Guest guest Posted June 19, 2002 Report Share Posted June 19, 2002 Hi Francesca and all, Apologies that I didn't have time to get some research into that last post! Even thought Xylitol isn't completely devoid of calories, I think it is quite amazing that they've found a nature-given substance that prevents bone loss. Given my osteo scare, I'm definitely going to use it, and with the money I'll also save from the dentist, take a weekend holiday in celebration! best to all MM <http://www.ncbi.nlm.nih.gov:80/corehtml/transparent.gif> 1: Calcif Tissue Int 1995 Mar;56(3):232-5 Related Articles, Books, LinkOut Diminished bone resorption in rats after oral xylitol administration: a dose-response study. Mattila P, Svanberg M, Knuuttila M. Institute of Dentistry, University of Oulu, Finland. The effects of 5, 10, and 20% dietary xylitol supplementations on the resorption of bone were studied. The resorption was measured by the urinary excretion of [3H] radioactivity from [3H]tetracycline-prelabeled rats. The 10 and 20% oral xylitol administrations caused a significant decrease in the excretion of [3H] as compared with the control group with no xylitol supplementation. The effect was detected as early as 2 days after the beginning of xylitol-feeding and was maintained throughout the experimental period of 31 days. The retarding effect on bone resorption was about 25% in the 10% xylitol group, about 40% in the 20% xylitol group, and undetectable in the 5% xylitol group. The amount of preserved [3H] radioactivity in the tibiae of the 10 and 20% xylitol groups after the experiment clearly exceeded the values of the control group. The mechanism of the retarded bone resorption caused by dietary xylitol still remains obscure, but an increased absorption of calcium may be involved. In conclusion, dietary xylitol supplementation in rats seems to retard the bone resorption in a dose-dependent way. The effect is achieved rapidly and is maintained at least over a period of 1 month xylitol feeding. PMID: 7750030 [PubMed - indexed for MEDLINE] Write to the Help Desk NCBI | NLM | NIH Department of Health & Human Services Freedom of Information Act | Disclaimer i686-pc-linux-gnu Jun 12 2002 10:20:00 [NCBI] [PubMed] PubMed Nucleotide Protein Genome Structure PopSet Taxonomy OMIM Books Search for <http://www.ncbi.nlm.nih.gov:80/corehtml/transparent.gif> 1: Gerontology 2001 Nov-Dec;47(6):300-5 Related Articles, Books, LinkOut [Click here to read] Increased bone volume and bone mineral content in xylitol-fed aged rats. Mattila PT, Svanberg MJ, Knuuttila ML. Oral and Maxillofacial Department, Oulu University Hospital, Oulu, Finland. ptm@... BACKGROUND: Our previous studies have shown that dietary xylitol supplementation protects against the loss of bone mineral after ovariectomy. The ovariectomy-induced decrease in trabecular bone volume is significantly retarded by dietary xylitol. Objective: To study whether dietary xylitol can protect against bone loss also during aging, a long-term experimental study was performed with rats. METHODS: Twenty-four male Sprague-Dawley rats were divided into two groups. The rats in the control group were fed a basal RM1 diet, while the rats in the experimental group were continuously fed the same diet supplemented with 10% (w/w) xylitol. The rats were killed after 20 months. Their tibiae were used for the analyses of bone density and trabecular bone volume, and their femurs were used for the scanning analyses with peripheral quantitative computed tomography (pQCT). RESULTS: The tibial density of the xylitol-fed aged group (1.73 +/- 0.14 g/mm(3)) was significantly greater than that of the aged group without xylitol (1.56 +/- 0.14 g/ mm(3)). The trabecular bone volume of the xylitol-fed rats was 21.2 +/- 4.0%. It was significantly greater than that of the rats not receiving xylitol (9.3 +/- 4.3%). The pQCT-measured cortical bone mineral density and the pQTC-measured cortical bone mineral content of the femoral diaphysis were significantly greater in the xylitol-fed group than in the control group. The trabecular bone mineral density and the trabecular bone mineral content of the femoral distal metaphysis were also significantly greater in the xylitol-fed group than in the non-xylitol group. The total bone mineral density and the total bone mineral content of the femoral neck in the xylitol-fed aged group significantly exceeded those in the aged group without xylitol supplementation. CONCLUSIONS: A continuous moderate dietary xylitol supplementation leads to increased bone volume and increased bone mineral content in the long bones of aged rats. This indicates a xylitol-induced protection against aging-related osteoporotic changes. Copyright 2001 S. Karger AG, Basel PMID: 11721142 [PubMed - indexed for MEDLINE] Write to the Help Desk NCBI | NLM | NIH Department of Health & Human Services Freedom of Information Act | Disclaimer i686-pc-linux-gnu Jun 12 2002 10:20:00 Dietary xylitol in the prevention of experimental osteoporosis Beneficial effects on bone resorption, structure and biomechanics i Mattila Institute of Dentistry, University of Oulu Academic Dissertation to be presented with the assent of the Faculty of Medicine, University of Oulu, for public discussion in the Auditorium of the Department of Anatomy and Cell Biology, on March 26th, 1999, at 12 noon. Copyright © 1999 University of Oulu Manuscript received 16 February 1999 Manuscript accepted 25 February 1999 Communicated by Docent Juha Tuukkanen Doctor Mauri Hämäläinen UNIVERSITY OF OULU, OULU FINLAND 1999 ISBN 951-42-5158-X URN:ISBN:951425158X Abstract Dietary xylitol supplementation increases bone calcium and phosphorus concentrations in healthy rats, as well as protects against the decrease of bone minerals and bone density during experimental osteoporosis. This suggests that dietary xylitol might have a favorable effect on the prevention of osteoporosis. However, before any conclusions can be drawn about the usefulness of a compound, studies including structural evaluation and biomechanical testing of bones must first be performed. Thus, the aim of the present study was to clarify whether dietary xylitol affects bone resorption, bone structure, and bone biomechanics in healthy rats, and whether dietary xylitol offers some preventive effects against the increased bone resorption, decreased bone trabeculation, and weakened bone biomechanical properties during experimental osteoporosis. Dietary xylitol reduced bone resorption in 3-mo old healthy male rats, and protected significantly against the increase of bone resorption in 3-mo old ovariectomized rats, as measured by the urinary excretion of 3H following [3H]tetracycline-prelabeling. In addition, increased trabecular bone volume of proximal tibia in 4-mo old healthy male rats was detected after a 1-mo xylitol feeding period, and significant protection against the decrease of trabecular bone volume in 6-mo old ovariectomized rats was observed after a 3-mo xylitol feeding period. Furthermore, dietary xylitol increased the strength properties of long bones in 6-mo old healthy male rats after a 3-mo feeding period, without affecting the bone elastic properties as tested by three-point bending of tibia, torsion of femur, and loading of femoral neck. Accordingly, dietary xylitol protected significantly against the weakening of bone biomechanical properties in 6-mo old ovariectomized rats after a 3-mo feeding period. In conclusion, the above results strongly support the hypothesis that oral administration of xylitol protects effectively against the progression of experimental osteoporosis. Dietary xylitol was effective both in increasing bone mass in healthy rats, and in preventing bone loss in ovariectomized rats, suggesting a favorable effect of xylitol on both main targets in the prevention of osteoporosis. As dietary xylitol was effective also in protecting against the experimental osteoporosis-caused changes in bone structure and weakening of bone biomechanical properties, oral xylitol administration seems to provide interesting possibilities when searching for new physiological choices for the prevention of osteoporosis. Keywords: bone metabolism, ovariectomy, polyols, rat * Publication in Adobe PDF-format 1.78 MB * Publication in HTML-format This publication is available in printed form [serieslogo] Acta Universitatis Ouluensis Medica D 510 ISBN 951-42-5150-4 ISSN 0355-3221 Other publications from University of Oulu ants and xylitol chewing gum are equal in caries prevention. Alanen P, Holsti ML, Pienihakkinen K. Institute of Dentistry, University of Turku, Finland. pentti.alanen@... Sealants and xylitol have been demonstrated to prevent dental decay, but their effect has never been compared in the same study. Regular use of xylitol chewing gum during 2 or 3 school years was compared with application of occlusal sealants in a randomized study. The reliability of the clinical observations was controlled by examining the presence of dental decay in the same teeth from bitewing radiographs in a blind study. After 5 years, no statistically significant differences between the sealant and xylitol groups were found. The results were in line with the results from separate studies with sealants or xylitol. There were no great differences between the costs of the measures. The selection between the compared preventive measures has to be made on the basis of practical aspects such as caries occurrence, availability of personnel and other resources, opportunity costs, cooperation with schools, and other local conditions. Publication Types: * Clinical trial * Randomized controlled trial PMID: 11196404 [PubMed - indexed for MEDLINE] ------------------------------------------------------------------------ CoOccurrence of dental decay in children after maternal consumption of xylitol chewing gum, a follow-up from 0 to 5 years of age. Isokangas P, Soderling E, Pienihakkinen K, Alanen P. Ylivieska Health Care Center, University of Turku, Finland. Studies have shown that prevention of mutans streptococci (MS) colonization in early childhood can lead to prevention of dental decay. In the microbiological part of the present study in Ylivieska, Finland, with 195 mothers with high salivary MS levels, regular maternal use of xylitol chewing gum resulted in a statistically significant reduction in MS colonization in their children's teeth at the age of 2 years compared with teeth in children whose mothers received fluoride or chlorhexidine varnish treatment. The children did not chew gum or receive varnish treatments. For the present study, the children were examined annually for caries occurrence by experienced clinicians who did not know whether the children were colonized with MS. Regardless of the maternal prevention group, the presence of MS colonization in children at the age of 2 years was significantly related to each child's age at the first caries attack in the primary dentition. In children at the age of 5 years, the dentinal caries (dmf) in the xylitol group was reduced by about 70% as compared with that in the fluoride or chlorhexidine group. We conclude that maternal use of xylitol chewing gum can prevent dental caries in their children by prohibiting the transmission of MS from mother to child. Maintaining mutans streptococci suppression with xylitol chewing gum. Hildebrandt GH, Sparks BS. School of Dentistry, University of Minnesota, Minneapolis 55455-0348, USA. .H.Hildebrandt1@... BACKGROUND: One strategy for treating dental caries is to suppress oral mutans streptococci, or MS, with chlorhexidine, or CHX, mouthrinse. Oral MS levels, however, tend to quickly return to baseline values without further intervention. In this clinical study, the authors evaluated the effect of xylitol chewing gum on MS regrowth. METHODS: The authors selected 151 subjects with elevated oral MS levels (> or = 105 colony-forming units per milliliter, or CFU/mL, of paraffin-stimulated saliva). Subjects rinsed with 0.12 percent CHX gluconate mouthrinse twice daily for 14 days. The authors then randomly assigned the subjects to one of three groups. Those in the test group (n = 51) chewed a commercial xylitol gum three times daily for a minimum of five minutes each time for three months. The placebo group subjects (n = 50) used a commercial sorbitol gum, and the control group subjects (n = 50) did not chew gum. The authors estimated MS load on the dentition using paraffin-stimulated saliva samples. The authors serially diluted the samples, plated them on selective media and incubated them anaerobically; they then enumerated the colonies under a stereomicroscope. RESULTS: MS levels were not significantly different between the three groups at baseline (mean log CFU/mL +/- standard deviation: 5.4 +/- 0.7, 5.4 +/- 0.8, 5.2 +/- 0.7, respectively) nor after CHX therapy (2.7 +/- 0.8, 3.1 +/- 1.1, 3.0 +/- 1.1, respectively). After three months of gum chewing, the test group subjects had significantly lower salivary MS levels (3.6 +/- 1.2) than did the placebo (4.7 +/- 1.2) or control (4.4 +/- 1.3) group subjects. CONCLUSIONS: Xylitol chewing gum appears to have the ability to prolong the effect of CHX therapy on oral MS. CLINICAL IMPLICATIONS: Maintaining long-term caries-pathogen suppression is feasible with currently available commercial products and can be expected to result in significant caries inhibition. Publication Types: * Clinical trial * Randomized controlled trial PMID: 10916329 [PubMed - indexed for MEDLINE] Influence of maternal xylitol consumption on acquisition of mutans streptococci by infants. Soderling E, Isokangas P, Pienihakkinen K, Tenovuo J. Institute of Dentistry, University of Turku, Finland. eva.soderling@... Xylitol is effective as a non-cariogenic sugar substitute. Habitual xylitol consumption appears to select for mutans streptococci (MS) with impaired adhesion properties, i.e., they shed easily to saliva from plaque. One hundred sixty-nine mother-child pairs participated in a two-year study exploring whether the mothers' xylitol consumption could be used to prevent mother-child transmission of mutans streptococci. All mothers showed high salivary levels of mutans streptococci during pregnancy. The mothers in the xylitol group (n = 106) were requested to chew xylitol-sweetened gum (65% w/w) at least 2 or 3 times a day, starting three months after delivery. In the two control groups, the mothers received either chlorhexidine (n = 30) or fluoride (n = 33) varnish treatments at 6, 12, and 18 months after delivery. The children did not chew gum or receive varnish treatments. MS were assessed from the mothers' saliva at half-year intervals and from the children's plaque at the one- and two-year examinations. The MS were cultured on Mitis salivarius agars containing bacitracin. The salivary MS levels of the mothers remained high and not significantly different among the three study groups throughout the study. At two years of age, 9.7% of the children in the xylitol, 28.6% in the chlorhexidine, and 48.5% in the fluoride varnish group showed a detectable level of MS. In conclusion, therefore, habitual xylitol consumption by mothers was associated with a statistically significant reduction of the probability of mother-child transmission of MS assessed at two years of age. The effect was superior to that obtained with either chlorhexidine or fluoride varnish treatments performed as single applications at six-month intervals. Publication Types: * Clinical trial * Randomized controlled trial PMID: 10765964 [PubMed - indexed for MED Long-term tolerance of healthy human subjects to high amounts of xylitol and fructose: general and biochemical findings. Makinen KK. Three groups of volunteers, totalling 125, lived for two years on strict diets so that comparisons might be made with regard to the sweeteners: fructose (F), sucrose (S), and xylitol (X). The sizes of the test groups were: S, 35; F, 38; X, 52. The average monthly amounts of the sugars consumed in a varied assortment of foods were: S, 2.2 kg; F, 2.1 kg; X, 1.5 kg. The highest daily doses of fructose and xylitol were 200 - 400 g (maximum 430 g xylitol). Serum samples were analyzed for several chemical parameters. The dietary regimens did not result in clinically significant changes between the sugar groups. The ability of X to produce osmotic diarrhoea and flatulence was found to depend on the individual physiological responses of each volunteer. In many cases no symptoms were found although high amounts (200 - 400 g) of X were consumed. All pregnancies and deliveries in the F and X groups were normal. Practically all the volunteers accepted the F and X foods (almost 100 varities) and adhered to the dietary regimen for two years. This was due in the main to the fact that most F and X products were comparable to those containing sucros Effect of xylitol on growth of Streptococcus pneumoniae in the presence of fructose and sorbitol. Tapiainen T, Kontiokari T, Sammalkivi L, Ikaheimo I, Koskela M, Uhari M. Department of Pediatrics, University of Oulu, Oulu, Finland. ttapiai@... Xylitol is effective in preventing acute otitis media by inhibiting the growth of Streptococcus pneumoniae. To clarify this inhibition we used fructose, which is known to block similar growth inhibition observed in Streptococcus mutans. In addition, we evaluated the efficacy of sorbitol in inhibiting the growth of pneumococci, as sorbitol is widely used for indications similar to those for which xylitol is used. The addition of 5% xylitol to the growth medium resulted in marked growth inhibition, an effect which was totally eliminated in the presence of 1, 2.5, or 5% fructose but not in the presence of 1 or 5% glucose, 1% galactose, or 1% sucrose. This finding implies that xylitol-induced inhibition of pneumococcal growth is mediated via the fructose phosphotransferase system in a way similar to that in which mutans group streptococcal growth is inhibited. The addition of sorbitol at concentrations of 1, 2.5, or 5% to the growth medium did not affect the growth of pneumococci and neither inhibited nor enhanced the xylitol-induced growth impairment. Thus, it seems that xylitol is the only commercially used sugar substitute proven to have an antimicrobial effect on pneumococci. Antiadhesive effects of xylitol on otopathogenic bacteria. Kontiokari T, Uhari M, Koskela M. Department of Paediatrics, University of Oulu, Finland. The exposure of either epithelial cells or pneumococci or both to 5% xylitol reduced the adherence of pneumococci. Exposure of epithelial cells or bacteria alone to xylitol did not reduce the adherence of Haemophilus influenzae, although the exposure of both cells and bacteria to xylitol reduced the adherence significantly. The adherence of Moraxella catarrhalis remained low irrespective of the exposure. _________________________________________________________________ Join the world’s largest e-mail service with MSN Hotmail. http://www.hotmail.com Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 20, 2002 Report Share Posted June 20, 2002 on 6/19/2002 3:09 AM, Mambo Mambo at mambomambo@... wrote: > Even thought Xylitol isn't completely devoid of calories, I think it is > quite amazing that they've found a nature-given substance that prevents bone > loss. MM: one more question: how's the taste? Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 20, 2002 Report Share Posted June 20, 2002 To my experience, xylitol tastes great. I actually like it better than white sugar. I have used it to flavor smoothies, to bake muffins, and tasted it straight. It is really very good. I order it under the name birch bark sugar from ultimatelife.org, a company website that some on this list might find interesting. It is a bit pricey, and corresponds one to one with table sugar, but I find it worth the cost. It is all natural and is not known/suspected to have any detrimental health effects, excepting the calories. I have read it actually has half the calories of regular sugar, someone posted that it was 2/3. Also, it metabolizes very slowly making it totally safe for diabetics, and anyone else concerned about blood sugar spikes. I myself am very sensitive to any high-glycemic index foods and have never had any problem with xylitol. Lerner jmlpiano@... IOn Wednesday, June 19, 2002, at 07:19 PM, Francesca Skelton wrote: > on 6/19/2002 3:09 AM, Mambo Mambo at mambomambo@... wrote: > > > Even thought Xylitol isn't completely devoid of calories, I think it > is > > quite amazing that they've found a nature-given substance that > prevents bone > > loss. > > MM: one more question: how's the taste? > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 20, 2002 Report Share Posted June 20, 2002 Hi Jeffry I tried the address you gave and had trouble finding the website. My web browser found the company at ultimatelife.com and the most direct address seems to be the one below since it places you at the products and price page from which you can click to see pictures of the products. http://www.flexbase.com/ul/servlet/FlexEngine?page=PagePurchase It looks interesting. I think I might like to try a sample of it although for now I am committed to Warren's sucralose order. http://www.flexbase.com/ul/servlet/FlexEngine?page=PagePurchase In a message dated 6/20/2002 4:47:50 AM Pacific Daylight Time, jmlpiano@... writes: To my experience, xylitol tastes great. I actually like it better than white sugar. I have used it to flavor smoothies, to bake muffins, and tasted it straight. It is really very good. I order it under the name birch bark sugar from ultimatelife.org, a company website that some on this list might find interesting. It is a bit pricey, and corresponds one to one with table sugar, but I find it worth the cost. It is all natural and is not known/suspected to have any detrimental health effects, excepting the calories. I have read it actually has half the calories of regular sugar, someone posted that it was 2/3. Also, it metabolizes very slowly making it totally safe for diabetics, and anyone else concerned about blood sugar spikes. I myself am very sensitive to any high-glycemic index foods and have never had any problem with xylitol. Lerner jmlpiano@... Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 20, 2002 Report Share Posted June 20, 2002 Sorry, it's been a while since I ordered from the site. The address to get information about the sweetener is http://www.flexbase.com/ul/servlet/FlexEngine?page=CatSweet You are right, the web address is ultimatelife.com The product is called ultimate sweetener. To order click the " purchase " tab at the bottom of the description page. Good Luck, Lerner jmlpiano@... On Thursday, June 20, 2002, at 08:40 AM, kcover wrote: > Hi there, > > > I tried to find the website for ultimatelife.org and my server could not > locate it. A search turned up UltimateLife.com, but I did not find the > xylitol. Could you send their complete website url, if you have time. > Thank you for sharing your experiences with this substance. > > Best wishes, > Kayce Cover > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 21, 2002 Report Share Posted June 21, 2002 Hi Francesca and all Somewhere I downloaded a study that said that between 4 and 6 teaspoons of X per day had bone building effects. I'll keep looking for it. The taste is " cooler " than sugar but very sweet. One can cook with it as well. best to all MM _________________________________________________________________ Join the world’s largest e-mail service with MSN Hotmail. http://www.hotmail.com Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 1, 2002 Report Share Posted September 1, 2002 Various xylitol products at http://xylitolnow.com/ Iris Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 1, 2002 Report Share Posted September 1, 2002 Hello all, Here are a few papers on Xylitol supplementation and bone resorption, as well as Xylitol's enhancement of Calcium citrate supplementation. I'll try to find out how much one needs to take per/lb for it to be effective. Somewhere in the back of my mind I remember 6 teaspoons. best wishes! MM ps. could someone check these American chewing gums out for me? I found this statement on one of the sites I visited: " Chew gum containing xylitol, for a minimum of five minutes after each meal. Xylitol will: retard the growth of oral bacteria, neutralizing plaque acids to fight cavities and remineralize tooth enamel. It is found in Trident™ Original, Bubblegum, Trident for Kids gum, Biotene gum and Advantage. " http://www.xylitol.org/faqs.htm http://www.xylitol.org/Publications.htm Gerontology 2001 Nov-Dec;47(6):300-5 Related Articles, Links Increased bone volume and bone mineral content in xylitol-fed aged rats. Mattila PT, Svanberg MJ, Knuuttila ML. Oral and Maxillofacial Department, Oulu University Hospital, Oulu, Finland. ptm@... BACKGROUND: Our previous studies have shown that dietary xylitol supplementation protects against the loss of bone mineral after ovariectomy. The ovariectomy-induced decrease in trabecular bone volume is significantly retarded by dietary xylitol. Objective: To study whether dietary xylitol can protect against bone loss also during aging, a long-term experimental study was performed with rats. METHODS: Twenty-four male Sprague-Dawley rats were divided into two groups. The rats in the control group were fed a basal RM1 diet, while the rats in the experimental group were continuously fed the same diet supplemented with 10% (w/w) xylitol. The rats were killed after 20 months. Their tibiae were used for the analyses of bone density and trabecular bone volume, and their femurs were used for the scanning analyses with peripheral quantitative computed tomography (pQCT). RESULTS: The tibial density of the xylitol-fed aged group (1.73 +/- 0.14 g/mm(3)) was significantly greater than that of the aged group without xylitol (1.56 +/- 0.14 g/ mm(3)). The trabecular bone volume of the xylitol-fed rats was 21.2 +/- 4.0%. It was significantly greater than that of the rats not receiving xylitol (9.3 +/- 4.3%). The pQCT-measured cortical bone mineral density and the pQTC-measured cortical bone mineral content of the femoral diaphysis were significantly greater in the xylitol-fed group than in the control group. The trabecular bone mineral density and the trabecular bone mineral content of the femoral distal metaphysis were also significantly greater in the xylitol-fed group than in the non-xylitol group. The total bone mineral density and the total bone mineral content of the femoral neck in the xylitol-fed aged group significantly exceeded those in the aged group without xylitol supplementation. CONCLUSIONS: A continuous moderate dietary xylitol supplementation leads to increased bone volume and increased bone mineral content in the long bones of aged rats. This indicates a xylitol-induced protection against aging-related osteoporotic changes. Copyright 2001 S. Karger AG, Basel PMID: 11721142 [PubMed - indexed for MEDLINE] Dietary xylitol protects against weakening of bone biomechanical properties in ovariectomized rats. Mattila PT, Svanberg MJ, Pokka P, Knuuttila ML. Institute of Dentistry, University of Oulu, 90220 Oulu, Finland. The effects of dietary xylitol (xyl) on bone biomechanical properties in ovariectomized rats (ovx) were studied. Forty-two 3-mo-old female Wistar rats were divided into three groups of 14. Rats in two groups were ovariectomized, while those in the control group underwent a sham operation. All rats received a basal diet, and half of the ovx were given an additional 10 g/100 g dietary xyl supplementation. Three months later the rats were killed and their tibias, femurs and humeri were prepared. The tibias were used for analyses of bone density and trabecular bone volume (BV/TV) and for the three-point bending test. The femurs were used for the torsion test and for the loading test of the femoral neck. The humeri were used for analyses of bone ash weight and bone concentrations of calcium and phosphorus. Dietary xyl gave a significant protection against ovariectomy-caused decline of tibial stress in the three-point bending test, of femoral shear stress in the torsion test, and of stress of the femoral neck, without affecting bone elasticity values. Xyl restricted the ovariectomy-caused reduction in bone density, in bone ash weight and in concentrations of bone calcium and phosphorus. Furthermore, trabecular bone loss in ovx was significantly suppressed by dietary xyl. These results indicate that a 10% dietary supplementation of xyl in ovx has a protective effect against the weakening of bone biomechanical properties. This is related to greater BV/TV and maintained bone mineral content. PMID: 9772154 [PubMed - indexed for MEDLINE] Comparison of the effect of gluconate, lactose, and xylitol on bone recalcification in calcium-deficient rats. Hamalainen MM, Knuuttila M, Svanberg M, Koskinen T. Institute of Dentistry, University of Turku, Finland. The therapeutic value of three calcium absorption promoting carbohydrates, lactose, gluconate and xylitol, in bone calcification was evaluated in 7-week-old male rats which were fed on a semisynthetic Ca-deficient diet for 3 weeks. Lactose + CaCO3, xylitol + CaCO3, Ca-gluconate, or CaCO3 alone were administered to the Ca-deficient rats for 2 weeks; the carbohydrate and Ca contents of the diets were 5% and 0.5%, respectively. The Ca-deficient rats showed a decrease in serum total Ca and ionized Ca2+ and in tibial Ca, Mg, P and density, with a concomitant increase in bone hydroxyproline concentration. Bone and serum tartrate-resistant acid phosphatase activities were increased 2-fold and the serum 1,25(OH)2D3 level 5-fold. Smaller increases were found in serum calcitonin, PTH, alkaline phosphatase and osteocalcin levels. These changes (except calcitonin) were reversed by the administration of Ca and the carbohydrates. It was observed that all three agents improved the recalcification of bones compared with the effect of CaCO3 alone. The effect of lactose and xylitol was superior to that of gluconate. These results suggest advantages in the use of xylitol in Ca-supplements. PMID: 2078437 [PubMed - indexed for MEDLINE] Miner Electrolyte Metab 1993;19(2):103-8 Related Articles, Links Citric acid concentration compared to serum parathyroid hormone, 1,25(OH)2D3 and calcitonin during dietary Ca deficiency and rehabilitation enhanced with xylitol in rats. Svanberg M, Knuuttila M, Hamalainen M. Institute of Dentistry, University of Oulu, Finland. Young male Wistar rats were fed on a Ca-deficient diet for 3 weeks, after which dietary Ca was restored with either CaCO3 or CaCO3 + xylitol (5% per weight). Citric acid, Ca, Mg, Zn and P were determined in the tibia and femur at the beginning and after 2 and 4 weeks of rehabilitation, and serum and urinary citric acid and serum 1,25(OH)2D3, parathyroid hormone (PTH) and calcitonin were measured at the same points in time. The diminished bone Ca (p < 0.001) after 3 weeks of deficiency did not reduce the bone citric acid concentration, although serum citrate increased markedly. Simultaneously the serum 1,25(OH)2D3 concentration more than doubled and PTH increased (p < 0.01). Rehabilitation with CaCO3 + xylitol reduced the 1,25(OH)2D3 concentration to below the control level (p < 0.05), while serum citric acid remained elevated. CaCO3 alone normalized the elevated hormone and citric acid levels in the serum. Dietary CaCO3 and CaCO3 + xylitol normalized the PTH concentration equally well. The gain in bone Ca after 4 weeks of rehabilitation was significantly greater when xylitol was added compared with CaCO3 alone (p < 0.05). Only the 4-week CaCO3 + xylitol group attained the bone Ca concentration of the controls. Xylitol supplementation seems to affect the serum citric acid concentration independent of 1,25(OH)2D3 and PTH concentrations. The elevated citric acid concentration could be associated with increasing bone Ca. PMID: 8377724 [PubMed - indexed for MEDLINE] Dietary xylitol in the prevention of experimental osteoporosis Beneficial effects on bone resorption, structure and biomechanics i Mattila Institute of Dentistry, University of Oulu Academic Dissertation to be presented with the assent of the Faculty of Medicine, University of Oulu, for public discussion in the Auditorium of the Department of Anatomy and Cell Biology, on March 26th, 1999, at 12 noon. UNIVERSITY OF OULU, OULU FINLAND 1999 ISBN 951-42-5158-X URN:ISBN:951425158X Abstract Dietary xylitol supplementation increases bone calcium and phosphorus concentrations in healthy rats, as well as protects against the decrease of bone minerals and bone density during experimental osteoporosis. This suggests that dietary xylitol might have a favorable effect on the prevention of osteoporosis. However, before any conclusions can be drawn about the usefulness of a compound, studies including structural evaluation and biomechanical testing of bones must first be performed. Thus, the aim of the present study was to clarify whether dietary xylitol affects bone resorption, bone structure, and bone biomechanics in healthy rats, and whether dietary xylitol offers some preventive effects against the increased bone resorption, decreased bone trabeculation, and weakened bone biomechanical properties during experimental osteoporosis. Dietary xylitol reduced bone resorption in 3-mo old healthy male rats, and protected significantly against the increase of bone resorption in 3-mo old ovariectomized rats, as measured by the urinary excretion of 3H following [3H]tetracycline-prelabeling. In addition, increased trabecular bone volume of proximal tibia in 4-mo old healthy male rats was detected after a 1-mo xylitol feeding period, and significant protection against the decrease of trabecular bone volume in 6-mo old ovariectomized rats was observed after a 3-mo xylitol feeding period. Furthermore, dietary xylitol increased the strength properties of long bones in 6-mo old healthy male rats after a 3-mo feeding period, without affecting the bone elastic properties as tested by three-point bending of tibia, torsion of femur, and loading of femoral neck. Accordingly, dietary xylitol protected significantly against the weakening of bone biomechanical properties in 6-mo old ovariectomized rats after a 3-mo feeding period. In conclusion, the above results strongly support the hypothesis that oral administration of xylitol protects effectively against the progression of experimental osteoporosis. Dietary xylitol was effective both in increasing bone mass in healthy rats, and in preventing bone loss in ovariectomized rats, suggesting a favorable effect of xylitol on both main targets in the prevention of osteoporosis. As dietary xylitol was effective also in protecting against the experimental osteoporosis-caused changes in bone structure and weakening of bone biomechanical properties, oral xylitol administration seems to provide interesting possibilities when searching for new physiological choices for the prevention of osteoporosis. _________________________________________________________________ Join the world’s largest e-mail service with MSN Hotmail. http://www.hotmail.com Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 13, 2002 Report Share Posted September 13, 2002 Hi , The more information I am getting back, the more I think I will pass on the Kefo. It is very expensive also. Another question. What do you think of Xylitol as a sweetener? Even Dr. Mercola had nothing bad to say about it, but would like more opinions.' Thanks, Kat http://www.katking.com ----- Original Message ----- From: " Idol " <Idol@...> < > Sent: Thursday, September 12, 2002 9:06 AM Subject: Re: Keto Sweet > Kat- > > >Has anyone heard of Keto Sweet? > > Unfortunately, the third ingredient is " natural flavor " , which pretty much > translates to " excitotoxin " . Otherwise it might be OK. I don't think > there's anything wrong with a bit of glycine, and ace k might be a > relatively innocuous sweetener, though saccharine is the only one on the > market that can pretty much be relied upon to be completely > safe. Certainly ace k is better than aspartame, sucralose and maltodextrin. > > I haven't tried ace k yet myself because I can't find it in a formulation > without any problematic fillers or other sweeteners. > > > > > - > > > > Quote Link to comment Share on other sites More sharing options...
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