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帕金森病灵长类动物和左旋多巴诱导异动症啮齿动物中D3多巴胺受体致敏的体内证据。

In vivo evidence of D3 dopamine receptor sensitization in parkinsonian primates and rodents with l-DOPA-induced dyskinesias.

作者信息

Sánchez-Pernaute Rosario, Jenkins Bruce G, Choi Ji-Kyung, Iris Chen Yin-Ching, Isacson Ole

机构信息

McLean Hospital/Harvard University Udall Parkinson's Disease Research Center of Excellence, McLean Hospital, 115 Mill St., Belmont, MA 02478, USA.

出版信息

Neurobiol Dis. 2007 Aug;27(2):220-7. doi: 10.1016/j.nbd.2007.04.016. Epub 2007 May 18.

Abstract

A growing body of evidence indicates a role for D(3) receptors in l-DOPA-induced dyskinesias. This involvement could be amenable to non-invasive in vivo analysis using functional neuroimaging. With this goal, we examined the hemodynamic response to the dopamine D(3)-preferring agonist 7-hydroxy-N,N-di-n-propyl-2 aminotetralin (7-OHDPAT) in naïve, parkinsonian and l-DOPA-treated, dyskinetic rodents and primates using pharmacological MRI (phMRI) and relative cerebral blood volume (rCBV) mapping. Administration of 7-OHDPAT induced minor negative changes of rCBV in the basal ganglia in naïve and parkinsonian animals. Remarkably, the hemodynamic response was reversed (increased rCBV) in the striatum of parkinsonian animals rendered dyskinetic by repeated l-DOPA treatment. Such increase in rCBV is consistent with D(1) receptor-like signaling occurring in response to D(3) stimulation, demonstrates a dysregulation of dopamine receptor function in dyskinesia and provides a potentially novel means for the characterization and treatment of l-DOPA-induced dyskinesia in patients.

摘要

越来越多的证据表明D(3)受体在左旋多巴诱发的异动症中起作用。这种作用可以通过使用功能神经成像的非侵入性体内分析来研究。为了实现这一目标,我们使用药物磁共振成像(phMRI)和相对脑血容量(rCBV)映射,研究了未用药、患帕金森病以及经左旋多巴治疗出现异动症的啮齿动物和灵长类动物对多巴胺D(3)偏好激动剂7-羟基-N,N-二正丙基-2-氨基四氢萘(7-OHDPAT)的血流动力学反应。在未用药和患帕金森病的动物中,给予7-OHDPAT会导致基底神经节的rCBV出现轻微的负向变化。值得注意的是,在经反复左旋多巴治疗而出现异动症的帕金森病动物的纹状体中,血流动力学反应发生了逆转(rCBV增加)。这种rCBV的增加与D(3)刺激后出现的D(1)受体样信号传导一致,表明异动症中多巴胺受体功能失调,并为患者左旋多巴诱发异动症的表征和治疗提供了一种潜在的新方法。

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