Evidence map›Paper›PMID 26048986›Full record

ArticleThe Journal of biological chemistry2015

Pregnancy and Smoothelin-like Protein 1 (SMTNL1) Deletion Promote the Switching of Skeletal Muscle to a Glycolytic Phenotype in Human and Mice.

Beata Lontay, Khaldon Bodoor, Adrienn Sipos, Douglas H Weitzel, David Loiselle, Rachid Safi, Donghai Zheng, James Devente, Robert C Hickner, Donald P McDonnell and 2 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
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

11 citing papers in PubMed, 24 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

12 authors at 6 institutions in 3 countries.

Beata LontayDepartment of Pharmacology, Duke University Medical Center, Durham, North Carolina 27710; Department of Medical Chemistry, Faculty of Medicine, University of Debrecen, Debrecen-4032, Hungary.
Khaldon BodoorDepartment of Pharmacology, Duke University Medical Center, Durham, North Carolina 27710.
Adrienn SiposDepartment of Medical Chemistry, Faculty of Medicine, University of Debrecen, Debrecen-4032, Hungary.
Douglas H WeitzelDepartment of Pharmacology, Duke University Medical Center, Durham, North Carolina 27710.
David LoiselleDepartment of Pharmacology, Duke University Medical Center, Durham, North Carolina 27710.
Rachid SafiDepartment of Pharmacology, Duke University Medical Center, Durham, North Carolina 27710.
Donghai ZhengDepartments of Kinesiology, East Carolina University, Greenville, North Carolina 27858.
James DeventeDepartment of Obstetrics and Gynecology, East Carolina University, Greenville, North Carolina 27834.
Robert C HicknerDepartments of Kinesiology, East Carolina University, Greenville, North Carolina 27858; Department of Biokinetics, Exercise, and Leisure Sciences, University of KwaZulu-Natal, Durban 4000, South Africa.
Donald P McDonnellDepartment of Pharmacology, Duke University Medical Center, Durham, North Carolina 27710.
Thomas RibarDuke iPSC Shared Resource Facility, Duke University Medical Center, Durham, North Carolina 27710.
Timothy A HaysteadDepartment of Pharmacology, Duke University Medical Center, Durham, North Carolina 27710. Electronic address: timothy.haystead@duke.edu.
Duke Medical Center · USDuke University · USEast Carolina University · USDuke University Hospital · USUniversity of Debrecen · HUUniversity of KwaZulu-Natal · ZA

Funding

Calcium desensitization in Smooth MuscleR01DK065954 · NIDDK · DUKE UNIVERSITY · PI HAYSTEAD, TIMOTHY A · 2006 to 2009
$1.2M
NIDDK NIH HHS R01 DK065954NIDDK NIH HHS R01DK065954-05
6 · The paper itself

Abstract

Pregnancy promotes physiological adaptations throughout the body, mediated by the female sex hormones progesterone and estrogen. Changes in the metabolic properties of skeletal muscle enable the female body to cope with the physiological challenges of pregnancy and may also be linked to the development of insulin resistance. We conducted global microarray, proteomic, and metabolic analyses to study the role of the progesterone receptor and its transcriptional regulator, smoothelin-like protein 1 (SMTNL1) in the adaptation of skeletal muscle to pregnancy. We demonstrate that pregnancy promotes fiber-type changes from an oxidative to glycolytic isoform in skeletal muscle. This phenomenon is regulated through an interaction between SMTNL1 and progesterone receptor, which alters the expression of contractile and metabolic proteins. smtnl1(-/-) mice are metabolically less efficient and show impaired glucose tolerance. Pregnancy antagonizes these effects by inducing metabolic activity and increasing glucose tolerance. Our results suggest that SMTNL1 has a role in mediating the actions of steroid hormones to promote fiber switching in skeletal muscle during pregnancy. Our findings also bear on the management of gestational diabetes that develops as a complication of pregnancy in ~4% of women.

Indexed as

Gene DeletionGlycolysisAnimalsCalponinsEstrogen Receptor alphaFemaleGene Expression RegulationGlucose Tolerance TestHumansInsulin ResistanceMiceMuscle ProteinsMuscle, SkeletalOxygen ConsumptionPhosphoproteinsPregnancyCalponinsEstrogen Receptor alphaMuscle ProteinsPhosphoproteinsprogesterone receptor BReceptors, ProgesteroneSMTNL1 protein, humanSMTNL1 protein, mousegene expressionpregnancyproteomicsskeletal musclesmoothelin-like protein 1steroid hormone receptor

Identifiers

PMID26048986
PMCPMC4505045
OpenAlexW1415958099

What OpenQuestion 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 OpenQuestion graph.