4.7 Article

Regulation of signaling molecules associated with insulin action, insulin secretion and pancreatic β-cell mass in the hypoglycemic effects of Korean red ginseng in Goto-Kakizaki rats

Journal

JOURNAL OF ETHNOPHARMACOLOGY
Volume 142, Issue 1, Pages 53-58

Publisher

ELSEVIER IRELAND LTD
DOI: 10.1016/j.jep.2012.04.012

Keywords

Korean red ginseng (KRG); Goto-Kakizaki rats; Diabetes; Insulin action; Insulin secretion; beta-Cell mass

Funding

  1. Korea Food Research Institute [E0121203]
  2. Korean Government [NRF-2010-0024475]
  3. Korea Research Foundation

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Ethnopharmacological relevance: Korean red ginseng (KRG) has long history as herbal remedy for antidiabetic effect. Aim of the study: To study molecular mechanisms by which KRG ameliorates diabetes mellitus, we investigated whether the supplementation with the aqueous extract of KRG as a dietary admixture (1%, w/w) regulates the expressions of signaling molecules that are associated with insulin action, insulin secretion and pancreatic beta-cell mass in spontaneously diabetic Goto-Kakizaki (GK) rats. Methods: An aqueous extract of KRG was supplemented for the estimated dosage to be 0.2 g/kg rat/day beginning at 5 weeks of age for 12 weeks in male GK rats. Plasma glucose levels were measured every 4 weeks. The expressions of signaling molecules that are associated with insulin action, insulin secretion and beta-cell mass in tissues were determined by Western blotting. Results: The 12-week supplementation with KRG significantly (P < 0.05) decreased blood glucose compared to control. It up-regulated the expression of glucose transporter (GLUT) 4 in adipose tissue, and down-regulated the expression of protein tyrosine phosphatases (PTP)-1B in adipose tissue and skeletal muscle. It also up-regulated the expression of insulin and down-regulated the expression of uncoupling protein (UCP) 2, Bax and poly (ADP-ribose) polymerase (PARP) in pancreas. Conclusions: These results suggest that GLUT4, PTP-1B, insulin, UCP2. Bax and PARP may be the primary targets of KRG that result in increase in insulin action and in insulin secretion, and decrease in beta-cell mass, and that cause the normalization in glucose homeostasis. (C) 2012 Elsevier Ireland Ltd. All rights reserved.

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