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pmid:37053002

NR5A2 as a potential target for exercise to improve metabolic syndrome.

Lingxiu Meng · Fusheng Dong · Junguo Deng

Aging · 2023 doi:10.18632/aging.204606

Paper

complete

Experiment

complete

Data

partial

Analysis

partial

Execution

absent

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Record details sci_version · id · kind · revision · content_hash · schema · created_at · updated_at · generator
id
pmid:37053002
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science-record
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sha256:24cf6ac3c29de50918199234dcecf7114ac5ea7a034c0164cfd28fbb9c925237
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created_at
2026-11-01T19:01:42Z
updated_at
2026-11-01T22:09:15Z
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paper object · 10 fields
state
complete
title
NR5A2 as a potential target for exercise to improve metabolic syndrome.
doi
10.18632/aging.204606
pmid
37053002
authors array · 3 items
[0]
Lingxiu Meng
[1]
Fusheng Dong
[2]
Junguo Deng
journal
Aging
year
2023
abstract
BACKGROUND: Metabolic syndrome is a syndrome of a variety of metabolic disorders. Exercise is beneficial to the human body. However, the association of NR5A2 and exercise with metabolic syndrome remains unclear. METHODS: Download the GSE10540 and GSE12385 from GEO database. Bioinformatics analysis was used to screen the hub molecular of the metabolic syndrome. Forty 3-week-old C57BL/6J male mice were used in this study. The mean body weight was (17.5 ± 2.1) g. After 10 days of adaptive feeding, they were randomly divided into 4 groups according to the random number table method: Model + Exercise (n = 10), Model (n = 10), Model/NR5A2-OE (n = 10), Model/NR5A2-KO (n = 10). Western Blotting was performed to detect the expression of hub genes and signaling pathway. RESULTS: There were 349 DEGs in GSE10540 and 49 DEGs in GSE12385. 10 core genes were obtained. GO showed that differentially expressed genes were mainly enriched in vascular morphogenesis, contractile fiber fraction, chemotaxis, and MAPK cascade regulation. KEGG showed that MAPK signaling pathway was a significant section in the metabolic syndrome. PIK3R2, STRA8, FLT1, DMRT1, FGF22, NR5A2, and FLT were up-regulated and PRDM14, POU5F1, and KDR were down-regulated in metabolic syndrome after exercise. CONCLUSION: The expression of NR5A2 is down-regulated in metabolic syndrome, and exercise can increase the expression level of NR5A2. NR5A2 might be used as a potential target for exercise to improve metabolic syndrome.
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Students’ T test or Fisher test were used for comparison.
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methodological
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null
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sections[13] "Statistics" paragraph 2
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Students’ T test or Fisher test were used for comparison.
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complete
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sections[14] "Availability of data and materials" paragraph 2
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The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.
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Western blot analysis showed that NR5A2, CYP7A1, and CYP8B1 were lowly expressed in metabolic syndrome, and their expression levels were up-regulated after exercise (P < 0.05).
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Western blot analysis showed that NR5A2, CYP7A1, and CYP8B1 were lowly expressed in metabolic syndrome, and their expression levels were up-regulated after exercise (P < 0.05) (Figure 10).
evidence array · 1 item
[0] object · 3 fields
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sections[25] "Western blot (WB)" paragraph 2
quote
Western blot analysis showed that NR5A2, CYP7A1, and CYP8B1 were lowly expressed in metabolic syndrome, and their expression levels were up-regulated after exercise (P < 0.05) (Figure 10).
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Western blot analysis showed that NR5A2, CYP7A1, and CYP8B1 were lowly expressed in metabolic syndrome, and their expression levels were up-regulated after exercise (P < 0.05).
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GSM266121
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GSM266124
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GSM266128
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GSM266129
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GSM266136
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GSM266310
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2986
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title
Transcriptional changes in blood from metabolic syndrome patients after a period of high intensity interval training
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2026-11-01T18:46:34Z
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GSM310770
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GSM310774
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GSM310775
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GSM310776
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GSM310777
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36
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4133
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Homo sapiens
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Gene expression changes in Peripheral Blood Mononuclear cells (PBMC) induced by physical activity
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2026-11-01T18:46:34Z
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identifier_resolution_only_no_download_no_licence_read
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The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.
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lic syndrome. Forty 3-week-old C57BL/6J male mice were used in this study. The mean body weight was
[1]
animal model Forty 3-week-old C57BL/6J male mice were used in this study. The mean body weight was
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A2-OE (n = 10), Model/NR5A2-KO (n = 10). All mice were fed with high-fat purified diet and high-sug
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Complete file
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Bioinformatics analysis was used to screen the hub molecular of the metabolic syndrome. Forty 3-week-old C57BL/6J male mice were used in this study. The mean body weight was (17.5 ± 2.1) g. After 10 days of adaptive feeding, they were randomly divided into 4 groups according to the random number table method: Model + Exercise (n = 10), Model (n = 10), Model/NR5A2-OE (n = 10), Model/NR5A2-KO (n = 10). Western Blotting was performed to detect the expression of hub genes and signaling pathway.\nRESULTS: There were 349 DEGs in GSE10540 and 49 DEGs in GSE12385. 10 core genes were obtained. GO showed that differentially expressed genes were mainly enriched in vascular morphogenesis, contractile fiber fraction, chemotaxis, and MAPK cascade regulation. KEGG showed that MAPK signaling pathway was a significant section in the metabolic syndrome. PIK3R2, STRA8, FLT1, DMRT1, FGF22, NR5A2, and FLT were up-regulated and PRDM14, POU5F1, and KDR were down-regulated in metabolic syndrome after exercise.\nCONCLUSION: The expression of NR5A2 is down-regulated in metabolic syndrome, and exercise can increase the expression level of NR5A2. 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