Little Karley Y, Ramssen Eric, Welchko Ryan, Volberg Vitaly, Roland Courtney J, Cassin Bader
Department of Psychiatry, Baylor College of Medicine, Houston, TX, United States.
Psychiatry Res. 2009 Aug 15;168(3):173-80. doi: 10.1016/j.psychres.2008.10.034. Epub 2009 Feb 23.
Cocaine use diminishes striatal and midbrain dopamine neuronal components in both post-mortem and in vivo human experiments. The diffuse nature of these declines suggests the possibility that cocaine use might cause a loss of dopamine neurons in humans. Previous rodent studies have not detected cocaine-induced dopamine cell damage. The present experiment involved counting midbrain dopamine neurons utilizing both melanin and tyrosine hydroxylase immunoreactivity. Well-preserved blocks ranging from +38 mm obex to +45 mm obex were examined in 10 cocaine users and 9 controls. Sections were also examined for signs of acute pathological injury by counting activated macrophages and microglia. Melanized cells at six midbrain levels were significantly reduced in cocaine users by both drug exposures. The estimated total number of melanized dopamine cells in the anterior midbrain was significantly reduced in cocaine users by 16%. Results with tyrosine hydroxylase immunoreactivity were less conclusive because of variability in staining. Both activated macrophages and activated microglia were significantly increased among cocaine users. Cocaine exposure may have neurotoxic effects on dopamine neurons in humans. The infiltration of phagocytic cells suggests that the lower number of dopamine cells found in cocaine users was a relatively recent effect. The loss of dopamine cells could contribute to and intensify cocaine dependence, as well as anhedonic and depressive symptoms, in some cocaine users. Further efforts at clarifying the pathophysiological mechanisms involved may help explain treatment refractoriness, and identify targets for therapeutic intervention.
在尸体解剖和人体活体实验中,使用可卡因会减少纹状体和中脑多巴胺神经元成分。这些下降的弥漫性表明,使用可卡因可能会导致人类多巴胺神经元丧失。先前的啮齿动物研究未检测到可卡因诱导的多巴胺细胞损伤。本实验涉及利用黑色素和酪氨酸羟化酶免疫反应性对中脑多巴胺神经元进行计数。在10名可卡因使用者和9名对照者中检查了从脑桥+38毫米到+45毫米保存完好的脑区。还通过计数活化的巨噬细胞和小胶质细胞来检查切片是否有急性病理损伤迹象。在可卡因使用者中,两种药物暴露都使六个中脑水平的黑色素化细胞显著减少。可卡因使用者中脑前部黑色素化多巴胺细胞的估计总数显著减少了16%。由于染色的变异性,酪氨酸羟化酶免疫反应性的结果不太具有决定性。在可卡因使用者中,活化的巨噬细胞和活化的小胶质细胞均显著增加。可卡因暴露可能对人类多巴胺神经元具有神经毒性作用。吞噬细胞的浸润表明,在可卡因使用者中发现的多巴胺细胞数量减少是相对近期的效应。多巴胺细胞的丧失可能导致并加剧一些可卡因使用者的可卡因依赖以及快感缺失和抑郁症状。进一步努力阐明其中涉及的病理生理机制可能有助于解释治疗难治性,并确定治疗干预的靶点。