Pinitol (3- O-methyl- D- CHIRO-inositol)
Pinitol is a natural product of the group of cyclitols.
Effects of Acute Pinitol Supplementation on Plasma
Pinitol Concentration, Whole Body Glucose Tolerance, and Activation of the
Skeletal Muscle Insulin Receptor in Older Humans.
Horm Metab Res. 2009 Feb 16. [ Stull AJ, Wood KV, Thyfault JP, Campbell WW.
1Department of Foods and Nutrition and Center on Aging and the Life Course,
Purdue University, West Lafayette, IN, USA.
Limited research with rodents and humans suggests that oral ingestion of pinitol
might positively influence glucose tolerance. This double-blinded,
placebo-controlled, and cross-over study assessed the effects of acute pinitol
supplementation on plasma pinitol concentration, glucose tolerance, insulin
sensitivity, and activation of the skeletal muscle insulin receptor. Fifteen
older, nondiabetic subjects completed four, 1-day trials. Subjects consumed a
non-nutritive beverage with nothing (placebo) or 1 000 mg pinitol. Sixty minutes
later, the subjects consumed beverages that were either energy- and
carbohydrate-free (Sham) or contained 75 g glucose (OGTT). For the OGTT trials
only, vastus lateralis samples were obtained before the placebo and pinitol
supplementation and 60 min after consuming the 75 g glucose beverage. Plasma
pinitol concentration increased and was maintained for 240 min. Pinitol did not
influence the fasting state and 180-min area under the curves for plasma glucose
and insulin during the Sham and OGTT trials or hepatic and whole-body insulin
sensitivities. Activation of the muscle insulin receptor was increased by 140%
with glucose ingestion but pinitol did not influence this response. Pinitol
supplement was quickly absorbed, but did not acutely influence indices of
whole-body glucose tolerance and insulin sensitivity, or the activation of the
skeletal muscle insulin receptor in older, nondiabetic humans.
Metabolic response of soy pinitol on lipid-lowering,
antioxidant and hepatoprotective action in hamsters fed-high fat and high
cholesterol diet.
Mol Nutr Food Res. 2009 Feb 9. Department of Food Science and Nutrition,
Kyungpook National University, Daegu, Korea.
This study was performed to investigate the lipid-lowering, antioxidant, and
hepato-protective effects of pinitol in dose-dependent manners in hamsters
fed-high fat and high cholesterol (HFHC) diet. Pinitol supplementation with an
HFHC diet (10% coconut oil plus 0.2% cholesterol) for 10 wks significantly
lowered the white adipose tissue weights, hepatic lipid droplets, plasma
glucose, total-cholesterol, nonHDL-cholesterol, total-cholesterol/HDL-cholesterol
ratio, and hepatic lipid levels. Whereas it significantly increased the brown
adipose tissue weight, plasma HDL-cholesterol, apolipoprotein A-I (apo A-I)
concentrations, paraoxonase (PON) activity, and/or mRNA expression, compared to
the HFHC control group. Plasma insulin and adiponectin levels were significantly
lower and higher. Dietary pinitol significantly inhibited hepatic HMG-CoA
reductase, acyl-CoA:cholesterol acyltransferase (ACAT), and cytochrome P4502E1
(CYP2E1) activities without altering their mRNA expressions compared to the
control group. Pinitol significantly elevated the hepatic antioxidant enzyme
activities, whereas it also significantly reduced the hepatic lipid peroxide and
H(2)O(2) production. Accordingly, these results indicate that pinitol
supplementation may improve the lipid and antioxidant metabolism in HFHC
diet-fed hamsters. In particular, pinitol supplementation was very effective on
the elevation of antiatherogenic factors, including plasma HDL-cholesterol, apo
A-I, adiponectin, and PON.
Pinitol is found in
Acacia nilotica herb
Pinitol is found in an aqueous extract of the heartwood
of Enterolobium cyclocarpum
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