Wakade A R, Wakade T D
Neurosci Lett. 1984 Sep 7;50(1-3):139-43. doi: 10.1016/0304-3940(84)90476-2.
The left adrenal gland of the rat was perfused in vitro via the adrenal vein with Krebs-bicarbonate solution to study accumulation of exogenous catecholamines and secretion of endogenous norepinephrine and epinephrine by exposing the gland to various sympathomimetic agents. Perfusions with high concentrations of norepinephrine for 30 min did not result in its accumulation over the endogenous norepinephrine content. High concentrations of dopamine, norepinephrine and phenylephrine failed to displace significant quantities of endogenous catecholamines in the perfusate over those secreted spontaneously. Agents known to release norepinephrine from sympathetic nerves, such as tyramine and ephedrine, were ineffective in causing secretion of catecholamines from the rat adrenal gland. We have concluded that chromaffin cells of the isolated rat adrenal gland do not exhibit an efficient uptake system across their membrane for transporting catecholamines.
通过肾上腺静脉用 Krebs - 碳酸氢盐溶液对大鼠的左肾上腺进行体外灌注,以研究外源性儿茶酚胺的积累以及通过将肾上腺暴露于各种拟交感神经药物来研究内源性去甲肾上腺素和肾上腺素的分泌。用高浓度去甲肾上腺素灌注 30 分钟并未导致其在内源性去甲肾上腺素含量之上的积累。高浓度的多巴胺、去甲肾上腺素和苯肾上腺素未能使灌注液中内源性儿茶酚胺的排出量超过自发分泌量。已知能从交感神经释放去甲肾上腺素的药物,如酪胺和麻黄碱,在引起大鼠肾上腺分泌儿茶酚胺方面无效。我们得出结论,分离的大鼠肾上腺嗜铬细胞在其细胞膜上不存在高效的儿茶酚胺转运摄取系统。