IIB   20738
INSTITUTO DE INVESTIGACIONES BIOLOGICAS
Unidad Ejecutora - UE
congresos y reuniones científicas
Título:
LA MALNUTRICIÓN PROTEICA DURANTE LA PROGRAMACIÓN FETAL PREDISPONE A SUFRIR NASH Y/O NAFLD EN LA ADULTEZ
Autor/es:
ECHARTE, EM; PODAZA E; A. CHISARI
Lugar:
Iguassu Falls
Reunión:
Congreso; I Panamerican Congress of Physiological Sciences; 2014
Institución organizadora:
Asociación americana de ciencias fisiologicas
Resumen:
09.085 - LIVER DAMAGE CAUSED BY MATERNAL PROTEIN MALNUTRITION ARE NOT RECOVERED BY RESTORING THE NORMAL DIET IN ADULT LIFE Stella Maris Echarte; Enrique Podaza; Andrea Nancy Chisari Iib-Unmdp-Conicet, Mar Del Plata, Argentina. Growth restriction in utero is associated with the development of obesity, hypertension, and diabetes in animal models. The current understanding is that intrauterine deprivation programs the individual for a deprived environment, and that such programming is maladaptive in a nondeprived environment. The liver plays an essential role in metabolism regulation. The aim of this work was study the effect of protein malnutrition during gestation and lactation on liver function offspring. And consider whether these changes can be reversed by refeeding with normal protein diet. Pregnant Wistar rats who were fed a diet containing 8% of proteins (M), malnourished group (M) or 20% control group (C). The male offspring of mothers M, after weaning, were fed diet 8% P (MM) or control diet (reversed group-MC). In addition, male offspring from mothers C were feed with Diet C (CC). At day 60 post-birth the rats were slaughtered, bled by cardiac puncture and the liver was dissected. Body weights and liver were lower in the MM. MC recovered body weight but have greater liver. MC presented high values of GPT and Ɣ-Glutamil transferase. MC did not reverse cholesterol levels, remain high. Histological studies showed MC and MM with alterations in nuclear morphology with apoptosis increased. Conclusion: The lack of protein during development compromises the integrity of the structural and functional liver, manifested in adulthood and not revert until the time studied.