Bodach E, Coceani F, Dumbrille A, Okpako D T, Olley P M
Br J Pharmacol. 1980;71(2):419-27. doi: 10.1111/j.1476-5381.1980.tb10954.x.
1 Responses of isolated ductus arteriosus preparations from near term guinea-pigs and lambs to transmural electrical stimulation and drugs were studied in a low oxygen medium (Po(2) 19 to 28 mmHg).2 Acetylcholine and noradrenaline contracted both vessels in a dose-dependent manner, their threshold being between 10(-8) and 10(-7) M. Transmural stimulation (pulse width 0.2 to 0.6 ms, typically 20 Hz) also contracted the vessels.3 Atropine and phentolamine or dibenzyline selectively blocked responses to acetylcholine and noradrenaline, respectively.4 In the guinea-pig ductus, part of the response to transmural stimulation was due to activation of intrinsic adrenergic nerves since the responses were reduced by alpha-adrenoceptor antagonists, bretylium or prior reserpine treatment, but not by atropine. The response of the lamp ductus to transmural stimulation varied greatly in magnitude and was inconsistently affected by alpha-adrenoceptor blocking drugs.5 There was no evidence that transmural stimulation activated cholinergic nerves in either species.6 After inactivation of alpha-adrenoceptors with dibenzyline, noradrenaline caused a beta-adrenoceptor-mediated relaxation. Both this effect and isoprenaline-mediated relaxation were blocked by propranolol. beta-Adrenoceptor activity was more prominent in the ductus of the guinea-pig than of the lamb.7 Raising the Po(2) from 19-28 to 92-98 mmHg increased the response of the guinea-pig ductus to transmural stimulation suggesting that, in this species, physiological elevation of oxygen tension at birth may increase transmitter release from intrinsic adrenergic nerves. Whether this mechanism would contribute to ductus closure remains an open question.8 We postulate that beta-adrenoceptor-mediated relaxation has a role in maintaining ductus patency in the guinea-pig foetus.
在低氧介质(氧分压19至28 mmHg)中研究了近足月豚鼠和羔羊离体动脉导管制剂对跨壁电刺激和药物的反应。
乙酰胆碱和去甲肾上腺素以剂量依赖方式使两种血管收缩,其阈值在10⁻⁸至10⁻⁷ M之间。跨壁刺激(脉冲宽度0.2至0.6 ms,通常为20 Hz)也使血管收缩。
阿托品和酚妥拉明或苄基乙胺分别选择性阻断对乙酰胆碱和去甲肾上腺素的反应。
在豚鼠动脉导管中,对跨壁刺激的部分反应是由于内在肾上腺素能神经的激活,因为α-肾上腺素能受体拮抗剂、溴苄铵或事先用利血平处理可使反应减弱,但阿托品则不能。羔羊动脉导管对跨壁刺激的反应在幅度上变化很大,且α-肾上腺素能阻断药物对其影响不一致。
没有证据表明跨壁刺激在这两个物种中激活了胆碱能神经。
用苄基乙胺使α-肾上腺素能受体失活后,去甲肾上腺素引起β-肾上腺素能受体介导的舒张。这种效应和异丙肾上腺素介导的舒张均被普萘洛尔阻断。β-肾上腺素能受体活性在豚鼠动脉导管中比在羔羊动脉导管中更明显。
将氧分压从19 - 28 mmHg提高到92 - 98 mmHg可增加豚鼠动脉导管对跨壁刺激的反应,这表明在该物种中,出生时氧张力的生理性升高可能增加内在肾上腺素能神经递质的释放。这种机制是否有助于动脉导管关闭仍是一个未解决的问题。
我们推测β-肾上腺素能受体介导的舒张在维持豚鼠胎儿动脉导管通畅中起作用。