Reches A, Wagner H R, Jackson-Lewis V, Yablonskaya-Alter E, Fahn S
Neurology. 1984 Sep;34(9):1208-12. doi: 10.1212/wnl.34.9.1208.
Refractory response to dopamine (DA) agonists is a common problem in the treatment of Parkinson's disease. In rats with unilateral lesions of the substantia nigra, denervation induced significant increases in striatal 3(H)-spiperone binding sites ipsilateral to the lesion. Chronic treatment with levodopa or with pergolide mesylate significantly decreased the number of 3(H)-spiperone striatal binding sites. Agonist-induced decreases were approximately equivalent in intact and denervated striata and did not appear to be affected by lesions. These results suggest that the poor response to DA agonist in certain parkinsonian patients with chronic drug exposure may be mediated by drug-induced DA receptor down-regulation.
对多巴胺(DA)激动剂的难治性反应是帕金森病治疗中的常见问题。在单侧黑质损伤的大鼠中,去神经支配导致损伤同侧纹状体3(H)-螺哌隆结合位点显著增加。左旋多巴或甲磺酸培高利特的长期治疗显著减少了3(H)-螺哌隆纹状体结合位点的数量。激动剂诱导的减少在完整和去神经支配的纹状体中大致相同,并且似乎不受损伤的影响。这些结果表明,某些长期药物暴露的帕金森病患者对DA激动剂反应不佳可能是由药物诱导的DA受体下调介导的。