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PMID: 15846800 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Alterations in metabolism and gap junction expression may determine the role of astrocytes as "good samaritans" or executioners.

Glia ·Vol. 50 ·No. 4 ·2005-06-00 ·Pages 351-61

Farahani R, Pina-Benabou MH, Kyrozis A, Siddiq A, Barradas PC, Chiu FC, Cavalcante LA, Lai JC, Stanton PK, Rozental R

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.

MeSH Terms
Astrocytes/metabolism,physiology Brain Ischemia/genetics,metabolism,prevention & control Cell Communication/genetics Connexins/biosynthesis,genetics,metabolism,physiology Gap Junctions/genetics,metabolism,physiology Gene Expression Regulation/physiology
Chemicals
Connexins
Authors & Affiliations
10 authors, click to expand affiliations / ORCID
Farahani Reza
Department of Pediatrics, Albert Einstein College of Medicine, Bronx, New York, USA.
Pina-Benabou Mara H
Kyrozis Andreas
Siddiq Ayesha
Barradas Penha C
Chiu Fung-Chow
Cavalcante Leny A
Lai James C K
Stanton Patric K
Rozental Renato
Article Info
Journal
Glia
Abbr.
Glia
ISSN
0894-1491
Published
2005-06-00
Pages
351-61
Language
English
Region
United States
NLM ID
8806785
Subset
IM
Grants
NINDS NIH HHS · NIH R21 NS42916 · United States
NINDS NIH HHS · R01 NS042152-01 · United States
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