Neuroprotection Abilities of Cytosolic Phospholipase A2 Inhibitors in Kainic acid-induced Neurodegeneration

Author(s): Akhlaq A. Farooqui, Wei-Yi Ong, Lloyd A. Horrocks

Journal Name: Current Drug Targets - Cardiovascular & Hematological Disorders
Continued as Cardiovascular & Hematological Disorders-Drug Targets

Volume 4 , Issue 1 , 2004


Phospholipases A 2 (PLA 2 )belong to a super-family of enzymes that hydrolyze membrane phospholipids at the sn -2 position to liberate free fatty acids and lysophospholipids.Different forms of PLA 2 are involved in inflammation,neurodegeneration,and intracellular and intercellular signaling related to neurotransmitter release,axonal growth and gene expression.The action of cytosolic PLA 2 (cPLA 2 )on phospholipid containing arachidonic acid at the sn -2 position releases arachidonic acid and lysophospholipids,precursors for various proinflammatory lipid mediators including prostaglandins, leukotrienes,thromboxanes,and platelet activating factor.During hypoxic / ischemic insults,alterations in calcium homeostasis and induction of cytokines results in stimulation of cPLA 2 and increased production of prostaglandins,leukotrienes,thromboxanes,and platelet activating factor.These metabolites cause atherosclerotic plaque development in cerebrovascular and coronary artery diseases in arterial walls and neuronal cell injury in brain tissue.Our studies on kainic acid-induced neurodegeneration in rat brain indicate that the stimulation of cPLA 2 increased generation of proinflammatory lipid mediators,and accumulation of 4- hydroxynonenal,a toxic aldehyde with neurodegenerative properties.Treatment of rat brain hippocampal slices with antimalarial drugs (non-specific cPLA 2 inhibitors),arachidonyl trifluoromethyl ketone (a specific cPLA 2 inhibitor),or surfactin (a non-specific cPLA 2 inhibitor)not only inhibits cPLA 2 activity but also blocks neurodegeneration suggesting that cPLA 2 inhibitors can be used as neuroprotective and anti- inflammatory agents in neurodegenerative diseases.

Keywords: Neuroprotection, neurodegenerative, proinflammatory lipid, cerebrovascular

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Article Details

Year: 2004
Page: [85 - 96]
Pages: 12
DOI: 10.2174/1568006043481239

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