In addition to integral proteins, neural membranes are composed of glycerophospholipids, sphingolipids,
and cholesterol, which provide membranes with structural integrity (suitable stability, fluidity, and permeability).
Kainic acid (KA), an excitotoxin, markedly upregulates glycerophospholipids, sphingolipids, and cholesterol
metabolism resulting not only in loss of essential lipids and inducing changes in neural membrane fluidity
and permeability, but also in elevations in glycerophospholipid, sphingolipid, and cholesterol-derived lipid mediators.
These processes result in depolarization, sustained increase in Ca2+ and stimulation of Ca2+-dependent enzymes
including PLA2, PLC, nitric oxide synthase, calpains, and endonucleases. Sustained stimulation of these
enzymes, generation, and interplay among glycerophospholipid-, sphingolipid-, and cholesterol-derived lipid mediators
along with mitochondrial dysfunction, decrease in ATP levels, changes in redox status of neural cell may
be responsible for neurodegeneration through apoptosis and necrosis in KA-mediated neurotoxicity. Other KAmediated
neurochemical changes include synaptic reorganization associated with recapitulation of hippocampal
development and synaptogenesis following KA-induced seizures.
Keywords: Lipid mediators; kainic acid-mediated neurotoxicity; glycerophospholipids, sphingolipids, cholesterol;
mitochondrial dysfunction
