Literature DB >> 1326973

The biochemical mechanisms of the excitotoxicity of kainic acid. Free radical formation.

A Y Sun1, Y Cheng, Q Bu, F Oldfield.   

Abstract

Kainic acid (KA) is a known potent neuroexcitotoxin, although the biochemical mechanism producing its underlying neurotoxic effect is not quite clear. Histopathological examination of gerbil brains 24 h after systemic injection of KA revealed severe neuronal lesions in different regions of the brain, especially the cerebellar and hippocampal areas. We have detected free radical formation in the brain 1 h after KA administration by using an in vivo spin trapping technique. We have also observed increased lipid peroxidation in the brain after KA-treatment by analyzing thiobarbituric acid reactive substances and conjugated diene formation. Diminished brain specific (Na+, K+)-ATPase activity was also found 2 h after KA injection and persisted to 24 h. It is possible that the free radical reaction is a primary cause of neuronal degeneration after KA administration.

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Year:  1992        PMID: 1326973     DOI: 10.1007/bf03159981

Source DB:  PubMed          Journal:  Mol Chem Neuropathol        ISSN: 1044-7393


  12 in total

1.  Propolis ameliorates tumor nerosis factor-α, nitric oxide levels, caspase-3 and nitric oxide synthase activities in kainic acid mediated excitotoxicity in rat brain.

Authors:  Mummedy Swamy; Dian Suhaili; K N S Sirajudeen; Zulkarnain Mustapha; Chandran Govindasamy
Journal:  Afr J Tradit Complement Altern Med       Date:  2014-08-23

Review 2.  Kainic acid-mediated excitotoxicity as a model for neurodegeneration.

Authors:  Qun Wang; Sue Yu; Agnes Simonyi; Grace Y Sun; Albert Y Sun
Journal:  Mol Neurobiol       Date:  2005       Impact factor: 5.590

3.  Spatial memory is enhanced in long-living Ames dwarf mice and maintained following kainic acid induced neurodegeneration.

Authors:  Sunita Sharma; James Haselton; Sharlene Rakoczy; Stephanie Branshaw; Holly M Brown-Borg
Journal:  Mech Ageing Dev       Date:  2010-06-16       Impact factor: 5.432

4.  Dimethyl sulfoxide and ebselen prevent convulsions induced by 5-aminolevulinic acid.

Authors:  Carlos André Prauchner; Adriano Neujahr Agostini; Akemi Morimoto; Paula Rossini Augusti; Taís Cristina Unfer; Gilson Zeni; Carlos Fernando Mello; Tatiana Emanuelli
Journal:  Neurochem Res       Date:  2004-10       Impact factor: 3.996

5.  Oxidative mechanisms involved in kainate-induced cytotoxicity in cortical neurons.

Authors:  Y Cheng; A Y Sun
Journal:  Neurochem Res       Date:  1994-12       Impact factor: 3.996

6.  Protective effect of resveratrol against kainate-induced temporal lobe epilepsy in rats.

Authors:  Zheng Wu; Qi Xu; Lei Zhang; Dehu Kong; Rong Ma; Liecheng Wang
Journal:  Neurochem Res       Date:  2009-02-14       Impact factor: 3.996

Review 7.  Free radicals as mediators of neuronal injury.

Authors:  F Facchinetti; V L Dawson; T M Dawson
Journal:  Cell Mol Neurobiol       Date:  1998-12       Impact factor: 5.046

8.  Sesamin ameliorates oxidative stress and mortality in kainic acid-induced status epilepticus by inhibition of MAPK and COX-2 activation.

Authors:  Peiyuan F Hsieh; Chien-Wei Hou; Pei-Wun Yao; Szu-Pei Wu; Yu-Fen Peng; Mei-Lin Shen; Ching-Huei Lin; Ya-Yun Chao; Ming-Hong Chang; Kee-Ching Jeng
Journal:  J Neuroinflammation       Date:  2011-05-24       Impact factor: 8.322

9.  Activation of Retinoid X Receptor increases dopamine cell survival in models for Parkinson's disease.

Authors:  Stina Friling; Maria Bergsland; Susanna Kjellander
Journal:  BMC Neurosci       Date:  2009-12-11       Impact factor: 3.288

10.  Red ginseng extract attenuates kainate-induced excitotoxicity by antioxidative effects.

Authors:  Jin-Yi Han; Sun-Young Ahn; Eun-Hye Oh; Sang-Yoon Nam; Jin Tae Hong; Ki-Wan Oh; Mi Kyeong Lee
Journal:  Evid Based Complement Alternat Med       Date:  2012-10-23       Impact factor: 2.629

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