Jump to content
RemedySpot.com

Treatment blocks pain without disrupting other functions

Rate this topic


Guest guest

Recommended Posts

Treatment blocks pain without disrupting other functions

By FMS Global News

Contact: Frazin

301-496-5924

http://fmsglobalnews.wordpress.com/2007/10/03/treatment-blocks-pain-

without-disrupting-other-functions/

NIH/National Institute of Neurological Disorders and Stroke

A combination of two drugs can selectively block pain-sensing

neurons in rats without impairing movement or other sensations such

as touch, according to a new study by National Institutes of Health

(NIH)-supported investigators. The finding suggests an improved way

to treat pain from childbirth and surgical procedures. It may also

lead to new treatments to help the millions of Americans who suffer

from chronic pain.

The study used a combination of capsaicin — the substance that makes

chili peppers hot — and a drug called QX-314. This combination

exploits a characteristic unique to pain-sensing neurons, also

called nociceptors, in order to block their activity without

impairing signals from other cells. In contrast, most pain relievers

used for surgical procedures block activity in all types of neurons.

This can cause numbness, paralysis and other nervous system

disturbances.

" The Holy Grail in pain science is to eliminate pathologic pain

without impairing thinking, alertness, coordination, or other vital

functions of the nervous system. This finding shows that a specific

combination of two molecules can block only pain-related neurons. It

holds the promise of major future breakthroughs for the millions of

persons who suffer with disabling pain, " says Story C. Landis,

Ph.D., director of the National Institute of Neurological Disorders

and Stroke (NINDS) at the NIH, which funds the investigators'

research along with the National Institute of Dental and

Craniofacial Research (NIDCR) and the National Institute of General

Medical Sciences (NIGMS). NINDS and NIDCR are co-chairs of the NIH

Pain Consortium. The study appears in the October 4, 2007, issue of

Nature.*

Lidocaine, the most commonly used local anesthetic, relieves pain by

blocking electric currents in all nerve cells. Although it is a

lidocaine derivative, QX-314 alone cannot get through cell membranes

to block their electrical activity.

That's where capsaicin comes in. It opens large pores called TRPV1

channels — found only within the cell membrane of pain-sensing

neurons. With these channels propped open by capsaicin, QX-314 can

pass through and selectively block the cells' activity.

The research team, led by Clifford J. Woolf, M.D., Ph.D., of

Massachusetts General Hospital and Harvard Medical School and Bruce

Bean, Ph.D., at Harvard Medical School, tested the combination of

capsaicin and QX-314 in neurons isolated in Petri dishes and found

that it blocked pain-sensing neurons without affecting other nerve

cells. They then injected the drugs into the paws of rats and found

that the treated animals could tolerate much more heat than usual.

They also injected the two drugs near the sciatic nerve that runs

down the hind leg. The treated rats did not show any signs of pain,

and five of the six animals continued to move and behave normally.

This showed that the drugs could block pain without impairing motor

neurons that control movement.

The drug combination took half an hour to fully block pain in the

rats. However, once it began, the pain relief lasted for several

hours.

" Current nerve blocks cause paralysis and total numbness, " Dr. Woolf

says. " This new strategy could profoundly change pain treatment in

the perioperative setting. "

The treatment tested in this study is unique in that it uses a type

of ion channel (TRPV1 channels) as an avenue to deliver medication.

Ion channels are pores in the cell membrane that control the flow of

electrically charged ions in and out of cells. " I'm not aware of any

other strategy that uses a channel within cells to deliver a drug to

a select set of cells, " Dr. Woolf says. The strategy builds on

research done since the 1970's, largely supported by NIH, that shows

how electrical signaling in the nervous system results from

expression of dozens of different types of ion channels. Some of

these ion channels are found only in specific types of neurons.

" This project is a nice illustration of how research trying to

understand very basic biological principles can have practical

applications, " says Dr. Bean. This type of treatment has great

potential to improve pain treatment during childbirth, dental

procedures, and surgery, the researchers say. " Surgical pain is the

obvious first application for this type of treatment, " Dr. Woolf

says. However, similar therapies might eventually be useful for

treating chronic pain, he adds. Chronic pain continues for weeks,

months, or even years and can cause severe problems, and is often

resistant to standard medical treatments.

While the researchers focused on finding a treatment for pain, this

strategy might also be useful for treating itch from eczema, poison

ivy rashes, and other conditions, Dr. Woolf says. Like pain

sensations, itch signals come from nociceptors. One problem with the

combination treatment is that the capsaicin can cause unpleasant

burning sensations until the QX-314 takes effect, Dr. Woolf says.

Administering the QX-314 ten minutes before the capsaicin minimized

this problem in rats. The investigators are now looking for ways to

open the TRPV1 channels without the burning sensations, perhaps by

finding an alternative to capsaicin. They also hope to find ways of

prolonging the pain relief. Eventually, they might be able to

develop pills that will stop pain signals without requiring

injections, Dr. Woolf adds.

###

The NINDS is the nation's primary funder of research on the brain

and nervous system. More information about pain and other

neurological disorders can be found on the NINDS web site,

http://www.ninds.nih.gov/. The NIDCR (http://www.nidcr.nih.gov/) is

the nation's leading funder of research on oral, dental, and

craniofacial health. The NIGMS (http://www.nigms.nih.gov) supports

basic biomedical research that is the foundation for advances in

disease diagnosis, treatment, and prevention. The NINDS, NIDCR, and

NIGMS are components of the National Institutes of Health (NIH). The

NIH Pain Consortium, co-chaired by the NIDCR, the National Institute

of Nursing Research, and the NINDS, strives to enhance pain research

and promote collaboration among researchers across the many NIH

Institutes and Centers that have programs and activities addressing

pain.

The NIH - The Nation's Medical Research Agency - includes 27

Institutes and Centers and is a component of the U. S. Department of

Health and Human Services. It is the primary Federal agency for

conducting and supporting basic, clinical, and translational medical

research, and it investigates the causes, treatments, and cures for

both common and rare diseases. For more information about NIH and

its programs, visit www.nih.gov.

*Binshtok AM, Bean BP, Woolf CJ. " Inhibition of nociceptors by TRPV1-

mediated entry of impermeant sodium channel blockers. " Nature,

October 4, 2007, Vol. 449, No. 7162, pp. 607-610.

Link to comment
Share on other sites

Not to be funny, but is her phone # there so we can sign up? Wait list, human

Guinea pig?

tigerpaw2c <tigerpaw2c@...> wrote: Treatment blocks pain without

disrupting other functions

By FMS Global News

Contact: Frazin

301-496-5924

http://fmsglobalnews.wordpress.com/2007/10/03/treatment-blocks-pain-

without-disrupting-other-functions/

NIH/National Institute of Neurological Disorders and Stroke

A combination of two drugs can selectively block pain-sensing

neurons in rats without impairing movement or other sensations such

as touch, according to a new study by National Institutes of Health

(NIH)-supported investigators. The finding suggests an improved way

to treat pain from childbirth and surgical procedures. It may also

lead to new treatments to help the millions of Americans who suffer

from chronic pain.

The study used a combination of capsaicin — the substance that makes

chili peppers hot — and a drug called QX-314. This combination

exploits a characteristic unique to pain-sensing neurons, also

called nociceptors, in order to block their activity without

impairing signals from other cells. In contrast, most pain relievers

used for surgical procedures block activity in all types of neurons.

This can cause numbness, paralysis and other nervous system

disturbances.

" The Holy Grail in pain science is to eliminate pathologic pain

without impairing thinking, alertness, coordination, or other vital

functions of the nervous system. This finding shows that a specific

combination of two molecules can block only pain-related neurons. It

holds the promise of major future breakthroughs for the millions of

persons who suffer with disabling pain, " says Story C. Landis,

Ph.D., director of the National Institute of Neurological Disorders

and Stroke (NINDS) at the NIH, which funds the investigators'

research along with the National Institute of Dental and

Craniofacial Research (NIDCR) and the National Institute of General

Medical Sciences (NIGMS). NINDS and NIDCR are co-chairs of the NIH

Pain Consortium. The study appears in the October 4, 2007, issue of

Nature.*

Lidocaine, the most commonly used local anesthetic, relieves pain by

blocking electric currents in all nerve cells. Although it is a

lidocaine derivative, QX-314 alone cannot get through cell membranes

to block their electrical activity.

That's where capsaicin comes in. It opens large pores called TRPV1

channels — found only within the cell membrane of pain-sensing

neurons. With these channels propped open by capsaicin, QX-314 can

pass through and selectively block the cells' activity.

The research team, led by Clifford J. Woolf, M.D., Ph.D., of

Massachusetts General Hospital and Harvard Medical School and Bruce

Bean, Ph.D., at Harvard Medical School, tested the combination of

capsaicin and QX-314 in neurons isolated in Petri dishes and found

that it blocked pain-sensing neurons without affecting other nerve

cells. They then injected the drugs into the paws of rats and found

that the treated animals could tolerate much more heat than usual.

They also injected the two drugs near the sciatic nerve that runs

down the hind leg. The treated rats did not show any signs of pain,

and five of the six animals continued to move and behave normally.

This showed that the drugs could block pain without impairing motor

neurons that control movement.

The drug combination took half an hour to fully block pain in the

rats. However, once it began, the pain relief lasted for several

hours.

" Current nerve blocks cause paralysis and total numbness, " Dr. Woolf

says. " This new strategy could profoundly change pain treatment in

the perioperative setting. "

The treatment tested in this study is unique in that it uses a type

of ion channel (TRPV1 channels) as an avenue to deliver medication.

Ion channels are pores in the cell membrane that control the flow of

electrically charged ions in and out of cells. " I'm not aware of any

other strategy that uses a channel within cells to deliver a drug to

a select set of cells, " Dr. Woolf says. The strategy builds on

research done since the 1970's, largely supported by NIH, that shows

how electrical signaling in the nervous system results from

expression of dozens of different types of ion channels. Some of

these ion channels are found only in specific types of neurons.

" This project is a nice illustration of how research trying to

understand very basic biological principles can have practical

applications, " says Dr. Bean. This type of treatment has great

potential to improve pain treatment during childbirth, dental

procedures, and surgery, the researchers say. " Surgical pain is the

obvious first application for this type of treatment, " Dr. Woolf

says. However, similar therapies might eventually be useful for

treating chronic pain, he adds. Chronic pain continues for weeks,

months, or even years and can cause severe problems, and is often

resistant to standard medical treatments.

While the researchers focused on finding a treatment for pain, this

strategy might also be useful for treating itch from eczema, poison

ivy rashes, and other conditions, Dr. Woolf says. Like pain

sensations, itch signals come from nociceptors. One problem with the

combination treatment is that the capsaicin can cause unpleasant

burning sensations until the QX-314 takes effect, Dr. Woolf says.

Administering the QX-314 ten minutes before the capsaicin minimized

this problem in rats. The investigators are now looking for ways to

open the TRPV1 channels without the burning sensations, perhaps by

finding an alternative to capsaicin. They also hope to find ways of

prolonging the pain relief. Eventually, they might be able to

develop pills that will stop pain signals without requiring

injections, Dr. Woolf adds.

###

The NINDS is the nation's primary funder of research on the brain

and nervous system. More information about pain and other

neurological disorders can be found on the NINDS web site,

http://www.ninds.nih.gov/. The NIDCR (http://www.nidcr.nih.gov/) is

the nation's leading funder of research on oral, dental, and

craniofacial health. The NIGMS (http://www.nigms.nih.gov) supports

basic biomedical research that is the foundation for advances in

disease diagnosis, treatment, and prevention. The NINDS, NIDCR, and

NIGMS are components of the National Institutes of Health (NIH). The

NIH Pain Consortium, co-chaired by the NIDCR, the National Institute

of Nursing Research, and the NINDS, strives to enhance pain research

and promote collaboration among researchers across the many NIH

Institutes and Centers that have programs and activities addressing

pain.

The NIH - The Nation's Medical Research Agency - includes 27

Institutes and Centers and is a component of the U. S. Department of

Health and Human Services. It is the primary Federal agency for

conducting and supporting basic, clinical, and translational medical

research, and it investigates the causes, treatments, and cures for

both common and rare diseases. For more information about NIH and

its programs, visit www.nih.gov.

*Binshtok AM, Bean BP, Woolf CJ. " Inhibition of nociceptors by TRPV1-

mediated entry of impermeant sodium channel blockers. " Nature,

October 4, 2007, Vol. 449, No. 7162, pp. 607-610.

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

Moody friends. Drama queens. Your life? Nope! - their life, your story.

Play Sims Stories at Games.

Link to comment
Share on other sites

I have no idea. Many articles have the reporters and or doctors

information or phone numbers.

KC

Treatment blocks pain

without disrupting other functions

> By FMS Global News

>

> Contact: Frazin

> 301-496-5924

>

> http://fmsglobalnews.wordpress.com/2007/10/03/treatment-blocks-

pain-

> without-disrupting-other-functions/

>

> NIH/National Institute of Neurological Disorders and Stroke

>

> A combination of two drugs can selectively block pain-sensing

> neurons in rats without impairing movement or other sensations

such

> as touch, according to a new study by National Institutes of

Health

> (NIH)-supported investigators. The finding suggests an improved

way

> to treat pain from childbirth and surgical procedures. It may also

> lead to new treatments to help the millions of Americans who

suffer

> from chronic pain.

>

> The study used a combination of capsaicin — the substance that

makes

> chili peppers hot — and a drug called QX-314. This combination

> exploits a characteristic unique to pain-sensing neurons, also

> called nociceptors, in order to block their activity without

> impairing signals from other cells. In contrast, most pain

relievers

> used for surgical procedures block activity in all types of

neurons.

> This can cause numbness, paralysis and other nervous system

> disturbances.

>

> " The Holy Grail in pain science is to eliminate pathologic pain

> without impairing thinking, alertness, coordination, or other

vital

> functions of the nervous system. This finding shows that a

specific

> combination of two molecules can block only pain-related neurons.

It

> holds the promise of major future breakthroughs for the millions

of

> persons who suffer with disabling pain, " says Story C. Landis,

> Ph.D., director of the National Institute of Neurological

Disorders

> and Stroke (NINDS) at the NIH, which funds the investigators'

> research along with the National Institute of Dental and

> Craniofacial Research (NIDCR) and the National Institute of

General

> Medical Sciences (NIGMS). NINDS and NIDCR are co-chairs of the NIH

> Pain Consortium. The study appears in the October 4, 2007, issue

of

> Nature.*

>

> Lidocaine, the most commonly used local anesthetic, relieves pain

by

> blocking electric currents in all nerve cells. Although it is a

> lidocaine derivative, QX-314 alone cannot get through cell

membranes

> to block their electrical activity.

>

> That's where capsaicin comes in. It opens large pores called TRPV1

> channels — found only within the cell membrane of pain-sensing

> neurons. With these channels propped open by capsaicin, QX-314 can

> pass through and selectively block the cells' activity.

>

> The research team, led by Clifford J. Woolf, M.D., Ph.D., of

> Massachusetts General Hospital and Harvard Medical School and

Bruce

> Bean, Ph.D., at Harvard Medical School, tested the combination of

> capsaicin and QX-314 in neurons isolated in Petri dishes and found

> that it blocked pain-sensing neurons without affecting other nerve

> cells. They then injected the drugs into the paws of rats and

found

> that the treated animals could tolerate much more heat than usual.

> They also injected the two drugs near the sciatic nerve that runs

> down the hind leg. The treated rats did not show any signs of

pain,

> and five of the six animals continued to move and behave normally.

> This showed that the drugs could block pain without impairing

motor

> neurons that control movement.

>

> The drug combination took half an hour to fully block pain in the

> rats. However, once it began, the pain relief lasted for several

> hours.

>

> " Current nerve blocks cause paralysis and total numbness, " Dr.

Woolf

> says. " This new strategy could profoundly change pain treatment in

> the perioperative setting. "

>

> The treatment tested in this study is unique in that it uses a

type

> of ion channel (TRPV1 channels) as an avenue to deliver

medication.

> Ion channels are pores in the cell membrane that control the flow

of

> electrically charged ions in and out of cells. " I'm not aware of

any

> other strategy that uses a channel within cells to deliver a drug

to

> a select set of cells, " Dr. Woolf says. The strategy builds on

> research done since the 1970's, largely supported by NIH, that

shows

> how electrical signaling in the nervous system results from

> expression of dozens of different types of ion channels. Some of

> these ion channels are found only in specific types of neurons.

>

> " This project is a nice illustration of how research trying to

> understand very basic biological principles can have practical

> applications, " says Dr. Bean. This type of treatment has great

> potential to improve pain treatment during childbirth, dental

> procedures, and surgery, the researchers say. " Surgical pain is

the

> obvious first application for this type of treatment, " Dr. Woolf

> says. However, similar therapies might eventually be useful for

> treating chronic pain, he adds. Chronic pain continues for weeks,

> months, or even years and can cause severe problems, and is often

> resistant to standard medical treatments.

>

> While the researchers focused on finding a treatment for pain,

this

> strategy might also be useful for treating itch from eczema,

poison

> ivy rashes, and other conditions, Dr. Woolf says. Like pain

> sensations, itch signals come from nociceptors. One problem with

the

> combination treatment is that the capsaicin can cause unpleasant

> burning sensations until the QX-314 takes effect, Dr. Woolf says.

> Administering the QX-314 ten minutes before the capsaicin

minimized

> this problem in rats. The investigators are now looking for ways

to

> open the TRPV1 channels without the burning sensations, perhaps by

> finding an alternative to capsaicin. They also hope to find ways

of

> prolonging the pain relief. Eventually, they might be able to

> develop pills that will stop pain signals without requiring

> injections, Dr. Woolf adds.

>

> ###

> The NINDS is the nation's primary funder of research on the brain

> and nervous system. More information about pain and other

> neurological disorders can be found on the NINDS web site,

> http://www.ninds.nih.gov/. The NIDCR (http://www.nidcr.nih.gov/)

is

> the nation's leading funder of research on oral, dental, and

> craniofacial health. The NIGMS (http://www.nigms.nih.gov) supports

> basic biomedical research that is the foundation for advances in

> disease diagnosis, treatment, and prevention. The NINDS, NIDCR,

and

> NIGMS are components of the National Institutes of Health (NIH).

The

> NIH Pain Consortium, co-chaired by the NIDCR, the National

Institute

> of Nursing Research, and the NINDS, strives to enhance pain

research

> and promote collaboration among researchers across the many NIH

> Institutes and Centers that have programs and activities

addressing

> pain.

>

> The NIH - The Nation's Medical Research Agency - includes 27

> Institutes and Centers and is a component of the U. S. Department

of

> Health and Human Services. It is the primary Federal agency for

> conducting and supporting basic, clinical, and translational

medical

> research, and it investigates the causes, treatments, and cures

for

> both common and rare diseases. For more information about NIH and

> its programs, visit www.nih.gov.

>

> *Binshtok AM, Bean BP, Woolf CJ. " Inhibition of nociceptors by

TRPV1-

> mediated entry of impermeant sodium channel blockers. " Nature,

> October 4, 2007, Vol. 449, No. 7162, pp. 607-610.

>

>

>

>

>

>

> ---------------------------------

> Moody friends. Drama queens. Your life? Nope! - their life, your

story.

> Play Sims Stories at Games.

>

>

Link to comment
Share on other sites

humm, capsiasin was used as a irritant to measure coughing in

hyperrective lings. just one of a few reasons why this may not help

with people woth MCI. seams that with limbic system damage our

tranmitters are not functioning right anyway. if I understand right,

our transmitters travel by way of myelin sheaths so if damaged, the

transmitters dont get to where they should be going anyway,even if

the limbic system wasn't damaged.

block activity in all types of neurons.

> This can cause numbness, paralysis and other nervous system

> disturbances.

Link to comment
Share on other sites

Join the conversation

You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.

Guest
Reply to this topic...

×   Pasted as rich text.   Paste as plain text instead

  Only 75 emoji are allowed.

×   Your link has been automatically embedded.   Display as a link instead

×   Your previous content has been restored.   Clear editor

×   You cannot paste images directly. Upload or insert images from URL.

Loading...
×
×
  • Create New...