Sinha J N, Gurtu S, Sharma D K, Bhargava K P
Naunyn Schmiedebergs Arch Pharmacol. 1985 Sep;330(3):163-8. doi: 10.1007/BF00572428.
Microinjection of noradrenaline and clonidine into lateral medullary pressor area (LMPA) of chloralose anaesthetized cats produced dose dependent decrease in blood pressure without affecting heart rate, while phenylephrine did not elicit any cardiovascular response. Selective alpha 2-adrenoceptor antagonists idazoxan and piperoxan, microinjected locally, blocked the effects of the agonists but prazosin and phenoxybenzamine, which are relatively selective for alpha 1-adrenoceptors, failed to do so. Clonidine did not elicit any response in guanethidine pretreated cats but noradrenaline microinjected into LMPA of these animals induced a pressor response which was blocked by prazosin pretreatment. It is concluded that catecholaminergic fibres impinging upon this area inhibit the activity of the inhibitory second order baroreceptor neurone by activating alpha 1-adrenoceptors while alpha 2-adrenoceptors situated presynaptically on these inhibitory catecholaminergic nerve terminals are responsible for the manifestation of the hypotensive effect of clonidine and exogenously administered noradrenaline.
向用氯醛糖麻醉的猫的延髓外侧加压区(LMPA)微量注射去甲肾上腺素和可乐定,可使血压呈剂量依赖性下降,而不影响心率,而苯肾上腺素未引起任何心血管反应。局部微量注射选择性α2肾上腺素能拮抗剂咪唑克生和哌罗克生可阻断激动剂的作用,但对α1肾上腺素能受体具有相对选择性的哌唑嗪和酚苄明则不能。可乐定对胍乙啶预处理的猫未引起任何反应,但向这些动物的LMPA微量注射去甲肾上腺素可诱发升压反应,该反应可被哌唑嗪预处理阻断。结论是,作用于该区域的儿茶酚胺能纤维通过激活α1肾上腺素能受体抑制抑制性二级压力感受器神经元的活动,而位于这些抑制性儿茶酚胺能神经末梢突触前的α2肾上腺素能受体则是可乐定和外源性给予的去甲肾上腺素降压作用表现的原因。