Betaine HCL
Betaine plays a critical role in the health of the
cardiovascular system. Betaine reduces
potentially toxic levels of homocysteine (Hcy), an amino acid found normally in the body.
Homocysteine metabolism is linked to that of several vitamins, especially folic acid, B6, and B12,
and deficiencies of those vitamins may cause elevated Hcy levels. In recent years, studies have
suggested that a high level of Hcy increases a person's chance of developing heart disease, stroke,
and peripheral vascular disease (reduced blood flow to the hands and feet).
Most people typically do not eat
enough fruits and vegetables, which may limit
their dietary intake of betaine and the B vitamins, thereby creating a potential need for
supplementation.
Betaine HCl may be beneficial in allergic rhinitis, asthma,
anemia, atherosclerosis, candidiasis, diarrhoea, food allergies, gallstones, heart disease,
rheumatoid arthritis, and thyroid disorders.
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Published
Clinical Studies
Betaine HCL
- Betaine lowers elevated s-adenosylhomocysteine levels
in hepatocyte from ethanol-fed rats.
- Carbon tetrachloride-induced nephrotoxicity and
protective effect of betaine in Sprague-Dawley rats.
Betaine lowers elevated s-adenosylhomocysteine
levels in hepatocytes from ethanol-fed rats.
Barak AJ, Beckenhauer HC, Mailliard ME, Kharbanda KK, Tuma
DJ.
VA Alcohol Research Center, Department of Veterans Affairs Medical
Center, Omaha, NE 68105, USA. ajbarak@yahoo.com
Previous studies showed that chronic ethanol administration
inhibits methionine synthase activity, resulting in impaired homocysteine remethylation to form
methionine. This defect in homocysteine remethylation was shown to increase plasma homocysteine and
to interfere with the production of hepatic S-adenosylmethionine (SAM) in ethanol-fed rats. These
changes were shown to be reversed by the administration of betaine, an alternative methylating
agent. This study was undertaken to determine additional effects of ethanol on methionine
metabolism and their functional consequences. The influences of methionine loading and betaine
supplementation were also evaluated. Adult Wistar rats were fed ethanol or a control Lieber-DeCarli
liquid diet for 4 wk, and metabolites of the methionine cycle were measured in vitro in isolated
hepatocytes under basal and methionine-supplemented conditions. S-Adenosylhomocysteine (SAH)
concentrations were elevated in hepatocytes isolated from ethanol-fed rats compared with controls
and in hepatocytes from both groups when supplemented with methionine. The addition of betaine to
the methionine-supplemented incubation media reduced the elevated SAH levels. The decrease in the
intracellular SAH:SAM ratio due to ethanol consumption inhibited the activity of the liver-specific
SAM-dependent methyltransferase, phosphatidylethanolamine methyltransferase. Our data indicate that
betaine, by remethylating homocysteine and removing SAH, overcomes the detrimental effects of
ethanol consumption on methionine metabolism and may be effective in correcting methylation defects
and treating liver diseases.
PMID: 12949375 [PubMed - indexed for MEDLINE]
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Carbon tetrachloride-induced nephrotoxicity
and protective effect of betaine in Sprague-Dawley rats.
Ozturk F, Ucar M, Ozturk IC, Vardi N, Batcioglu K.
Department of Histology-Embryology, Inonu University Faculty of
Medicine, Malatya, Turkey.
OBJECTIVES: To observe the changes in the antioxidative defense
enzymes and to detect the alterations of renal microscopy after carbon tetrachloride (CCl4)
administration in rats and to investigate the possible protective effects of betaine against
CCl4-induced renal damage. METHODS: Thirty-two adult Sprague-Dawley rats were divided into four
groups as follows: control group, betaine group, CCl4 group, and CCl4 + betaine group. CCl4 was
given subcutaneously at 1 mL/kg. In the CCl4 + betaine group, rats were pretreated with betaine,
then exposed to CCl4 at the same dose. Betaine group rats received concentrated betaine solution.
The rats were killed and the kidneys taken for enzyme analyses and histologic examination.
Glutathione peroxidase, superoxide dismutase, and catalase activities were measured in right kidney
homogenates. Left kidneys were processed for light microscopic evaluation. RESULTS: In the
CCl4-treated group, significant increases in kidney superoxide dismutase and catalase activities
and significant decrease in glutathione peroxidase activity were observed (P <0.01). These
changes were found to be normalized in the CCl4 + betaine group. Betaine did not change the enzyme
activities. Exposure to CCl4 resulted in glomerular and tubular alterations in the renal cortex.
These alterations were found to be prevented by betaine pretreatment. CONCLUSIONS: These results
indicate that exposure to CCl4 leads to renal damage in rats and betaine exerts an improvement on
nephrotoxic effects of CCl4.
PMID: 12893363 [PubMed - indexed for MEDLINE]
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References
- Micromedex Healthcare Series. Englewood, CO: MICROMEDEX
Inc.
- Martindale W. Martindale the Extra Pharmacopoeia.
Pharmaceutical Press, 1999.
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