Balbaa Mahmoud, El-Zeftawy Marwa, Ghareeb Doaa, Taha Nabil, Mandour Abdel Wahab
Biochemistry Department, Faculty of Science, Alexandria University, Alexandria 21511, Egypt.
Biochemistry Department, Faculty of Veterinary Medicine, Alexandria University, Alexandria, Egypt.
Oxid Med Cell Longev. 2016;2016:2492107. doi: 10.1155/2016/2492107. Epub 2016 Aug 4.
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.
黑孜然(黑种草)“NS”或其种子具有许多药理活性,如抗氧化、抗癌、抗高血压和抗糖尿病特性。在本研究中,用链脲佐菌素诱导建立糖尿病大鼠模型,给予高脂饮食,并每日用黑孜然籽油(NSO)进行治疗,以研究其对血糖、血脂谱、氧化应激参数以及一些胰岛素受体诱导信号分子基因表达的影响。该治疗还联合了一些药物(二甲双胍和格列美脲)以及胰岛素受体抑制剂I-OMe-AG538。与未接受NSO的大鼠相比,给予NSO显著诱导了胰岛素受体的基因表达。此外,它上调了胰岛素样生长因子-1和磷脂酰肌醇-3激酶的表达,而下调了ADAM-17的表达。通过对TIMP-3含量的分析证实了ADAM-17的表达情况。此外,NSO显著降低了血糖水平、血脂谱成分、氧化应激参数、血清胰岛素/胰岛素受体比值以及肿瘤坏死因子-α,证实NSO具有抗糖尿病活性。因此,在我们的大鼠模型中每日给予NSO治疗表明,NSO在糖尿病管理以及改善胰岛素诱导信号方面具有潜力。