Gaspo R, Yamaguchi N, De Champlain J
Groupe de Recherche sur le Système Nerveux Autonome, Faculté de Pharmacie, Université de Montréal, Québec, Canada.
Am J Physiol. 1993 Jul;265(1 Pt 2):R28-34. doi: 10.1152/ajpregu.1993.265.1.R28.
The effects of nifedipine and BAY K 8644 on the adrenal medullary secretion in response to direct splanchnic nerve stimulation were studied in anesthetized dogs. Supramaximal stimulation (12 V) was given on the left splanchnic nerve at a frequency of 2 Hz with three different pulse durations (0.2, 2, and 20 ms) for a total period of 1.5 min. Each stimulation was given for 30 s without interruption between each stimulation. Plasma concentrations of epinephrine and norepinephrine were measured in adrenal venous and aortic blood. In the vehicle control group, epinephrine and norepinephrine concentrations in adrenal venous blood proportionally increased with the lengthening of the pulse duration without significant changes in catecholamine concentrations in aortic blood. In dogs receiving nifedipine (100 micrograms/kg iv), the net increase in adrenal venous epinephrine concentration during stimulation with 20-ms pulse duration was attenuated by approximately 50% (P < 0.05). In dogs treated with BAY K 8644 (30 micrograms.kg-1.min-1 iv), both adrenal venous epinephrine and norepinephrine secretions evoked by stimulation with 20-ms pulse duration were significantly enhanced by approximately 50%. The present results suggest that the secretion of adrenal catecholamines under in vivo conditions is controlled through mechanism(s) involving dihydropyridine sensitive L-type Ca2+ channels presumably localized on the surface of adrenal medullary chromaffin cells.
在麻醉犬中研究了硝苯地平和BAY K 8644对直接刺激内脏神经时肾上腺髓质分泌的影响。以2Hz的频率对左侧内脏神经给予超强刺激(12V),采用三种不同的脉冲持续时间(0.2、2和20ms),共刺激1.5分钟。每次刺激持续30秒,每次刺激之间不间断。测量肾上腺静脉血和主动脉血中肾上腺素和去甲肾上腺素的血浆浓度。在溶剂对照组中,肾上腺静脉血中肾上腺素和去甲肾上腺素浓度随脉冲持续时间的延长成比例增加,而主动脉血中儿茶酚胺浓度无明显变化。在静脉注射硝苯地平(100μg/kg)的犬中,用20ms脉冲持续时间刺激时肾上腺静脉肾上腺素浓度的净增加量减弱了约50%(P<0.05)。在用BAY K 8644(30μg·kg-1·min-1静脉注射)治疗的犬中,用20ms脉冲持续时间刺激诱发的肾上腺静脉肾上腺素和去甲肾上腺素分泌均显著增强了约50%。目前的结果表明,体内条件下肾上腺儿茶酚胺的分泌是通过涉及二氢吡啶敏感的L型Ca2+通道的机制控制的,这些通道可能位于肾上腺髓质嗜铬细胞表面。