Nigella Sativa Inhibits Intestinal Glucose Absorption and Improves Glucose Tolerance in Rats
Overview
Authors
Affiliations
Aim Of The Study: Nigella sativa L. (Ranunculaceae) seeds have been used traditionally for centuries, notably for treating diabetes.
Materials And Methods: We studied the effects of the crude aqueous extract of Nigella sativa seeds on intestinal glucose absorption in vitro using a short-circuit current technique and in vivo using an oral glucose tolerance test.
Results: The aqueous extract of Nigella sativa (0.1 pg/ml to 100 ng/ml) exerted dose-dependent inhibition of sodium-dependent glucose transport across isolated rat jejunum. Maximal inhibition exceeded 80% and IC50 was close to 10 pg/ml. An oral glucose tolerance test was carried out in rats after the initial dose and after a 6-week treatment of Nigella sativa (2 g/(kg day)), and compared to metformin (300 mg/(kg day)). Chronic Nigella sativa treatment improved glucose tolerance as efficiently as metformin. Nigella sativa and metformin also reduced body weight without any toxic effect.
Conclusions: To our knowledge, this is the first demonstration that Nigella sativa directly inhibits the electrogenic intestinal absorption of glucose in vitro. Together with the observed improvement of glucose tolerance and body weight in rats after chronic oral administration in vivo, these effects further validate the traditional use of Nigella sativa seeds against diabetes.
Ethnopharmacological Study of and Its Antidiabetic Effect in Rats.
Estevez-Carmona M, Pablo-Perez S, Almanza-Cruz J, Melendez-Camargo M, Arrieta-Baez D, Cristobal-Luna J Plants (Basel). 2024; 13(22).
PMID: 39599444 PMC: 11598156. DOI: 10.3390/plants13223235.
A Comprehensive Review of Moroccan Medicinal Plants for Diabetes Management.
Boutaj H Diseases. 2024; 12(10).
PMID: 39452489 PMC: 11507334. DOI: 10.3390/diseases12100246.
ALSuhaymi N Oxid Med Cell Longev. 2024; 2024:5594090.
PMID: 39156220 PMC: 11330337. DOI: 10.1155/2024/5594090.
Demirel S World J Diabetes. 2024; 15(6):1122-1141.
PMID: 38983824 PMC: 11229960. DOI: 10.4239/wjd.v15.i6.1122.
Al Dhaheri A, Alkhatib D, Feehan J, Ismail L, Apostolopoulos V, Stojanovska L Nutrients. 2024; 16(11).
PMID: 38892617 PMC: 11175078. DOI: 10.3390/nu16111685.