Evidence map›Paper›PMID 23900719›Full record

ArticleJournal of molecular neuroscience : MN2013

Distinct expression of Mas1-related G-protein-coupled receptor B4 in dorsal root and trigeminal ganglia--implications for altered behaviors in acid-sensing ion channel 3-deficient mice.

Ya-Han Huang, Chin-Yu Chang, Chih-Cheng Chen, Chih-Dong Yang, Wei-Hsin Sun

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Article in Journal of molecular neuroscience : MN, 2013. 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
0.5field-weighted citation impact, top 41% 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, 8 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

5 authors at 3 institutions in 1 country.

Ya-Han HuangDepartment of Life Sciences, National Central University, Jhongda Road 300, 32054, Jhongli, Taiwan.
Chin-Yu Chang
Chih-Cheng Chen
Chih-Dong Yang
Wei-Hsin Sun
National Central University · TWInstitute of Biomedical Sciences, Academia Sinica · TWLandseed Hospital · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mas1-related G-protein-coupled receptors (Mrgprs), comprising more than 50 distinct members, are specifically expressed in primary sensory neurons. Reflecting the diversity and specificity of stimuli they detect, Mrgprs are involved in pain, touch, and itch-related behaviors. Sensory-neuron-specific acid-sensing ion channel 3 (ASIC3) is essential for touch and inflammatory pain, but mice lacking ASIC3 have complex behavioral alterations in various modalities of pain and touch. To understand whether Mrgprs are involved in complex behavioral alterations found in ASIC3-deficient mice, we examined Mrgpr gene expression in ASIC3(-/-) mice. Only MrgprB4 expression has shown significant change. MrgprB4 expression was increased in ASIC3(-/-) dorsal root ganglia (DRG) but decreased in ASIC3(-/-) trigeminal ganglia. The distinct alterations in DRG and trigeminal ganglia imply that MrgprB4 could have multiple functions. Given that MrgprB4 is expressed in neurons that may detect gentle touch and that ASIC3(-/-) mice have altered sensitivity of mechanoreceptors for light touch, the expression change of MrgprB4 is more likely related to the altered touch behaviors of ASIC3(-/-) mice.

Indexed as

Acid Sensing Ion ChannelsAnimalsGanglia, SpinalMaleMechanoreceptorsMiceMice, KnockoutNociceptorsProto-Oncogene MasReceptors, G-Protein-CoupledTouchTrigeminal GanglionAcid Sensing Ion ChannelsASIC3 protein, mouseMas1 protein, mouseMrgprB4 protein, mouseProto-Oncogene MasReceptors, G-Protein-Coupled

Identifiers

PMID23900719
OpenAlexW1980893943

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.