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Maternal low-protein diet decreases brain-derived neurotrophic factor expression in the brains of the neonatal rat offspring
Affiliation:1. Department of Biomedical Sciences, School of Medicine & Health Sciences, University of North Dakota, Grand Forks, ND 58203, USA;2. U.S. Department of Agriculture, Agricultural Research Service, Grand Forks Human Nutrition Research Center, Grand Forks, ND 58203, USA;1. Instituto de Investigaciones en Salud, Universidad de Costa Rica, Costa Rica;2. Instituto de Investigaciones Psicológicas, Universidad de Costa Rica, Costa Rica;3. Centro de Investigación en Neurociencias, Universidad de Costa Rica, Costa Rica;1. Biochemistry and Molecular Medicine Department, Universidad Autónoma de Nuevo León, College of Medicine, Monterrey, Mexico;2. Center for Research and Development in Health Sciences, Neurometabolism Unit, Universidad Autónoma de Nuevo León, Monterrey, Mexico;3. Facultad de Ciencias Biológicas, Laboratorio de Inmunología y Virología, Universidad Autónoma de Nuevo León, Monterrey, Mexico;4. Tecnologico de Monterrey, Escuela de Medicina y Ciencias de la Salud and The Institute for Obesity Research. Monterrey 64710, Mexico
Abstract:Prenatal exposure to a maternal low-protein (LP) diet has been known to cause cognitive impairment, learning and memory deficits. However, the underlying mechanisms have not been identified. Herein, we demonstrate that a maternal LP diet causes, in the brains of the neonatal rat offspring, an attenuation in the basal expression of the brain-derived neurotrophic factor (BDNF), a neurotrophin indispensable for learning and memory. Female rats were fed either a 20% normal protein (NP) diet or an 8% LP 3 weeks before breeding and during the gestation period. Maternal LP diet caused a significant reduction in the Bdnf expression in the brains of the neonatal rats. We further found that the maternal LP diet reduced the activation of the cAMP/protein kinase A/cAMP response element binding protein (CREB) signaling pathway. This reduction was associated with a significant decrease in CREB binding to the Bdnf promoters. We also show that prenatal exposure to the maternal LP diet results in an inactive or repressed exon I and exon IV promoter of the Bdnf gene in the brain, as evidenced by fluxes in signatory hallmarks in the enrichment of acetylated and trimethylated histones in the nucleosomes that envelop the exon I and exon IV promoters, causing the Bdnf gene to be refractory to transactivation. Our study is the first to determine the impact of a maternal LP diet on the basal expression of BDNF in the brains of the neonatal rats exposed prenatally to an LP diet.
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