Dotti C G, Taleisnik S
Eur J Pharmacol. 1984 Mar 16;99(1):9-14. doi: 10.1016/0014-2999(84)90426-6.
Previous studies have indicated that stimulation of the locus coeruleus (LC) produced inhibition of the release of LH induced by stimulation of the medial preoptic area (mPOA) in ovariectomized, estrogen-primed rats. A similar response following the application of drugs into the LC was taken as an index of activation of the LC neurons. The injection of the phenylethanolamine N-methyltransferase (PNMT) blocking-agent, 2,3- dichloromethylbenzylamine ( DCMB , 0.5 micrograms) into the LC, 2 and 1 h before starting the mPOA stimulation greatly attenuated the induced release of LH. Injection of saline had no effect. The reduced release of LH in DCMB -treated rats was restored to normal by injecting clonidine (0.5 micrograms) into the LC immediately before the mPOA stimulus started, but not by injecting phenylephrine (0.5 micrograms) or saline (0.5 microliter). The release of LH induced by mPOA stimulation was also blocked in rats in which the alpha 2-antagonist, piperoxane (0.5 micrograms) was injected into the LC but not in those injected with the alpha 1-antagonist, phenoxybenzamine (0.5 micrograms) or the beta-antagonist, propranolol (0.5 micrograms). It is concluded that adrenergic afferents into the LC tonically inhibited the activity of LC neurons and that this effect is mediated by alpha 2-adrenoceptors. Interference with the synthesis of epinephrine or blockade of alpha 2-adrenoceptors resulted in activation of LC neurons and thereby in inhibition of LH release.
先前的研究表明,在去卵巢并用雌激素预处理的大鼠中,刺激蓝斑(LC)会抑制由刺激内侧视前区(mPOA)诱导的促黄体生成素(LH)释放。向LC内注射药物后出现的类似反应被视为LC神经元激活的指标。在开始刺激mPOA前2小时和1小时,向LC内注射苯乙醇胺N-甲基转移酶(PNMT)阻断剂2,3-二氯甲基苄胺(DCMB,0.5微克),可大大减弱诱导的LH释放。注射生理盐水则无此作用。在开始刺激mPOA前立即向LC内注射可乐定(0.5微克)可使DCMB处理的大鼠中降低的LH释放恢复正常,但注射去氧肾上腺素(0.5微克)或生理盐水(0.5微升)则不能。在向LC内注射α2拮抗剂哌罗克生(0.5微克)的大鼠中,mPOA刺激诱导的LH释放也受到阻断,但在注射α1拮抗剂酚苄明(0.5微克)或β拮抗剂普萘洛尔(0.5微克)的大鼠中则未受阻断。得出的结论是,进入LC的肾上腺素能传入神经持续抑制LC神经元的活性,且这种作用是由α2肾上腺素能受体介导的。干扰肾上腺素的合成或阻断α2肾上腺素能受体会导致LC神经元激活,从而抑制LH释放。