Boksa P, Aitken D, Meaney M
Douglas Hospital Research Centre, Department of Psychiatry, McGill University, Montreal, Quebec, Canada.
Biochem Pharmacol. 1989 May 1;38(9):1491-8. doi: 10.1016/0006-2952(89)90189-5.
N-(2-Chloroethyl)-N-ethyl-2-bromobenzylamine (DSP-4) is an inhibitor of noradrenaline uptake and a neurotoxin known to deplete noradrenaline levels with little effect on dopamine, serotonin or adrenaline in the central nervous system. The present study tested the effects of DSP-4 on catecholamine uptake, release and content in cultures of isolated bovine adrenal chromaffin cells. DSP-4 selectively inhibited the acute uptake of [3H]noradrenaline with little or no effect on [3H]adrenaline or [3H]dopamine uptake. In cultures preloaded with [3H]catecholamines, DSP-4 stimulated the release of [3H]noradrenaline and, to a small extent, also [3H]adrenaline and [3H]dopamine. However, the drug did not stimulate the release of appreciable amounts of endogenous adrenaline, noradrenaline or dopamine. A high concentration of DSP-4 inhibited the carbachol-stimulated release of adrenaline, noradrenaline and dopamine from the cells. Following a 1-hr exposure to the drug, DSP-4 decreased adrenaline, noradrenaline and dopamine levels in the cells with no gross morphologic changes in the cells. Reductions in adrenaline and noradrenaline levels were almost equal in magnitude, while dopamine was depleted to a somewhat greater extent under some conditions. Longer exposure to DSP-4 resulted in morphological changes in the cells, suggesting that the drug is also toxic to chromaffin cells in culture.
N-(2-氯乙基)-N-乙基-2-溴苄胺(DSP-4)是一种去甲肾上腺素摄取抑制剂,也是一种神经毒素,已知其可降低中枢神经系统中的去甲肾上腺素水平,而对多巴胺、5-羟色胺或肾上腺素影响甚微。本研究测试了DSP-4对分离的牛肾上腺嗜铬细胞培养物中儿茶酚胺摄取、释放和含量的影响。DSP-4选择性抑制[3H]去甲肾上腺素的急性摄取,而对[3H]肾上腺素或[3H]肾上腺素或[3H]多巴胺摄取几乎没有影响。在预先加载[3H]儿茶酚胺的培养物中,DSP-4刺激[3H]去甲肾上腺素的释放,在较小程度上也刺激[3H]肾上腺素和[3H]多巴胺的释放。然而,该药物并未刺激大量内源性肾上腺素、去甲肾上腺素或多巴胺的释放。高浓度的DSP-4抑制了卡巴胆碱刺激的细胞中肾上腺素、去甲肾上腺素和多巴胺的释放。在暴露于该药物1小时后,DSP-4降低了细胞中的肾上腺素、去甲肾上腺素和多巴胺水平,而细胞没有明显的形态学变化。肾上腺素和去甲肾上腺素水平的降低幅度几乎相等,而在某些条件下多巴胺的消耗程度更大。长时间暴露于DSP-4会导致细胞出现形态学变化,这表明该药物对培养中的嗜铬细胞也具有毒性。