4.5 Article

Improving insulin resistance with Antrodia cinnamomea mycelium powder to induce a hypoglycemic effect in dexamethasone-induced insulin-resistant rats

期刊

MOLECULAR MEDICINE REPORTS
卷 17, 期 2, 页码 3260-3266

出版社

SPANDIDOS PUBL LTD
DOI: 10.3892/mmr.2017.8259

关键词

Antrodia cinnamomea; dexamethasone; free fatty acid; insulin signal transduction proteins; insulin resistance

资金

  1. Ministry of Science and Technology [104-2632-E-212-001]
  2. Taichung Veterans General Hospital [TCVGH-DYU-1058304]
  3. Da-Yeh University [TCVGH-DYU-1058304]
  4. Cheng Ching Hospital in Taiwan [CCGH-DYU-106-001, CCGH-DYU-104-001]
  5. Da-Yeh University in Taiwan [CCGH-DYU-106-001, CCGH-DYU-104-001]
  6. China Medical University under the Aim for Top University Plan of the Ministry of Education, Taiwan [CHM106-5-2]
  7. Taiwan Ministry of Health and Welfare Clinical Trial Center, Taiwan [MOHW106-TDU-B-212-113004]

向作者/读者索取更多资源

Insulin resistance is a major factor in type II diabetes development, occurring when insulin levels are normal, but do not have normal interactions with adipose, muscle or liver tissue. The present study aimed to explore the hypoglycemic effect of Antrodia cinnamomea (AC) mycelium powder by evaluating its impact on insulin resistance and plasma free fatty acid (FFA) levels in steroid-induced insulin-resistant (SIIR) rats. Male Wistar rats were administered dexamethasone for 5 days to induce insulin resistance. The SIIR rats were subsequently randomly assigned into three experimental groups (EGs) and a control group (CG), where saline was orally administered. The EGs were orally administered different doses of AC (100, 200 or 500 mg/kg) and an optimal dose for further study was determined. Changes in plasma insulin and glucose levels were calculated to investigate the hypoglycemic effect of AC. To evaluate insulin resistance, the homeostasis model assessment-estimated insulin resistance of the SIIR rats was determined. Changes in plasma FFA levels were detected and levels of insulin signal proteins (IRS-1, GLUT-4 and PI3K) were analyzed by western blot to elucidate AC's mechanism of action. The SIIR rats exhibited significantly decreased plasma glucose levels in the first 30 min, with plasma FFA levels displaying a marked downward trend (P<0.05) when they were administered the optimal dose of AC (200 mg/kg). The decrease in plasma glucose and FFA levels was significantly larger in the EG compared to the CG, and insulin signal protein levels were also significantly increased (P<0.05). The hypoglycemic effect observed may be due to decreased plasma FFA levels and increased expression of intracellular insulin signal proteins. Furthermore, insulin sensitivity was enhanced, indicating that AC acts as an insulin sensitizer in insulin resistant animal models.

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