Tomlinson D R
Med Biol. 1980 Apr;58(2):82-6.
The effects of the prostaglandin synthetase inhibitors aspirin, indomethacin and meclofenamic acid have been studied on the response of the rat isolated perfused vas deferens. None of these drugs, up to a concentration of 5 x 10(-5) M affected either phase of the biphasic constrictor response to 30 s periods of field stimulation. In the same preparations an inhibition of the response to field stimulation was seen in the presence of prostaglandin E1 at concentrations of 1 to 5 ng ml-1. All three prostaglandin synthetase inhibitors, at 5 x 10(-5) M, caused significant reduction of prostaglandin biosynthesis by homogenates of rat vas deferens. It is, therefore, suggested that stimuli which activate directly the noradrenergic nerves in the rat vas do not activate simultaneously a release of endogenous prostaglandins.
已经研究了前列腺素合成酶抑制剂阿司匹林、消炎痛和甲氯芬那酸对大鼠离体灌注输精管反应的影响。在浓度高达5×10⁻⁵M时,这些药物均未影响对30秒场刺激的双相收缩反应的任何一个阶段。在相同的制备物中,当存在浓度为1至5纳克/毫升的前列腺素E1时,可观察到对场刺激反应的抑制。所有三种前列腺素合成酶抑制剂在5×10⁻⁵M时,均可使大鼠输精管匀浆中的前列腺素生物合成显著减少。因此,有人提出,直接激活大鼠输精管中去甲肾上腺素能神经的刺激不会同时激活内源性前列腺素的释放。