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肉桂醛通过调节大鼠脂肪组织和肝组织自噬过程改善 STZ 诱导的糖尿病。

Cinnamaldehyde ameliorates STZ-induced diabetes through modulation of autophagic process in adipocyte and hepatic tissues on rats.

机构信息

Department of Biochemistry, Medical Research Institute, Alexandria University, 165 El-Horreya Avenue, EL-Hadara, POB 21561, Alexandria, Egypt.

出版信息

Sci Rep. 2024 May 2;14(1):10053. doi: 10.1038/s41598-024-60150-2.

Abstract

Type 2 diabetes mellitus is a worldwide public health issue. In the globe, Egypt has the ninth-highest incidence of diabetes. Due to its crucial role in preserving cellular homeostasis, the autophagy process has drawn a lot of attention in recent years, Therefore, the purpose of this study was to evaluate the traditional medication metformin with the novel therapeutic effects of cinnamondehyde on adipocyte and hepatic autophagy in a model of high-fat diet/streptozotocin-diabetic rats. The study was conducted on 40 male albino rats, classified into 2 main groups, the control group and the diabetic group, which was subdivided into 4 subgroups (8 rats each): untreated diabetic rats, diabetic rats received oral cinnamaldehyde 40 mg/kg/day, diabetic rats received oral metformin 200 mg/kg/day and diabetic rats received a combination of both cinnamaldehyde and metformin daily for 4 weeks. The outcomes demonstrated that cinnamaldehyde enhanced the lipid profile and glucose homeostasis. Moreover, Cinnamaldehyde had the opposite effects on autophagy in both tissues; by altering the expression of genes that control autophagy, such as miRNA 30a and mammalian target of rapamycin (mTOR), it reduced autophagy in adipocytes and stimulated it in hepatic tissues. It may be inferred that by increasing the treatment efficacy of metformin and lowering its side effects, cinnamaldehyde could be utilized as an adjuvant therapy with metformin for the treatment of type 2 diabetes.

摘要

2 型糖尿病是一个全球性的公共卫生问题。在全球范围内,埃及的糖尿病发病率位居第九。由于自噬过程在维持细胞内稳态方面的重要作用,近年来引起了广泛关注。因此,本研究旨在评估传统药物二甲双胍与新型肉桂醛在高脂肪饮食/链脲佐菌素诱导的糖尿病大鼠模型中对脂肪细胞和肝自噬的治疗效果。该研究共纳入 40 只雄性白化大鼠,分为 2 个主要组,对照组和糖尿病组,糖尿病组又分为 4 个亚组(每组 8 只):未治疗的糖尿病大鼠、每天给予肉桂醛 40mg/kg 的糖尿病大鼠、每天给予二甲双胍 200mg/kg 的糖尿病大鼠以及联合给予肉桂醛和二甲双胍的糖尿病大鼠。结果表明,肉桂醛改善了血脂谱和葡萄糖稳态。此外,肉桂醛对两种组织中的自噬均产生了相反的影响;通过改变控制自噬的基因(如 miRNA 30a 和雷帕霉素靶蛋白(mTOR))的表达,肉桂醛减少了脂肪细胞中的自噬,刺激了肝组织中的自噬。可以推断,通过提高二甲双胍的治疗效果并降低其副作用,肉桂醛可以作为二甲双胍治疗 2 型糖尿病的辅助治疗药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c2f/11066029/a1c47b2e37ed/41598_2024_60150_Fig1_HTML.jpg

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