Antidiabetic activity and toxicity of Zizyphus spina-christi leaves

J Ethnopharmacol. 2005 Oct 3;101(1-3):129-38. doi: 10.1016/j.jep.2005.04.007.

Abstract

The effect of the butanol extract of Zizyphus spina-christi (L.), Willd (Rhamnaceae) leaves and its major saponin glycoside, christinin-A, on the serum glucose and insulin levels was studied in non-diabetic control, type-I (insulin-dependent) and type-II (non-insulin-dependent) diabetic rats. Pretreatment either with 100 mg/kg butanol extract or christinin-A potentiated glucose-induced insulin release in non-diabetic control rats. In type-II but not in type-I diabetic rats pretreatment with the butanol extract or christinin-A improved the oral glucose tolerance and potentiated glucose-induced insulin release. Treatment either with 100 mg/kg butanol extract or christinin-A reduced the serum glucose level and increased the serum insulin level of non-diabetic control and type-II diabetic rats but not of type-I diabetic rats. Effects of the butanol extract and christinin-A were similar. Pretreatment of non-diabetic control and type-II diabetic rats either with 100 mg/kg butanol extract or christinin-A enhanced the glucose lowering and insulinotropic effects of 5 g/kg glibenclamide. The hyperglycemic and hypoinsulinemic effects of 30 mg/kg diazoxide in non-diabetic control and type-II diabetic rats were inhibited and antagonized, respectively by pretreatment with the butanol extract or christinin-A. The relaxant effects of different concentrations of diazoxide on the isolated norepinephrine-contracted aortic strips were inhibited by 100 micromol/l christinin-A or 10 micromol/l glibenclamide. The combination of glibenclamide and christinin-A led to complete inhibition of the relaxant effects of different concentrations of diazoxide. At a dose level much higher than that required to produce satisfactory insulinotropic and hypoglycemic effects, the butanol extract of Zizyphus spina-christi leaves produced a depressant effect on the central nervous system in rats. Treatment of rats with 100mg/kg butanol extract for 3 months produced no functional or structural disturbances in liver and kidney and no haematological changes. In addition, the oral LD50 of the butanol extract in mice was 3820 mg/kg, while that of glibenclamide was 3160 mg/kg. Thus, Zizyphusspina-christi leaves appears to be a safe alternative to lower blood glucose. The safe insulinotropic and subsequent hypoglycemic effects of Zizyphus spina-christi leaves may be due to a sulfonylurea-like activity.

MeSH terms

  • Animals
  • Aorta / drug effects
  • Aorta / physiology
  • Blood Glucose / analysis
  • Diabetes Mellitus, Type 2 / drug therapy
  • Glucose Tolerance Test
  • Glyburide / pharmacology
  • Hypoglycemic Agents / pharmacology*
  • Hypoglycemic Agents / toxicity
  • In Vitro Techniques
  • Insulin / blood
  • Male
  • Motor Activity / drug effects
  • Phytotherapy*
  • Plant Extracts / pharmacology*
  • Plant Leaves / chemistry*
  • Potassium Channels / drug effects
  • Rabbits
  • Rats
  • Rats, Wistar
  • Streptozocin / pharmacology
  • Ziziphus*

Substances

  • Blood Glucose
  • Hypoglycemic Agents
  • Insulin
  • Plant Extracts
  • Potassium Channels
  • mitochondrial K(ATP) channel
  • Streptozocin
  • Glyburide