Evidence map›Paper›PMID 18550869›Full record

ArticleAmerican journal of physiology. Regulatory, integrative and comparative physiology2008

Melanocortin-4 receptor mRNA expressed in sympathetic outflow neurons to brown adipose tissue: neuroanatomical and functional evidence.

C Kay Song, Cheryl H Vaughan, Erin Keen-Rhinehart, Ruth B S Harris, Denis Richard, Timothy J Bartness

Abstract read
In one paragraph

Article in American journal of physiology. Regulatory, integrative and comparative physiology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 79 papers.

0numbers the graph read from it
0cells of the map it votes in
79citing papers in PubMed
3.7field-weighted citation impact, top 6% 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

79 citing papers in PubMed, 143 citations in OpenAlex.

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  11. Oxytocin as an Anti-obesity Treatment.Frontiers in neuroscience · 2021
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  14. Incendiary Leptin.Nutrients · 2020
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  20. Review

19 more citing papers are in PubMed but not listed here.

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

6 authors at 1 institution in 1 country.

C Kay SongDepartment of Biology, Georgia State University, 24 Peachtree Center Ave. NE, Atlanta, GA 30302-4010, USA.
Cheryl H Vaughan
Erin Keen-Rhinehart
Ruth B S Harris
Denis Richard
Timothy J Bartness
Georgia State University · US

Funding

LEPTIN AND PERIPHERAL GLUCOSE METABOLISMR01DK053903 · NIDDK · UNIVERSITY OF GEORGIA (UGA) · PI HARRIS, RUTH B · 1999 to 2018
$4.6M
PHOTOPERIODIC CONTROL OF OBESITYR01DK035254 · NIDDK · WORCESTER FOUNDATION FOR BIOMEDICAL RES · PI XUE, BINGZHONG · 1988 to 2015
$3.3M
NIDDK NIH HHS R01 DK053903NIDDK NIH HHS R01-DK-35254
6 · The paper itself

Abstract

A precise understanding of neural circuits controlling lipid mobilization and thermogenesis remains to be determined. We have been studying the sympathetic nervous system (SNS) contributions to white adipose tissue (WAT) lipolysis largely in Siberian hamsters. Central melanocortins are implicated in the control of the sympathetic outflow to WAT, and, moreover, the melanocortin 4 receptors (MC4-R) appear to be principally involved. We previously found that acute third ventricular melanotan II (MTII; an MC3/4-R agonist) injections increase sympathetic drive (norepinephrine turnover) to interscapular brown adipose tissue (IBAT) and IBAT temperature. Here we tested whether MC4-R mRNA is expressed in IBAT SNS outflow neurons using in situ hybridization for the former and injections of the transneuronal viral retrograde tract tracer, pseudorabies virus (PRV) into IBAT, for the latter. Significant numbers of double-labeled cells for PRV and MC4-R mRNA were found across the neuroaxis (mean of all brain sites approximately 60%), including the hypothalamic paraventricular nucleus (PVH; approximately 80%). Acute parenchymal MTII microinjections into the PVH of awake, freely-moving hamsters, using doses below those able to increase IBAT temperature when injected into the third ventricle, increased IBAT temperature for as long as 4 h, as measured by temperature transponders implanted below the tissue. Collectively, these data add significant support to the view that central melanocortins are important in controlling IBAT thermogenesis via the SNS innervation of this tissue, likely through the MC4-Rs.

Indexed as

ThermogenesisAdipose Tissue, Brownalpha-MSHAnimalsCricetinaeHerpesvirus 1, SuidIn Situ HybridizationMaleMicroinjectionsNeurons, EfferentParaventricular Hypothalamic NucleusPeptides, CyclicPhodopusReceptor, Melanocortin, Type 4RNA, MessengerStaining and Labelingalpha-MSHmelanotan-IIPeptides, CyclicReceptor, Melanocortin, Type 4RNA, Messenger

Identifiers

PMID18550869
PMCPMC2519921
OpenAlexW2162977729

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.