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α1A - 肾上腺素能受体亚型介导大鼠尿道收缩。

Alpha 1A-adrenoceptor subtype mediates contraction of the rat urethra.

作者信息

Chess-Williams R, Aston N, Couldwell C

机构信息

Department of Biomedical Science, University of Sheffield, UK.

出版信息

J Auton Pharmacol. 1994 Dec;14(6):375-81. doi: 10.1111/j.1474-8673.1994.tb00618.x.

Abstract
  1. The alpha 1-adrenoceptor-mediated responses of the rat urethra to phenylephrine have been examined in vitro. Phenylephrine caused concentration-dependent contractions of the isolated urethra which were antagonized by WB4101 (3-30 nM) and prazosin (10-100 nM) but not idazoxan (1.5 microM). Schild plot analysis of the antagonism by prazosin and WB4101 yielded straight lines with slopes not significantly different from unity. The pA2 value of 9.0 for WB4101 was significantly greater than the value previously obtained at the alpha 1B-adrenoceptor of the rat spleen. 2. 5-Methylurapidil (30 nM) and abanoquil (1 nM) caused dextral shifts of concentration-response curves yielding pKB values of 8.3 and 9.4 respectively. Maximal responses to phenylephrine were also reduced by this concentration of abanoquil. 3. Preincubation with chloroethylclonidine (25 microM for 40 min) failed to alter responses, but removing extracellular calcium or the presence of nifedipine (1 microM) almost abolished contractions to phenylephrine. 4. These results indicate that the responses of the rat urethra to phenylephrine are mediated via the alpha 1A-adrenoceptor subtype and are dependent on the influx of extracellular calcium.
摘要
  1. 已在体外研究了大鼠尿道对去氧肾上腺素的α1 -肾上腺素能受体介导的反应。去氧肾上腺素引起离体尿道浓度依赖性收缩,这种收缩被WB4101(3 - 30 nM)和哌唑嗪(10 - 100 nM)拮抗,但不被咪唑克生(1.5 μM)拮抗。对哌唑嗪和WB4101拮抗作用的Schild图分析得到斜率与1无显著差异的直线。WB4101的pA2值为9.0,显著大于先前在大鼠脾脏α1B -肾上腺素能受体处获得的值。2. 5 -甲基尿嘧啶(30 nM)和阿巴诺喹(1 nM)使浓度 -反应曲线向右移位,pKB值分别为8.3和9.4。该浓度的阿巴诺喹也降低了对去氧肾上腺素的最大反应。3. 用氯乙可乐定(25 μM,40分钟)预孵育未能改变反应,但去除细胞外钙或存在硝苯地平(1 μM)几乎消除了对去氧肾上腺素的收缩。4. 这些结果表明,大鼠尿道对去氧肾上腺素的反应是通过α1A -肾上腺素能受体亚型介导的,并且依赖于细胞外钙的内流。

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