Key result
Capsaicin proportionally blocks inward and outward type I K+ currents in cultured rabbit Schwann cells.
Effect estimate: KD of 8.7 microM
Capsaicin blocks type I delayed rectifier K+ currents in rabbit Schwann cells with a KD of 8.7 microM.
No immediate clinical implications from rabbit Schwann cells; leaves open capsaicin effects on glial K+ currents in vivo.
Capsaicin, a lipophilic alkaloid, blocked type I K+ currents in rabbit cultured Schwann cells when applied by superfusion. The concentration-response relation at equilibrium was well described by a rectangular hyperbola, with a KD of 8.7 microM. The kinetics of block resembled an 'inactivation', the rate of blockade increasing with increasing concentrations of capsaicin (1-100 microM). Unlike internal tetraethylammonium (TEA) ions (5-10 mM), which preferentially reduced outward current in symmetrical high [K+], capsaicin reduced both inward and outward type I current by the same proportion. The block achieved by capsaicin during a voltage-clamp step that activated the current was relieved by subsequent hyperpolarization, and the rate of relief from block at -70 mV and -100 mV could be reasonably accounted for on the assumption that capsaicin had to unbind to allow the channels' to close.
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Baker et al. (1994) studied this question. Capsaicin vs. internal tetraethylammonium (TEA) ions was evaluated on Blockade of type I K+ currents (KD of 8.7 microM). Capsaicin blocked type I K+ currents in rabbit cultured Schwann cells with a KD of 8.7 microM, reducing both inward and outward currents by the same proportion.
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