Evidence map›Paper›PMID 27140610›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2016

Mesolimbic neuropeptide W coordinates stress responses under novel environments.

Toshiyuki Motoike, Jeffrey M Long, Hirokazu Tanaka, Christopher M Sinton, Amber Skach, S Clay Williams, Robert E Hammer, Takeshi Sakurai, Masashi Yanagisawa

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.0field-weighted citation impact, top 27% 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

11 citing papers in PubMed, 24 citations in OpenAlex.

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  7. Restriction of food intake by PPP1R17-expressing neurons in the DMH.Proceedings of the National Academy of Sciences of the United States of America · 2021
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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

9 authors at 6 institutions in 2 countries.

Toshiyuki MotoikeHoward Hughes Medical Institute, University of Texas Southwestern Medical Center, Dallas, TX 75390; Department of Molecular Genetics, University of Texas Southwestern Medical Center, Dallas, TX 75390; Exploratory Research for Advanced Technology, Yanagisawa Orphan Receptor Project, Japan Science and Technology Agency, Tokyo 135-0064, Japan;
Jeffrey M LongDepartment of Biochemistry, University of Texas Southwestern Medical Center, Dallas, TX 75390; Laboratory of Behavioral Neuroscience, National Institute on Aging, National Institutes of Health, Baltimore, MD 21224;
Hirokazu TanakaHoward Hughes Medical Institute, University of Texas Southwestern Medical Center, Dallas, TX 75390; Department of Molecular Genetics, University of Texas Southwestern Medical Center, Dallas, TX 75390; Exploratory Research for Advanced Technology, Yanagisawa Orphan Receptor Project, Japan Science and Technology Agency, Tokyo 135-0064, Japan;
Christopher M SintonArizona Respiratory Center, Department of Medicine, University of Arizona, Tucson, AZ 85724;
Amber SkachHoward Hughes Medical Institute, University of Texas Southwestern Medical Center, Dallas, TX 75390; Department of Molecular Genetics, University of Texas Southwestern Medical Center, Dallas, TX 75390;
S Clay WilliamsHoward Hughes Medical Institute, University of Texas Southwestern Medical Center, Dallas, TX 75390; Department of Molecular Genetics, University of Texas Southwestern Medical Center, Dallas, TX 75390;
Robert E HammerDepartment of Biochemistry, University of Texas Southwestern Medical Center, Dallas, TX 75390;
Takeshi SakuraiExploratory Research for Advanced Technology, Yanagisawa Orphan Receptor Project, Japan Science and Technology Agency, Tokyo 135-0064, Japan; Department of Molecular Neuroscience and Integrative Physiology, Faculty of Medicine, Institute of Medical, Pharmacological, and Health Sciences, Kanazawa University, Kanazawa 920-8640, Japan;
Masashi YanagisawaHoward Hughes Medical Institute, University of Texas Southwestern Medical Center, Dallas, TX 75390; Department of Molecular Genetics, University of Texas Southwestern Medical Center, Dallas, TX 75390; Exploratory Research for Advanced Technology, Yanagisawa Orphan Receptor Project, Japan Science and Technology Agency, Tokyo 135-0064, Japan; International Institute for Integrative Sleep Medicine, University of Tsukuba, Tsukuba 305-8575, Japan yanagisawa.masa.fu@u.tsukuba.ac.jp.
Southwestern Medical Center · USThe University of Texas Southwestern Medical Center · USJapan Science and Technology Agency · JPNational Institute on Aging · USUniversity of Arizona · USUniversity of Tsukuba · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neuropeptide B (NPB) and neuropeptide W (NPW) are endogenous neuropeptide ligands for the G protein-coupled receptors NPBWR1 and NPBWR2. Here we report that the majority of NPW neurons in the mesolimbic region possess tyrosine hydroxylase immunoreactivity, indicating that a small subset of dopaminergic neurons coexpress NPW. These NPW-containing neurons densely and exclusively innervate two limbic system nuclei in adult mouse brain: the lateral bed nucleus of the stria terminalis and the lateral part of the central amygdala nucleus (CeAL). In the CeAL of wild-type mice, restraint stress resulted in an inhibition of cellular activity, but this stress-induced inhibition was attenuated in the CeAL neurons of NPW(-/-) mice. Moreover, the response of NPW(-/-) mice to either formalin-induced pain stimuli or a live rat (i.e., a potential predator) was abnormal only when they were placed in a novel environment: The mice failed to show the normal species-specific self-protective and aversive reactions. In contrast, the behavior of NPW(-/-) mice in a habituated environment was indistinguishable from that of wild-type mice. These results indicate that the NPW/NPBWR1 system could play a critical role in the gating of stressful stimuli during exposure to novel environments.

Indexed as

Avoidance LearningBehavior, AnimalAnimalsCentral Amygdaloid NucleusDopaminergic NeuronsMiceMice, KnockoutNeuropeptidesPainRatsReceptors, G-Protein-CoupledReceptors, NeuropeptideTyrosine 3-MonooxygenaseNeuropeptidesneuropeptide W, mouseNpbwr1 protein, mouseReceptors, G-Protein-CoupledReceptors, NeuropeptideTyrosine 3-Monooxygenaseamygdaladopaminergicfearmousepain

Identifiers

PMID27140610
PMCPMC4889355
OpenAlexW2346122327

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.