Evidence map›Paper›PMID 28104917›Full record

ArticleInternational journal of obesity (2005)2017

Overexpression of bone morphogenetic protein-3b (BMP-3b) in adipose tissues protects against high-fat diet-induced obesity.

J Hino, M Nakatani, Y Arai, K Tsuchida, M Shirai, M Miyazato, K Kangawa

Abstract read
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In one paragraph

Article in International journal of obesity (2005), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 1 pooled it
1.5field-weighted citation impact, top 19% 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

19 citing papers in PubMed, 1 synthesis or guideline pooled it, 35 citations in OpenAlex.

  1. Pooled it
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  10. Transgenic Expression ofInternational journal of molecular sciences · 2021
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  12. Deficiency of bone morphogenetic protein-3b induces metabolic syndrome and increases adipogenesis.American journal of physiology. Endocrinology and metabolism · 2020
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  14. Review
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  16. Beyond the bone: Bone morphogenetic protein signaling in adipose tissue.Obesity reviews : an official journal of the International Association for the Study of Obesity · 2019
    Review
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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

7 authors at 2 institutions in 1 country.

J HinoDepartment of Biochemistry, National Cerebral and Cardiovascular Center Research Institute, Suita, Japan.
M NakataniDivision for Therapies against Intractable Diseases, Institute for Comprehensive Medical Science, Fujita Health University, Toyoake, Japan.
Y AraiDepartment of Bioscience and Genetics, National Cerebral and Cardiovascular Center Research Institute, Suita, Japan.
K TsuchidaDivision for Therapies against Intractable Diseases, Institute for Comprehensive Medical Science, Fujita Health University, Toyoake, Japan.
M ShiraiDepartment of Cardiac Physiology, National Cerebral and Cardiovascular Center Research Institute, Suita, Japan.
M MiyazatoDepartment of Biochemistry, National Cerebral and Cardiovascular Center Research Institute, Suita, Japan.
K KangawaDepartment of Biochemistry, National Cerebral and Cardiovascular Center Research Institute, Suita, Japan.
National Cerebral and Cardiovascular Center · JPFujita Health University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBone morphogenetic protein-3b (BMP-3b) is a member of the transforming growth factor-β superfamily and has several activities that differ from those of other BMPs. We previously found that BMP-3b is highly expressed in adipocytes, its level is increased during obesity, and it inhibits adipogenesis by suppressing peroxisome proliferator-activated receptor γ (PPARγ) in vitro. However, the function of BMP-3b in adipose tissues in vivo remains unknown.

methodsTo determine the role of BMP-3b overexpression in adipose tissues in vivo, we generated transgenic mice (BMP-3b Tg) by using a conditional overexpression approach in fatty acid-binding protein 4-expressing adipocytes. We examined BMP-3b Tg mice fed a high-fat diet to elucidate the effects of BMP-3b on obesity. Adipocyte function was evaluated as expression of adipogenic and lipogenic markers in adipose tissue. We also performed glucose and insulin tolerance tests (GTT and ITT, respectively), and biochemical analysis of serum and measured energy expenditure by indirect calorimetry.

resultsBMP-3b Tg mice fed a high-fat diet showed decreases in weight gain, fat-pad mass and adipocyte area, compared with wild-type mice. The adipose tissues of BMP-3b Tg mice showed downregulated expression of PPARγ and its target gene encoding fatty acid translocase/CD36. In addition, BMP-3b Tg mice had decreased blood glucose levels on GTT and ITT, and their serum leptin levels were decreased and adiponectin concentrations were increased. These changes in BMP-3b Tg mice were accompanied by increased energy expenditure, indicated as increased locomotor activity and oxygen consumption.

conclusionsThese results provide in vivo evidence that BMP-3b regulates adipocyte function to cause an anti-obesity effect.

Indexed as

3T3-L1 CellsAdipogenesisAdipose TissueAnimalsDiet, High-FatDisease Models, AnimalEnergy MetabolismGrowth Differentiation Factor 10MaleMiceMice, Inbred C57BLMice, TransgenicObesityPPAR gammaThermogenesisGrowth Differentiation Factor 10PPAR gamma

Identifiers

PMID28104917
OpenAlexW2579485914

What OpenQuestion holds

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Read underepoch 390

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.