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Catecholamine secretion by isolated adrenal cells.

作者信息

Hochman J, Perlman R L

出版信息

Biochim Biophys Acta. 1976 Jan 14;421(1):168-75. doi: 10.1016/0304-4165(76)90180-x.

DOI:10.1016/0304-4165(76)90180-x
PMID:174736
Abstract

Isolated adrenal cells were prepared by collagenase digestion of guinea pig adrenal glands. Acetylcholine stimulates the secretion of catecholamines by these isolated adrenal cells. Acetylcholine-stimulated catecholamine secretion is inhibited by cholinergic blocking agents (atropine and hexamethonium) and by local anaesthetics (tetracaine), and is dependent upon the concentration of Ca2+ in the incubation medium. In the presence of Ca2+, catecholamine secretion is also stimulated by two divalent cation ionophores, A23187 and X-537A. Cyclic nucleotides and 5'-nucleotides cause a small, non-specific stimulation of catecholamine secretion. These results indicate that isolated adrenal cells are a useful system in which to study catecholamine secretion, and support the hypothesis that increased Ca2+ entry into chromaffin cells is a sufficient stimulus for catecholamine secretion.

摘要

相似文献

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Catecholamine secretion by isolated adrenal cells.
Biochim Biophys Acta. 1976 Jan 14;421(1):168-75. doi: 10.1016/0304-4165(76)90180-x.
2
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引用本文的文献

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Primary culture of bovine chromaffin cells.牛嗜铬细胞的原代培养。
Nat Protoc. 2007;2(5):1248-53. doi: 10.1038/nprot.2007.136.
2
Modulation of calcium current by ATP in guinea-pig adrenal chromaffin cells.ATP对豚鼠肾上腺嗜铬细胞钙电流的调节作用。
Pflugers Arch. 1996 Jan;431(3):402-7. doi: 10.1007/BF02207278.
3
Inhibitory effects of caffeine on secretagogue-induced catecholamine secretion from adrenal chromaffin cells of the guinea-pig.咖啡因对豚鼠肾上腺嗜铬细胞促分泌素诱导的儿茶酚胺分泌的抑制作用。
Br J Pharmacol. 1994 Mar;111(3):935-41. doi: 10.1111/j.1476-5381.1994.tb14829.x.
4
A reassessment of the modulatory role of cyclic AMP in catecholamine secretion by chromaffin cells.对环磷酸腺苷在嗜铬细胞儿茶酚胺分泌中调节作用的重新评估。
Br J Pharmacol. 1995 Jan;114(2):517-23. doi: 10.1111/j.1476-5381.1995.tb13257.x.
5
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J Physiol. 1983 Aug;341:153-67. doi: 10.1113/jphysiol.1983.sp014798.
6
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Br J Pharmacol. 1984 Apr;81(4):599-610. doi: 10.1111/j.1476-5381.1984.tb16124.x.
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