Brambilla F, Lampertico M, Panerai A E, Sali L, Salerno F, Müller E E
Psychiatry Res. 1984 Dec;13(4):295-304. doi: 10.1016/0165-1781(84)90077-5.
Neuroendocrine effects of intravenous injections of clonidine, 0.15 mg, were investigated in 13 heroin addicts and 14 normal control subjects. The study was designed to determine whether continuous opiate administration leads to the development of hypersensitive alpha 2-adrenergic receptors. The peak increments in levels of plasma growth hormone (GH) and beta-endorphin induced by clonidine did not differ between heroin addicts and normal control subjects. At no time interval could the clonidine-induced rise in GH levels in addicts be differentiated from that induced by placebo. Clonidine failed to alter plasma prolactin, gonadotropin, or thyrotropin levels in either heroin addicts or controls. Since clonidine's neuroendocrine effects are reportedly due to the activation of postsynaptic alpha 2-adrenoceptors, it appears that (1) continuous opiate use does not lead to the development of hypersensitive alpha 2-adrenergic receptors involved in neuroendocrine mechanisms and (2) brain norepinephrine does not play a role in the regulation of tonic prolactin, gonadotropin, and thyrotropin secretion in man.
对13名海洛因成瘾者和14名正常对照者研究了静脉注射0.15毫克可乐定的神经内分泌效应。该研究旨在确定持续给予阿片类药物是否会导致超敏α2 - 肾上腺素能受体的形成。可乐定诱导的血浆生长激素(GH)和β-内啡肽水平的峰值增量在海洛因成瘾者和正常对照者之间没有差异。在任何时间间隔,成瘾者中可乐定诱导的GH水平升高都无法与安慰剂诱导的升高区分开来。可乐定未能改变海洛因成瘾者或对照组的血浆催乳素、促性腺激素或促甲状腺激素水平。由于据报道可乐定的神经内分泌效应是由于突触后α2 - 肾上腺素能受体的激活,因此似乎(1)持续使用阿片类药物不会导致参与神经内分泌机制的超敏α2 - 肾上腺素能受体的形成,并且(2)脑去甲肾上腺素在人类紧张性催乳素、促性腺激素和促甲状腺激素分泌的调节中不起作用。