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

Yi Wen Chen, Ang Doma Sherpa, Chiye Aoki

Research output: Contribution to journalArticle

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.

Original languageEnglish (US)
JournalInternational Journal of Eating Disorders
DOIs
StateAccepted/In press - Jan 1 2018

Fingerprint

Ketamine
Anorexia
Anxiety
Eating
Injections
Food
Running
Weight Gain
Weight Loss
Body Weight
Weights and Measures

Keywords

  • ABA
  • adolescence
  • anxiety-like behavior
  • body weight
  • C57BL6/J
  • EPM
  • food intake
  • hyperactivity
  • ketamine
  • rodent

ASJC Scopus subject areas

  • Psychiatry and Mental health

Cite this

@article{05c4ecc0493e41f5b00658278b307d89,
title = "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",
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.",
keywords = "ABA, adolescence, anxiety-like behavior, body weight, C57BL6/J, EPM, food intake, hyperactivity, ketamine, rodent",
author = "Chen, {Yi Wen} and Sherpa, {Ang Doma} and Chiye Aoki",
year = "2018",
month = "1",
day = "1",
doi = "10.1002/eat.22937",
language = "English (US)",
journal = "International Journal of Eating Disorders",
issn = "0276-3478",
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T1 - 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

AU - Chen, Yi Wen

AU - Sherpa, Ang Doma

AU - Aoki, Chiye

PY - 2018/1/1

Y1 - 2018/1/1

N2 - 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.

AB - 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.

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