Miñano F J, McMillen B A, Myers R D
Department of Pharmacology, East Carolina University School of Medicine, Greenville, NC 27858.
Alcohol. 1989 Mar-Apr;6(2):133-7. doi: 10.1016/0741-8329(89)90038-4.
The effects of the 1-aromatic amino acid decarboxylase inhibitor, Ro 4-4602 (benserazide), was determined on alcohol drinking induced in the rat by tetrahydropapaveroline (THP) injected by the intracerebroventricular (ICV) route. After ICV guide cannulae were implanted stereotaxically in 19 Sprague-Dawley rats, an artificial CSF solution containing 5.0 ng/micrograms THP was infused twice daily for 3 days in a volume of 5.0 microliters. Following a standard self-selection procedure, concentrations of alcohol which ranged from 3-30% were presented to the rats. A single maximally preferred solution, which in these rats ranged from 9-12% alcohol, was then offered in the presence of water. After a 4-day pretest in which alcohol intakes had stabilized, either 50 or 100 micrograms Ro 4-4602 plus THP were infused ICV to the animal during a 3-day period. Both doses of Ro 4-4602 significantly antagonized the g amount and proportional intakes of alcohol, but the higher dose was nearly twice as potent as the lower. During the 4-day postdrug test period, alcohol drinking continued to be suppressed. When THP was infused ICV over a 3-day period following the injections of Ro 4-4602, the predrug alcohol intake was partially reinstated, suggesting that this TIQ, when delivered directly into the brain, partly reversed the potent central action of Ro 4-4602. These results show that interference with the functional activity of central catecholamine pathways in the rat, by means of the inhibition of dopamine synthesis, serves to modify markedly the mechanisms underlying alcohol drinking in this species.(ABSTRACT TRUNCATED AT 250 WORDS)
研究了1-芳香氨基酸脱羧酶抑制剂罗4-4602(苄丝肼)对脑室内(ICV)注射四氢罂粟碱(THP)诱导大鼠饮酒的影响。在19只Sprague-Dawley大鼠中立体定位植入ICV引导套管后,每天两次以5.0微升的体积注入含5.0纳克/微克THP的人工脑脊液溶液,持续3天。按照标准的自我选择程序,向大鼠提供浓度范围为3%-30%的酒精。然后在有水的情况下提供单一的最优选溶液,在这些大鼠中,该溶液含9%-12%的酒精。在进行了4天的酒精摄入量稳定的预试验后,在3天内给动物ICV注入50或100微克罗4-4602加THP。两种剂量的罗4-4602均显著拮抗酒精的摄入量和摄入比例,但高剂量的效力几乎是低剂量的两倍。在停药后4天的试验期内,饮酒量持续受到抑制。在注射罗4-4602后3天内ICV注入THP时,给药前的酒精摄入量部分恢复,这表明这种TIQ直接注入脑内时,部分逆转了罗4-4602强大的中枢作用。这些结果表明,通过抑制多巴胺合成来干扰大鼠中枢儿茶酚胺途径的功能活性,可显著改变该物种饮酒的潜在机制。(摘要截短至250字)