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脯氨酰-亮氨酰-甘氨酰胺可降低小鼠的攻击性,并阻断失败诱导的阿片类镇痛作用。

Prolyl-leucyl-glycinamide reduces aggression and blocks defeat-induced opioid analgesia in mice.

作者信息

Teskey G C, Kavaliers M

出版信息

Peptides. 1985 Mar-Apr;6(2):165-7. doi: 10.1016/0196-9781(85)90034-8.

Abstract

The effects of Prolyl-leucyl-glycinamide (PLG, MIF-1) and the exogenous opiate antagonist naloxone, on aggressive interactions and defeat-induced analgesia were examined in male mice. Both substances reduced the number of bites required to obtain defeat in subordinate mice during aggressive encounters as well as blocking the subsequent defeat-induced analgesia. These results suggest that MIF-1 may function as an endogenous opioid antagonist and have an inhibitory influence on aggression.

摘要

研究了脯氨酰 - 亮氨酰 - 甘氨酰胺(PLG,MIF - 1)和外源性阿片拮抗剂纳洛酮对雄性小鼠攻击性行为和战败诱导性镇痛的影响。这两种物质均减少了从属小鼠在攻击性遭遇中获得战败所需的撕咬次数,并阻断了随后的战败诱导性镇痛。这些结果表明,MIF - 1可能作为内源性阿片拮抗剂发挥作用,并对攻击行为产生抑制性影响。

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