Muraki T, Ishii K, Kato R
Arch Int Pharmacodyn Ther. 1986 Apr;280(2):264-74.
Effects of clonidine and yohimbine on plasma cyclic nucleotide levels were investigated in both clonidine-naive and clonidine-treated male mice. Clonidine increased plasma cyclic GMP but decreased slightly cyclic AMP levels in clonidine-naive mice. Clonidine treatment for 10-14 days in the drinking water did not decrease the cyclic GMP response to clonidine indicating that no tolerance develops to the effect of clonidine on plasma cyclic GMP. alpha 2-Agonists, such as clonidine, oxymetazoline and naphazoline, were more potent than phenylephrine, an alpha 1-agonist, in increasing cyclic GMP, although azepexole, a weak alpha 2-agonist, had no effect. Inhibition of clonidine-induced increase in plasma cyclic GMP by yohimbine, hexamethonium and atropine, but not by prazosin suggests that the effect of clonidine is mediated by the central alpha 2-adrenoceptors, activating the muscarinic receptor-linked guanylate cyclase through the stimulation of vagal activity. Yohimbine increased plasma cyclic AMP levels in clonidine-naive mice. Inhibition of this effect by hexamethonium and propranolol suggests that yohimbine increases plasma cyclic AMP through increasing the sympathetic tone. The increase in plasma cyclic AMP elicited by yohimbine was potentiated by chronic clonidine treatment. Enhancement of the cyclic AMP effect of yohimbine found in clonidine-treated mice may be regarded as a precipitated withdrawal symptom and indicate development of dependence on clonidine.
在未使用可乐定的雄性小鼠和使用过可乐定的雄性小鼠中,研究了可乐定和育亨宾对血浆环核苷酸水平的影响。在未使用可乐定的小鼠中,可乐定可提高血浆环鸟苷酸(cGMP)水平,但会使环磷酸腺苷(cAMP)水平略有下降。在饮用水中给予可乐定治疗10 - 14天,并未降低对可乐定的环鸟苷酸反应,这表明对可乐定对血浆环鸟苷酸的作用不会产生耐受性。α2激动剂,如可乐定、羟甲唑啉和萘甲唑啉,在提高环鸟苷酸方面比α1激动剂去氧肾上腺素更有效,尽管弱α2激动剂阿泽哌唑没有作用。育亨宾、六甲铵和阿托品可抑制可乐定诱导的血浆环鸟苷酸升高,但哌唑嗪则无此作用,这表明可乐定的作用是由中枢α2肾上腺素能受体介导的,通过刺激迷走神经活动激活与毒蕈碱受体相连的鸟苷酸环化酶。育亨宾可提高未使用可乐定小鼠的血浆环磷酸腺苷水平。六甲铵和普萘洛尔对这种作用的抑制表明,育亨宾通过增加交感神经张力来提高血浆环磷酸腺苷水平。长期使用可乐定治疗可增强育亨宾引起的血浆环磷酸腺苷升高。在使用可乐定的小鼠中发现育亨宾的环磷酸腺苷作用增强,可能被视为一种戒断症状,并表明对可乐定产生了依赖性。