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GluR6‐containing KA receptor mediates the activation of p38 MAP kinase in rat hippocampal CA1 region during brain ischemia injury
Author(s) -
Chen Juan,
Li Chong,
Pei DongSheng,
Han Dong,
Liu XiaoMei,
Jiang HaiXia,
Wang XiaoTian,
Guan QiuHua,
Wen XiangRu,
Hou XiaoYu,
Zhang GuangYi
Publication year - 2009
Publication title -
hippocampus
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.767
H-Index - 155
eISSN - 1098-1063
pISSN - 1050-9631
DOI - 10.1002/hipo.20479
Subject(s) - mitogen activated protein kinase , p38 mitogen activated protein kinases , chemistry , neuroscience , ischemia , map kinase kinase kinase , ask1 , microbiology and biotechnology , hippocampal formation , kinase , pharmacology , biology , protein kinase a , mitogen activated protein kinase kinase , medicine
Our previous study showed that kainate (KA) receptor subunit GluR6 played an important role in ischemia‐induced MLK3 and JNK activation and neuronal degeneration through the GluR6‐PSD95‐MLK3 signaling module. However, whether the KA receptors subunit GluR6 is involved in the activation of p38 MAP kinase during the transient brain ischemia/reperfusion (I/R) in the rat hippocampal CA1 subfield is still unknown. In this present study, we first evaluated the time‐course of phospho‐p38 MAP kinase at various time‐points after 15 min of ischemia and then observed the effects of antagonist of KA receptor subunit GluR6, GluR6 antisence oligodeoxynucleotides on the phosphorylation of p38 MAP kinase induced by I/R. Results showed that inhibiting KA receptor GluR6 or suppressing the expression of KA receptor GluR6 could down‐regulate the elevation of phospho‐p38 MAP kinase induced by I/R. These drugs also reduced the phosphorylation of MLK3, MKK3/MKK6, MKK4, and MAPKAPK2. Additionally, our results indicated administration of three drugs, including p38 MAP kinase inhibitor before brain ischemia significantly decreased the number of TUNEL‐positive cells detected at 3 days of reperfusion and increased the number of the surviving CA1 pyramidal cells at 5 days of reperfusion after 15 min of ischemia. Taken together, we suggest that GluR6‐contained KA receptors can mediate p38 MAP kinase activation through a kinase cascade, including MLK3, MKK3/MKK6, and MKK4 and then induce increased phosphorylation of MAPKAPK‐2 during ischemia injury and ultimately result in neuronal cell death in the rat hippocampal CA1 region. © 2008 Wiley‐Liss, Inc.