Sandyk R
Life Sci. 1985 Nov 4;37(18):1655-63. doi: 10.1016/0024-3205(85)90292-9.
The endogenous opioid peptides have for some time been implicated in the regulation of motor behavior in animals. Recently, however, there is increased evidence to suggest a role for these peptides in the control of human motor functions as well as in the pathophysiology of abnormal movement disorders. Degeneration of opioid peptide-containing neurons in the basal ganglia has been demonstrated in Parkinson's disease and Huntington's chorea, but the clinical significance of these findings is largely unknown. On the other hand, there is evidence that excessive opioid activity may be important in the pathophysiology of some movement disorders such as tardive dyskinesia, progressive supra-nuclear palsy, and a subgroup of Tourette's patients. These findings indicate that diseases of the basal ganglia are possibly associated with alterations in opioid peptide activity, and that these alterations may be useful in designing experimental therapeutic strategies in these conditions.
内源性阿片肽在一段时间以来一直被认为与动物的运动行为调节有关。然而,最近有越来越多的证据表明,这些肽在人类运动功能的控制以及异常运动障碍的病理生理学中也发挥着作用。在帕金森病和亨廷顿舞蹈病中,已证实基底神经节中含阿片肽的神经元发生退化,但这些发现的临床意义在很大程度上尚不清楚。另一方面,有证据表明,在某些运动障碍如迟发性运动障碍、进行性核上性麻痹以及一部分图雷特氏综合征患者的病理生理学中,阿片活性过高可能很重要。这些发现表明,基底神经节疾病可能与阿片肽活性的改变有关,而且这些改变可能有助于设计针对这些病症的实验性治疗策略。