4.5 Article

Astrocytes from adult Wistar rats aged in vitro show changes in glial functions

期刊

NEUROCHEMISTRY INTERNATIONAL
卷 90, 期 -, 页码 93-97

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.neuint.2015.07.016

关键词

Adult astrocytes; Astrocytes aged in vitro; Brain aging; Glucose uptake; Glutamine synthetase activity; Glutathione

资金

  1. Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq)
  2. Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior (CAPES)
  3. Fundacao de Amparo a Pesquisa do Estado do Rio Grande do Sul (FAPERGS)
  4. Financiadora de Estudos e Projetos (FINEP) - IBN Net (Instituto Brasileiro de Neurociencias) [01.06.0842-00]
  5. Federal University of Rio Grande do Sul (UFRGS)
  6. Instituto Nacional de Ciencia e Tecnologia paraExcitotoxicidade e Neuroprotecao (INCTEN/CNPq)

向作者/读者索取更多资源

Astrocytes, the most versatile cells of the central nervous system, play an important role in the regulation of neurotransmitter homeostasis, energy metabolism, antioxidant defenses and the anti-inflammatory response. Recently, our group characterized cortical astrocyte cultures from adult Wistar rats. In line with that work, we studied glial function using an experimental in vitro model of aging astrocytes (30 days in vitro after reaching confluence) from newborn (NB), adult (AD) and aged (AG) Wistar rats. We evaluated metabolic parameters, such as the glucose uptake, glutamine synthetase (GS) activity, and glutathione (GSH) content, as well as the GFAP, GLUT-1 and xCT expression. AD and AG astrocytes take up less glucose than NB astrocytes and had decreased GLUT1 expression levels. Furthermore, AD and AG astrocytes exhibited decreased GS activity compared to NB cells. Simultaneously, AD and AG astrocytes showed an increase in GSH levels, along with an increase in xCT expression. NB, AD and AG astrocytes presented similar morphology; however, differences in GFAP levels were observed. Taken together, these results improve the knowledge of cerebral senescence and represent an innovative tool for brain studies of aging. (C) 2015 Elsevier Ltd. All rights reserved.

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