Hodge C W, Niehus J S, Samson H H
Department of Physiology and Pharmacology, Wake Forest University, Bowman Gray School of Medicine, Winston-Salem, N.C. 27157, USA.
Psychopharmacology (Berl). 1995 May;119(2):186-92. doi: 10.1007/BF02246160.
The opiate agonist morphine has been shown to increase ethanol intake and mesolimbic dopamine (DA) levels. Conversely, the 5-HT3/4 antagonist tropisetron has been shown to decrease ethanol intake and morphine-induced increases in mesolimbic DA levels. This study was designed to test the effects of acutely administered tropisetron on morphine-induced changes in ethanol (6% v/v) and water intake in a two-bottle test procedure. Ten water restricted male rats were injected with combinations of morphine (0.0, 0.56, 1.0, 1.5, 10.0, and 17.0 mg/kg, SC) and tropisetron (0.0, 1.0, 10.0, and 17.0 mg/kg, SC) prior to test sessions. Morphine (1.0 and 1.5 mg/kg) significantly increased absolute (g/kg) and relative ethanol intake (ethanol/total fluid). Tropisetron alone did not affect ethanol or water intake. When tropisetron (10.0 and 17.0 mg/kg) was administered in combination with morphine (1.5 mg/kg), the increase in ethanol intake induced by morphine was attenuated. Tropisetron (1.0 mg/kg) reversed a decrease in ethanol intake induced by morphine (17.0 mg/kg). The two highest doses of tropisetron partially attenuated a significant decrease in water intake produced by morphine (17.0 mg/kg). These data suggest that opiate and 5-HT3 mechanisms could interact in the regulation of ethanol intake. However, the doses of tropisetron tested were high and, therefore, the potential involvement of 5-HT4 receptors or other neurotransmitter systems in regulating ethanol intake is discussed.
阿片类激动剂吗啡已被证明可增加乙醇摄入量和中脑边缘多巴胺(DA)水平。相反,5-HT3/4拮抗剂托烷司琼已被证明可减少乙醇摄入量以及吗啡诱导的中脑边缘DA水平升高。本研究旨在通过双瓶测试程序,测试急性给予托烷司琼对吗啡诱导的乙醇(6% v/v)和水摄入量变化的影响。在测试前,对10只限水雄性大鼠注射吗啡(0.0、0.56、1.0、1.5、10.0和17.0 mg/kg,皮下注射)和托烷司琼(0.0、1.0、10.0和17.0 mg/kg,皮下注射)的组合。吗啡(1.0和1.5 mg/kg)显著增加绝对(g/kg)和相对乙醇摄入量(乙醇/总液体量)。单独使用托烷司琼不影响乙醇或水的摄入量。当托烷司琼(10.0和17.0 mg/kg)与吗啡(1.5 mg/kg)联合使用时,吗啡诱导的乙醇摄入量增加被减弱。托烷司琼(1.0 mg/kg)逆转了吗啡(17.0 mg/kg)诱导的乙醇摄入量减少。托烷司琼的两个最高剂量部分减弱了吗啡(17.0 mg/kg)引起的水摄入量显著减少。这些数据表明,阿片类和5-HT3机制可能在乙醇摄入的调节中相互作用。然而,所测试的托烷司琼剂量较高,因此讨论了5-HT4受体或其他神经递质系统在调节乙醇摄入中的潜在作用。