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首页> 外文期刊>International Journal of Pharmaceutical Sciences and Research >BEHAVIORAL STUDIES OF DASATINIB AND RESVERATROL IN ROTENONE INDUCED PARKINSON’S RAT MODEL
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BEHAVIORAL STUDIES OF DASATINIB AND RESVERATROL IN ROTENONE INDUCED PARKINSON’S RAT MODEL

机译:鱼藤酮诱导帕金森病大鼠模型中达沙替尼和白藜芦醇的行为研究

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摘要

Neurodegeneration accounts for diseases like Parkinson’s disease, Alzheimer’s disease, Huntington’s disease, etc. that come under neurodegenerative diseases. Parkinson’s disease is the second most common neurodegenerative disease. The main hallmarks of Parkinson’s disease are progressive loss of motor control and cognitive dysfunction. Current treatments are of reducing the symptoms, do not address the long term complications like motor and cognitive dysfunction and have serious side effects as well. Recent research has linked tyrosine kinase activity dysfunction and mitochondrial dysfunctions to the main etiologies of Parkinson’s disease of familial and sporadic origin. Since Parkinson’s disease occur due to multiple etiologies, using a combination of drugs that target different etiologies could be an ideal strategy to address neurodegeneration. In the present study, the neuroprotective efficacy of a combination of tyrosine kinase inhibitor; dasatinib and natural antioxidant resveratrol were studied. Stereotaxic infusion of rotenone was given to rats to induce Parkinson’s disease, with nine treatment groups. The neuroprotective efficacy of the drug combinations was evaluated in different treatment groups by checking, behavioral studies, like learning and memory using radial arm maze, anxiety level using elevated plus maze and muscle grip strength using rotarod. The drug combination results were more inclined towards the sham control and found to be significant for all three experiments compared to rotenone group. Further, the results demonstrated that the drug combinations are potent candidates for rescuing the neurons from neurodegeneration.
机译:神经退行性疾病是帕金森氏病,阿尔茨海默氏病,亨廷顿氏病等疾病的归因于神经退行性疾病。帕金森氏病是第二大最常见的神经退行性疾病。帕金森氏病的主要标志是运动控制的逐步丧失和认知功能障碍。当前的治疗方法是减轻症状,不能解决运动和认知功能障碍等长期并发症,并且还具有严重的副作用。最近的研究已将酪氨酸激酶活性功能障碍和线粒体功能障碍与帕金森氏家族和散发性疾病的主要病因联系起来。由于帕金森氏病是由多种病因引起的,因此使用针对不同病因的药物组合可能是解决神经变性的理想策略。在本研究中,联合使用酪氨酸激酶抑制剂的神经保护作用;研究了达沙替尼和天然抗氧化剂白藜芦醇。将鱼藤酮立体定向输注给大鼠,以诱发帕金森氏病,共有9个治疗组。通过检查,行为研究,如使用radial臂迷宫的学习和记忆,使用升高的迷宫和高架迷宫的焦虑水平以及使用旋转脚架的肌肉抓地力,对药物组合的神经保护功效进行了评估。药物组合的结果更倾向于假对照,与鱼藤酮组相比,在所有三个实验中均具有显着意义。此外,结果证明药物组合是从神经变性中拯救神经元的有效候选物。

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