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首页> 外文期刊>International Journal of Neuroscience >Melatonin premedication attenuates isoflurane anesthesia-induced β-amyloid generation and cholinergic dysfunction in the hippocampus of aged rats
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Melatonin premedication attenuates isoflurane anesthesia-induced β-amyloid generation and cholinergic dysfunction in the hippocampus of aged rats

机译:褪黑素的前药治疗可减轻异氟烷麻醉引起的老龄大鼠海马中β-淀粉样蛋白生成和胆碱能功能障碍

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摘要

Melatonin plays an important role in aging and relevant neurodegeneration as an antioxidant and neuroprotector. It can interact with β-amyloid (Aβ) generation, inhibit formation of β-sheet and amyloid fibrils, modulate apoptosis, and protect cholinergic system function in Alzheimer's disease animal model. Recently, its effects on anesthetic-induced neurodegeneration have received more attention, and in this investigation, we explored whether melatonin can attenuate Aβ1-40 generation and cholinergic dysfunction in the hippocampus of aged rats induced by isoflurane through enzyme-linked immunosorbent assay, Western blot, immunohistochemistry, and immunofluorescence. The results showed that isoflurane increased Aβ1-40 generation and caused cholinergic dysfunction through decreasing choline acetyltransferase (ChAT) expression in the hippocampus in a dose-dependent way, and intraperitoneal melatonin premedication attenuated the neurodegeneration through inhibiting Aβ1-40 generation and increasing ChAT expression, and its effects were more obvious in high-concentration isoflurane group. Collectively, our results provide evidence for the therapeutic value of melatonin on isoflurane-induced neurodegeneration, including Aβ1-40 generation and cholinergic dysfunction, and further work is necessary to clarify its target sites and detailed mechanisms.
机译:褪黑素作为抗氧化剂和神经保护剂,在衰老和相关的神经退行性变中起重要作用。它可以与β-淀粉样蛋白(Aβ)生成相互作用,抑制β-折叠和淀粉样蛋白原纤维的形成,调节细胞凋亡,并保护阿尔茨海默氏病动物模型中的胆碱能系统功能。近年来,其对麻醉药引起的神经变性的作用已引起更多关注,在这项研究中,我们通过酶联免疫吸附法,蛋白质印迹法研究了褪黑激素是否能减轻异氟烷所致衰老大鼠海马中Aβ1-40的生成和胆碱能功能障碍。 ,免疫组织化学和免疫荧光。结果表明,异氟烷通过减少海马中胆碱乙酰转移酶(ChAT)的表达来增加Aβ1-40的生成并引起胆碱能功能障碍,并且腹膜内褪黑素的预处理通过抑制Aβ1-40的生成和增加ChAT的表达来减轻神经变性。在高浓度异氟醚组中其作用更为明显。总的来说,我们的结果提供了褪黑激素对异氟烷诱导的神经变性包括Aβ1-40生成和胆碱能功能障碍的治疗价值的证据,还需要进一步的工作来阐明其靶位和详细的机制。

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