Hermansson L E, Johansson P
Br J Pharmacol. 1986 Nov;89(3):447-52. doi: 10.1111/j.1476-5381.1986.tb11143.x.
The nature of the vascular alpha-adrenoceptors has been studied in the herring gull, Larus argentatus. In the anaesthetized herring gull, both phenylephrine and clonidine elicited dose-dependent increases in arterial blood pressure. The alpha 1-adrenoceptor antagonist prazosin was a better antagonist of phenylephrine than were the alpha 2-adrenoceptor antagonists yohimbine and rauwolscine. Yohimbine and rauwolscine were better antagonists of clonidine than was prazosin. The maximum response to phenylephrine, but not clonidine, was lower in reserpine-treated birds, indicating that phenylephrine in high doses liberates endogenous catecholamines, which contribute to the effect. It is concluded that the herring gull possesses postsynaptic, vascular alpha-adrenoceptors, of both the alpha 1- and alpha 2-subtypes, similar to those found in mammals.
已对银鸥(Larus argentatus)血管α-肾上腺素能受体的性质进行了研究。在麻醉的银鸥中,去氧肾上腺素和可乐定均引起动脉血压的剂量依赖性升高。α1-肾上腺素能受体拮抗剂哌唑嗪比α2-肾上腺素能受体拮抗剂育亨宾和萝芙木碱更有效地拮抗去氧肾上腺素。育亨宾和萝芙木碱比哌唑嗪更有效地拮抗可乐定。利血平处理的鸟类对去氧肾上腺素(而非可乐定)的最大反应较低,这表明高剂量的去氧肾上腺素会释放内源性儿茶酚胺,从而产生该效应。得出的结论是,银鸥拥有与哺乳动物中发现的类似的α1和α2亚型的突触后血管α-肾上腺素能受体。