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Received for publication June 2, 2005.
Revised July 25, 2005.
Accepted for publication August 15, 2005.
The mechanisms underlying the acute neurophysiological and behavioral effects of volatile organic compounds (VOCs) remain to be elucidated. However, the function of neuronal ion channels is perturbed by VOCs. The present study examined effects of toluene (TOL), trichloroethylene (TCE) and perchloroethylene (PERC) on whole cell calcium current (ICa) in nerve growth factor-differentiated pheochromocytoma (PC12) cells. All three VOCs affected ICa in a reversible, concentration-dependent manner. At +10 mV test potentials, VOCs inhibited ICa, whereas at test potentials of -20 and -10 mV, they potentiated it. The order of potency for inhibition (IC50) was PERC (270 µM) > TOL (720 µM) > TCE (1525 µM). VOCs also changed ICa inactivation kinetics from a single to double exponential function. Voltage-ramp experiments suggested that VOCs shifted ICa activation in a hyperpolarizing direction; this was confirmed by calculating the half maximal voltage of activation (V1/2, act) in the absence and presence of VOCs using the Boltzman equation. V1/2,act was shifted from ~ -2 mV in control to -11, -12 and -16 mV by TOL, TCE and PERC, respectively. Similarly, VOCs shifted the half-maximal voltage of steady-state inactivation (V1/2, inact) from ~ -16 mV in control to -32, -35 and -20 mV in the presence of TOL, TCE and PERC, respectively. Inhibition of ICa by TOL was confirmed in primary cultures of cortical neurons, where 827 µM TOL inhibited current by 61%. These data demonstrate that VOCs perturb voltage-sensitive Ca2+ channel function in neurons, an effect that could contribute to the acute neurotoxicity of these compounds.
Key words:
calcium channel, neurotoxicology, perchloroethylene, solvent, toluene, trichloroethylene
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