Carr L A, Rowell P P, Pierce W M
Department of Pharmacology and Toxicology, University of Louisville, Kentucky 40292.
Neurochem Res. 1989 Jun;14(6):511-5. doi: 10.1007/BF00964911.
Nicotine was administered acutely and subchronically (14 days) to determine whether various synaptic mechanisms are selectively altered in the nigrostriatal and mesolimbic dopaminergic systems in the rat. When added to tissue preparations in vitro, nicotine had no effects on tyrosine hydroxylase, synaptosomal uptake of [3H]dopamine or binding of [3H]spiperone to D2 receptors in either system. However, acute treatment in vivo stimulated tyrosine hydroxylase activity in the nucleus accumbens. This effect was prevented by pretreatment with a nicotinic antagonist, suggesting that it was mediated by nicotinic receptors. Since subchronic exposure to nicotine had no effect on tyrosine hydroxylase, it appears that tolerance develops to this action. In vivo treatment with nicotine did not alter dopamine uptake or receptor binding. The results suggest that, in doses which result in moderate plasma levels, nicotine has selective stimulant actions on nerve terminals of the mesolimbic system.
对大鼠急性和亚慢性(14天)给予尼古丁,以确定大鼠黑质纹状体和中脑边缘多巴胺能系统中各种突触机制是否被选择性改变。当体外添加到组织制剂中时,尼古丁对任一系统中的酪氨酸羟化酶、[3H]多巴胺的突触体摄取或[3H]螺哌隆与D2受体的结合均无影响。然而,体内急性治疗可刺激伏隔核中的酪氨酸羟化酶活性。烟碱拮抗剂预处理可阻止此效应,提示其由烟碱受体介导。由于亚慢性暴露于尼古丁对酪氨酸羟化酶无影响,似乎对此作用产生了耐受性。尼古丁体内治疗未改变多巴胺摄取或受体结合。结果表明,在导致中等血浆水平的剂量下,尼古丁对中脑边缘系统的神经末梢具有选择性刺激作用。