Evidence map›Paper›PMID 28939592›Full record

ArticleFASEB journal : official publication of the Federation of American Societies for Experimental Biology2018

α-Ketoglutarate prevents skeletal muscle protein degradation and muscle atrophy through PHD3/ADRB2 pathway.

Xingcai Cai, Yexian Yuan, Zhengrui Liao, Kongping Xing, Canjun Zhu, Yaqiong Xu, Lulu Yu, Lina Wang, Songbo Wang, Xiaotong Zhu and 5 more

Erratum issuedOpen access · bronzeAbstract read
In one paragraph

Article in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

30 citing papers in PubMed, 64 citations in OpenAlex.

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  13. Impact ofFrontiers in microbiology · 2024
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors at 2 institutions in 2 countries.

Xingcai CaiGuangdong Provincial Key Laboratory of Animal Nutritional Control, South China Agricultural University, Guangzhou, China.
Yexian YuanGuangdong Provincial Key Laboratory of Animal Nutritional Control, South China Agricultural University, Guangzhou, China.
Zhengrui LiaoGuangdong Provincial Key Laboratory of Animal Nutritional Control, South China Agricultural University, Guangzhou, China.
Kongping XingGuangdong Provincial Key Laboratory of Animal Nutritional Control, South China Agricultural University, Guangzhou, China.
Canjun ZhuGuangdong Provincial Key Laboratory of Animal Nutritional Control, South China Agricultural University, Guangzhou, China.
Yaqiong XuGuangdong Provincial Key Laboratory of Animal Nutritional Control, South China Agricultural University, Guangzhou, China.
Lulu YuGuangdong Provincial Key Laboratory of Animal Nutritional Control, South China Agricultural University, Guangzhou, China.
Lina WangGuangdong Provincial Key Laboratory of Animal Nutritional Control, South China Agricultural University, Guangzhou, China.
Songbo WangGuangdong Provincial Key Laboratory of Animal Nutritional Control, South China Agricultural University, Guangzhou, China.
Xiaotong ZhuGuangdong Provincial Key Laboratory of Animal Nutritional Control, South China Agricultural University, Guangzhou, China.
Ping GaoGuangdong Provincial Key Laboratory of Animal Nutritional Control, South China Agricultural University, Guangzhou, China.
Yongliang ZhangGuangdong Provincial Key Laboratory of Animal Nutritional Control, South China Agricultural University, Guangzhou, China.
Qingyan JiangGuangdong Provincial Key Laboratory of Animal Nutritional Control, South China Agricultural University, Guangzhou, China.
Pingwen XuDepartment of Pediatrics, Baylor College of Medicine, Houston, Texas, USA.
Gang ShuGuangdong Provincial Key Laboratory of Animal Nutritional Control, South China Agricultural University, Guangzhou, China; shugang@scau.edu.cn.
South China Agricultural University · CNBaylor College of Medicine · US

Funding

Medial amygdala ERα neurocircuits in the regulation of physical activityK99DK107008 · NIDDK · BAYLOR COLLEGE OF MEDICINE · PI XU, PINGWEN · 2016 to 2017
$178k
NIDDK NIH HHS K99 DK107008
6 · The paper itself

Abstract

Skeletal muscle atrophy due to excessive protein degradation is the main cause for muscle dysfunction, fatigue, and weakening of athletic ability. Endurance exercise is effective to attenuate muscle atrophy, but the underlying mechanism has not been fully investigated. α-Ketoglutarate (AKG) is a key intermediate of tricarboxylic acid cycle, which is generated during endurance exercise. Here, we demonstrated that AKG effectively attenuated corticosterone-induced protein degradation and rescued the muscle atrophy and dysfunction in a Duchenne muscular dystrophy mouse model. Interestingly, AKG also inhibited the expression of proline hydroxylase 3 (PHD3), one of the important oxidoreductases expressed under hypoxic conditions. Subsequently, we identified the β

Indexed as

AnimalsCorticosteroneDisease Models, AnimalKetoglutaric AcidsMaleMetabolic Networks and PathwaysMiceMice, Inbred C57BLMice, Inbred mdxMuscle Fibers, SkeletalMuscle ProteinsMuscle, SkeletalMuscular AtrophyMuscular Dystrophy, DuchenneProcollagen-Proline DioxygenaseProtein StabilityCorticosteroneKetoglutaric AcidsMuscle ProteinsPHD3 protein, mouseProcollagen-Proline DioxygenaseReceptors, Adrenergic, beta-2Duchenne muscular dystrophymetabolismmetabolitetricarboxylic acid cycle

Identifiers

PMID28939592
PMCPMC6266637
OpenAlexW2758622699

What Socratic 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 Socratic graph.