Apolipoprotein A-I Protects Against Pregnancy-Induced Insulin Resistance in Rats.


Journal

Arteriosclerosis, thrombosis, and vascular biology
ISSN: 1524-4636
Titre abrégé: Arterioscler Thromb Vasc Biol
Pays: United States
ID NLM: 9505803

Informations de publication

Date de publication:
06 2019
Historique:
pubmed: 26 4 2019
medline: 6 2 2020
entrez: 26 4 2019
Statut: ppublish

Résumé

Objective- Insulin resistance and inflammation in pregnancy are risk factors for gestational diabetes mellitus. Increased plasma HDL (high-density lipoprotein) and apo (apolipoprotein) A-I levels have been reported to improve glucose metabolism and inhibit inflammation in animals and humans. This study asks whether increasing plasma apoA-I levels improves insulin sensitivity and reduces inflammation in insulin-resistant pregnant rats. Approach and Results- Insulin-resistant pregnant rats received intravenous infusions of lipid-free apoA-I (8 mg/kg) or saline on days 6, 9, 12, 15, and 18 of pregnancy. The rats were then subjected to a euglycemic-hyperinsulinemic clamp. Glucose uptake was increased in white and brown adipose tissue by 57±13% and 32±10%, respectively ( P<0.05 for both), and in quadriceps and gastrocnemius muscle by 35±9.7% and 47±14%, respectively ( P<0.05 for both), in the apoA-I-treated pregnant rats relative to saline-infused pregnant rats. The pregnant rats that were treated with apoA-I also had reduced plasma TNF-α (tumor necrosis factor-α) levels by 57±8.4%, plasma IL (interleukin)-6 levels by 67±9.5%, and adipose tissue macrophage content by 54±8.2% ( P<0.05 for all) relative to the saline-treated pregnant rats. Conclusions- These studies establish that apoA-I protects against pregnancy-induced insulin resistance in rats by increasing insulin sensitivity in adipose tissue and skeletal muscle and inhibiting inflammation. This identifies apoA-I as a potential target for preventing pregnancy-induced insulin resistance and reducing the incidence of gestational diabetes mellitus.

Identifiants

pubmed: 31018664
doi: 10.1161/ATVBAHA.118.312282
doi:

Substances chimiques

Anti-Inflammatory Agents 0
Apolipoprotein A-I 0
Biomarkers 0
Blood Glucose 0
Hypoglycemic Agents 0
Il6 protein, rat 0
Inflammation Mediators 0
Insulin 0
Interleukin-6 0
Tumor Necrosis Factor-alpha 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1160-1171

Subventions

Organisme : Austrian Science Fund FWF
ID : W 1226
Pays : Austria

Auteurs

Ben J Wu (BJ)

From the Lipid Research Group, School of Medical Sciences, University of New South Wales Sydney, Australia (B.J.W., Y.S., K.-L.O., Y.L., S.T., P.J.B., K.-A.R.).

Yidan Sun (Y)

From the Lipid Research Group, School of Medical Sciences, University of New South Wales Sydney, Australia (B.J.W., Y.S., K.-L.O., Y.L., S.T., P.J.B., K.-A.R.).
Division of Immunology and Pathophysiology, Otto Loewi Research Center for Vascular Biology, Immunology and Inflammation, Medical University of Graz, Austria (Y.S.).

Kwok-Leung Ong (KL)

From the Lipid Research Group, School of Medical Sciences, University of New South Wales Sydney, Australia (B.J.W., Y.S., K.-L.O., Y.L., S.T., P.J.B., K.-A.R.).

Yue Li (Y)

From the Lipid Research Group, School of Medical Sciences, University of New South Wales Sydney, Australia (B.J.W., Y.S., K.-L.O., Y.L., S.T., P.J.B., K.-A.R.).

Shudi Tang (S)

From the Lipid Research Group, School of Medical Sciences, University of New South Wales Sydney, Australia (B.J.W., Y.S., K.-L.O., Y.L., S.T., P.J.B., K.-A.R.).

Philip J Barter (PJ)

From the Lipid Research Group, School of Medical Sciences, University of New South Wales Sydney, Australia (B.J.W., Y.S., K.-L.O., Y.L., S.T., P.J.B., K.-A.R.).

Kerry-Anne Rye (KA)

From the Lipid Research Group, School of Medical Sciences, University of New South Wales Sydney, Australia (B.J.W., Y.S., K.-L.O., Y.L., S.T., P.J.B., K.-A.R.).

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Classifications MeSH