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J Dev Orig Health Dis ; 8(2): 236-243, 2017 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-28004624

RESUMEN

It has been demonstrated that intrauterine growth restriction (IUGR) can program increase cardiometabolic risk. There are also evidences of the correlation between IUGR with low-grade inflammation and, thus can contribute to development of several cardiometabolic comorbidities. Therefore, we investigated the influence of IUGR on circulating mitochondrial DNA (mtDNA)/Toll-like receptor 9 (TLR9) and TNF-α expression in adult offspring. Considering that the aerobic training has anti-inflammatory actions, we also investigated whether aerobic training would improve these inflammatory factors. Pregnant Wistar rats received ad libitum or 50% of ad libitum diet throughout gestation. At 8 weeks of age, male offspring from both groups were randomly assigned to control, trained control, restricted and trained restricted. Aerobic training protocol was performed on a treadmill and after that, we evaluated circulating mtDNA, cardiac protein expression of TLR9, plasma and cardiac TNF-α levels, and left ventricle (LV) mass. We found that IUGR promoted an increase in the circulating mtDNA, TLR9 expression and plasma TNF-α levels. Further, our results revealed that aerobic training can restore mtDNA/TLR9 content and plasma levels of TNF-α among restricted rats. The cardiac TNF-α content and LV mass were not influenced either by IUGR or aerobic training. In conclusion, IUGR can program mtDNA/TLR9 content, which may lead to high levels of TNF-α. However, aerobic training was able to normalize these alterations. These findings evidenced that the association of IUGR and aerobic training seems to exert an important interaction effect regarding pro-inflammatory condition and, aerobic training may be used as a strategy to reduce deleterious adaptations in IUGR offspring.


Asunto(s)
Cardiomegalia/prevención & control , ADN Mitocondrial/genética , Retardo del Crecimiento Fetal/fisiopatología , Condicionamiento Físico Animal/métodos , Efectos Tardíos de la Exposición Prenatal/fisiopatología , Receptor Toll-Like 9/metabolismo , Adaptación Fisiológica , Animales , Animales Recién Nacidos , Cardiomegalia/etiología , ADN Mitocondrial/sangre , Femenino , Masculino , Embarazo , Ratas , Ratas Wistar
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