Maternal Hypermethioninemia Affects Neurons Number,Neurotrophins Levels,Energy Metabolism,and Na+,K+-ATPase Expression/Content in Brain of Rat Offspring |
| |
Authors: | Bruna M. Schweinberger André F. Rodrigues Elias Turcatel Paula Pierozan Leticia F. Pettenuzzo Mateus Grings Giselli Scaini Mariana M. Parisi Guilhian Leipnitz Emilio L. Streck Florencia M. Barbé-Tuana Angela T. S. Wyse |
| |
Affiliation: | 1.Postgraduate Program in Biological Sciences—Biochemistry, Department of Biochemistry, Institute of Health Basic Sciences,Federal University of Rio Grande do Sul,Porto Alegre,Brazil;2.Postgraduate program in Health Sciences, Laboratory of Bioenergetics,University of Southern Santa Catarina,Criciúma,Brazil |
| |
Abstract: | In the current study, we verified the effects of maternal hypermethioninemia on the number of neurons, apoptosis, nerve growth factor, and brain-derived neurotrophic factor levels, energy metabolism parameters (succinate dehydrogenase, complex II, and cytochrome c oxidase), expression and immunocontent of Na+,K+-ATPase, edema formation, inflammatory markers (tumor necrosis factor-alpha and interleukin-6), and mitochondrial hydrogen peroxide levels in the encephalon from the offspring. Pregnant Wistar rats were divided into two groups: the first one received saline (control) and the second group received 2.68 μmol methionine/g body weight by subcutaneous injections twice a day during gestation (approximately 21 days). After parturition, pups were killed at the 21st day of life for removal of encephalon. Neuronal staining (anti-NeuN) revealed a reduction in number of neurons, which was associated to decreased nerve growth factor and brain-derived neurotrophic factor levels. Maternal hypermethioninemia also reduced succinate dehydrogenase and complex II activities and increased expression and immunocontent of Na+,K+-ATPase alpha subunits. These results indicate that maternal hypermethioninemia may be a predisposing factor for damage to the brain during the intrauterine life. |
| |
Keywords: | |
本文献已被 SpringerLink 等数据库收录! |
|