Evidence map›Paper›PMID 26404873›Full record

ArticleNeuroscience2015

Contribution of regional brain melanocortin receptor subtypes to elevated activity energy expenditure in lean, active rats.

C Shukla, L G Koch, S L Britton, M Cai, V J Hruby, M Bednarek, C M Novak

Open access · greenAbstract read
In one paragraph

Article in Neuroscience, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.6field-weighted citation impact, top 38% 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

6 citing papers in PubMed, 7 citations in OpenAlex.

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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

7 authors at 4 institutions in 1 country.

C ShuklaDepartment of Biological Sciences, Kent State University, Kent, OH, United States; Harvard Medical School - VA Boston Healthcare System, Boston, MA, United States. Electronic address: charu_shukla@hms.harvard.edu.
L G KochDepartment of Anesthesiology, University of Michigan, Ann Arbor, MI, United States; Department of Molecular & Integrative Physiology, University of Michigan, Ann Arbor, MI, United States.
S L BrittonDepartment of Anesthesiology, University of Michigan, Ann Arbor, MI, United States; Department of Molecular & Integrative Physiology, University of Michigan, Ann Arbor, MI, United States.
M CaiDepartment of Chemistry and Biochemistry, University of Arizona, Tucson, AZ, United States.
V J HrubyDepartment of Chemistry and Biochemistry, University of Arizona, Tucson, AZ, United States.
M BednarekMedImmune Limited, Cambridge, United Kingdom.
C M NovakDepartment of Biological Sciences, Kent State University, Kent, OH, United States.
University of Arizona · USUniversity of Michigan–Ann Arbor · USHarvard University · USKent State University · US

Funding

STRUCTURE AND FUNCTION OF NUCLEIC ACIDSR01GM010840 · NIGMS · UNIVERSITY OF CALIFORNIA BERKELEY · PI TINOCO, IGNACIO · 1985 to 2015
$7.1M
Brain Mechanisms of Non-Exercise Activity ThermogenesisR01NS055859 · NINDS · MAYO CLINIC ROCHESTER · PI NOVAK, COLLEEN M · 2007 to 2010
$1.3M
Supplement for "Designing Novel Melanotropins for New Applications for the Melanocortin System"R01GM108040 · NIGMS · UNIVERSITY OF ARIZONA · PI CAI, MINYING, HRUBY, VICTOR J · 2014 to 2017
$1.2M
Resource for Rat Genetic Models of Aerobic CapacityR24OD010950 · OD · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI BRITTON, STEVEN LOYAL · 2012 to 2013
$1.0M
Brain Melanocortin Control of Activity Energy Expenditure and Obesity ResistanceR15DK097644 · NIDDK · KENT STATE UNIVERSITY · PI NOVAK, COLLEEN M · 2013 to 2013
$384k
NIDDK NIH HHS R15 DK097644NIDDK NIH HHS R15DK097644-01A1NIGMS NIH HHS R01 GM010840NIGMS NIH HHS R01 GM108040NIH HHS R24 OD010950NIH HHS R24OD010950NINDS NIH HHS R01 NS055859NINDS NIH HHS R01NS055859
6 · The paper itself

Abstract

Physical activity and non-exercise activity thermogenesis (NEAT) are crucial factors accounting for individual differences in body weight, interacting with genetic predisposition. In the brain, a number of neuroendocrine intermediates regulate food intake and energy expenditure (EE); this includes the brain melanocortin (MC) system, consisting of MC peptides as well as their receptors (MCR). MC3R and MC4R have emerged as critical modulators of EE and food intake. To determine how variance in MC signaling may underlie individual differences in physical activity levels, we examined behavioral response to MC receptor agonists and antagonists in rats that show high and low levels of physical activity and NEAT, that is, high- and low-capacity runners (HCR, LCR), developed by artificial selection for differential intrinsic aerobic running capacity. Focusing on the hypothalamus, we identified brain region-specific elevations in expression of MCR 3, 4, and also MC5R, in the highly active, lean HCR relative to the less active and obesity-prone LCR. Further, the differences in activity and associated EE as a result of MCR activation or suppression using specific agonists and antagonists were similarly region-specific and directly corresponded to the differential MCR expression patterns. The agonists and antagonists investigated here did not significantly impact food intake at the doses used, suggesting that the differential pattern of receptor expression may by more meaningful to physical activity than to other aspects of energy balance regulation. Thus, MCR-mediated physical activity may be a key neural mechanism in distinguishing the lean phenotype and a target for enhancing physical activity and NEAT.

Indexed as

Energy MetabolismMotor ActivityAnimalsBody WeightEatingFemaleHypothalamusMaleRatsReceptors, MelanocortinRNA, MessengerReceptors, MelanocortinRNA, MessengerHCR/LCRnon-exercise activity thermogenesis (NEAT)obesityspontaneous physical activity

Identifiers

PMID26404873
PMCPMC4633328
OpenAlexW1792489984

What OpenQuestion holds

Textmetadata
LicenceTDM
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.