Literature DB >> 8281126

Induction of glucose regulated protein (grp78) and inducible heat shock protein (hsp70) mRNAs in rat brain after kainic acid seizures and focal ischemia.

S Wang1, F M Longo, J Chen, M Butman, S H Graham, K G Haglid, F R Sharp.   

Abstract

Specific probes were obtained using PCR cloning from rat brain for the 78 kDa glucose regulated (grp78), inducible 72 kDa (hsp70) as well as constitutive 73 kDa (hsc73) heat shock mRNAs. Grp78 and hsc73 were expressed in normal rat brain whereas hsp70 was not. Subcutaneous injection kainic acid (10 mg/kg) produced seizures and induced all three mRNAs. The induction of grp78 and hsp70 mRNAs occurred within 2 h, peaked between 6-8 h, persisted for 48 h, and returned to control levels by 72 h. Expression of the grp78 and hsp70 mRNAs after focal ischemia progressively increased with occlusion durations from 15-120 min in the cerebral cortex. Though grp78 and hsp70 mRNAs were induced modestly in the striatum by 15 min of ischemia, longer durations of ischemia were characterized by little change in the grp78 mRNA levels and relatively lower levels of hsp70 expression. This result indicates that progressive increases in the duration of ischemia in brain, prior to infarction, may produce proportional increases in transcription of the heat shock genes. However, once the duration of ischemia is long enough to produce infarction, this severely limits the availability of ATP which blocks transcription of the heat shock genes. In conclusion, concurrent induction of the heat shock genes suggests that kainic acid seizures and focal ischemia induce several different stress responses in brain cells caused by denaturation of proteins, changes of protein synthesis, and changes of protein glycosylation.

Entities:  

Mesh:

Substances:

Year:  1993        PMID: 8281126     DOI: 10.1016/0197-0186(93)90106-f

Source DB:  PubMed          Journal:  Neurochem Int        ISSN: 0197-0186            Impact factor:   3.921


  8 in total

1.  Protein misfolding induces hypoxic preconditioning via a subset of the unfolded protein response machinery.

Authors:  Xianrong R Mao; C Michael Crowder
Journal:  Mol Cell Biol       Date:  2010-08-23       Impact factor: 4.272

2.  Overexpressing GRP78 influences Ca2+ handling and function of mitochondria in astrocytes after ischemia-like stress.

Authors:  Yi-Bing Ouyang; Li-Jun Xu; John F Emery; Amy S Lee; Rona G Giffard
Journal:  Mitochondrion       Date:  2010-11-01       Impact factor: 4.160

3.  Subcellular stress response and induction of molecular chaperones and folding proteins after transient global ischemia in rats.

Authors:  Jessie S Truettner; Kurt Hu; Cindy L Liu; W Dalton Dietrich; Bingren Hu
Journal:  Brain Res       Date:  2008-10-28       Impact factor: 3.252

Review 4.  Molecular mechanisms of apoptosis in cerebral ischemia: multiple neuroprotective opportunities.

Authors:  Venkata Prasuja Nakka; Anchal Gusain; Suresh L Mehta; Ram Raghubir
Journal:  Mol Neurobiol       Date:  2007-12-08       Impact factor: 5.590

Review 5.  Loss of endoplasmic reticulum Ca2+ homeostasis: contribution to neuronal cell death during cerebral ischemia.

Authors:  Ankur Bodalia; Hongbin Li; Michael F Jackson
Journal:  Acta Pharmacol Sin       Date:  2012-10-29       Impact factor: 6.150

6.  Cellular and Subcellular Localization of Endoplasmic Reticulum Chaperone GRP78 Following Transient Focal Cerebral Ischemia in Rats.

Authors:  Xuyan Jin; Dong Kyu Kim; Tae-Ryong Riew; Hong Lim Kim; Mun-Yong Lee
Journal:  Neurochem Res       Date:  2018-05-17       Impact factor: 3.996

7.  Spatiotemporal Expression of GRP78 in the Blood Vessels of Rats Treated With 3-Nitropropionic Acid Correlates With Blood-Brain Barrier Disruption.

Authors:  Xuyan Jin; Tae-Ryong Riew; Hong Lim Kim; Soojin Kim; Mun-Yong Lee
Journal:  Front Cell Neurosci       Date:  2018-11-20       Impact factor: 5.505

8.  Transgenic overexpression of 14-3-3 zeta protects hippocampus against endoplasmic reticulum stress and status epilepticus in vivo.

Authors:  Gary P Brennan; Eva M Jimenez-Mateos; Ross C McKiernan; Tobias Engel; Guri Tzivion; David C Henshall
Journal:  PLoS One       Date:  2013-01-24       Impact factor: 3.240

  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.