Liao Zuozhuang, Wang Jinni, Tan Hongdi, Wei Limei
Affiliated Hospital of YouJiang Medical University for Nationalities, Baise, Guangxi 533000, PR China; The Second Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi 530007, PR China.
YouJiang Medical University for Nationalities, Baise, Guangxi 533000, PR China.
Gene. 2017 Sep 5;627:519-523. doi: 10.1016/j.gene.2017.07.014. Epub 2017 Jul 8.
In the current study, we aimed to investigate the potential hypoglycemic bioactivity of cinnamon extracts (CES) on streptozotocin (STZ)-induced hyperglycemia in mice. In biological methods, glucose metabolic ability of all mice was evaluated by glucose tolerance testing (GTT). Blood levels of pancreas-produced insulin, glucagon, inflammation-associated interleukin-6 (IL-6), tumor necrosis factor-α (TNF-α) were determined via enzyme-linked immunosorbent assay (ELISA). In gene level, intrapancreatic mRNA expressions of insulin, TNF-α and nuclear-factor kappa B (NF-κB) were assayed by reverse transcription polymerase chain reaction (RT-PCR). Meanwhile, intracellular insulin-immunoactive cells in the pancreas were analyzed by using immunohistochemical staining. In addition, the protein levels of intrapancreatic NF-κB, IκB (p-IκB) and IKK were tested by western blotting. As a result, CES-treated mice showed increased body weight, blood glucose and insulin, reduced IL-6 and TNF-α contents in sera. Further, the TNF-α and NF-κB mRNA expressions in the CES-treated pancreas were down-regulated at a dose-dependent manner, while insulin mRNA was elevated. Moreover, the reduced intrapancreatic NF-κB, IκB (p-IκB) and IKK expression were observed in CES-treated pancreas, respectively. Taken together, our current findings indicate that CES-mediated intrapancreatic cytoprotection is linked to the molecular mechanism that may be through inhibiting inflammatory stress and promoting insulin secretion in the pancreas.
在本研究中,我们旨在探究肉桂提取物(CES)对链脲佐菌素(STZ)诱导的小鼠高血糖的潜在降血糖生物活性。在生物学方法中,通过葡萄糖耐量试验(GTT)评估所有小鼠的葡萄糖代谢能力。通过酶联免疫吸附测定(ELISA)测定胰腺产生的胰岛素、胰高血糖素、炎症相关白细胞介素-6(IL-6)、肿瘤坏死因子-α(TNF-α)的血液水平。在基因水平上,通过逆转录聚合酶链反应(RT-PCR)检测胰腺内胰岛素、TNF-α和核因子κB(NF-κB)的mRNA表达。同时,使用免疫组织化学染色分析胰腺内胰岛素免疫活性细胞。此外,通过蛋白质印迹法检测胰腺内NF-κB、IκB(p-IκB)和IKK的蛋白质水平。结果显示,CES处理的小鼠体重、血糖和胰岛素增加,血清中IL-6和TNF-α含量降低。此外,CES处理的胰腺中TNF-α和NF-κB的mRNA表达以剂量依赖性方式下调,而胰岛素mRNA升高。此外,在CES处理的胰腺中分别观察到胰腺内NF-κB、IκB(p-IκB)和IKK表达降低。综上所述,我们目前的研究结果表明,CES介导的胰腺内细胞保护作用与可能通过抑制炎症应激和促进胰腺胰岛素分泌的分子机制有关。