Evidence map›Paper›PMID 37897141›Full record

ArticleJournal of cachexia, sarcopenia and muscle2023

Gastric inhibitory polypeptide receptor antagonism suppresses intramuscular adipose tissue accumulation and ameliorates sarcopenia.

Yuya Takahashi, Hiroki Fujita, Yusuke Seino, Satoko Hattori, Shihomi Hidaka, Tsuyoshi Miyakawa, Atsushi Suzuki, Hironori Waki, Daisuke Yabe, Yutaka Seino and 1 more

Open access · goldAbstract read
In one paragraph

Article in Journal of cachexia, sarcopenia and muscle, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
3.2field-weighted citation impact, top 7% 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

17 citing papers in PubMed, 18 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

11 authors at 3 institutions in 1 country.

Yuya TakahashiDepartment of Metabolism and Endocrinology, Akita University Graduate School of Medicine, Akita, Japan.
Hiroki FujitaDepartment of Metabolism and Endocrinology, Akita University Graduate School of Medicine, Akita, Japan.ORCID 0000-0003-0404-605X
Yusuke SeinoDepartment of Endocrinology, Diabetes and Metabolism, Fujita Health University, Toyoake, Japan.
Satoko HattoriDivision of Systems Medical Science, Center for Medical Science, Fujita Health University, Toyoake, Japan.
Shihomi HidakaDepartment of Endocrinology, Diabetes and Metabolism, Fujita Health University, Toyoake, Japan.
Tsuyoshi MiyakawaDivision of Systems Medical Science, Center for Medical Science, Fujita Health University, Toyoake, Japan.
Atsushi SuzukiDepartment of Endocrinology, Diabetes and Metabolism, Fujita Health University, Toyoake, Japan.
Hironori WakiDepartment of Metabolism and Endocrinology, Akita University Graduate School of Medicine, Akita, Japan.
Daisuke YabeYutaka Seino Distinguished Center for Diabetes Research, Kansai Electric Power Medical Research Institute, Kyoto, Japan.
Yutaka SeinoYutaka Seino Distinguished Center for Diabetes Research, Kansai Electric Power Medical Research Institute, Kyoto, Japan.
Yuichiro YamadaYutaka Seino Distinguished Center for Diabetes Research, Kansai Electric Power Medical Research Institute, Kyoto, Japan.
Fujita Health University · JPAkita University · JPKansai Electric Power (Japan) · JP

Funding

Japan Agency for Medical Research and Development (AMED) JP20ek0210111JSPS KAKENHI 16H06276JSPS KAKENHI 22H04922JSPS KAKENHI 23K16764MEXT Promotion of Distinctive Joint Research Center Program JPMXP0618217663MEXT Promotion of Distinctive Joint Research Center Program JPMXP0621467949Suzuken Memorial Foundation 21-092
6 · The paper itself

Abstract

backgroundIntramuscular adipose tissue (IMAT) formation derived from muscle fibro-adipogenic progenitors (FAPs) has been recognized as a pathological feature of sarcopenia. This study aimed to explore whether genetic and pharmacological gastric inhibitory polypeptide (GIP) receptor antagonism suppresses IMAT accumulation and ameliorates sarcopenia in mice.

methodsWhole body composition, grip strength, skeletal muscle weight, tibialis anterior (TA) muscle fibre cross-sectional area (CSA) and TA muscle IMAT area were measured in young and aged male C57BL/6 strain GIP receptor (Gipr)-knockout (Gipr

resultsBody composition analysis revealed that 104-week-old Gipr

conclusionsGIP promotes the differentiation of muscle FAPs into adipocytes and its receptor antagonism suppresses IMAT accumulation and promotes muscle regeneration. Pharmacological GIP receptor antagonism may serve as a novel therapeutic approach for sarcopenia.

Indexed as

SarcopeniaAdipose TissueAnimalsGlycerolMaleMiceMice, Inbred C57BLReceptors, Gastrointestinal HormoneReceptors, G-Protein-Coupledgastric inhibitory polypeptide receptorGipr protein, mouseGlycerolReceptors, Gastrointestinal HormoneReceptors, G-Protein-Coupledagingfibro-adipogenic progenitorsGIP receptorintramuscular adipose tissuesarcopenia

Identifiers

PMID37897141
PMCPMC10751449
OpenAlexW4387996575

What OpenQuestion holds

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LicenceCC BY
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.