N-acetylcysteine inhibits lipid accumulation in mouse embryonic adipocytes
Oxidative stress plays critical roles in the pathogenesis of diabetes, hypertension, and atherosclerosis; some authors reported that fat accumulation correlates to systemic oxidative stress in human and mice, but cellular redox environment effect on lipid accumulation is still unclear. In our labora...
| Autores: | , , , , , |
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| Tipo de recurso: | artículo |
| Estado: | Versión publicada |
| Fecha de publicación: | 2016 |
| País: | Argentina |
| Institución: | Consejo Nacional de Investigaciones Científicas y Técnicas |
| Repositorio: | CONICET Digital (CONICET) |
| Idioma: | inglés |
| OAI Identifier: | oai:ri.conicet.gov.ar:11336/24037 |
| Acceso en línea: | http://hdl.handle.net/11336/24037 |
| Access Level: | acceso abierto |
| Palabra clave: | TRIGLYCERIDES INHIBITION ADIPOCYTES N-ACETYLCYSTEINE https://purl.org/becyt/ford/1.6 https://purl.org/becyt/ford/1 |
| Sumario: | Oxidative stress plays critical roles in the pathogenesis of diabetes, hypertension, and atherosclerosis; some authors reported that fat accumulation correlates to systemic oxidative stress in human and mice, but cellular redox environment effect on lipid accumulation is still unclear. In our laboratory we used mouse embryonic fibroblasts (undifferentiated cells: CC), which are capable of differentiating into ma- ture adipocytes (differentiated cells: DC) and accumulate lipids, as obesity model. Here we analyzed the role of the well-known antioxidant and glutathione precursor N-acetylcysteine (NAC) in cellular MAPK modulation and lipid accumulation. We evaluated the effect of NAC on the adipogenic differentiation pathway using different doses: 0.01, 0.1, 1 and 5 mM; no toxic doses in these cells. A dose of 5 mM NAC [DCN-5] provoked a significant decrease in triglyceride accumulation (72710 [DCN-5] vs 169715 [DC], po0.01), as well in Oil Red O stained neutral lipid content (12072 [DCN-5] vs 139712 [DC], po0.01). Molecular mechanisms responsible for adipogenic differentiation involve increase of the expression of phosphoERK1⁄2 and phosphoJNK, 5 mM NAC treatment inhibited both pERK1⁄2 and pJNK protein levels. We also evaluated the mitotic clonal expansion (MCE) which takes place during adipogenesis and observed an increase in DC at a rate of 1.5 cells number compared to CC at day 2, whereas the highest doses of NAC significantly inhibited MCE. Our results suggest that NAC inhibits lipid accumulation and the MAPK phosphorylation in mouse embryonic fibroblasts during adipogenic differentiation and further con- tribute to probe the importance of cellular redox environment in adipogenesis. |
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