Perlmutter J S, Stambuk M K, Markham J, Black K J, McGee-Minnich L, Jankovic J, Moerlein S M
Department of Neurology, Washington University School of Medicine, St. Louis, Missouri 63110, USA.
J Neurosci. 1997 Jan 15;17(2):843-50. doi: 10.1523/JNEUROSCI.17-02-00843.1997.
In this study we have investigated the pathophysiology of two idiopathic focal dystonias: hand cramp with excessive cocontractions of agonist and antagonist hand or forearm muscles during specific tasks, such as writing, and facial dystonia manifested by involuntary eyelid spasms (blepharospasm) and lower facial and jaw spasms (oromandibular dystonia). We used positron emission tomography (PET) to measure the in vivo binding of the dopaminergic radioligand [18F]spiperone in putamen in 21 patients with these two focal dystonias and compared the findings with those from 13 normals. We measured regional cerebral blood flow and blood volume in each subject as well as the radiolabeled metabolites of [18F]spiperone in arterial blood. A stereotactic method of localization, independent of the appearance of the images, was used to identify the putamen in all of the PET images. We analyzed the PET and arterial blood data with a validated nonsteady-state tracer kinetic model representing the in vivo behavior of the radioligand. An index of binding called the combined forward rate constant was decreased by 29% in dystonics, as compared with normals (p < 0.05). There were no significant differences between dystonics and normals in regional blood flow, blood volume, nonspecific binding, permeability-surface area product of [18F]spiperone or the dissociation rate constant. These findings are consistent with a decrease of dopamine D2-like binding in putamen and are the first demonstration of a receptor abnormality in idiopathic dystonia. These results have important implications for the pathophysiology of dystonia as well as for function of the basal ganglia.
在本研究中,我们调查了两种特发性局灶性肌张力障碍的病理生理学:一种是书写等特定任务期间手部痉挛,伴有手部或前臂的主动肌和拮抗肌过度共同收缩;另一种是面部肌张力障碍,表现为不自主的眼睑痉挛(睑痉挛)以及面部下部和下颌痉挛(口下颌肌张力障碍)。我们使用正电子发射断层扫描(PET)测量了21例患有这两种局灶性肌张力障碍患者壳核中多巴胺能放射性配体[18F]司哌隆的体内结合情况,并将结果与13名正常人的结果进行了比较。我们测量了每个受试者的局部脑血流量和血容量以及动脉血中[18F]司哌隆的放射性标记代谢产物。采用一种与图像外观无关的立体定向定位方法来识别所有PET图像中的壳核。我们使用一个经过验证的非稳态示踪剂动力学模型分析PET和动脉血数据,该模型代表了放射性配体的体内行为。与正常人相比,肌张力障碍患者中一个称为联合前向速率常数的结合指数降低了29%(p < 0.05)。肌张力障碍患者与正常人在局部血流量、血容量、非特异性结合、[18F]司哌隆的通透表面积乘积或解离速率常数方面没有显著差异。这些发现与壳核中多巴胺D2样结合减少一致,并且是特发性肌张力障碍中受体异常的首次证明。这些结果对肌张力障碍的病理生理学以及基底神经节的功能具有重要意义。