Antidiabetic activity of Kalanchoe pinnata in streptozotocin-induced diabetic rats by glucose independent insulin secretagogue action

Pharm Biol. 2013 Nov;51(11):1411-8. doi: 10.3109/13880209.2013.794364. Epub 2013 Jul 19.

Abstract

Context: Kalanchoe pinnata Lam. (Crassulaceae) is used as a traditional medicine worldwide to treat several ailments, including diabetes. However, the mechanism for the antihyperglycemic action is unknown.

Objective: The present study evaluates the antihyperglycemic and insulin secretagogue potential of Kalanchoe pinnata and assessment of the probable mechanism of action.

Materials and methods: Steam distillate of Kalanchoe pinnata leaves was subjected to solvent fractionation and antidiabetic activity was detected in dichloromethane (DCM) fraction. In the in vivo studies, rats were treated with 5 and 10 mg/kg body weight of DCM fraction for 45 days orally. Lipid profile and other biochemical parameters were estimated. The probable mechanism for insulin secretagogue action was evaluated through studies using diazoxide and nifedipine. The bioactive component from DCM fraction was studied using HPTLC, GCMS and IR.

Results and discussion: Fasting blood glucose values were reduced to 116 mg/dl from 228 mg/dl on treatment with 10 mg/kg body weight of DCM fraction, while glycated hemoglobin improved to 8.4% compared with 12.9% in diabetic controls. The insulin level and lipid profile values were close to normal values. In vitro studies demonstrated a dose-dependent insulin secretagogue action. Insulin secretion was 3.29-fold higher at 10 µg/ml as compared to the positive control. The insulin secretagogue activity was glucose independent and K(+)-ATP channel dependent. The bioactive component of the DCM fraction was identified to be a phenyl alkyl ether derivative.

Conclusion: The DCM fraction of Kalanchoe pinnata demonstrates excellent insulin secretagogue action and can be useful in treatment of diabetes mellitus.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Biomarkers / blood
  • Blood Glucose / drug effects*
  • Blood Glucose / metabolism
  • Diabetes Mellitus, Experimental / blood
  • Diabetes Mellitus, Experimental / chemically induced
  • Diabetes Mellitus, Experimental / drug therapy*
  • Dose-Response Relationship, Drug
  • Ethers / pharmacology
  • Glycated Hemoglobin / metabolism
  • Hypoglycemic Agents / pharmacology*
  • Insulin / blood
  • Insulin / metabolism*
  • Insulin Secretion
  • Islets of Langerhans / drug effects*
  • Islets of Langerhans / metabolism
  • KATP Channels / metabolism
  • Kalanchoe*
  • Lipids / blood
  • Male
  • Phytotherapy
  • Plant Extracts / pharmacology*
  • Plant Leaves
  • Plants, Medicinal
  • Rats
  • Rats, Wistar
  • Solvents / chemistry
  • Streptozocin
  • Time Factors
  • Tissue Culture Techniques

Substances

  • Biomarkers
  • Blood Glucose
  • Ethers
  • Glycated Hemoglobin A
  • Hypoglycemic Agents
  • Insulin
  • KATP Channels
  • Lipids
  • Plant Extracts
  • Solvents
  • Streptozocin