抗阻训练和叶酸纳米脂质体对阿尔茨海默病大鼠脑海马多巴胺受体的同步影响

F. Nameni, Fatemeh Firuzmand
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引用次数: 0

摘要

背景:阿尔茨海默病是伴有神经细胞丧失的进行性痴呆。体育活动和纳米药物补充剂的使用可能会阻止阿尔茨海默氏症的发展。本研究旨在探讨抗阻训练和叶酸纳米脂质体对阿尔茨海默病大鼠海马组织D1和D2受体表达的影响。方法:从巴斯德研究所制备8周龄雄性Wistar大鼠33只,随机分为5组(健康对照组、阿尔茨海默病对照组、阿尔茨海默病+阻力训练组、阿尔茨海默病+叶酸纳米脂质体组、阿尔茨海默病+阻力训练组)。诱导阿尔茨海默氏症,并注射叶酸纳米脂质体作为补充。这些动物被麻醉,并在最后一次训练后分析海马体。最后,采用单因素方差分析估计组间差异(P≤0.05)。结果:单因素方差分析结果显示,各组D1 mRNA和D2 mRNA含量差异有统计学意义(P≤0.000)。根据Bonferroni事后检验结果,对照组与阿尔茨海默病、阿尔茨海默病+阻力训练和阿尔茨海默病+叶酸纳米脂质体之间存在显著差异。同样,阿尔茨海默病组与阿尔茨海默病+抗阻训练、阿尔茨海默病+抗阻训练+叶酸纳米脂质体之间也存在显著差异(P≤0.05)。结论:抗阻训练和叶酸纳米脂质体可改变阿尔茨海默病诱导后脑内D1和D2的含量。这些变化可能部分是由于身体活动和纳米药物在预防或减少病理条件的有害影响方面的协同作用。在神经退行性疾病的活动和运动中,炎症因子似乎与神经营养因子有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Simultaneous Effect of Resistance Training and Folate Nano-liposome on Dopamine Receptors in the Brain Hippocampus of Alzheimer’s Rats
Background: Alzheimer’s is progressive dementia with loss of nerve cells. Physical activity and the use of nano-pharmaceutical supplements may prevent the progression of Alzheimer’s. The aim of this study was to investigate the effects of resistance training and Folate nano-liposome on the expression of D1 and D2 receptors in the hippocampal tissue of Alzheimer’s rats. Methods: Thirty-three male Wistar rats at the age of eight weeks were prepared from Pasteur Institute and randomly divided into 5 groups (healthy control, Alzheimer’s control, Alzheimer+resistance training, Alzheimer+Folate nano-liposomes, and Alzheimer+resistance training+Folate nano-liposomes). Alzheimer’s was induced, and Folate nano-liposomes were injected as a supplement. The animals were anesthetized, and the hippocampus was analyzed after the last training session. Eventually, a one-way ANOVA test was used to estimate the differences between groups (P≤0.05). Results: The results of one-way ANOVA showed a significant difference between the groups in terms of D1 mRNA and D2 mRNA (P≤0.000). Based on the results of the Bonferroni post hoc test, there was a significant difference between the control group and the Alzheimer’s, Alzheimer’s+resistance training, and Alzheimer’s+Folate nano-liposomes. Similarly, a significant difference was found between the Alzheimer’s group and Alzheimer’s+resistance training and Alzheimer’s+resistance training+Folate nano-liposomes (P≤0.05). Conclusion: Resistance training and Folate nano-liposomes changed the content of D1 and D2 in the brain after Alzheimer’s induction. These changes may be partly due to the synergistic effect of physical activity and nano-pharmaceuticals on preventing or reducing the detrimental effects of pathological conditions. Inflammatory factors appear to be associated with neurotrophic factors during activity and exercise in neurodegenerative diseases.
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