Evidence map›Paper›PMID 29697769›Full record

ArticleEndocrinology2018

Carnitine Acetyltransferase in AgRP Neurons Is Required for the Homeostatic Adaptation to Restricted Feeding in Male Mice.

Alex Reichenbach, Mathieu Mequinion, Jacqueline A Bayliss, Sarah H Lockie, Moyra B Lemus, Randall L Mynatt, Romana Stark, Zane B Andrews

Open access · bronzeAbstract read
In one paragraph

Article in Endocrinology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.4field-weighted citation impact, top 37% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
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  3. Article
  4. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 3 institutions in 2 countries.

Alex ReichenbachMonash Biomedicine Discovery Institute, Monash University, Clayton, Victoria, Australia.
Mathieu MequinionMonash Biomedicine Discovery Institute, Monash University, Clayton, Victoria, Australia.
Jacqueline A BaylissMonash Biomedicine Discovery Institute, Monash University, Clayton, Victoria, Australia.
Sarah H LockieMonash Biomedicine Discovery Institute, Monash University, Clayton, Victoria, Australia.
Moyra B LemusMonash Biomedicine Discovery Institute, Monash University, Clayton, Victoria, Australia.
Randall L MynattGene Nutrient Interactions Laboratory, Pennington Biomedical Research Center, Louisiana State University System, Baton Rouge, Louisiana.
Romana StarkMonash Biomedicine Discovery Institute, Monash University, Clayton, Victoria, Australia.
Zane B AndrewsMonash Biomedicine Discovery Institute, Monash University, Clayton, Victoria, Australia.
Monash University · AUAustralian Regenerative Medicine Institute · AUPennington Biomedical Research Center · US

Funding

Research BaseP30DK072476 · NIDDK · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI Peter Todd Katzmarzyk · 2005 to 2026
$26.5M
Mentoring Obesity and Diabetes Research in LouisianaP20GM103528 · NIGMS · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI GETTYS, THOMAS W · 2012 to 2015
$8.8M
NIDDK NIH HHS P30 DK072476NIGMS NIH HHS P20 GM103528
6 · The paper itself

Abstract

Behavioral adaptation to periods of varying food availability is crucial for survival, and agouti-related protein (AgRP) neurons have been associated with entrainment to temporal restricted feeding. We have shown that carnitine acetyltransferase (Crat) in AgRP neurons enables metabolic flexibility and appropriate nutrient partitioning. In this study, by restricting food availability to 3 h/d during the light phase, we examined whether Crat is a component of a food-entrainable oscillator (FEO) that helps link behavior to food availability. AgRP Crat knockout (KO) mice consumed less food and regained less body weight but maintained blood glucose levels during the 25-day restricted feeding protocol. Importantly, we observed no difference in meal latency, food anticipatory activity (FAA), or brown adipose tissue temperature during the first 13 days of restricted feeding. However, as the restricted feeding paradigm progressed, we noticed an increased FAA in AgRP Crat KO mice. The delayed increase in FAA, which developed during the last 12 days of restricted feeding, corresponded with elevated plasma levels of corticosterone and nonesterified fatty acids, indicating it resulted from greater energy debt incurred by KO mice over the course of the experiment. These experiments highlight the importance of Crat in AgRP neurons in regulating feeding behavior and body weight gain during restricted feeding but not in synchronizing behavior to food availability. Thus, Crat within AgRP neurons forms a component of the homeostatic response to restricted feeding but is not likely to be a molecular component of FEO.

Indexed as

Caloric RestrictionAdaptation, PhysiologicalAgouti-Related ProteinAnimalsCarnitine O-AcetyltransferaseFeeding BehaviorHomeostasisMaleMiceMice, Inbred C57BLMice, KnockoutNeuronsPhysical Conditioning, AnimalAgouti-Related ProteinCarnitine O-Acetyltransferase

Identifiers

PMID29697769
PMCPMC6692886
OpenAlexW2801825287

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.