Anti-diabetic and spasmolytic potential of Farsetia hamiltonii Royle from Cholistan desert

J Ethnopharmacol. 2014 Oct 28:156:347-52. doi: 10.1016/j.jep.2014.08.038. Epub 2014 Sep 9.

Abstract

Ethnopharmacological relevance: Folk herbal practitioners of the Cholistan desert claim Farsetia hamiltonii Royle (Brassicaceae) to treat diabetes, oxidative damages, diarrhea, fever, and abdominal cramps. The aim of this study was to scientifically find the potential of Farsetia hamiltonii in treating diabetes and gastrointestinal diseases.

Materials and methods: In vivo anti-diabetic activity of Farsetia hamiltonii was studied on alloxan induced diabetic rats to justify its traditional use. The in vitro antispasmodic activity on isolated tissues of rabbit jejunum was also evaluated. In addition, several enzyme inhibition studies (lipoxygenase, tyrosinase, acetylcholinesterase (AchE), carbonic II anhydrase and phosphodiesterase I) and antioxidant activity of plant extracts were also conducted.

Results: In vivo experiments, Farsetia hamiltonii methanol extract (300 mg/kg) significantly lowered the fasting blood glucose (107.6 ± 1.249 mg/dL up to 4th day) comparable to positive control (Glibenclamide) throughout the study period. The in vitro antispasmodic activity on isolated tissues of rabbit jejunum on methanol extract showed concentration dependent (0.01-0.3 mg/ml) relaxation of spontaneous contractions with EC₅₀ value 0.011 µM and high K(+) (80 mM) induced contraction (0.01-0.1 mg/ml) with EC₅₀ value 0.066 mg/ml. Farsetia hamiltonii DCM and methanol extracts exhibited some antilipoxygenase activities while tyrosinase, acetylcholinesterase (AchE), carbonic II anhydrase, phosphodiesterase I, and antioxidant activity of plant extracts were not significant.

Conclusions: Our results validate the traditional use of Farsetia hamiltonii for the traditional therapeutic potential in treating diabetes and gastrointestinal diseases.

Keywords: Anti-diabetic; Antispasmodic; Apigenin (CID: 5280443); Apigenin-7-O-β-D-glucopyranoside (CID: 5280704); Betulin (CID: 72326); Biological activities; Farsetia hamiltonii; Friedelin (CID: 91472); Isorhamnetin (CID: 5281654); Kaempferol (CID: 5280863); Kaempferol 3,7-dirhamnoside (CID 5486199); Kaempferol-3,7-di-O-α -L –rhamnopyranoside (CID 12305419); Scopoletin (CID: 5280460); β-Amyrin (CID: 73145).

MeSH terms

  • Alloxan / pharmacology
  • Animals
  • Blood Glucose / drug effects
  • Brassicaceae / chemistry*
  • Diabetes Mellitus, Experimental / drug therapy*
  • Female
  • Hypoglycemic Agents / pharmacology*
  • Jejunum / drug effects
  • Male
  • Parasympatholytics / pharmacology*
  • Plant Extracts / pharmacology*
  • Rabbits
  • Rats
  • Rats, Sprague-Dawley

Substances

  • Blood Glucose
  • Hypoglycemic Agents
  • Parasympatholytics
  • Plant Extracts
  • Alloxan