myelin-basic-protein and benzyloxycarbonylvalyl-alanyl-aspartyl-fluoromethyl-ketone

Oligodendrocyte (OLG) death plays a major role in white matter dysfunction and demyelination following injury to the CNS. Axonal contact, communication, and neuronal activity appear to promote OLG survival and function in cell culture and during development. The application of electrical stimulation to mixed neural cultures has been shown to promote OLG differentiation and the formation of myelin in vitro. Here we show that OLG viability can be significantly enhanced in mixed cortical cultures by applying biphasic pulses of electrical stimulation (ESTIM). Enhanced survival via ESTIM requires the presence of neurons and is suppressed by inhibition of voltage-gated sodium channels. Additionally, contact between the axon and OLG is necessary for ESTIM to promote OLG survival. This report suggests that patterned neuronal activity could repress delayed progression of white matter injury and promote CNS repair in neurological conditions that involve white matter damage.

Topics: Amino Acid Chloromethyl Ketones; Analysis of Variance; Anesthetics, Local; Animals; Antigens; Biophysics; Bromodeoxyuridine; Caspase 3; Cell Count; Cell Differentiation; Cell Proliferation; Cell Survival; Cells, Cultured; Cerebral Cortex; Cysteine Proteinase Inhibitors; Electric Stimulation; Female; Galactosylceramidase; Glial Fibrillary Acidic Protein; Myelin Basic Protein; Neurons; Oligodendroglia; Phosphopyruvate Hydratase; Pregnancy; Proteoglycans; Rats; Rats, Sprague-Dawley; Stem Cells; Tetrodotoxin