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首页> 外文期刊>Experimental Neurology >Effect of acute L-Dopa pretreatment on apomorphine-induced rotational behavior in a rat model of Parkinson's disease.
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Effect of acute L-Dopa pretreatment on apomorphine-induced rotational behavior in a rat model of Parkinson's disease.

机译:在帕金森氏病大鼠模型中,急性左旋多巴预处理对阿扑吗啡诱导的旋转行为的影响。

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摘要

Currently, reduction of apomorphine-induced rotational behavior in the 6-hydroxydopamine (6-OHDA) lesioned rat is the most utilized drug-induced paradigm for assessing functional efficacy in a rat model of Parkinson's disease (PD). Any clinically predictive animal model of PD should include a positive response to l-dopa, the standard pharmacotherapy for PD. However, the acute interaction between L-dopa and apomorphine has never been studied to determine if L-dopa pretreatment could reduce apomorphine-induced rotational behavior in a 6-OHDA lesioned rat. The present study was designed to explore whether, indeed, pretreatment with subrotational doses of L-dopa could inhibit apomorphine-induced rotations. The data indicate that L-dopa significantly reduced apomorphine-induced rotational behavior only at one dose (5.0 mg/kg) for 12 min. Based on these and other data, it is concluded that although the apomorphine-induced rotational paradigm may continue to be utilized as one additional indicator of efficacy in the 6-OHDA rat model of PD, it is not in itself a completely valid functional assay. Copyright 2000 Academic Press.
机译:目前,在6-羟基多巴胺(6-OHDA)病变大鼠中减少阿扑吗啡诱导的旋转行为是评估帕金森氏病(PD)大鼠模型中功能功效的最常用的药物诱导范例。 PD的任何临床预测动物模型都应包括对PD的标准药物治疗l-多巴的阳性反应。然而,从未研究过左旋多巴与阿朴吗啡之间的急性相互作用来确定左旋多巴预处理是否可以降低6-OHDA损伤大鼠中阿扑吗啡诱导的旋转行为。本研究旨在探讨是否确实可以对亚旋转剂量的左旋多巴进行预处理是否能抑制阿扑吗啡诱导的旋转。数据表明左旋多巴仅以一种剂量(5.0 mg / kg)持续12分钟即可显着降低阿扑吗啡诱导的旋转行为。基于这些和其他数据,可以得出结论,尽管阿扑吗啡诱导的旋转范例可能继续被用作PD的6-OHDA大鼠模型中功效的另一个指标,但它本身并不是一种完全有效的功能测定方法。版权所有2000学术出版社。

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