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在链脲佐菌素诱导的 2 型糖尿病小鼠中表现出抗糖尿病潜力:一项联合生化和体内研究。

Exhibits Anti-Diabetic Potential in Streptozotocin-Induced Diabetes Mellitus Type 2 Mice: A Combined Biochemical and In Vivo Study.

机构信息

Department of Healthcare Biotechnology, Atta-Ur-Rahman School of Applied Biosciences (ASAB), National University of Sciences and Technology (NUST), Islamabad 44000, Pakistan.

出版信息

Nutrients. 2022 Aug 29;14(17):3561. doi: 10.3390/nu14173561.

Abstract

Type 2 diabetes mellitus (T2DM) is a complex metabolic disorder that is characterized by hyperglycemia, insulin resistance, and lack of insulin production. It has been previously reported that has therapeutic potential against many diseases. To investigate the antidiabetic action of , this study aimed to analyze its restorative impact in diabetic mice, in which it was administered in diet. Diabetes was induced in BALB/c mice fed with a high-fat diet and two intraperitoneal injections of streptozotocin. With the onset of diabetes, the mice were administered daily with aqueous extract of (500 mg/kg/d and 800 mg/kg/d) for 4 weeks. Body weight and fasting blood glucose levels were measured after every 1 week of the treatment. Subsequently, intraperitoneal glucose tolerance and insulin tolerance tests were conducted. In addition, liver tissue was isolated for assessment in terms of levels of gene expression of the , , and gene. Treatment with the aqueous extract of was found to be significantly effective in controlling hyperglycemia and improving glucose and insulin tolerance. Predictable with these impacts, the extract of upregulated the expression at the mRNA level, as well as upregulating the expression of and gene. Histopathological examination of the liver, kidney, and pancreas also revealed the restorative impact in terms of cellular morphology. The results hence demonstrated that oral administration of aqueous extract of can potentially attenuate hyperglycemia in the liver muscle of streptozotocin (STZ)-induced diabetic mice via and upregulation.

摘要

2 型糖尿病(T2DM)是一种复杂的代谢紊乱疾病,其特征是高血糖、胰岛素抵抗和胰岛素缺乏。先前有报道称,[药物名称]对许多疾病都具有治疗潜力。为了研究[药物名称]的抗糖尿病作用,本研究旨在分析其在糖尿病小鼠中的恢复作用,在该研究中,[药物名称]以饮食的形式给予。通过给予高脂肪饮食和两次链脲佐菌素腹腔注射,在 BALB/c 小鼠中诱导糖尿病。在糖尿病发作时,每天给予[药物名称]的水提物(500mg/kg/d 和 800mg/kg/d)4 周。在治疗的每 1 周后测量体重和空腹血糖水平。随后,进行腹腔内葡萄糖耐量和胰岛素耐量试验。此外,还分离肝脏组织,评估 、 和 基因的表达水平。[药物名称]的水提物的治疗被发现可显著有效控制高血糖并改善葡萄糖和胰岛素耐量。可预测的是,[药物名称]的提取物在 mRNA 水平上上调了 的表达,同时还上调了 和 基因的表达。肝、肾和胰腺的组织病理学检查也显示出在细胞形态方面的恢复作用。因此,研究结果表明,口服[药物名称]的水提物可通过上调 和 来潜在减轻链脲佐菌素(STZ)诱导的糖尿病小鼠肝脏中的高血糖。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/50d7/9460602/43973d068966/nutrients-14-03561-g001.jpg

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