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急性补充松醇对老年人血浆松醇浓度、全身葡萄糖耐量及骨骼肌胰岛素受体激活的影响。

Effects of acute pinitol supplementation on plasma pinitol concentration, whole body glucose tolerance, and activation of the skeletal muscle insulin receptor in older humans.

作者信息

Stull A J, Wood K V, Thyfault J P, Campbell W W

机构信息

Department of Foods and Nutrition and Center on Aging and the Life Course, Purdue University, West Lafayette, IN 47907-2059, USA.

出版信息

Horm Metab Res. 2009 May;41(5):381-6. doi: 10.1055/s-0028-1128140. Epub 2009 Feb 16.

DOI:10.1055/s-0028-1128140
PMID:19221977
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4562028/
Abstract

Limited research with rodents and humans suggests that oral ingestion of pinitol (3- O-methyl- D- CHIRO-inositol) 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 (62+/-1 years, mean+/-SEM) 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). Blood samples were collected frequently over the 240-min testing period. 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 (placebo 0.83+/-0.08; pinitol 0.80+/-0.08) and whole-body (placebo 6.10+/-0.54; pinitol 6.22+/-0.52) insulin sensitivities. Activation of the muscle insulin receptor was increased by 140% with glucose ingestion (Pre 0.62+/-0.12; Post 1.49+/-0.35), but pinitol did not influence this response. These results show that the 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.

摘要

对啮齿动物和人类进行的有限研究表明,口服松醇(3 - O - 甲基 - D - 手性肌醇)可能对葡萄糖耐量产生积极影响。这项双盲、安慰剂对照的交叉研究评估了急性补充松醇对血浆松醇浓度、葡萄糖耐量、胰岛素敏感性以及骨骼肌胰岛素受体激活的影响。15名年龄较大的非糖尿病受试者(62±1岁,平均值±标准误)完成了四项为期1天的试验。受试者饮用不含任何成分(安慰剂)或含有1000毫克松醇的无营养饮料。60分钟后,受试者饮用不含能量和碳水化合物的饮料(假对照)或含有75克葡萄糖的饮料(口服葡萄糖耐量试验)。在240分钟的测试期内频繁采集血样。仅在口服葡萄糖耐量试验中,于补充安慰剂和松醇之前以及饮用75克葡萄糖饮料60分钟后采集股外侧肌样本。血浆松醇浓度升高并维持240分钟。在假对照和口服葡萄糖耐量试验期间,松醇对空腹状态以及血浆葡萄糖和胰岛素曲线下180分钟面积均无影响,对肝脏(安慰剂组0.83±0.08;松醇组0.80±0.08)和全身(安慰剂组6.10±0.54;松醇组6.22±0.52)胰岛素敏感性也无影响。葡萄糖摄入使肌肉胰岛素受体激活增加了140%(摄入前0.62±0.12;摄入后1.49±0.35),但松醇对此反应无影响。这些结果表明,松醇补充剂吸收迅速,但对老年非糖尿病人类的全身葡萄糖耐量、胰岛素敏感性指标以及骨骼肌胰岛素受体激活并无急性影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/729c/4562028/4ac4fa5b8a0d/nihms719472f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/729c/4562028/67ec1c3c9ba9/nihms719472f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/729c/4562028/91c820f8effe/nihms719472f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/729c/4562028/09b063804235/nihms719472f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/729c/4562028/4ac4fa5b8a0d/nihms719472f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/729c/4562028/67ec1c3c9ba9/nihms719472f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/729c/4562028/91c820f8effe/nihms719472f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/729c/4562028/09b063804235/nihms719472f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/729c/4562028/4ac4fa5b8a0d/nihms719472f4.jpg

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Diabetes Res Clin Pract. 2007 Sep;77 Suppl 1:S247-51. doi: 10.1016/j.diabres.2007.01.066. Epub 2007 Apr 27.
2
Contraction of insulin-resistant muscle normalizes insulin action in association with increased mitochondrial activity and fatty acid catabolism.胰岛素抵抗肌肉的收缩通过增加线粒体活性和脂肪酸分解代谢使胰岛素作用恢复正常。
Am J Physiol Cell Physiol. 2007 Feb;292(2):C729-39. doi: 10.1152/ajpcell.00311.2006. Epub 2006 Oct 18.
3
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Int J Mol Med. 2018 Apr;41(4):1826-1834. doi: 10.3892/ijmm.2018.3408. Epub 2018 Jan 19.
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Angew Chem Int Ed Engl. 2016 Jan 26;55(5):1614-50. doi: 10.1002/anie.201502227. Epub 2015 Dec 22.
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