Anti-diabetic effect mediated by Ramulus mori polysaccharides

Carbohydr Polym. 2015 Mar 6:117:63-69. doi: 10.1016/j.carbpol.2014.09.052. Epub 2014 Sep 28.

Abstract

Diabetes mellitus is a complicated metabolic disease, whose pathogenesis is related to apoptosis within pancreatic tissue. In this study, the potential therapeutic benefits of Ramulus mori polysaccharides (RMP) on streptozotocin (STZ)-induced diabetic mice were evaluated. Our experiments indicated that RMP lowered hyperglycemia and increased insulin levels in diabetic mice. Histopathological examination revealed that RMP contributed to the reduction of STZ-lesioned pancreatic cells. In addition, the serum level of HbA1c was decreased. RMP treatment also showed increased Bcl-2 expression and reduced Bax protein level in pancreatic tissue. Furthermore, intrapancreatic expressions of p-JNK, p-p38 and cleaved-caspase-3 were down-regulated by RMP treatment. Collectively, the findings demonstrate that RMP exerts the pronounced hypoglycemic effect via regulation of the intrapancreatic JNK/p38 pathway to protect against STZ-induced apoptosis in pancreatic tissue, eventually ameliorating metabolic function in the pancreas.

Keywords: Apoptosis; Hyperglycemia; Metabolism; Ramulus mori polysaccharides.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis / drug effects
  • Body Weight / drug effects
  • Caspase 3 / metabolism
  • Diabetes Mellitus, Experimental / blood
  • Diabetes Mellitus, Experimental / drug therapy
  • Diabetes Mellitus, Experimental / metabolism
  • Diabetes Mellitus, Experimental / pathology
  • Fasting / blood
  • Gene Expression Regulation, Enzymologic / drug effects
  • Glycated Hemoglobin / metabolism
  • Hypoglycemic Agents / pharmacology*
  • Hypoglycemic Agents / therapeutic use
  • Insulin / blood
  • JNK Mitogen-Activated Protein Kinases / metabolism
  • Male
  • Mice
  • Morus / chemistry*
  • Pancreas / drug effects
  • Pancreas / metabolism
  • Phosphoproteins / metabolism
  • Polysaccharides / pharmacology*
  • Polysaccharides / therapeutic use
  • Proteolysis / drug effects
  • Up-Regulation / drug effects
  • p38 Mitogen-Activated Protein Kinases / metabolism

Substances

  • Glycated Hemoglobin A
  • Hypoglycemic Agents
  • Insulin
  • Phosphoproteins
  • Polysaccharides
  • JNK Mitogen-Activated Protein Kinases
  • p38 Mitogen-Activated Protein Kinases
  • Caspase 3