Frischknecht H R, Siegfried B
Institute of Pharmacology, University of Zurich, Switzerland.
Physiol Behav. 1988;44(3):383-8. doi: 10.1016/0031-9384(88)90041-8.
Mice of the inbred strain DBA/2, when exposed to a social conflict, developed a low intensity, naloxone-insensitive analgesia after 15 bites, and a more pronounced naloxone-sensitive analgesia after 45 bites. The effective inhibition of the antinociceptive response following low and high number of bites by the alkylating opiate antagonist beta-chlornaltrexamine suggests participation of opioid mechanisms at both stress levels. Emergence of an increased tail-flick latency was indicated by the occurrence of defensive upright postures upon contact with the opponent, while animals displaying full analgesic response during the period of bite 31-45 increased their escape reactions without being in contact with the aggressor. Suppression of social conflict analgesia in mice by pretreatment with opiate antagonists facilitated the occurrence of these escape reactions. The display of panic escape responses is discussed in the context of increased fear and helplessness that developed under conditions of sustained attacks.
近交系DBA/2小鼠在遭遇社会冲突时,被咬15次后会产生低强度、纳洛酮不敏感的镇痛作用,被咬45次后会产生更明显的纳洛酮敏感的镇痛作用。烷基化阿片拮抗剂β-氯诺啡胺对低次数和高次数咬伤后的抗伤害感受反应的有效抑制表明,在这两种应激水平下阿片机制均有参与。与对手接触时出现防御性直立姿势表明甩尾潜伏期增加,而在第31 - 45次咬伤期间表现出完全镇痛反应的动物在未与攻击者接触的情况下增加了逃避反应。用阿片拮抗剂预处理抑制小鼠的社会冲突镇痛作用,促进了这些逃避反应的发生。在持续攻击条件下产生的恐惧和无助感增加的背景下,讨论了恐慌逃避反应的表现。