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A Soxhlet Extract of Gongronema latifolium Retains Moderate Blood Glucose Lowering Effect and Produces Structural Recovery in the Pancreas of STZ-Induced Diabetic Rats.

Authors :
Al-Hindi B
Yusoff NA
Atangwho IJ
Ahmad M
Asmawi MZ
Yam MF
Source :
Medical sciences (Basel, Switzerland) [Med Sci (Basel)] 2016 Apr 25; Vol. 4 (2). Date of Electronic Publication: 2016 Apr 25.
Publication Year :
2016

Abstract

Background: Gongronema latifolium Benth. (GL) possesses considerable glucose lowering effects able to be utilized on a large-scale. This paper investigates the effects of a Soxhlet extract on hyperglycemia, Langerhans islets and glucose uptake by abdominal muscles.<br />Methods: Ethanol and a Soxhlet apparatus were used to obtain GL ethanolic Soxhlet extract (GLES). It was then administered to randomly-segregated male Sprague-Dawley , normal and STZ-induced diabetic rats, using oral gavage to evaluate blood glucose levels (BGLs), serum lipid profile, insulin levels and the pancreas post-treatment.<br />Results: GLES significantly ( p < 0.05) decreased BGLs of normal rats in glucose tolerance testing at a dose of 2 g/kg b.w. but failed to do so in diabetic rats undergoing acute 7-h treatment. Given twice-daily, 1 g/kg b.w. of GLES moderately controlled diabetic BGLs starting from day 10. After 14 days of treatment, 1 g/kg and 0.5 g/kg b.w. of GLES caused 44% and 50% respective increases in the average area of Langerhans islets compared to DC. Using isolated rat abdominal muscle, GLES was found to be a mild insulin-sensitizer. GC-MS analysis revealed the presence of the known glucose-lowering phytosterol, Sitostenone.<br />Conclusion: Despite retaining moderate antidiabetic activity, Soxhlet extraction of Gongronema latifolium probably leads to the destruction of active heat-liable compounds.

Details

Language :
English
ISSN :
2076-3271
Volume :
4
Issue :
2
Database :
MEDLINE
Journal :
Medical sciences (Basel, Switzerland)
Publication Type :
Academic Journal
Accession number :
29083373
Full Text :
https://doi.org/10.3390/medsci4020009