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Alleviating Effects of Bushen-Yizhi Formula on Ibotenic Acid-Induced Cholinergic Impairments in Rat

机译:补肾益智方对异戊二烯酸致胆碱能障碍的缓解作用

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This study explored the curative effect and underlying mechanisms of a traditional Chinese medicine compound prescription, Bushen-Yizhi formula (BSYZ), in ibotenic acid (IBO)-induced rats. Morris water maze and novel object recognition tests showed that BSYZ significantly improved spatial and object memory. Brain immunohistochemistry staining showed that BSYZ significantly up-regulated expression of choline acetyltransferase (ChAT) and nerve growth factor (NGF) in the hippocampus and cortex. The protein tyrosine kinase high-affinity receptor TrkA was slightly increased in the hippocampus and cortex, and significantly enhanced in the nucleus basalis of Meynert (NBM) after BSYZ intervention. The immunoreactivity of the p75 low-affinity receptor in BSYZ-treated rats was significantly strengthened in the cortex. Similar expression trends of nerve growth factor (NGF), TrkA, and p75 mRNA were observed in the hippocampus and cortex. Additionally, BSYZ reversed IBO-induced disorders of acetylcholine (ACh) levels, ChAT, and cholinesterase (ChE) in the cortex, which was consistent with the changes in mRNA levels of ChAT and acetylcholinesterase (AChE). Expression of ChAT and AChE proteins and mRNA in the hippocampus was up-regulated, whereas the apoptosis-relative protein cleaved caspase-3 was decreased after administration of BSYZ. Moreover, changes in cell death were confirmed by histological morphology. Thus, the results indicated that the BSYZ formula could ameliorate memory impairments in IBO-induced rats, and it exerted its therapeutic action probably by modulating cholinergic pathways, NGF signaling, and anti-apoptosis. Overall, it is suggested that the BSYZ formula might be a potential therapeutic approach for the treatment of Alzheimer's disease (AD) and other cholinergic impairment-related diseases.
机译:这项研究探讨了传统中药复方补肾益智配方(BSYZ)在依波酸(IBO)诱导的大鼠中的疗效和潜在机制。莫里斯水迷宫和新颖的物体识别测试表明,BSYZ可显着改善空间和物体记忆。脑免疫组织化学染色显示,BSYZ明显上调海马和皮质中胆碱乙酰转移酶(ChAT)和神经生长因子(NGF)的表达。在BSYZ干预后,蛋白酪氨酸激酶高亲和力受体TrkA在海马和皮质中略有增加,在Meynert(NBM)的基底核中显着增强。在BSYZ治疗的大鼠中,p75低亲和力受体的免疫反应性在皮质中显着增强。在海马和皮质中观察到神经生长因子(NGF),TrkA和p75 mRNA的相似表达趋势。此外,BSYZ逆转了IBO诱导的皮质中乙酰胆碱(ACh)水平,ChAT和胆碱酯酶(ChE)的紊乱,这与ChAT和乙酰胆碱酯酶(AChE)mRNA水平的变化一致。给予BSYZ后海马ChAT和AChE蛋白及mRNA的表达上调,而凋亡相关蛋白裂解的caspase-3减少。此外,通过组织学形态学​​证实了细胞死亡的变化。因此,该结果表明,BSYZ配方可以减轻IBO诱导的大鼠的记忆障碍,并且可能通过调节胆碱能途径,NGF信号传导和抗凋亡发挥其治疗作用。总体而言,建议BSYZ公式可能是治疗阿尔茨海默氏病(AD)和其他胆碱能减退相关疾病的潜在治疗方法。

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