使用不同抗糖尿病药物控制血糖对实验诱导的 2DM 型糖尿病患者认知功能的影响:一项比较研究

Omnia Ameen, Safaa M. Saleh, Gerges S. Yousef, R. Yassien, Nasra D. Raslan, Essam O. Hendya
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摘要

背景:神经认知障碍被认为是 2 型糖尿病(T2DM)的第四大微血管并发症。目的:比较血糖控制对糖尿病大鼠认知功能的影响:比较使用不同抗糖尿病药物控制血糖对糖尿病大鼠认知功能的影响。材料与方法:将 50 只雄性白化大鼠平均分为三组:对照组、捷诺美组、糖尿病未治疗组、糖尿病+胰岛素组和糖尿病+捷诺美组。4周后,使用莫里斯水迷宫(MWM)和Y迷宫测试进行神经认知评估。收集血液样本以评估血糖状态、血脂状况和总抗氧化能力水平(TAC)。提取大鼠大脑。右半脑用于测量脂质过氧化标记物(MDA)、肿瘤坏死因子α(TNF-α)、超氧化物歧化酶(SOD)和白细胞介素1B(IL-B)。左半部分用于海马组织的组织病理学研究。结果:糖尿病组的 FBG、HBA1C、HOMA-IR、总胆固醇、甘油三酯、MDA、TNF-α 和 IL-1B 显著升高,而血清胰岛素、高密度脂蛋白、TAC 和 SOD 下降。糖尿病大鼠的神经认知功能也明显受损,海马发生退行性改变。与糖尿病+胰岛素组相比,糖尿病+捷诺美组在生物标志物测量和神经行为测试方面有显著改善,海马组织结构得到恢复。然而,糖尿病+ Janumet 组与糖尿病+ 胰岛素组在血脂指标方面的差异不明显。对照组和捷诺美组在所有测量参数方面均无显著差异。结论胰岛素和杰诺迈特药物都能缓解与 T2DM 相关的代谢、神经认知障碍和海马体变化。然而,与胰岛素治疗相比,Janumet 治疗的改善效果更为明显。Janumet成分的协同降糖、抗氧化和抗炎作用可能是这种改善的原因。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effect of Glycemic Control Using Different Antidiabetic Drugs on Cognitive Functions in Experimentally-Induced Type 2DM: A Comparative Study
Background : Neurocognitive impairment is recognized as the fourth microvascular complications of type 2 diabetes mellitus (T2DM). Objectives: To compare the effect of glycemic control on cognitive functions in diabetic rats by using different anti-diabetic drugs. Materials and Methods: Fifty male albino rats were equally categorized into: Control group, Janumet group, Diabetic non-treated group, Diabetic+Insulin group and Diabetic+Janumet group. At the end of 4 weeks, neurocognitive assessment was done by using Morris water maze (MWM) and Y-maze tests. Blood samples were collected to estimate glycemic state, lipid profile and total antioxidant capacity level (TAC). Rats' brains were extracted. The right half of the brain was utilized for lipid peroxidation marker (MDA), tumor necrosis factor alpha (TNF-α), superoxide dismutase (SOD), and interleukin 1B (IL-B) measurement. The left half was utilized for histopathological study of the hippocampal tissue. Results : Diabetic group showed significant increase in FBG, HBA1C, HOMA-IR, total cholesterol, triglyceride, MDA, TNF-alpha and IL-1B, and decrease in serum insulin, HDL, TAC and SOD. Neurocognitive impairment and hippocampal degenerative changes were also obvious in diabetic rats. Diabetic+ Janumet group demonstrated significant improvement in the measured biomarkers and neurobehavioral tests with restoration of the hippocampal tissue structure in comparison with Diabetic+ Insulin group. However, there was an insignificant difference in lipid profile markers between Diabetic+ Janumet group and Diabetic+ Insulin group. Insignificant difference between Control and Janumet groups regarding all measured parameters was detected. Conclusion: Both insulin and Janumet drugs alleviates the metabolic, neurocognitive impairment and hippocampal changes associated with T2DM. However, the improvement was more pronounced with Janumet treatment than insulin treatment. The synergistic hypoglycemic, anti-oxidant and anti-inflammatory effects of Janumet's components may account for this improvement.
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