Nigella sativa Relieves the Altered Insulin Receptor Signaling in Streptozotocin-Induced Diabetic Rats Fed with a High-Fat Diet.
Mahmoud BalbaaMarwa El-ZeftawyDoaa Ahmad GhareebNabil TahaAbdel Wahab MandourPublished in: Oxidative medicine and cellular longevity (2016)
The black cumin (Nigella sativa) "NS" or the black seeds have many pharmacological activities such as antioxidant, anticarcinogenic, antihypertensive, and antidiabetic properties. In this work, streptozotocin-induced diabetic rats fed with a high-fat diet were treated daily with NS oil (NSO) in order to study the effect on the blood glucose, lipid profile, oxidative stress parameters, and the gene expression of some insulin receptor-induced signaling molecules. This treatment was combined also with some drugs (metformin and glimepiride) and the insulin receptor inhibitor I-OMe-AG538. The administration of NSO significantly induced the gene expression of insulin receptor compared to rats that did not receive NSO. Also, it upregulated the expression of insulin-like growth factor-1 and phosphoinositide-3 kinase, whereas the expression of ADAM-17 was downregulated. The expression of ADAM-17 is corroborated by the analysis of TIMP-3 content. In addition, the NSO significantly reduced blood glucose level, components of the lipid profile, oxidative stress parameters, serum insulin/insulin receptor ratio, and the tumor necrosis factor-α, confirming that NSO has an antidiabetic activity. Thus, the daily NSO treatment in our rat model indicates that NSO has a potential in the management of diabetes as well as improvement of insulin-induced signaling.
Keyphrases
- diabetic rats
- oxidative stress
- type diabetes
- glycemic control
- high fat diet
- blood glucose
- gene expression
- insulin resistance
- poor prognosis
- ischemia reperfusion injury
- dna damage
- induced apoptosis
- high glucose
- cardiovascular disease
- blood pressure
- adipose tissue
- physical activity
- metabolic syndrome
- risk assessment
- weight loss
- zika virus
- quantum dots
- visible light
- drug induced
- combination therapy
- highly efficient