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青春期中期单次注射氯胺酮可通过增加食物摄入和减弱过度活跃及类似焦虑样行为,促进雌性小鼠对抗活动限制型厌食症的持久恢复能力。

Single injection of ketamine during mid-adolescence promotes long-lasting resilience to activity-based anorexia of female mice by increasing food intake and attenuating hyperactivity as well as anxiety-like behavior.

机构信息

Center for Neural Science, New York University, New York, New York.

Neuroscience Institute, Langone Medical Center, New York University, New York, New York.

出版信息

Int J Eat Disord. 2018 Aug;51(8):1020-1025. doi: 10.1002/eat.22937. Epub 2018 Aug 13.

DOI:10.1002/eat.22937
PMID:30102796
Abstract

OBJECTIVE

This study tested the effects of ketamine on vulnerability of female adolescent mice to activity-based anorexia (ABA).

METHOD

Twenty-four female C57Bl/6 J mice underwent ABA induction, which involved exposing wheel-acclimated adolescent mice to two bouts of food restriction (FR)-the first ABA (P41-44, mid-adolescence) and the second ABA (P55-59, late adolescence), with recovery in between. Ketamine (3 or 30 mg/kg) or vehicle was given once, on the second day of FR of the first ABA (P42). Food consumption, body weight and wheel running activity were measured daily. Anxiety-like behaviors were accessed by elevated plus maze on P49 and P62, after weight restoration during the recovery phase.

RESULTS

Ketamine (30 mg/kg) increased food intake during the first ABA (+38%, p = .015) and facilitated weight gain during recovery (+42%, p = .003). During the second ABA, the effect was manifested as increased food intake (+38%, p = .001) and weight gain (+47%, p = .001) while attenuating FR-induced wheel running activity (-24%, p = .09) and weight loss (-17%, p = .056). Ketamine also reduced anxiety-like behaviors.

DISCUSSION

Thus, single injection of ketamine during mid-adolescence effectively attenuates vulnerability of female mice to repeated ABA exposures.

摘要

目的

本研究测试了氯胺酮对雌性青春期小鼠易患基于活动的厌食症(ABA)的影响。

方法

24 只 C57Bl/6 J 雌性小鼠接受 ABA 诱导,包括使适应轮的青春期小鼠经历两次食物限制(FR)-第一次 ABA(P41-44,青春期中期)和第二次 ABA(P55-59,青春期后期),中间有恢复期。氯胺酮(3 或 30mg/kg)或载体在第一次 ABA 的 FR 的第二天(P42)给予一次。每天测量食物消耗、体重和轮跑活动。在恢复期间体重恢复后,在 P49 和 P62 通过高架十字迷宫测量焦虑样行为。

结果

氯胺酮(30mg/kg)增加了第一次 ABA 期间的食物摄入量(增加 38%,p=0.015)并促进了恢复期间的体重增加(增加 42%,p=0.003)。在第二次 ABA 中,这种作用表现为增加食物摄入量(增加 38%,p=0.001)和体重增加(增加 47%,p=0.001),同时减轻 FR 诱导的轮跑活动减少(减少 24%,p=0.09)和体重减轻(减少 17%,p=0.056)。氯胺酮还降低了焦虑样行为。

讨论

因此,青春期中期单次注射氯胺酮可有效减轻雌性小鼠对重复 ABA 暴露的易感性。

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