Kilpatrick D L, Slepetis R J, Corcoran J J, Kirshner N
J Neurochem. 1982 Feb;38(2):427-35. doi: 10.1111/j.1471-4159.1982.tb08647.x.
The uptake of 45Ca2+ and secretion of catecholamines by primary cultures of adrenal medulla cells were studied. Nicotine, veratridine, potassium, and Ionomycin stimulate both the accumulation of 45Ca2+ and the secretion of catecholamines. Nicotinic antagonists block 45Ca2+ uptake induced by nicotine, tetrodotoxin blocks 45Ca2+ uptake induced by veratridine, and D600 or secretion induced by Ionomycin. The EC50 for nicotine is 3 microM for catecholamine secretion and 10 microM for 45Ca2+ uptake, while the EC50s for veratridine-stimulated uptake and secretion are approximately the same (75 microM). Kinetic studies show that the uptake of Ca2+ is rapid and appears to precede the secretion of catecholamines, and that the rate of uptake declines rapidly. The 50 mM-K+ show saturation kinetics with respect to external calcium concentrations at about 2 mM. On the other hand, the uptake of 45Ca2+ stimulated by nicotine does not become saturated at external calcium concentrations of 10 mM although the secretion of catecholamines reaches a maximum at external calcium concentrations of 2 mM. The data suggest that depolarizing agents such as veratridine and 50 mM-K+ stimulate 45Ca2+ entry through voltage-sensitive calcium channels, while nicotinic agonists stimulate calcium entry through the acetylcholine receptor ion channels as well as through voltage-sensitive calcium channels.
对肾上腺髓质细胞原代培养物摄取(45Ca2+)和分泌儿茶酚胺的情况进行了研究。尼古丁、藜芦碱、钾离子和离子霉素均可刺激(45Ca2+)的积累以及儿茶酚胺的分泌。烟碱拮抗剂可阻断尼古丁诱导的(45Ca2+)摄取,河豚毒素可阻断藜芦碱诱导的(45Ca2+)摄取,而D600可阻断离子霉素诱导的(45Ca2+)摄取或分泌。尼古丁刺激儿茶酚胺分泌的(EC50)为(3)微摩尔,刺激(45Ca2+)摄取的(EC50)为(10)微摩尔,而藜芦碱刺激摄取和分泌的(EC50)大致相同((75)微摩尔)。动力学研究表明,(Ca2+)的摄取迅速,似乎先于儿茶酚胺的分泌,且摄取速率迅速下降。(50)毫摩尔/升的钾离子在外部钙浓度约为(2)毫摩尔时呈现饱和动力学。另一方面,尼古丁刺激的(45Ca2+)摄取在外部钙浓度为(10)毫摩尔时未达到饱和,尽管儿茶酚胺的分泌在外部钙浓度为(2)毫摩尔时达到最大值。数据表明,藜芦碱和(50)毫摩尔/升的钾离子等去极化剂通过电压敏感钙通道刺激(45Ca2+)内流,而烟碱激动剂则通过乙酰胆碱受体离子通道以及电压敏感钙通道刺激钙内流。