Shepperson N B
Br J Pharmacol. 1984 Oct;83(2):463-9. doi: 10.1111/j.1476-5381.1984.tb16508.x.
Alpha 1 but not alpha 2-adrenoceptors mediate contractions of the cat nictitating membrane. The contractions of this tissue evoked by alpha 1-adrenoceptor agonists, but not those evoked by angiotensin II, are potentiated by pre-dosing with alpha 2-adrenoceptor agonists. This potentiation is reversed by the alpha 2-adrenoceptor antagonist, WY 26392. Pressor responses evoked by alpha 1-adrenoceptor agonists or angiotensin II were not affected by alpha 2-adrenoceptor agonists. Contractions of the nictitating membrane evoked by noradrenaline were reduced by pretreatment with WY 26392. These results suggest that in some tissues the role of alpha 2-adrenoceptors may be to modulate responses to alpha 1-adrenoceptors, rather than to evoke a discrete response themselves.
α1 肾上腺素能受体而非 α2 肾上腺素能受体介导猫瞬膜的收缩。α1 肾上腺素能受体激动剂诱发的该组织收缩,而非血管紧张素 II 诱发的收缩,会因预先给予 α2 肾上腺素能受体激动剂而增强。这种增强作用可被 α2 肾上腺素能受体拮抗剂 WY 26392 逆转。α1 肾上腺素能受体激动剂或血管紧张素 II 诱发的升压反应不受 α2 肾上腺素能受体激动剂影响。用 WY 26392 预处理可降低去甲肾上腺素诱发的瞬膜收缩。这些结果表明,在某些组织中,α2 肾上腺素能受体的作用可能是调节对 α1 肾上腺素能受体的反应,而非自身引发离散反应。