4.6 Article

Herbal constituent sequoyitol improves hyperglycemia and glucose intolerance by targeting hepatocytes, adipocytes, and β-cells

出版社

AMER PHYSIOLOGICAL SOC
DOI: 10.1152/ajpendo.00479.2011

关键词

insulin resistance; diabetes; hyperglycemia

资金

  1. National Institutes of Health (NIH) [DK065122, DK073601, 5P60 DK20572, 5 P30 CA46592, P30AG013283, DK34933]
  2. American Diabetes Association [1-09-RA-156]
  3. Chinese Academy of Science/SAFEA
  4. National Natural Science Foundation [30728024]
  5. Michigan Diabetes Research and Training Center
  6. University of Michigan's Cancer Center
  7. University of Michigan Nathan Shock Center
  8. University of Michigan Gut Peptide Research Center

向作者/读者索取更多资源

Herbal constituent sequoyitol improves hyperglycemia and glucose intolerance by targeting hepatocytes, adipocytes, and beta-cells. Am J Physiol Endocrinol Metab 302: E932-E940, 2012. First published January 31, 2012; doi:10.1152/ajpendo.00479.2011.-The prevalence of insulin resistance and type 2 diabetes increases rapidly; however, treatments are limited. Various herbal extracts have been reported to reduce blood glucose in animals with either genetic or dietary type 2 diabetes; however, plant extracts are extremely complex, and leading compounds remain largely unknown. Here we show that 5-O-methyl-myo-inositol (also called sequoyitol), a herbal constituent, exerts antidiabetic effects in mice. Sequoyitol was chronically administrated into ob/ob mice either orally or subcutaneously. Both oral and subcutaneous administrations of sequoyitol decreased blood glucose, improved glucose intolerance, and enhanced insulin signaling in ob/ob mice. Sequoyitol directly enhanced insulin signaling, including phosphorylation of insulin receptor substrate-1 and Akt, in both HepG2 cells (derived from human hepatocytes) and 3T3-L1 adipocytes. In agreement, sequoyitol increased the ability of insulin to suppress glucose production in primary hepatocytes and to stimulate glucose uptake into primary adipocytes. Furthermore, sequoyitol improved insulin signaling in INS-1 cells (a rat beta-cell line) and protected INS-1 cells from streptozotocin-or H2O2-induced injury. In mice with streptozotocin-induced beta-cell deficiency, sequoyitol treatments increased plasma insulin levels and decreased hyperglycemia and glucose intolerance. These results indicate that sequoyitol, a natural, water-soluble small molecule, ameliorates hyperglycemia and glucose intolerance by increasing both insulin sensitivity and insulin secretion. Sequoyitol appears to directly target hepatocytes, adipocytes, and beta-cells. Therefore, sequoyitol may serve as a new oral diabetes medication.

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