Abstract | OBJECTIVE: METHODS: Cardiomyocyte hypertrophy induced by high glucose (25.5 mmol/L) and insulin (0.1 μmol/L) (HGI) was characterized in rat primary cardiomyocytes by measuring the cell surface area, protein content, and atrial natriuretic factor mRNA expression level. Protein and mRNA expressions were measured by Western blotting and real time RT-PCR, respectively. A spectrophotometric assay was used to measure the enzymatic concentration of endothelial NO synthase (eNOS), and the Griess assay measured the NO concentration. RESULTS: HGI induced significant cardiomyocyte hypertrophy and decreased the expression of PPARγ, AKT and eNOS at the mRNA and protein levels, which occurred in parallel with declining eNOS activity and NO concentration (P<0.05). The effects of HGI were inhibited by rosiglitazone (0.1 μmol/L), a selective PPARγ agonist (P<0.05). However, GW9662, a selective PPARγ antagonist, abolished the effects of rosiglitazone (P<0.05). LY294002, a PI3K/AKT inhibitor, and N(G)-nitro-L-arginine-methyl ester, an NOS inhibitor, partially blocked the effects of rosiglitazone (P<0.05). CONCLUSION: These results suggest that the PPARγ-PI3K/AKT-NO signal transduction pathway might be involved in HGI-induced cardiomyocyte hypertrophy.
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Authors | Xiaofeng Peng, Rongchun Chen, Yang Wu, Bo Huang, Cuiping Tang, Jiafei Chen, Quanhua Wang, Qin Wu, Junqing Yang, Hongmei Qiu, Qingsong Jiang |
Journal | Journal of diabetes and its complications
(J Diabetes Complications)
Vol. 29
Issue 6
Pg. 755-60
(Aug 2015)
ISSN: 1873-460X [Electronic] United States |
PMID | 26045205
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | Copyright © 2015 Elsevier Inc. All rights reserved. |
Chemical References |
- Insulin
- PPAR gamma
- Nitric Oxide
- Phosphatidylinositol 3-Kinases
- Proto-Oncogene Proteins c-akt
- Glucose
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Topics |
- Animals
- Cells, Cultured
- Glucose
(pharmacology)
- Hyperglycemia
(complications)
- Hyperinsulinism
(complications)
- Hypertrophy
(etiology)
- Insulin
(pharmacology)
- Myocytes, Cardiac
(drug effects, metabolism, pathology)
- Nitric Oxide
(metabolism)
- PPAR gamma
(metabolism)
- Phosphatidylinositol 3-Kinases
(metabolism)
- Proto-Oncogene Proteins c-akt
(metabolism)
- Rats
- Rats, Sprague-Dawley
- Signal Transduction
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