Pan J T, Hooth M J, Lookingland K J, Moore K E, Marks T A
Department of Pharmacology and Toxicology, Michigan State University, East Lansing 48824.
Toxicol Appl Pharmacol. 1993 Nov;123(1):26-33. doi: 10.1006/taap.1993.1217.
The purpose of this study was to examine the effects of both acute and chronic administration of the peripheral sympatholytic antihypertensive agent losulazine on central dopaminergic, noradrenergic, and 5-hydroxytryptaminergic neurons in the rat. For comparison, the acute effects of reserpine were also examined. Acute systemic administration of losulazine produced marked dose- and time-dependent decreases in dopamine and norepinephrine concentrations in regions outside the blood-brain barrier (i.e., the median eminence, intermediate lobe, and neural lobe), that were accompanied by an increase in plasma concentrations of prolactin and alpha-melanocyte-stimulating hormone. By comparison, losulazine caused a relatively modest, transient depletion of dopamine and norepinephrine (but not 5-hydroxytryptamine) in regions of the brain protected by the blood-brain barrier (i.e., the striatum, nucleus accumbens, and dorsomedial nucleus of the hypothalamus). In contrast to losulazine, acute systemic administration of reserpine caused a prolonged depletion of dopamine, norepinephrine, and 5-hydroxytryptamine in all brain and pituitary regions examined. These results suggest that regional differences in the response of aminergic neurons to acute administration of losulazine and reserpine reflect differences in the ability of these drugs to penetrate the blood-brain barrier. Chronic systemic administration of losulazine produced a similar decrease in dopamine and norepinephrine in the median eminence, intermediate lobe, and neural lobe, suggesting that tolerance does not develop to the ability of losulazine to deplete catecholamines in these regions. Chronic losulazine administration also decreased dopamine concentrations in the striatum, and norepinephrine concentrations in the dorsomedial nucleus, suggesting that losulazine may have cumulative effects on central catecholamine neurons terminating in these brain regions.
本研究的目的是考察外周交感神经阻滞性抗高血压药物洛苏拉嗪急性和慢性给药对大鼠中枢多巴胺能、去甲肾上腺素能和5-羟色胺能神经元的影响。为作比较,还考察了利血平的急性作用。急性全身给予洛苏拉嗪后,血脑屏障外区域(即正中隆起、中间叶和神经叶)的多巴胺和去甲肾上腺素浓度出现显著的剂量和时间依赖性降低,同时催乳素和α-黑素细胞刺激素的血浆浓度升高。相比之下,洛苏拉嗪使血脑屏障保护区域(即纹状体、伏隔核和下丘脑背内侧核)的多巴胺和去甲肾上腺素(但不包括5-羟色胺)出现相对适度的短暂耗竭。与洛苏拉嗪不同,急性全身给予利血平导致所有检测脑区和垂体区域的多巴胺、去甲肾上腺素和5-羟色胺出现长期耗竭。这些结果表明,胺能神经元对洛苏拉嗪和利血平急性给药反应的区域差异反映了这些药物穿透血脑屏障能力的差异。慢性全身给予洛苏拉嗪使正中隆起、中间叶和神经叶的多巴胺和去甲肾上腺素出现类似降低,表明对洛苏拉嗪在这些区域耗竭儿茶酚胺的能力不会产生耐受性。慢性给予洛苏拉嗪还降低了纹状体中的多巴胺浓度以及背内侧核中的去甲肾上腺素浓度,表明洛苏拉嗪可能对终止于这些脑区的中枢儿茶酚胺能神经元具有累积效应。