copper per day, the amount thought to be

required by adults (Klevay, 1982).

Tissue distribution

Copper is widely distributed in biological tissues, where it

occurs largely in the form of organic complexes, many of which are

metalloproteins and function as enzymes. Copper enzymes are involved in a

variety of metabolic reactions, such as the utilization of oxygen during

cell respiration and energy utilization. They are also involved in the

synthesis of essential compounds, such as the complex proteins of connective

tissues of the skeleton and blood vessels, and in a range of neuroactive

compounds concerned in nervous tissue function. It has been estimated that

the adult human body contains 80 mg of copper, with a range of 50-120 mg.

Tissue copper levels range from < 1 ug/g (dry weight) in many organs to > 10

ug/g (dry weight) in the liver and brain. Copper levels in the fetus and

young infant differ from those in the adult. Concentrations of copper may be

6-10-fold greater in the liver of infants where, during the first 2 months

of postnatal life, it presumably serves as a store of copper to tide the

infant over the period when intake from breast milk is relatively small.

Copper in human blood is principally distributed between the

erythrocytes and the plasma. In erythrocytes, most copper (60%) occurs as

the copper-zinc metalloenzyme superoxide dismutase, the remaining 40% being

loosely bound to other proteins and amino acids. Total erythrocyte copper in

normal humans is around 0.9-1.0 ug/ml of packed red cells.

In plasma, about 93% of copper is firmly bound to the enzyme

ceruloplasmin, believed to be involved in iron mobilization by maintaining

the supply of oxidized iron transported after its incorporation into

transferrin. The remaining plasma copper (7%) is bound less firmly to

albumin and amino acids, and constitutes transport copper capable of

reacting with receptor proteins or of diffusing, probably in the form of

charged complexes, across cell membranes. Plasma or serum copper in normal

humans is in the range 0.8-1.2 ug/ml and is not significantly influenced by

cyclical rhythms or by feeding. The mean value for females is about 10%

higher than that for males and is elevated by a factor of up to 3 in late

pregnancy and in women taking estrogen-based oral contraceptives.

a.. References for Copper (Cu)

a.. Back to the Minerals introduction

a.. Back to the Minerals list

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>DC NutritionI have been researching copper deficiency the last few days as my

father has an aneurysm. Itseems the aortic wall is inflamed and lacks elastin

both have a common denominator..low copper.

There is also the issue of low sulfates! It seems in autism a lot of the

minerals are messed up. Now this could be lack of stuff in the

diet, and it could also be malabsorption. It could also be

how the body handles it (celiacs are typically low calcium

but have calcium *deposits* in the wrong places, regardless

of how much of it they eat). Or it could be a vicious spiral ...

inflamed intestines don't absorb minerals right.

-- Heidi

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I am not sure about american supplements as I live in Germany.

I can tell you though that most copper supplements were taken off

the market last year due to new EU guidelines!!!!!!!!

Sound suspicious. I think so!!!!!!!

in Germany

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The menkes kinky hair syndrome part caught my eye... I have a head of

very thick hair that I am often complimented on, but within that,

there are little kinky hairs. I can run my fingers through my hair

and find them (sometimes I do that as a stim!LOL!) but what bothers

me is that I see that my son has A LOT of these kinky hairs, too.

When his hair is wet and I comb it, I can see them more readily.

Hmmm...

But, he doesn't have retarded growth--he's average/tall for his age.

W

> >

> Menkes' Kinky Hair Syndrome is thought to be a sex-

linked recessive defect of copper absorption. The affected infants

exhibit retarded growth, defective keratin formation and loss of hair

pigment, low body temperature, degeneration and fracture of aortic

elastin (aneurysms), arthritis in the growth plate of long bones, and

a progressive mental deterioration (brain tissue is totally free of

the essential enzyme Cytochrome c oxidase). Because of absorption

problems of metallic copper, injections of copper are useful.

>

>

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This is interesting because the first time I had my RBC essential

elements tested, copper came out extremely low. They were afraid I

would have an aneurysm and had me supplement copper, but I didn't do

well on that. At least I think I didn't but I was taking so many

other things at once, I stopped everything they gave me.

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And Don't forget the pesticides that are used in some apts., libraries,

churches, schools, and restaurants -- especially those which are not

following the principles of IPM (integrated pest management). And many

communites in US are sprayed with pesticides to control mosquitoes (call

your local mayor and health dept. and inquire- some states do not have laws

requiring that the public be notified in advance of mosquito spraying).

Mosquito control Alternatives do exist - Bti larvacide is considered a less

toxic control method for communities to use.

Autism and LOW copper

> Not only the pesticides that are used on the crops, lawns, etc. but

> what about the flea and tick products used on the dogs and cats?

> Not only those that are a spray or a dip, but also the spot ons like

> Revolution, BioSpot, and Frontline and there are others.

>

> Jackie Noel

> www.sagaciousairedales.com

> www.sagaciousdogcountry.com

>

>

>

>

>

>

>

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