Soubrié P, Jobert A, Thiebot M H
Psychopharmacology (Berl). 1980;69(1):101-5. doi: 10.1007/BF00426529.
The effects of naloxone on diazepam-induced release of behavior in aversive situations were investigated in rats. Naloxone (0.5 and 1 mg/kg-1) suppressed diazepam-induced eating in an unfamiliar situation and reduced (1 mg/kg-1) spontaneous food intake. Naloxone (1 mg/kg-1) canceled the increased lever pressing produced by diazepam in a conflict procedure in which one electric shock was delivered at each seventh press. Naloxone (1 mg/kg-1) failed to reverse the enhanced responding for food induced by diazepam in the presence of a signal previously paired with electric foot shocks. In this situation, naloxone alone reinforced the behavioral suppression. These results suggest that transmission mediated by opiate peptides may be involved in only some 'disinhibitory' effects of benzodiazepines. In addition, such a peptidergic transmission may play a role in the control of stress-induced behavioral suppression.
在大鼠中研究了纳洛酮对厌恶情境中地西泮诱导的行为释放的影响。纳洛酮(0.5和1毫克/千克-1)在陌生情境中抑制地西泮诱导的进食,并减少(1毫克/千克-1)自发食物摄入量。纳洛酮(1毫克/千克-1)在一种冲突程序中消除了地西泮产生的杠杆按压增加,在该程序中每第七次按压会施加一次电击。在存在先前与足部电击配对的信号的情况下,纳洛酮(1毫克/千克-1)未能逆转地西泮诱导的对食物的增强反应。在这种情况下,单独使用纳洛酮会增强行为抑制。这些结果表明,阿片肽介导的传递可能仅参与苯二氮䓬类药物的某些“去抑制”作用。此外,这种肽能传递可能在应激诱导的行为抑制的控制中起作用。