Sandi C, Borrell J, Guaza C
Department of Psychobiology, Cajal Institute, Madrid, Spain.
Physiol Behav. 1989 Jan;45(1):87-92. doi: 10.1016/0031-9384(89)90169-8.
Attention has been focused on the possibility of an interaction between the endorphinergic system and ethanol intake. In the present study, the effects of subcutaneous (SC) administration of beta-endorphin (beta-E) (0.25, 1 and 5 micrograms/kg) and/or naloxone (NX) (1 or 2.5 mg/kg) on ethanol preference (EP) have been investigated in rats. Under our procedural conditions, rats developed ethanol preference (EP) by a forced ethanol drinking session (conditioning session). Preconditioning administration of beta-E (1 microgram/kg) reduced later EP. When beta-E was administered postconditioning, the opioid affects ethanol preference depending on the dose: both 0.25 micrograms/kg and 5 microgram/kg reduced EP, but the dose of 1 microgram/kg did not alter it. Administration of beta-E (1 and 5 micrograms/kg) before the first testing session attenuated EP. NX antagonized the effects of beta-E on EP in the three experimental procedures used, indicating that mu-opioid receptors might be involved in the beta-E-induced reductions on EP. Our results provide further evidences for a beta-endorphinergic system involvement on the mechanism leading to consumption of ethanol.
内啡肽能系统与乙醇摄入之间相互作用的可能性已受到关注。在本研究中,研究了皮下注射β-内啡肽(β-E)(0.25、1和5微克/千克)和/或纳洛酮(NX)(1或2.5毫克/千克)对大鼠乙醇偏好(EP)的影响。在我们的实验条件下,大鼠通过强制乙醇饮用期(适应期)形成乙醇偏好(EP)。预处理给予β-E(1微克/千克)可降低后期的EP。当在适应期后给予β-E时,阿片类药物对乙醇偏好的影响取决于剂量:0.25微克/千克和5微克/千克均降低了EP,但1微克/千克的剂量未改变它。在第一次测试前给予β-E(1和5微克/千克)可减弱EP。在所用的三个实验过程中,NX拮抗了β-E对EP的影响,表明μ-阿片受体可能参与了β-E诱导的EP降低。我们的结果为内啡肽能系统参与导致乙醇消耗的机制提供了进一步的证据。