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CART modulates the effects of levodopa in rat model of Parkinson's disease

机译:推车调节Levodopa在帕金森病的大鼠模型中的影响

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Parkinson's disease (PD) is an age-related disorder characterized by a progressive degeneration of dopaminergic neurons of substantia nigra (SN). The neuropeptide cocaine- and amphetamine-regulated transcript (CART) is known to closely interact with the dopamine system and regulate psychomotor activity. We screened the effectiveness of CART in reversing the symptoms of PD in a rat model. PD like condition was induced by administering 6-hydroxydopamine (6-OHDA) directly in the SN of the right side. Fifteen days later, intraperitoneal (IP) treatment with apomorphine hydrochloride to these rats, resulted in contralateral rotations in the rotation test chamber suggesting induction of PD-like symptoms. This action of apomorphine was significantly attenuated by intracerebroventricular (ICV) treatment with CART and potentiated by CART antibody. IP treatment with levodopa also produced contralateral rotation in PD induced rats, and showed anti-Parkinson-like action. Prior treatment with CART via ICV route potentiated the anti-Parkinsonian effects of levodopa, while CART antibody produced opposite effects. CART treatment per se, to PD induced rats produced ipsilateral rotations, suggesting that the peptide may promote the endogenous release of dopamine from intact neurons. While CART-immunoreactivity in arcuate nucleus, paraventricular nucleus, striatum, substantia nigra, ventral tegmental area and locus coeruleus was reduced in the PD induced rats, levodopa treatment restored the expression of CART-immunoreactivity in these nuclei. These results suggest that endogenous CART might closely interact with the dopamine containing SN-striatal pathway which is known to profoundly influence the motor system. The study underscores the importance of CART as a potential therapeutic agent in the treatment of PD. (C) 2015 Elsevier B.V. All rights reserved.
机译:帕金森病(PD)是一种与年龄相关的疾病,其特征,其特征是体积NIGRA(SN)的多巴胺能神经元进行性渐变。已知神经肽可卡因和安非他明调节的转录物(推车)与多巴胺系统密切相关并调节精神运动活性。我们筛选了推车在大鼠模型中逆转PD症状的有效性。通过直接在右侧的SN中施用6-羟基多胺(6-OHDA)诱导PD。十五天后,腹膜内(IP)用盐酸盐酸盐酸盐处理,导致旋转试验室中的对侧旋转,表明PD样症状的诱导。通过用推车的脑室(ICV)治疗和用购物车抗体调节,该酮啡的这种作用显着减弱。用左旋多巴的IP治疗也产生了PD诱导的大鼠对侧旋转,并显示出抗帕金森的作用。通过ICV路线提前处理推车有强调左司泮的抗帕金纳抗帕辛尼亚效应,而推车抗体产生相反的效果。本身的推车治疗本身,对Pd诱导的大鼠产生同侧旋转,表明肽可以从完整神经元中促进多巴胺的内源性释放。在PD诱导的大鼠中降低了弧形核中,椎间盘核,纹状体,脊髓岩,脊髓植物,基因群,腹侧三核,脊髓瘤和基因座菌,腹腔治疗恢复了这些核中的推车 - 免疫反应性表达。这些结果表明内源性推车可能与含有SN薄层途径的多巴胺密切相互作用,该途径已知对电动机系统深入影响。该研究强调了推车作为潜在治疗剂治疗PD的潜在治疗剂的重要性。 (c)2015 Elsevier B.v.保留所有权利。

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