牙买加水青叶提取物对N,N ' -二甲基-4,4 ' -二氯化联吡啶诱导的成年Wistar大鼠帕金森病海马和前额皮质的改善作用

H. Akpan, E. M. Adesegun, M. Adebola, M. Onasanya, J. Enya, M. Amadi
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引用次数: 0

摘要

帕金森病(PD)是继阿尔茨海默病之后的世界第二大神经退行性疾病,其特征是多巴胺能神经元的退化。本研究旨在评估牙买加水青树叶提取物对百草枯诱导帕金森病海马和前额叶皮层的组织学和形态学特性的影响。雄性成年Wistar大鼠28只(180 ~ 240g),分为N,N ' -二甲基-4,4 ' -二氯化联吡啶(百草枯,P)组、百草枯加牙买加水青虫(PSJ)组、牙买加水青虫(SJ)组和对照(CTR)组。在整个过程中,动物可以随意饮水和进食,并定期测量体重。P组和PSJ组小鼠腹腔注射8.4 mg/kg体重百草枯,每周2次,连续3周;PSJ进一步接受SJ叶水提取物两周。采用巴恩斯迷宫法进行空间学习记忆的神经行为评估。实验结束时处死动物,切除脑标本,对海马和前额叶皮层进行组织学和生化分析。结果表明,百草枯引起大鼠锥体和颗粒状神经元变性,海马和前额叶皮层输出功能失调。多巴胺能神经元的明显缺失主要发生在P组。另一方面,SJ叶提取物保留了大部分神经元。综上所述,SJ叶提取物对百草枯诱导的帕金森病模型海马和前额叶皮层有明显的积极作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Ameliorative Effects of Stachytarpheta jamaicensis Aqueous Leaf Extract on the Hippocampus and Prefrontal Cortex of N,N′-dimethyl-4,4′-bipyridinium dichloride-Induced Parkinson’s Disease in Adult Wistar Rats
Parkinson’s disease (PD) is the world’s second neurodegenerative disorder after Alzheimer’s dise-ase, and degeneration of dopaminergic neurons is the hallmark. This novel management approach for Parkinson’s disease with Stachytarpheta jamaic-ensis was to assess the role of leaf extract on the histological and morphological properties of the hippocampus and prefrontal cortex in Paraquat-induced Parkinson’s disease. Twenty-eight adult Wistar rats of both sexes (180 - 240g) were assigned to four groups: N,N′-dimethyl-4,4′-bipyridinium dichloride (Paraquat, P), Paraquat and Stachytarpheta jamaicensis (PSJ), only S. jamaicensis (SJ) and control (CTR). Animals were allowed water and food ad libitum throughout, and the weights were taken periodically. Parkinson’s-like disease was induced by intraperitoneal injection of 8.4 mg/kg body weight of Paraquat twice weekly for three weeks in the P and PSJ groups; The PSJ further received SJ aqueous leaf extract for another two weeks. Neurobehavioural assessment using Barnes maze for spatial learning and memory was carried out. Animals were sacrificed at the end of the experiment, and brain specimens were excised and processed for histological and biochemical analyses of the hippocampus and prefrontal cortex. The results showed that paraquat caused the degeneration of pyramidal and granular neurons, as well as dysfunctional output of the hippocampus and prefrontal cortex. There was a significant loss of dopaminergic neurons mainly in the P group. On the other hand, SJ leaf extract preserved most of the neurons. In conclusion, SJ leaf extract produced observable positive effects on the hippocampus and prefrontal cortex of the paraquat-induced Parkinson’s disease model.
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