Majoon-e-Nisyan (一种传统的多草药乌纳尼配方)对学习和记忆动物模型的影响

M. Shaikh, Mohd Urooj, Uzma Viquar, G. Javed, M. H. Kazmi, G. M. Husain
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摘要

根据古典尤那尼文献,多成分传统尤那尼配方 majoon-e-nisyan 可用于治疗健忘症和认知障碍。本研究的目的是评估 Majoon-e-nisyan 在改善认知功能方面的效果。用被动回避测试和水迷宫实验对小鼠的认知功能进行了评估。在记忆保持试验中记录的被动回避数据显示,与东莨菪碱对照组(阴性对照组)相比,1000 毫克/千克体重(体重)(p < 0.05)和 1500 毫克/千克体重(体重)(p < 0.001)的 Majoon-e-Nisyan 以及阳性对照组(p < 0.001)的转移潜伏期显著延长。水迷宫实验数据显示,与药物对照组相比,中剂量(1000 毫克/千克体重)和高剂量(1500 毫克/千克体重)试验药物在平台象限附近停留的时间显著增加(p < 0.01)。研究结果表明,在 1000 毫克/千克体重和 1500 毫克/千克体重的测试剂量水平下,马琼恩-伊-尼斯延对两种模型的认知功能都有益处。然而,500 毫克/千克体重的剂量则无效。目前的研究成功地利用两种有效的小鼠模型证明了 "majoon-e-nisyan "的有效性。我们的研究结果提供了更多证据,证明传统乌纳尼医学中使用的热性药物治疗痴呆症的概念是正确的。这种配方可用作传统痴呆症药物的替代品。
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Effect of Majoon‐e‐Nisyan (a traditional polyherbal Unani formulation) in animal models of learning and memory
According to classical Unani literature, the multicomponent traditional Unani formulation majoon‐e‐nisyan is used to treat amnesia and cognitive impairment. The purpose of the current study was to evaluate majoon‐e‐nisyan's effectiveness in improving cognitive function.Majoon‐e‐Nisyan was prepared as per traditional method. The cognitive function was evaluated using the passive avoidance test and the water maze experiment in mice. The effectiveness of the test drug was compared to that of the positive control drug, piracetam.Passive avoidance data recorded during the memory retention trial showed that transfer latency was significantly increased by majoon‐e‐nisyan at 1000 mg/kg bw (body weight) (p < 0.05) and at 1500 mg/kg bw (p < 0.001) as well as by the positive control (p < 0.001) compared to scopolamine control (negative control). Data of the water maze experiment showed a significant increase (p < 0.01) in time spent near the platform quadrant following treatment with the test drug at mid‐dose (1000 mg/kg bw) and high dose (1500 mg/kg bw) in comparison with vehicle control. A significant increase in time spent in the platform quadrant was also observed in the piracetam group (p < 0.01).The study indicated that majoon‐e‐nisyan had a beneficial effect on cognitive functions at tested dose levels of 1000 and 1500 mg/kg bw in both models. However, the dose of 500 mg/kg bw was ineffective. The current study was successful in demonstrating the effectiveness of majoon‐e‐nisyan using two validated mouse models. Our findings provide more evidence in favor of the concept of hot‐tempered medications used in traditional Unani medicine to treat dementia. This formulation may be used as an alternative to conventional dementia medications.
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