4.7 Article

Activation of p38 MAPK participates in brain ischemic tolerance induced by limb ischemic preconditioning by up-regulating HSP 70

Journal

EXPERIMENTAL NEUROLOGY
Volume 224, Issue 2, Pages 347-355

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.expneurol.2010.04.009

Keywords

Brain ischemic tolerance; Limb ischemic preconditioning; p38 MAPK; HSP 70; Hippocampus

Categories

Funding

  1. National Natural Science Foundation of China [30770738]
  2. Ministry of Education, PR China [20050089001]
  3. Natural Science Foundation of Hebei Province, PR China [C200500720, C2008001042]
  4. Grant for Department of Science and Technology of Hebei Province [072761901]
  5. Health Department of Hebei Province [20090313]
  6. Foundation of scientific backbone breeding plan of Hebei Medical University

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This study investigates whether activation of p38 MAPK by the up-regulation of HSP 70 participates in the induction of brain ischemic tolerance by limb ischemic preconditioning (LIP). Western blot and immunohistochemical assays indicated that p38 MAPK activation occurred earlier than HSP 70 induction in the CA1 region of the hippocampus after LIP. P-p38 MAPK expression was up-regulated at 6 h and reached its peak 12 h after LIP, while HSP 70 expression was not significantly increased until 1 day and peaked 2 days after LIP. Neuropathological evaluation by thionin staining showed that quercetin (4 ml/kg, 50 mg/kg, intraperitoneal injection), an inhibitor of HSP 70, blocked the protective effect of LIP against delayed neuronal death that is normally induced by lethal brain ischemic insult, indicating that HSP 70 participates in the induction of brain ischemic tolerance by LIP. Furthermore, SB 203580, an inhibitor of HSP 70, inhibited HSP 70 activation in the CA1 region of the hippocampus induced by LIP either with or without the presence of subsequent brain ischemic insult. Based on the above results, it can be concluded that activation of p38 MAPK participates in the brain ischemic tolerance induced by LIP at least partly by the up-regulation of HSP 70 expression. (C) 2010 Elsevier Inc. All rights reserved.

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