Wood J M
Psychopharmacology (Berl). 1980 Jan;67(1):67-72. doi: 10.1007/BF00427597.
Brain 5-hydroxytryptamine (5-HT) was depleted in rats by intraventricular injection with 5,7-dihyroxytryptamine (5,7-DHT) prior to feeding rats a liquid diet containing ethanol. After withdrawal of ethanol, withdrawal reactions were significantly less severe in 5-HT-depleted rats than control rats. Sleeping times after a standard dose of ethanol or pentobarbitone were significantly prolonged in 5-HT-depleted rats. However, metabolic and pharmacodynamic tolerance developed to a similar extent in 5-HT-depleted rats as in control rats. It was concluded that 5-hydroxytryptaminergic neurons are not directly involved in the development of physical dependence on or tolerance to ethanol. Depletion of brain 5-HT by 5,7-DHT appears to result in a non-specific central nervous system depression that potentiates the depressant actions of ethanol and pentobarbitone and antagonises the hyperexcitability of ethanol withdrawal.
在给大鼠喂食含乙醇的液体饲料之前,通过脑室内注射5,7 - 二羟基色胺(5,7 - DHT)使大鼠脑内5 - 羟色胺(5 - HT)耗竭。乙醇戒断后,5 - HT耗竭的大鼠戒断反应明显比对照大鼠轻。给予标准剂量的乙醇或戊巴比妥后,5 - HT耗竭的大鼠睡眠时间显著延长。然而,5 - HT耗竭的大鼠与对照大鼠在代谢和药效学耐受性方面的发展程度相似。得出的结论是,5 - 羟色胺能神经元不直接参与对乙醇的身体依赖性或耐受性的形成。5,7 - DHT导致脑内5 - HT耗竭似乎会引起非特异性的中枢神经系统抑制,这种抑制增强了乙醇和戊巴比妥的抑制作用,并拮抗了乙醇戒断时的过度兴奋。