Ketogenic Food Ameliorates Activity-Based Anorexia of Adult Female Mice.

IF 4.7 2区 医学 Q1 NUTRITION & DIETETICS
Yiru Dong, Yuki Lin, Latika Khatri, Moses Chao, Chiye Aoki
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引用次数: 0

Abstract

Objective: Genome-wide association studies implicate metabo-psychiatric origins for anorexia nervosa (AN). There are two case reports totaling six adult females who experienced complete remission of AN following a treatment comprised of ketogenic diet (targeting metabolism) with ketamine infusions (targeting psychiatric origins), but no study has determined the efficacy of ketogenic diet, alone. We addressed this gap in knowledge, with exploration of potential molecular mechanisms, using an animal model.

Method: Adult C57BL6 female mice underwent 2 or 3 cycles of activity-based anorexia (ABA1, ABA2, ABA3), an animal model of AN relapse, in which AN-like maladaptive behaviors of hyperactivity and voluntary food restriction are elicited when wheel access is combined with food restriction. ABA was categorized as severe, based on weight loss ≥ 20%, food restriction-evoked increase in wheel counts > 10,000/6 h, and crouching/grimace, and compared across two groups: (1) KG, fed ketogenic food continuously (N = 25); and (2) CON, fed standard diet (N = 28).

Results: 86% of CON versus none of the KG were crouching with grimace during ABA1. 93% of CON versus 11% of KG lost weight severely during ABA2 (p < 0.001, 8% difference of group mean weights). Severe hyperactivity was prevalent among CON (86%) and rare for KG (4%) during ABA2 (p < 0.001 on all food-restricted days). ABA up-regulated BDNF (brain-derived neurotrophic factor) in the hippocampus of both groups but ketone body, β-hydroxybutyrate, in urine was increased only among KG.

Discussion: Ketogenic diet may reduce severity of AN relapse through reduction of compulsive exercise, via mechanisms that are in addition to BDNF up-regulation and involve β-hydroxybutyrate.

生酮食物可改善成年雌性小鼠基于活动的厌食症。
目的:全基因组关联研究表明,神经性厌食症(AN)与代谢-精神疾病有关。有两份病例报告称,共有六名成年女性在接受生酮饮食(针对代谢)和氯胺酮输注(针对精神疾病)治疗后,神经性厌食症完全缓解。我们利用动物模型探索潜在的分子机制,填补了这一知识空白:方法:成年 C57BL6 雌性小鼠接受 2 或 3 个周期的活动性厌食(ABA1、ABA2、ABA3),这是一种 AN 复发的动物模型。根据体重减轻≥20%、食物限制引起的车轮计数增加> 10,000/6 h和蹲下/咧嘴,ABA被归类为严重ABA,并在两组中进行比较:(1) KG组,连续喂食生酮食物(N = 25);(2) CON组,喂食标准饮食(N = 28):结果:ABA1期间,86%的CON和没有一个KG都面无表情地蹲下。93%的CON和11%的KG在ABA2期间体重严重下降(p 讨论:生酮饮食可通过减少强迫性运动来降低自闭症复发的严重程度,其机制除上调BDNF外,还涉及β-羟丁酸。
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来源期刊
CiteScore
10.00
自引率
12.70%
发文量
204
审稿时长
4-8 weeks
期刊介绍: Articles featured in the journal describe state-of-the-art scientific research on theory, methodology, etiology, clinical practice, and policy related to eating disorders, as well as contributions that facilitate scholarly critique and discussion of science and practice in the field. Theoretical and empirical work on obesity or healthy eating falls within the journal’s scope inasmuch as it facilitates the advancement of efforts to describe and understand, prevent, or treat eating disorders. IJED welcomes submissions from all regions of the world and representing all levels of inquiry (including basic science, clinical trials, implementation research, and dissemination studies), and across a full range of scientific methods, disciplines, and approaches.
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