Effects of Apilarnil on Type 2 Diabetes-Induced IRS-1/PI3K/Akt Mediated Insulin Resistance in Male Rats

阿皮拉尼尔对2型糖尿病诱导的雄性大鼠IRS-1/PI3K/Akt介导的胰岛素抵抗的影响

阅读:1

Abstract

Diabetes is one of the most important chronic and metabolic health problems seen as an epidemic of the 21st century. The incidence of diabetes is gradually increasing, and different methods are used to treat it. Apitherapy products such as honey, propolis, royal jelly, and bee venom can be used as an alternative to treat diabetes and reduce symptoms. One of these apitherapy products is Apilarnil, which has not yet become popular. The hypolipidemic, hepatoprotective, androgenic, anabolic, and immune system enhancing properties of Apilarnil indicate that it may be effective in the treatment of type 2 diabetes or in reducing the symptoms. The study aimed to determine the therapeutic effect of Apilarnil on insulin resistance and the possible underlying mechanism. In the study, 40 8 week-old male Wistar albino rats were used. The rats were divided into 5 groups as Control, Diabetes, Diabetes + Api1 (125 mg/kg/day lyophilized Apilarnil), Diabetes + Api2 (250 mg/kg/day lyophilized Apilarnil) and Diabetes + Api3 (500 mg/kg/day lyophilized Apilarnil). Each group consisted of 8 rats. Apilarnil doses were administered by oral gavage with 1 mL of distilled water, 5 days in a week, during the last 6 weeks. The levels of Nrf2, NF-κB, TNF-α, total IRS-1, p-IRS-1, PI3K p85, total Akt, p-Akt, IL-1B, and GLUT4 proteins were determined in target tissues by Western blotting. Alanine aminotransferase (ALT), aspartate aminotransferase (AST), high-density lipoprotein (HDL), low-density lipoprotein (LDL), total cholesterol (TC), and triglyceride (TG) levels were detected in the serum. Serum superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GSH-Px), malondialdehyde (MDA), and insulin levels were determined by the ELISA method. According to the data obtained in the study, the application of Apilarnil, compared to the diabetes group, balanced some findings, but did not demonstrate a fully antidiabetic effect.

特别声明

1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。

2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。

3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。

4、投稿及合作请联系:info@biocloudy.com。