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大鼠主动脉α_1肾上腺素能受体激活引起Ca~(2+)内流的特性
引用本文:徐济良,关永源,陈克敏,贺华,孙家钧.大鼠主动脉α_1肾上腺素能受体激活引起Ca~(2+)内流的特性[J].中国药理学通报,1994,10(2):101-104.
作者姓名:徐济良  关永源  陈克敏  贺华  孙家钧
作者单位:中山医科大学药理教研室,南通医学院药理教研室
摘    要:在大鼠主动脉平滑肌标本上,0.5μmol.L-1硝苯吡啶能完全阻断由100mmol·L-1KCl引起的血管收缩和45Ca内流;并部分抑制苯肾上腺素引起的血管收缩效应和45Ca内流;6mmol·L-1普鲁卡因能完全阻断无钙Krebs液中苯肾上腺素引起的血管收缩和45Ca外溢,且部分阻断正常Krebs液中苯肾上腺素引起的血管收缩和45Ca内流;0.5μmol·L-1硝苯吡啶和6mmol·L-1普鲁卡因合用能阻断苯肾上腺素引起的Ca2+内流。提示:α1受体兴奋后引起的细胞外Ca2+内流可分为硝苯吡啶敏感和不敏感两部分,而后者受细胞内Ca2+释放调节。

关 键 词:Ca~(2+)内流,Ca~(2+)释放,α_1肾上腺素能受体血管平滑肌

Character of the Ca ̄(2+) entry induced by activation of α_1-adrenoceptor in rat aorta
XU Ji-Liang, GUAN Yong-Yuan, CHEN Ke-Ming et al.Character of the Ca ̄(2+) entry induced by activation of α_1-adrenoceptor in rat aorta[J].Chinese Pharmacological Bulletin,1994,10(2):101-104.
Authors:XU Ji-Liang  GUAN Yong-Yuan  CHEN Ke-Ming
Abstract:In rat aorta, 0.5μmol. L-1nifedipine(Nif) completely blocked the contractile response and 45Ca influx induced by 100mmol. L-1 KCl and partially inhibited phenylephrine(PHE) -induced contractile response and 45Ca influx. 6 mmol. L-1 procaine competely blocked the contractile response and 45Ca efflux in Ca2+ free Krebs solution and partially inhibited contractile response and 45Ca influx in normal krebs solution induced by PHE. 0.5μmol. L-1 Nif plus 6 mmol. L-1 procaine completely blocked PHE-induced Ca2+ entry. These results suggest that the extracellular Ca2+ entry induced by activation of α1-adrenoceptor contains two components, sensitive to Nif and insensitive to Nif; The latter is partially regulated by intracel lular Ca2+ release.
Keywords:Ca ̄(2+) influx  Ca ̄(2+) release  α_1- adrenoceptor  smooth muslce(vascular )
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