Bond R A, Charlton K G, Clarke D E
J Pharmacol Exp Ther. 1986 Feb;236(2):408-15.
The mode of action of clonidine and norepinephrine (NE) has been investigated in the isolated transmurally stimulated guinea-pig ileum preparation using rauwolscine, idazoxan and benextramine as antagonists. Both clonidine and NE produced concentration-dependent inhibition of the cholinergically induced twitch response and were antagonized by rauwolscine and idazoxan, but only clonidine was antagonized in a truly competitive fashion. Benextramine, an irreversible alpha adrenoceptor antagonist, in a concentration of 10(-5) M, inhibited the effect of clonidine completely but only partially antagonized the inhibitory action of NE. The antagonism of NE by rauwolscine and benextramine was most pronounced after reserpine pretreatment and blockade of neuronal and extraneuronal uptake. Under these conditions, the concentration-effect curve to NE remaining after treatment with benextramine showed an IC50 of about 3 X 10(-7) M and an intrinsic activity of 0.6. This curve was resistant to further inhibition by clonidine (10(-5) M), phentolamine (3 X 10(-6) M), rauwolscine (3 X 10(-6) M), prazosin (10(-6) M) and propranolol (1.2 X 10(-5) M). Thus, alpha and beta adrenergic receptors do not appear to be involved. It is postulated that NE-induced inhibition of the guinea-pig ileum twitch response is mediated by two distinct sites: one is the classical alpha-2 adrenoceptor (the site of action of clonidine and the alpha adrenoceptor antagonists) whereas the other is a site seemingly unrelated to the alpha and beta subtypes.
使用萝芙木碱、咪唑克生和苄胺唑啉作为拮抗剂,在离体经壁刺激的豚鼠回肠制备物中研究了可乐定和去甲肾上腺素(NE)的作用方式。可乐定和NE均产生浓度依赖性抑制胆碱能诱导的抽搐反应,且被萝芙木碱和咪唑克生拮抗,但只有可乐定以真正竞争性方式被拮抗。苄胺唑啉是一种不可逆的α肾上腺素能受体拮抗剂,浓度为10⁻⁵ M时,可完全抑制可乐定的作用,但仅部分拮抗NE的抑制作用。在利血平预处理以及神经元和非神经元摄取被阻断后,萝芙木碱和苄胺唑啉对NE的拮抗作用最为明显。在这些条件下,苄胺唑啉处理后剩余的NE浓度-效应曲线显示IC50约为3×10⁻⁷ M,内在活性为0.6。该曲线对可乐定(10⁻⁵ M)、酚妥拉明(3×10⁻⁶ M)、萝芙木碱(3×10⁻⁶ M)、哌唑嗪(10⁻⁶ M)和普萘洛尔(1.2×10⁻⁵ M)的进一步抑制具有抗性。因此,α和β肾上腺素能受体似乎未参与其中。据推测,NE诱导的豚鼠回肠抽搐反应抑制是由两个不同位点介导的:一个是经典的α₂肾上腺素能受体(可乐定和α肾上腺素能受体拮抗剂的作用位点),而另一个位点似乎与α和β亚型无关。