Harvey J A, McMaster S E, Romano A G
Department of Pharmacology, Medical College of Pennsylvania, Philadelphia 19129.
Brain Res. 1993 Aug 13;619(1-2):1-14. doi: 10.1016/0006-8993(93)91590-o.
This study employed immunocytochemistry to visualize the neurotoxic effects of methylenedioxyamphetamine hydrochloride (MDA) on serotonergic projections to brainstem structures. Separate groups of animals were injected twice a day, for 4 consecutive days, with: saline; MDA (40 mg/kg/day); or fluoxetine hydrochloride (10 mg/kg) prior to each injection of MDA. In agreement with previous reports, MDA produced a pronounced loss of 5-HT immunoreactivity in the forebrain, most notably in neocortex and hippocampus. However, our results revealed that MDA also produced a loss of 5-HT fibers in brainstem that was as severe as that seen in any region of forebrain. Regions most severely affected included: superior colliculus; superior olivary complex; trigeminal sensory complex and vestibular nuclei. The brains of animals treated with MDA demonstrated a relative absence of fine 5-HT axon terminals within these forebrain and brainstem regions, while thicker axonal elements were still present. The neurotoxic effects of MDA on serotonergic projections to forebrain and brainstem were completely blocked by the prior administration of the 5-HT reuptake inhibitor, fluoxetine. It was suggested that the denervation of the superior colliculus, superior olive and vestibular nuclei could alter visually guided eye movements and the vestibulo-ocular reflex while the loss of serotonergic inputs to the trigeminal sensory complex might be expected to alter tactual reflexes.
本研究采用免疫细胞化学方法来观察盐酸亚甲二氧基苯丙胺(MDA)对投射至脑干结构的5-羟色胺能神经纤维的神经毒性作用。将动物分成不同组,连续4天每天注射两次:生理盐水;MDA(40毫克/千克/天);或在每次注射MDA前先注射盐酸氟西汀(10毫克/千克)。与之前的报道一致,MDA导致前脑5-羟色胺免疫反应性显著丧失,最明显的是在新皮层和海马体。然而,我们的结果显示,MDA还导致脑干中5-羟色胺纤维丧失,其严重程度与在前脑任何区域所见相当。受影响最严重的区域包括:上丘;上橄榄复合体;三叉神经感觉复合体和前庭核。用MDA处理的动物大脑在这些前脑和脑干区域内显示出5-羟色胺轴突终末细丝相对缺失,而较粗的轴突成分仍然存在。MDA对投射至前脑和脑干的5-羟色胺能神经纤维的神经毒性作用被预先给予的5-羟色胺再摄取抑制剂氟西汀完全阻断。有人提出,上丘、上橄榄和前庭核的去神经支配可能会改变视觉引导的眼球运动和前庭眼反射,而三叉神经感觉复合体5-羟色胺能输入的丧失可能会改变触觉反射。