摘要
Isatin was a potent endogenous monoamine oxidase (MAO) inhibitor that is more active against MAO-B than MAO-A. The acute effects of isatin on apomorphine (APO)-induced rotations were evaluated in Parkinsonian rats induced by 6-hydroxydopamine (6-OHDA) lesion. Furthermore, the effects of isatin on DA release in caudate putamen (CPu) of model and normal rats were monitored using fast cyclic vohammetry (FCV).
出处
《青岛大学医学院学报》
CAS
2002年第2期132-132,共1页
Acta Academiae Medicinae Qingdao Universitatis
