Frankhuijzen A L, Wardeh G, Hogenboom F, Mulder A H
Department of Pharmacology, Medical Faculty, Free University, Amsterdam, The Netherlands.
Naunyn Schmiedebergs Arch Pharmacol. 1988 Mar;337(3):255-60. doi: 10.1007/BF00168835.
Possible local interactions between noradrenergic and serotonergic systems in the dorsal raphe region of the rat were investigated by studying the effects of various drugs on depolarization (20 mmol/l K+)-induced release of [3H]5-hydroxytryptamine (5-HT) and [3H]noradrenaline (NA) in vitro using a superfusion method. Exogenous 5-HT did not influence the release of [3H]NA. However, NA (in the presence of 10 mumol/l desipramine) as well as the selective alpha 2-adrenoceptor agonists clonidine and oxymetazoline strongly inhibited [3H]5-HT release. The selective alpha 1-adrenoceptor agonists phenylephrine and methoxamine did not affect the release of either [3H]5-HT or [5H]NA. The inhibition by NA of both [3H]5-HT and [3H]NA release was not affected by the beta-adrenoceptor antagonist sotalol nor by the selective alpha 1-adrenoceptor antagonist prazosin. However, phentolamine and the selective alpha 2-adrenoceptor antagonists yohimbine and rauwolscine competitively antagonized the inhibitory effect of NA on [3H]NA release (respective pA2-values 7.5 and 8.3) and on [3H]5-HT release (respective pA2-values 7.7 and 8.2). Moreover, the release of [3H]NA and also, but to a lesser extent, that of [3H]5-HT were increased by the antagonists. It is concluded that the release of both 5-HT and NA in the dorsal raphe region may be subject to presynaptic inhibition by NA via activation of alpha 2-adrenoceptors.
通过使用灌流法研究各种药物对去极化(20 mmol/l K+)诱导的[3H]5-羟色胺(5-HT)和[3H]去甲肾上腺素(NA)在体外释放的影响,对大鼠中缝背核区域去甲肾上腺素能和5-羟色胺能系统之间可能的局部相互作用进行了研究。外源性5-HT不影响[3H]NA的释放。然而,NA(在存在10 μmol/l地昔帕明的情况下)以及选择性α2-肾上腺素能受体激动剂可乐定和羟甲唑啉强烈抑制[3H]5-HT的释放。选择性α1-肾上腺素能受体激动剂去氧肾上腺素和甲氧明不影响[3H]5-HT或[3H]NA的释放。NA对[3H]5-HT和[3H]NA释放的抑制作用不受β-肾上腺素能受体拮抗剂索他洛尔或选择性α1-肾上腺素能受体拮抗剂哌唑嗪的影响。然而,酚妥拉明以及选择性α2-肾上腺素能受体拮抗剂育亨宾和萝芙木碱竞争性拮抗NA对[3H]NA释放(各自的pA2值为7.5和8.3)和对[3H]5-HT释放(各自的pA2值为7.7和8.2)的抑制作用。此外,拮抗剂增加了[3H]NA的释放,也增加了[3H]5-HT的释放,但程度较小。结论是,中缝背核区域5-HT和NA的释放可能通过α2-肾上腺素能受体的激活受到NA的突触前抑制。