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类固醇17-α-雌二醇对肾上腺儿茶酚胺释放的膜介导作用。

Membrane-mediated effects of the steroid 17-alpha-estradiol on adrenal catecholamine release.

作者信息

López M G, Abad F, Sancho C, de Pascual R, Borges R, Maroto R, Dixon W, Garcia A G

机构信息

Departamento de Farmacología, Facultad de Medicina, Universidad Autónoma de Madrid, Spain.

出版信息

J Pharmacol Exp Ther. 1991 Oct;259(1):279-85.

PMID:1920120
Abstract

The effects of 17-alpha-estradiol on the secretion of catecholamines from the perfused bovine and cat adrenal gland and bovine chromaffin cells in culture elicited by dimethylphenylpiperazinium (DMPP), methacholine and high potassium were studied. In perfused cat adrenal glands, secretion of catecholamines evoked by pulses of DMPP (1 microM for 30 sec) was decreased by 17-alpha-estradiol at concentrations of 1 and 10 microM by 50 and 80%, respectively. However, secretion evoked by pulses of methacholine (3 microM for 30 sec) was not affected by 1 microM of 17-alpha-estradiol and was affected to a variable extent by 10 microM 17-alpha-estradiol. Catecholamine secretion evoked by higher concentrations of methacholine (100 microM for 60 sec) was reduced by 50% by 10 microM 17-alpha-estradiol. 17-alpha-Estradiol decreased secretion evoked by pulses of 120 mM K+ for 10 sec to a similar extent in the perfused bovine and cat adrenal gland. The 45Ca++ uptake into bovine chromaffin cells in culture stimulated by DMPP (100 microM for 10 sec) or high K+ (59 mM for 10 sec) was almost inhibited completely by 100 microM 17-alpha-estradiol. The rapid action precludes a classical genomic mechanism and suggests effects at the cell membrane.

摘要

研究了17-α-雌二醇对灌注的牛和猫肾上腺以及培养的牛嗜铬细胞在二甲基苯基哌嗪鎓(DMPP)、乙酰甲胆碱和高钾刺激下儿茶酚胺分泌的影响。在灌注的猫肾上腺中,DMPP脉冲(1微摩尔/升,持续30秒)诱发的儿茶酚胺分泌在17-α-雌二醇浓度为1微摩尔/升和10微摩尔/升时分别降低了50%和80%。然而,乙酰甲胆碱脉冲(3微摩尔/升,持续30秒)诱发的分泌不受1微摩尔/升17-α-雌二醇影响,而受10微摩尔/升17-α-雌二醇不同程度影响。较高浓度乙酰甲胆碱(100微摩尔/升,持续60秒)诱发的儿茶酚胺分泌在10微摩尔/升17-α-雌二醇作用下降低了50%。在灌注的牛和猫肾上腺中,17-α-雌二醇使120毫摩尔/升钾离子脉冲(持续10秒)诱发的分泌降低到相似程度。培养的牛嗜铬细胞中,DMPP(100微摩尔/升,持续10秒)或高钾(59毫摩尔/升,持续10秒)刺激的45Ca++摄取在100微摩尔/升17-α-雌二醇作用下几乎完全被抑制。这种快速作用排除了经典的基因组机制,提示其作用于细胞膜。

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