ALAMETHICIN-EVOKED CATECHOLAMINE RELEASE FROM CAT ADRENAL-GLANDS

被引:13
作者
ARTALEJO, AR [1 ]
MONTIEL, C [1 ]
SANCHEZGARCIA, P [1 ]
UCEDA, G [1 ]
GUANTES, JM [1 ]
GARCIA, AG [1 ]
机构
[1] UNIV AUTONOMA MADRID,FAC MED,DEPT FARMACOL & TERAPEUT,E-28029 MADRID,SPAIN
关键词
D O I
10.1016/0006-291X(90)92024-T
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Alamethicin enhances the rate of catecholamine output from perfused cat adrenal glands in a concentration-dependent manner. At 37°C, catecholamine released went from 4.29±0.25 to 20.51±0.63 ug/stimulus at ionophore concentrations ranging from 20 to 100 ug/ml. Secretion was abolished at 22°C or in the absence of extracellular Ca. The time-course of secretion (quick activation followed by a decline) evoked by alamethicin considerably differs from the catecholamine release pattern seen with A23187, X537A or ionomycin, which evoke a slowly developing, non-inactivating secretory response. In fact, its transient secretion pattern resembles that of nicotinic or high-K stimulation of cat adrenal glands, thus suggesting that alamethicin might form Ca permeable artificial channels in chromaffin cell plasma membranes. © 1990.
引用
收藏
页码:1204 / 1210
页数:7
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