Evidence map›Paper›PMID 24574718›Full record

ArticleWorld journal of gastroenterology2014

Deletion of Gpr128 results in weight loss and increased intestinal contraction frequency.

Ying-Yin Ni, Yan Chen, Shun-Yuan Lu, Bi-Ying Sun, Fang Wang, Xiao-Lin Wu, Su-Ying Dang, Guo-Hua Zhang, Hong-Xin Zhang, Yin Kuang and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in World journal of gastroenterology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.1field-weighted citation impact, top 45% 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

7 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
  2. Targeting of ELMO2 by thebioRxiv : the preprint server for biology · 2026
    Article
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  4. Adhesion G protein-coupled receptors.Pharmacological reviews · 2026
    Review
  5. Article
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  7. Article
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

14 authors at 1 institution in 1 country.

Ying-Yin NiYing-Yin Ni, Yan Chen, Fang Wang, Xiao-Lin Wu, Su-Ying Dang, Ming-Min Gu, Zhu-Gang Wang, Department of Medical Genetics, E-Institutes of Shanghai Universities, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China.
Yan ChenYing-Yin Ni, Yan Chen, Fang Wang, Xiao-Lin Wu, Su-Ying Dang, Ming-Min Gu, Zhu-Gang Wang, Department of Medical Genetics, E-Institutes of Shanghai Universities, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China.
Shun-Yuan LuYing-Yin Ni, Yan Chen, Fang Wang, Xiao-Lin Wu, Su-Ying Dang, Ming-Min Gu, Zhu-Gang Wang, Department of Medical Genetics, E-Institutes of Shanghai Universities, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China.
Bi-Ying SunYing-Yin Ni, Yan Chen, Fang Wang, Xiao-Lin Wu, Su-Ying Dang, Ming-Min Gu, Zhu-Gang Wang, Department of Medical Genetics, E-Institutes of Shanghai Universities, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China.
Fang WangYing-Yin Ni, Yan Chen, Fang Wang, Xiao-Lin Wu, Su-Ying Dang, Ming-Min Gu, Zhu-Gang Wang, Department of Medical Genetics, E-Institutes of Shanghai Universities, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China.
Xiao-Lin WuYing-Yin Ni, Yan Chen, Fang Wang, Xiao-Lin Wu, Su-Ying Dang, Ming-Min Gu, Zhu-Gang Wang, Department of Medical Genetics, E-Institutes of Shanghai Universities, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China.
Su-Ying DangYing-Yin Ni, Yan Chen, Fang Wang, Xiao-Lin Wu, Su-Ying Dang, Ming-Min Gu, Zhu-Gang Wang, Department of Medical Genetics, E-Institutes of Shanghai Universities, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China.
Guo-Hua ZhangYing-Yin Ni, Yan Chen, Fang Wang, Xiao-Lin Wu, Su-Ying Dang, Ming-Min Gu, Zhu-Gang Wang, Department of Medical Genetics, E-Institutes of Shanghai Universities, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China.
Hong-Xin ZhangYing-Yin Ni, Yan Chen, Fang Wang, Xiao-Lin Wu, Su-Ying Dang, Ming-Min Gu, Zhu-Gang Wang, Department of Medical Genetics, E-Institutes of Shanghai Universities, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China.
Yin KuangYing-Yin Ni, Yan Chen, Fang Wang, Xiao-Lin Wu, Su-Ying Dang, Ming-Min Gu, Zhu-Gang Wang, Department of Medical Genetics, E-Institutes of Shanghai Universities, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China.
Jian FeiYing-Yin Ni, Yan Chen, Fang Wang, Xiao-Lin Wu, Su-Ying Dang, Ming-Min Gu, Zhu-Gang Wang, Department of Medical Genetics, E-Institutes of Shanghai Universities, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China.
Ming-Min GuYing-Yin Ni, Yan Chen, Fang Wang, Xiao-Lin Wu, Su-Ying Dang, Ming-Min Gu, Zhu-Gang Wang, Department of Medical Genetics, E-Institutes of Shanghai Universities, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China.
Wei-Fang RongYing-Yin Ni, Yan Chen, Fang Wang, Xiao-Lin Wu, Su-Ying Dang, Ming-Min Gu, Zhu-Gang Wang, Department of Medical Genetics, E-Institutes of Shanghai Universities, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China.
Zhu-Gang WangYing-Yin Ni, Yan Chen, Fang Wang, Xiao-Lin Wu, Su-Ying Dang, Ming-Min Gu, Zhu-Gang Wang, Department of Medical Genetics, E-Institutes of Shanghai Universities, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China.
Shanghai Liangyou (China) · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimTo generate a Gpr128 gene knockout mouse model and to investigate its phenotypes and the biological function of the Gpr128 gene.

methodsBacterial artificial chromosome-retrieval methods were used for constructing the targeting vector. Using homologous recombination and microinjection technology, a Gpr128 knockout mouse model on a mixed 129/BL6 background was generated. The mice were genotyped by polymerase chain reaction (PCR) analysis of tail DNA and fed a standard laboratory chow diet. Animals of both sexes were used, and the phenotypes were assessed by histological, biochemical, molecular and physiological analyses. Semi-quantitative reverse transcription-PCR and Northern blotting were used to determine the tissue distribution of Gpr128 mRNA. Beginning at the age of 4 wk, body weights were recorded every 4 wk. Food, feces, blood and organ samples were collected to analyze food consumption, fecal quantity, organ weight and constituents of the blood and plasma. A Trendelenburg preparation was utilized to examine intestinal motility in wild-type (WT) and Gpr128(-/-) mice at the age of 8 and 32 wk.

resultsGpr128 mRNA was highly and exclusively detected in the intestinal tissues. Targeted deletion of Gpr128 in adult mice resulted in reduced body weight gain, and mutant mice exhibited an increased frequency of peristaltic contraction and slow wave potential of the small intestine. The Gpr128(+/+) mice gained more weight on average than the Gpr128(-/-) mice since 24 wk, being 30.81 ± 2.84 g and 25.74 ± 4.50 g, respectively (n = 10, P < 0.01). The frequency of small intestinal peristaltic contraction was increased in Gpr128(-/-) mice. At the age of 8 wk, the frequency of peristalsis with an intraluminal pressure of 3 cmH2O was 6.6 ± 2.3 peristalsis/15 min in Gpr128(-/-) intestine (n = 5) vs 2.6 ± 1.7 peristalsis/15 min in WT intestine (n = 5, P < 0.05). At the age of 32 wk, the frequency of peristaltic contraction with an intraluminal pressure of 2 and 3 cmH2O was 4.6 ± 2.3 and 3.1 ± 0.8 peristalsis/15 min in WT mice (n = 8), whereas in Gpr128(-/-) mice (n = 8) the frequency of contraction was 8.3 ± 3.0 and 7.4 ± 3.1 peristalsis/15 min, respectively (2 cmH2O: P < 0.05 vs WT; 3 cmH2O: P < 0.01 vs WT). The frequency of slow wave potential in Gpr128(-/-) intestine (35.8 ± 4.3, 36.4 ± 4.2 and 37.1 ± 4.8/min with an intraluminal pressure of 1, 2 and 3 cmH2O, n = 8) was also higher than in WT intestine (30.6 ± 4.2, 31.4 ± 3.9 and 31.9 ± 4.5/min, n = 8, P < 0.05).

conclusionWe have generated a mouse model with a targeted deletion of Gpr128 and found reduced body weight and increased intestinal contraction frequency in this animal model.

Indexed as

Gene DeletionAge FactorsAnimalsFemaleGene Expression RegulationGenotypeJejunumMaleMiceMice, 129 StrainMice, Inbred C57BLMice, KnockoutMuscle ContractionPeristalsisPhenotypePressureGpr128 protein, mouseReceptors, G-Protein-CoupledRNA, MessengerGpr128G-protein-coupled receptorsIntestinal contraction frequencyKnockout mouseWeight loss

Identifiers

PMID24574718
PMCPMC3923024
OpenAlexW2083043385

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Registered trials

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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.