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丙泊酚麻醉后米诺环素对老年大鼠认知障碍、海马炎症反应及海马阿尔茨海默病相关蛋白的影响。

Effects of Minocycline on Cognitive Impairment, Hippocampal Inflammatory Response, and Hippocampal Alzheimer's Related Proteins in Aged Rats after Propofol Anesthesia.

机构信息

Department of Neurology, Tianjin Fourth Central Hospital, Tianjin 300140, China.

Department of Neurology, Xianyang Hospital of Yan 'an University, Xianyang Shanxi 712000, China.

出版信息

Dis Markers. 2022 Apr 26;2022:4709019. doi: 10.1155/2022/4709019. eCollection 2022.

Abstract

The aim of this study was to evaluate the effect of minocycline preadministration on cognitive dysfunction, hippocampal inflammatory response, and hippocampal senile dementia-related proteins induced by propofol anesthesia in aged rats. Sixty male SD rats, aged 20 months and weighing 340-410 g, were randomly divided into three groups: normal saline (NC) group, propofol group (prop), and minocycline (M) group. Prop group rats were injected intraperitoneally with 100 mg/kg propofol. The rats in group M were injected intraperitoneally with 50 mg/kg minocycline 30 minutes before injection of 100 mg/kg propofol, and the rest were the same as prop group. The rats in NC group were received intraperitoneal injection of the same amount of normal saline. The results indicated that compared with group C, the expressions of GSK-3, acetyl-NF-B (Lys310), Tau, and Amlyoid-beta were upregulated, the levels of TNF-, IL-1, and IL-6 were increased, the escape incubation period was prolonged, and the exploration time was shortened in prop group, while the expression of GSK-3, acetyl-NF-B (Lys310), Tau, and Amlyoid-beta in minocycline group was downregulated, the levels of TNF-, IL-1, and IL-6 were decreased, the escape incubation period was shortened, and the exploration time was shortened. In conclusion, preadministration of minocycline can improve cognitive impairment induced by propofol anesthesia in aged rats, and its mechanism of action may be related to minocycline inhibiting hippocampal inflammatory reaction and downregulating the expression of GSK-3, acetyl-NF-B (Lys310), Tau, and Amlyoid-beta proteins in hippocampus.

摘要

本研究旨在评估米诺环素预先给药对丙泊酚麻醉诱导的老年大鼠认知功能障碍、海马炎性反应和海马与衰老性痴呆相关蛋白的影响。

将 60 只 20 月龄、体重 340-410g 的雄性 SD 大鼠随机分为三组:生理盐水(NC)组、丙泊酚(prop)组和米诺环素(M)组。prop 组大鼠腹腔注射 100mg/kg 丙泊酚。M 组大鼠在注射 100mg/kg 丙泊酚前 30 分钟腹腔注射 50mg/kg 米诺环素,其余与 prop 组相同。NC 组大鼠接受等量的生理盐水腹腔注射。

结果表明,与 C 组相比,prop 组大鼠的 GSK-3、乙酰-NF-B(Lys310)、Tau 和 Amlyoid-beta 表达上调,TNF-、IL-1 和 IL-6 水平升高,逃避潜伏期延长,探索时间缩短,而米诺环素组大鼠的 GSK-3、乙酰-NF-B(Lys310)、Tau 和 Amlyoid-beta 表达下调,TNF-、IL-1 和 IL-6 水平降低,逃避潜伏期缩短,探索时间延长。

综上所述,预先给予米诺环素可改善丙泊酚麻醉诱导的老年大鼠认知障碍,其作用机制可能与米诺环素抑制海马炎性反应和下调海马中 GSK-3、乙酰-NF-B(Lys310)、Tau 和 Amlyoid-beta 蛋白表达有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ce8/9064516/0c16050f51b5/DM2022-4709019.001.jpg

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