Alterations in metabolism and gap junction expression may determine the role of astrocytes as “good samaritans” or executioners
- 21 April 2005
- Vol. 50 (4) , 351-361
- https://doi.org/10.1002/glia.20213
Abstract
Our knowledge of astroglia and their physiological and pathophysiological role(s) in the central nervous system (CNS) has grown during the past decade, revealing a complex picture. It is becoming increasingly clear that glia play a significant role in the homeostasis and function of the CNS and that neurons should no longer be considered the only cell type that responds, both rapidly and slowly, to electrochemical activity. We discuss recent advances in the field with an emphasis on the impact of hypoxia and ischemia on astrocytic metabolism and the functional relationship between glucose metabolism and gap junctions in astrocytes. We also address the controversy over whether astrocytic gap junctions mediate protection or killing of neurons during or after hypoxic or ischemic insults.Keywords
This publication has 89 references indexed in Scilit:
- Endothelin‐1 stimulates the translocation and upregulation of both glucose transporter and hexokinase in astrocytes: relationship with gap junctional communicationJournal of Neurochemistry, 2004
- Brain regional development of the activity of α-ketoglutarate dehydrogenase complex in the ratDevelopmental Brain Research, 2000
- Temporal expression of neuronal connexins during hippocampal ontogenyBrain Research Reviews, 2000
- Gap junctions in the nervous systemBrain Research Reviews, 2000
- Metabolic trafficking through astrocytic gap junctionsGlia, 1997
- Octanol, a gap junction uncoupling agent, changes intracellular [H+] in rat astrocytesGlia, 1996
- NMR spectroscopic study of cell cultures of astrocytes and neurons exposed to hypoxia: Compartmentation of astrocyte metabolismNeurochemistry International, 1994
- Quantitative immunohistochemical and biochemical correlates of connexin43 localization in rat brainGlia, 1992
- Exchange between hamster cells in cultureExperimental Cell Research, 1968
- Biochemically marked variants of the syrian hamster fibroblast cell line BHK21 and its derivativesExperimental Cell Research, 1965