Livett B G, Marley P D
Br J Pharmacol. 1986 Oct;89(2):327-34. doi: 10.1111/j.1476-5381.1986.tb10264.x.
The effect of opioid peptides and morphine on histamine-induced catecholamine secretion has been studied in monolayer cultures of dispersed, bovine adrenal chromaffin cells. Histamine-induced a dose-dependent secretion of both adrenaline and noradrenaline with a threshold dose of approximately 5 nM, an EC50 of 150 nM and maximal secretion at 10 microM. Catecholamine secretion induced by 1 microM histamine was completely dependent on extracellular calcium, was inhibited in a dose-dependent manner by mepyramine (1 nM-1 microM), and was unaffected by cimetidine (10 microM) and hexamethonium (0.1 mM). Dynorphin-1-13 (1 nM-20 microM), metorphamide (0.1 nM-10 microM), morphine (1 nM-0.1 mM) and diprenorphine (1 nM-0.1 mM) each had no effect on adrenaline or noradrenaline secretion induced by 1 microM histamine. The characteristics of histamine-induced catecholamine secretion from bovine adrenal chromaffin cells were similar to those reported previously for cat and rat adrenal medulla being calcium-dependent and mediated by H1 histamine-receptors. The results with opioid peptides and morphine suggest that endogenous adrenal opioid peptides do not act on the opioid binding sites found on adrenal medullary chromaffin cells to modify their secretory response to histamine.
在分散的牛肾上腺嗜铬细胞单层培养物中,研究了阿片肽和吗啡对组胺诱导的儿茶酚胺分泌的影响。组胺以剂量依赖性方式诱导肾上腺素和去甲肾上腺素分泌,阈值剂量约为5 nM,半数有效浓度(EC50)为150 nM,在10 μM时分泌量最大。1 μM组胺诱导的儿茶酚胺分泌完全依赖于细胞外钙,被美吡拉敏(1 nM - 1 μM)以剂量依赖性方式抑制,而不受西咪替丁(10 μM)和六甲铵(0.1 mM)影响。强啡肽 -1-13(1 nM - 20 μM)、甲硫啡肽(0.1 nM - 10 μM)、吗啡(1 nM - 0.1 mM)和二丙诺啡(1 nM - 0.1 mM)对1 μM组胺诱导的肾上腺素或去甲肾上腺素分泌均无影响。牛肾上腺嗜铬细胞组胺诱导的儿茶酚胺分泌特征与先前报道的猫和大鼠肾上腺髓质相似,即依赖钙且由H1组胺受体介导。阿片肽和吗啡的研究结果表明,内源性肾上腺阿片肽并不作用于肾上腺髓质嗜铬细胞上发现的阿片类结合位点来改变它们对组胺的分泌反应。