Evidence map›Paper›PMID 30201044›Full record

ArticleBiology of sex differences2018

Sex-specific differences in hepatic steatosis in obese spontaneously hypertensive (SHROB) rats.

Qingming Dong, Michael S Kuefner, Xiong Deng, Dave Bridges, Edwards A Park, Marshall B Elam, Rajendra Raghow

Open access · goldAbstract read
In one paragraph

Article in Biology of sex differences, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.1field-weighted citation impact, top 21% 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

8 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
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  6. Transcriptional Responses of Copper-Transport-Related GenesInternational journal of molecular sciences · 2022
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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.

Qingming DongDepartment of Veterans Affairs Medical Center, 1030 Jefferson Avenue, Memphis, TN, 38104, USA.
Michael S KuefnerDepartment of Veterans Affairs Medical Center, 1030 Jefferson Avenue, Memphis, TN, 38104, USA.
Xiong DengDepartment of Veterans Affairs Medical Center, 1030 Jefferson Avenue, Memphis, TN, 38104, USA.
Dave BridgesDepartment of Nutritional Sciences, University of Michigan School of Public Health, Ann Arbor, MI, 48109, USA.
Edwards A ParkDepartment of Veterans Affairs Medical Center, 1030 Jefferson Avenue, Memphis, TN, 38104, USA.
Marshall B ElamDepartment of Veterans Affairs Medical Center, 1030 Jefferson Avenue, Memphis, TN, 38104, USA.
Rajendra RaghowDepartment of Veterans Affairs Medical Center, 1030 Jefferson Avenue, Memphis, TN, 38104, USA. rraghow@uthsc.edu.
University of Tennessee Health Science Center · USUniversity of Michigan–Ann Arbor · US

Funding

Regional Pilot And Feasibility Study Grants ProgramP30DK020572 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI DAVID P OLSON · 2013 to 2026
$24.3M
Regulation of Lipid Storage by mTORC1R01DK107535 · NIDDK · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI BRIDGES, DAVE · 2016 to 2020
$1.7M
BLRD VA I01 BX002408BLRD VA I01 BX002409NIDDK NIH HHS P30 DK020572NIDDK NIH HHS R01 DK107535
6 · The paper itself

Abstract

backgroundPatients with metabolic syndrome, who are characterized by co-existence of insulin resistance, hypertension, hyperlipidemia, and obesity, are also prone to develop non-alcoholic fatty liver disease (NAFLD). Although the prevalence and severity of NAFLD is significantly greater in men than women, the mechanisms by which gender modulates the pathogenesis of hepatic steatosis are poorly defined. The obese spontaneously hypertensive (SHROB) rats represent an attractive model of metabolic syndrome without overt type 2 diabetes. Although pathological manifestation caused by the absence of a functional leptin receptor has been extensively studied in SHROB rats, it is unknown whether these animals elicited sex-specific differences in the development of hepatic steatosis.

methodsWe compared hepatic pathology in male and female SHROB rats. Additionally, we examined key biochemical and molecular parameters of signaling pathways linked with hyperinsulinemia and hyperlipidemia. Finally, using methods of quantitative polymerase chain reaction (qPCR) and western blot analysis, we quantified expression of 45 genes related to lipid biosynthesis and metabolism in the livers of male and female SHROB rats.

resultsWe show that all SHROB rats developed hepatic steatosis that was accompanied by enhanced expression of SREBP1, SREBP2, ACC1, and FASN proteins. The livers of male rats also elicited higher induction of Pparg, Ppara, Slc2a4, Atox1, Skp1, Angptl3, and Pnpla3 mRNAs. In contrast, the livers of female SHROB rats elicited constitutively higher levels of phosphorylated JNK and AMPK and enhanced expression of Cd36.

conclusionBased on these data, we conclude that the severity of hepatic steatosis in male and female SHROB rats was mainly driven by increased de novo lipogenesis. Moreover, male and female SHROB rats also elicited differential severity of hepatic steatosis that was coupled with sex-specific differences in fatty acid transport and esterification.

Indexed as

HypertensionNon-alcoholic Fatty Liver DiseaseObesitySex CharacteristicsAcyltransferasesAnimalsCD36 AntigensFatty AcidsFemaleLipogenesisLiverMaleMembrane ProteinsPhospholipases A2Phospholipases A2, Calcium-IndependentProto-Oncogene Proteins c-aktAcyltransferasesCD36 AntigensFatty AcidsMembrane ProteinsPhospholipases A2Phospholipases A2, Calcium-IndependentPNPLA3 protein, ratProto-Oncogene Proteins c-akt

Identifiers

PMID30201044
PMCPMC6131947
OpenAlexW2890279529

What Socratic holds

Textmetadata
LicenceCC BY
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.