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阿扑吗啡持续刺激治疗帕金森病:受体脱敏作为运动反应降低的一种可能机制

Apomorphine continuous stimulation in Parkinson's disease: receptor desensitization as a possible mechanism of reduced motor response.

作者信息

Maggio R, Barbier P, Corsini G U

机构信息

Istituto di Farmacologia, Scuola Medica, Università di Pisa, Italy.

出版信息

J Neural Transm Suppl. 1995;45:133-6.

PMID:8748618
Abstract

Apomorphine is a potent nonselective agonist at D1 and D2 dopamine receptors. The utility of apomorphine in Parkinson's disease (PD) is well asserted but its clinical use is reduced because of its short half-life and numerous side-effects. The disabling "on-off" fluctuations are among the most frequent and troublesome complications of chronic levodopa therapy in PD. Apomorphine is effective to reverse refractory L-dopa induced "off" periods, but a reduced motor response after repeated administrations has also been described with this drug. The loss of response to apomorphine, when the drug is administered repeatedly, is well fitted by the processes of receptor phosphorylation and down regulation. Elucidation of the molecular bases of dopaminergic receptors desensitization may lead to a better understanding of the mechanisms of dopaminergic regulation, and to a more appropriate treatment of PD.

摘要

阿扑吗啡是一种强效的、对D1和D2多巴胺受体无选择性的激动剂。阿扑吗啡在帕金森病(PD)中的效用已得到充分证实,但其临床应用因半衰期短和副作用众多而受到限制。致残性的“开-关”波动是PD慢性左旋多巴治疗中最常见且棘手的并发症之一。阿扑吗啡可有效逆转难治性左旋多巴诱导的“关”期,但也有报道称该药物反复给药后运动反应会降低。当反复给药时,阿扑吗啡反应丧失的情况与受体磷酸化和下调过程高度吻合。阐明多巴胺能受体脱敏的分子基础可能有助于更好地理解多巴胺能调节机制,并为PD提供更恰当的治疗。

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