Evidence map›Paper›PMID 29288408›Full record

ArticleJournal of physiology and biochemistry2018

Muscle-specific deletion of Prkaa1 enhances skeletal muscle lipid accumulation in mice fed a high-fat diet.

Weiche Wu, Ziye Xu, Ling Zhang, Jiaqi Liu, Jie Feng, Xinxia Wang, Tizhong Shan, Yizhen Wang

Abstract read
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In one paragraph

Article in Journal of physiology and biochemistry, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

12 citing papers in PubMed, 17 citations in OpenAlex.

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  12. Role of miRNAs in skeletal muscle aging.Clinical interventions in aging · 2018
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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

8 authors at 1 institution in 1 country.

Weiche WuCollege of Animal Science, Zhejiang University, No. 866 Yuhangtang Road, Hangzhou, Zhejiang, 310058, People's Republic of China.
Ziye XuCollege of Animal Science, Zhejiang University, No. 866 Yuhangtang Road, Hangzhou, Zhejiang, 310058, People's Republic of China.
Ling ZhangDepartment of Neurobiology, School of Basic Medical Sciences, Key Laboratory of Medical Neurobiology (Ministry of Health of China), Key Laboratory of Neurobiology of Zhejiang Province, Zhejiang University School of Medicine, Hangzhou, Zhejiang Province, 310058, China.
Jiaqi LiuCollege of Animal Science, Zhejiang University, No. 866 Yuhangtang Road, Hangzhou, Zhejiang, 310058, People's Republic of China.
Jie FengCollege of Animal Science, Zhejiang University, No. 866 Yuhangtang Road, Hangzhou, Zhejiang, 310058, People's Republic of China.
Xinxia WangCollege of Animal Science, Zhejiang University, No. 866 Yuhangtang Road, Hangzhou, Zhejiang, 310058, People's Republic of China.
Tizhong ShanCollege of Animal Science, Zhejiang University, No. 866 Yuhangtang Road, Hangzhou, Zhejiang, 310058, People's Republic of China. tzshan@zju.edu.cn.
Yizhen WangCollege of Animal Science, Zhejiang University, No. 866 Yuhangtang Road, Hangzhou, Zhejiang, 310058, People's Republic of China. yzwang321@zju.edu.cn.
Zhejiang University · CN

Funding

Ministry of Agriculture of the People's Republic of China 2014ZX0800949BMinistry of Science and Technology of the People's Republic of China 2012CB124705
6 · The paper itself

Abstract

Excessive intramyocellular triacylglycerols (IMTGs, muscle lipids) are associated with the abnormal energy metabolism and insulin resistance of skeletal muscle. AMP-activated protein kinase (AMPK), a crucial cellular energy sensor, consists of α, β and γ subunits. Researchers have not clearly determined whether Prkaa1 (also known as AMPKα1) affects IMTG accumulation in skeletal muscle. Here, we show an important role of Prkaa1 in skeletal muscle lipid metabolism. Deletion of muscle Prkaa1 leads to the delayed development of skeletal muscles but does not affect glucose tolerance or insulin sensitivity in animals fed a normal diet. Notably, when animals are fed a high-fat diet, the skeletal muscle of muscle-specific Prkaa1 knockout mice accumulates more lipids than the skeletal muscle of wild-type (WT) mice, with concomitant upregulation of adipogenic gene expressions and downregulation of the expression of genes associated with mitochondrial oxidation. Muscle-specific Prkaa1 ablation also results in hyperlipidemia, which may contribute to the increased IMTG levels. Furthermore, Prkaa1 deletion activates skeletal muscle mTOR signalling, which has a central role in lipid metabolism and mitochondrial oxidation. Collectively, our study provides new insights into the role of Prkaa1 in skeletal muscle. This knowledge may contribute to the treatment of related metabolic diseases.

Indexed as

Diet, High-FatLipid MetabolismAMP-Activated Protein KinasesAnimalsCell LineEnergy MetabolismGene DeletionInsulin ResistanceMaleMice, KnockoutMuscle, SkeletalReal-Time Polymerase Chain ReactionSignal TransductionTOR Serine-Threonine KinasesUp-RegulationAMP-Activated Protein KinasesmTOR protein, mousePrkaa1 protein, mouseTOR Serine-Threonine KinasesLipid metabolismMitochondrial oxidationmTORPrkaa1Skeletal muscle

Identifiers

PMID29288408
OpenAlexW2779517268

What OpenQuestion holds

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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.