Couldwell C, Jackson A, O'Brien H, Chess-Williams R
Department of Biomedical Science, University of Sheffield, UK.
J Pharm Pharmacol. 1993 Oct;45(10):922-4. doi: 10.1111/j.2042-7158.1993.tb05623.x.
The alpha 1-adrenoceptor-mediated responses of the rat prostate to phenylephrine have been examined in-vitro. Phenylephrine induced concentration-dependent contractions of the isolated prostate gland which were antagonized by WB4101 (1-30 nM). Schild plot analysis of the antagonism yielded a straight line with a slope not significantly different from unity. The pKB value of 9.2 was similar to that obtained for WB4101 on the rat vas deferens (9.4) but was greater than that obtained on the rat spleen (8.4). Chloroethylclonidine depressed responses to phenylephrine of the rat spleen but not the prostate or the vas deferens. These results indicate that the rat prostate gland possesses a typical alpha 1A-adrenoceptor similar to that found in the vas deferens.
已在体外研究了大鼠前列腺对去氧肾上腺素的α1-肾上腺素能受体介导的反应。去氧肾上腺素可诱导离体前列腺产生浓度依赖性收缩,而这种收缩可被WB4101(1 - 30 nM)拮抗。对这种拮抗作用进行的Schild图分析得到一条直线,其斜率与1无显著差异。9.2的pKB值与在大鼠输精管上得到的WB4101的pKB值(9.4)相似,但大于在大鼠脾脏上得到的pKB值(8.4)。氯乙可乐定可抑制大鼠脾脏对去氧肾上腺素的反应,但不影响前列腺或输精管。这些结果表明,大鼠前列腺具有与输精管中发现的典型α1A-肾上腺素能受体相似的受体。