Effect of Kainic Acid on the Phosphorylation of Mitogen Activated Protein Kinases in Rat Hippocampus

  • Won, Je-Seong (Department of Pharmacology and Institute of Natural Medicine, College of Medicine, Hallym University) ;
  • Lee, Jin-Koo (Department of Pharmacology and Institute of Natural Medicine, College of Medicine, Hallym University) ;
  • Choi, Seong-Soo (Department of Pharmacology and Institute of Natural Medicine, College of Medicine, Hallym University) ;
  • Song, Dong-Keun (Department of Pharmacology and Institute of Natural Medicine, College of Medicine, Hallym University) ;
  • Huh, Sung-Oh (Department of Pharmacology and Institute of Natural Medicine, College of Medicine, Hallym University) ;
  • Kim, Yung-Hi (Department of Pharmacology and Institute of Natural Medicine, College of Medicine, Hallym University) ;
  • Suh, Hong-Won (Department of Pharmacology and Institute of Natural Medicine, College of Medicine, Hallym University)
  • Published : 2001.12.21

Abstract

In rat hippocampus, kainic acid (KA; 10 mg/kg; i.p.) increased the phosphorylated forms of ERK1/2 (p-ERK1/2) and Jun kinase1 (p-JNK1), but not p-JNK2 and p38 (p-p38). The preadministration with cycloheximide (CHX; 5 mg/kg; i.p.) inhibited KA-induced increase of p-JNK1, but not p-ERK1/2. Surprisingly, the phosphorylated upstream MAP kinase kinases (p-MKKs) were not correlated with their downstream MAP kinases. The basal p-MKK1/2 levels were completely abolished by KA, which were reversed by CHX. In addition, p-MKK4 and p-MKK3/6 levels were enhanced by CHX alone, but were attenuated by KA. Thus, our results showed that KA increased the p-ERK and p-JNK levels in rat hippocampus, which were not parallel with their classical upstreamal kinases.

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