Frischknecht H R, Siegfried B
Institute of Pharmacology, University of Zurich, Switzerland.
Psychopharmacology (Berl). 1989;97(2):160-2. doi: 10.1007/BF00442241.
The relationship between analgesia and behavior during and after an aggressive encounter was investigated in saline- and opiate antagonist-treated DBA mice. A low number of bites induced an analgesia that was reversed by beta-chlornaltrexamine but not by naloxone, and that correlated positively with increased displays of defensive upright and immobility upon contact with the opponent. Extended attacks induced a naloxone-sensitive analgesia that was linked to a delayed occurrence of "panic" escape behavior. In the post-conflict phase, the degree of immobility and analgesia correlated positively in attacked mice. Naltrexone prevented this analgesia and lowered immobility. Endogenous opioids released during social conflict may induce analgesia and immobility in DBA mice.
在生理盐水和阿片类拮抗剂处理的DBA小鼠中,研究了攻击性遭遇期间及之后镇痛与行为之间的关系。少量撕咬会诱导一种镇痛作用,这种镇痛作用可被β-氯代纳曲胺逆转,但不能被纳洛酮逆转,且与接触对手时防御性直立和不动行为的增加呈正相关。长时间攻击会诱导一种对纳洛酮敏感的镇痛作用,这种作用与“恐慌”逃避行为的延迟出现有关。在冲突后阶段,受攻击小鼠的不动程度和镇痛程度呈正相关。纳曲酮可预防这种镇痛作用并降低不动程度。社会冲突期间释放的内源性阿片类物质可能会在DBA小鼠中诱导镇痛和不动行为。