鱼藤酮口服与腹腔注射诱导神经行为改变的比较研究

Suchitra Kavuri, Senthilkumar Sivanesan
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摘要

帕金森病是世界范围内常见的主要神经系统疾病之一,与许多运动和非运动症状有关。鱼藤酮引起的运动和行为障碍可能涉及肠-脑轴,这在最近的一些研究中得到了强调。探讨口服和腹腔注射鱼藤酮毒性对Wistar大鼠神经行为改变的影响。比较研究了雄性Wistar大鼠腹腔注射(3 mg/kg体重21 d)和口服(50 mg/kg体重28 d)鱼藤酮对其旋转、体温、饲养行为和升高+迷宫等神经行为参数的影响。神经行为学研究,如旋转杆测试、饲养行为、高架加迷宫(EPM)和温度计,按照标准公布的方案并利用研究所现有的设施进行。采用Kruskal-Wallis单因素方差分析和Student-Newman-Keul多重比较。研究发现,与各自的对照组相比,口服和腹腔鱼藤酮治疗对神经行为参数有显著影响。虽然在研究设定的行为参数中,腹腔注射和口服鱼藤酮治疗之间几乎没有差异,但差异并不显著。研究结果表明,口服或腹腔注射鱼藤酮毒性引起的神经行为改变是显著的。事实上,口服鱼藤酮毒性与肠-脑轴相关的问题也可能在pd相关的运动/运动和焦虑行为障碍中起作用。
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A comparative study of neurobehavioral changes induced by rotenone through oral and intraperitoneal administration
Parkinson’s disease is one of the major neurological disorders seen worldwide and associated with many motor and nonmotor symptoms. Rotenone-induced motor and behavior impairments could involve the gut-brain axis which is emphasized in several recent works. To explore how oral and intraperitoneal rotenone toxicity impacts neurobehavioral alterations in Wistar rats. The effect of intraperitoneal (3 mg/kg body weight 21 days) and oral (50 mg/kg body weight for 28 days) rotenone toxicity in male Wistar rats on various neurobehavioral parameters viz., rotarod, actophotometer, rearing behavior and elevated plus maze was comparatively studied. The neurobehavioral studies such as the Rota-rod test, rearing behavior, Elevated plus maze (EPM), and Actophotometer were performed by following standard published protocols and by utilizing the facilities available at the Institution. Kruskal-Wallis one- way ANOVA on ranks with Student-Newman-Keul’s multiple comparisons was used. It was found that both oral and intraperitoneal rotenone treatments had a significant impact on neurobehavioral parameters when compared to their respective controls. Although there were few differences observed in the study set behavioral parameters between intraperitoneal and oral rotenone treatments, it was not significant. The study findings suggest that neurobehavioral alterations caused by oral or intraperitoneal rotenone toxicity are found to be significant. The fact that oral rotenone toxicity has gut-brain axis- related problems can also have a role in PD-related motor/movement and anxiety behavior dysfunctions.
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