Literature DB >> 8898692

Induction of Na+/myo-inositol cotransporter mRNA after focal cerebral ischemia: evidence for extensive osmotic stress in remote areas.

T Yamashita1, E Kohmura, A Yamauchi, S Shimada, T Yuguchi, T Sakaki, A Miyai, M Tohyama, T Hayakawa.   

Abstract

Myo-inositol is one of the major organic osmolytes in the brain. It is accumulated into cells through an Na+/ myo-inositol cotransporter (SMIT) that is regulated by extracellular tonicity. To investigate the role of SMIT in the brain after cerebral ischemia, we examined expression of SMIT mRNA in the rat brain after middle cerebral artery occlusion, which would reflect alteration of extracellular tonicity. The expression of SMIT mRNA was markedly increased 12 h after surgery in the cortex of the affected side and lasted until the second day. Increased expression was also found in the contralateral cingulate cortex. Up-regulated expression was found predominantly in the neurons in remote areas, although nonneuronal cells adjacent to the ischemic core also expressed this mRNA. These results suggest that cerebral ischemia causes extensive osmotic stress in brain and that the neuronal cells respond to this stress by increasing SMIT expression.

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Year:  1996        PMID: 8898692     DOI: 10.1097/00004647-199611000-00014

Source DB:  PubMed          Journal:  J Cereb Blood Flow Metab        ISSN: 0271-678X            Impact factor:   6.200


  2 in total

1.  High cerebral scyllo-inositol: a new marker of brain metabolism disturbances induced by chronic alcoholism.

Authors:  A Viola; F Nicoli; B Denis; S Confort-Gouny; Y Le Fur; J-P Ranjeva; P Viout; P J Cozzone
Journal:  MAGMA       Date:  2004-08-31       Impact factor: 2.310

2.  Deletion of TRAAK potassium channel affects brain metabolism and protects against ischemia.

Authors:  Christophe Laigle; Sylviane Confort-Gouny; Yann Le Fur; Patrick J Cozzone; Angèle Viola
Journal:  PLoS One       Date:  2012-12-28       Impact factor: 3.240

  2 in total

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