Effects of prenatal stress and postnatal high fat diet feeding on BALB/c mice metabolism

• Autores: Quiroga, Sofia; Juárez, Yamila R.; Tellechea, Mariana L.; Genaro, Ana María; Burgueño, Adriana Laura
• Año de publicación: 2019
• Idioma: inglés
• Tipo de recurso: documento de conferencia
• Fuente: Medicina Buenos Aires. 2019, 79 (Supl. IV)
• Materia: ESTRES PRENATAL
• Institución: Pontificia Universidad Católica Argentina

Fil: Quiroga, Sofia. Pontificia Universidad Católica Argentina. Facultad de Ciencias Médicas. Instituto de Investigaciones Científicas; Argentina
Fil: Juárez, Yamila Raquel. Pontificia Universidad Católica Argentina. Facultad de Ciencias Médicas. Instituto de Investigaciones Científicas; Argentina
Fil: Tellechea, Mariana L. Consejo Nacional de Investigaciones Científicas y Tecnicas. Centro de Investigaciones Endocrinólogas Dr. César Bergadá; Argentina
Fil: Genaro, Ana María. Pontificia Universidad Católica Argentina. Facultad de Ciencias Médicas. Instituto de Investigaciones Científicas; Argentina
Fil: Burgueño, Adriana. Pontificia Universidad Católica Argentina. Facultad de Ciencias Médicas. Instituto de Investigaciones Científicas; Argentina
Resumen: In-utero exposure to maternal stress increases short and long term risk of suffering metabolic diseases. Exposure to stressful events leads to an increase in glucocorticoids release by activation of the HPA axis, therefore early programming of the HPA axis has emerged as a key underlying mechanism of stress-related disorders. Evidence suggests that a stressful prenatal environment seems to favour adverse metabolic conditions. To test this hypothesis in BALB/c mice, a strain susceptible to stress but resistant to metabolic effects of a high fat diet (HFD), we exposed female pregnant mice to restraint stress during the last week of pregnancy (2 h/day). Offspring were fed with HFD between weeks 4 and 28 of age. Prenatally stressed (PS) females and males fed with HFD showed higher body weight (females: p<0.001, n= 8; males: p<0.01, n= 8) and adipose tissue content (adipose tissue weight/body weight, both sexes: p<0.001, n= 8). Females were hyperinsulinemic (p<0.001, n= 5), with decreased expression of Foxo1 (Forkhead box protein O1) a transcription factor that plays important roles in regulation of gluconeogenesis and glycogenolysis by insulin signaling (p<0.05, n= 5) and Adiponectin (p<0.05, n= 5) in adipose tissue. On the other hand, PS males (fed with standard or HFD) had hypertriglyceridemia (p<0.001, n= 8) and hypercholesterolemia (p<0.001, n= 8). PS per se, in males, decreased the expression of Adiponectin (p<0.01, n= 5). PS animals showed a great susceptibility to develop obesity. We conclude that PS may give rise to some adverse effects, and abnormal phenotype may be provoked by or exacerbated in a later life nutritional challenge. We intend to continue our research by evaluating whether epigenetic alterations are responsible for the observed gene expression alterations.