二甲双胍与塞来吉兰对利血平帕金森病模型的神经保护作用:α突触核蛋白与抗氧化剂对大鼠行为改变的相互作用

G. Soliman, Ghada Hashem, Monica Gamal Fawzy, Walaa M. Ibrahim
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引用次数: 0

摘要

目的:本研究旨在评价二甲双胍与selegiline(单用或联用)对利血平帕金森病模型大鼠的神经保护作用,并进一步探讨二甲双胍通过其抗氧化作用或α突触核蛋白的遗传识别作用及其对行为改变的影响作用机制。方法:共分为7组。第一种,第二种(对照组和利血平诱导)。第三、第四和第五组分别给予二甲双胍(100、250 mg/kg)和塞来吉兰(0.25 mg/kg),第六和第七组分别给予塞来吉兰和二甲双胍两种剂量。从第一天开始用药,持续21天。Morris水迷宫、吊丝和强迫游泳测试分别于第1、11、21天进行记忆变化、运动评估和抑郁评估。取血清后处死大鼠,测定血清血糖;他们的大脑被解剖,均质化以测量多巴胺、α突触核蛋白、丙二醛、还原型谷胱甘肽的水平。结果:利血平治疗组对帕金森模型的诱导作用较对照组显著,各治疗组帕金森模型均有改善,其中二甲双胍治疗组的改善效果明显优于塞来吉兰治疗组,尤其是同时使用100 mg/kg二甲双胍和塞来吉兰治疗组。塞来吉兰治疗组出现低血糖,而二甲双胍治疗组未出现低血糖。结论:低剂量二甲双胍可通过抗氧化和遗传机制增强PD患者的神经保护作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Neuroprotective Effects of Metformin Versus Selegiline on Parkinson’s Disease Model By Reserpine through the Interrelation of α Synuclein and Antioxidants on Behavioral Changes in Rats
Aim: This study aimed to assess the neuroprotective effects of metformin compared to selegiline, (each drug alone or in combination) on Parkinson’s disease model by reserpine in rats also, it was extended to investigate the mechanisms through which metformin could produce such effect either by its antioxidant effect or genetic recognized by α synuclein and such impact on behavioral changes. Methods: Seven groups were included in the study. The first, second (control and reserpine induced). The third, fourth and fifth were treated with metformin (100, 250 mg/kg), selegiline, (0.25 mg/kg), six and seventh were treated with both selegiline and metformin both doses respectively. Drugs initiated from the first day for 21 days. Morris water maze, hang wire and forced swim tests were done on days 1, 11, 21 to estimate memory changes, motor assessment and depression respectively. Rats were then sacrificed after taking serum samples to assess serum blood glucose; their brains were dissected, homogenized to measure dopamine, α synuclein, malondialdehyde, reduced glutathione levels. Results: reserpine treated group were significant compared to control proving the induction of parkinsonian model which were improved on treatment in all groups with much more improvement in those treated with metformin than selegiline especially those treated by both metformin 100 mg/kg and selegiline. Selegiline treated showed hypoglycemia that was not observed in metformin treated. Conclusion: Metformin on low dose can serve as an add on therapy with selegiline through antioxidant and genetic mechanisms to enhance the neuroprotection in PD patients.
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