二甲双胍对asprosin和FBN1表达的影响:2型糖尿病大鼠胰岛素敏感性之外的潜在机制

Q2 Agricultural and Biological Sciences
Ali Dashtkar, Mansour Karajibani, Mohsen Saravani, Roya Zanganeh, Hamed Fanaei
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引用次数: 0

摘要

背景:阿司匹林是一种在空腹条件下释放的新型脂肪因子,可能在2型糖尿病(T2DM)的病理生理学中发挥重要作用。本研究的目的是探讨二甲双胍对雄性大鼠血清阿司匹林水平和白色脂肪组织中 FBN1 基因表达的影响:将 32 只雄性 Wistar 大鼠随机平均分为四组(n = 8):1.对照组(CON):2. 非糖尿病二甲双胍组(CON + MET):2.非糖尿病二甲双胍组(CON + MET):摄入标准食物,并接受二甲双胍(400 毫克/千克/天)治疗四周;3.糖尿病组(DM):诱发 T2DM;和 4.糖尿病二甲双胍组(DM + MET):诱发 T2DM 并接受二甲双胍(400 毫克/千克/天)治疗四周。最后,测定血清天冬氨酸水平、血脂概况、空腹血糖和胰岛素浓度。使用实时定量聚合酶链式反应(qRT-PCR)对白色脂肪组织中 FBN1 基因的表达水平进行了量化:结果:与 CON 组和 CON + MET 组相比,DM 组的血清天冬氨酸水平明显升高(P 讨论):我们对糖尿病雄性大鼠的研究结果表明,二甲双胍治疗可显著下调 FBN1 基因的表达,并降低血清中的酪氨酸水平,这表明二甲双胍的潜在治疗机制不仅仅是改善胰岛素敏感性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Metformin's impact on asprosin and FBN1 expression: Potential mechanisms beyond insulin sensitivity in type 2 diabetes in rats.

Background: Asprosin, a novel adipokine released under fasting conditions, may play a significant role in the pathophysiology of type 2 diabetes mellitus (T2DM). The objective of this study is to investigate the effects of metformin on serum asprosin levels and FBN1 gene expression in white adipose tissue in male rats.

Methods: Thirty-two male Wistar rats were randomly and equally divided into four groups (n = 8): 1. Control Group (CON): Received standard food; 2. Non-Diabetic Metformin Group (CON + MET): Received standard food and were treated with metformin (400 mg/kg/day) for four weeks; 3. Diabetic Group (DM): Induced with T2DM; and 4. Diabetic Metformin Group (DM + MET): Induced with T2DM and treated with metformin (400 mg/kg/day) for four weeks. Finally, serum asprosin levels, lipid profiles, fasting glucose, and insulin concentrations were measured. The expression level of the FBN1 gene in white adipose tissue was quantified using quantitative real-time polymerase chain reaction (qRT-PCR).

Results: Serum asprosin levels were significantly higher in the DM group compared to both the CON and CON + MET groups (P < 0.0001). However, serum asprosin levels were significantly lower in the DM + MET group than in the DM group (P = 0.0003). Additionally, the FBN1 gene expression level in white adipose tissue was significantly higher in the DM group compared to the CON group (P = 0.0053), while FBN1 gene expression was significantly lower in the DM + MET group than in the DM group (P < 0.0001). Furthermore, lipid profile, insulin resistance, and fasting blood sugar improved in the CON + MET and DM + MET groups compared to the CON and DM groups, respectively.

Discussion: Our findings in diabetic male rats reveal that metformin treatment significantly downregulates FBN1 gene expression and reduces serum asprosin levels, suggesting a potential mechanism for its therapeutic benefits beyond improving insulin sensitivity.

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来源期刊
Current Research in Pharmacology and Drug Discovery
Current Research in Pharmacology and Drug Discovery Agricultural and Biological Sciences-Animal Science and Zoology
CiteScore
6.40
自引率
0.00%
发文量
65
审稿时长
40 days
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