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1. Mitochondrial uncouplers are potent stimulants of the carotid body. We have therefore investigated their effects upon isolated type I cells. Both 2,4-dinitrophenol (DNP) and carbonyl cyanide p-trifluoromethoxyphenyl hydrazone (FCCP) caused an increase in [Ca2+]i which was largely inhibited by removal of extracellular Ca2+ or Na+, or by the addition of 2 mM Ni2+. Methoxyverapamil (D600) also partially inhibited the [Ca2+]i response. 2. In perforated-patch recordings, the rise in [Ca2+]i coincided with membrane depolarization and was greatly reduced by voltage clamping the cell to -70 mV. Uncouplers also inhibited a background K+ current and induced a small inward current. 3. Uncouplers reduced pHi by 0.1 unit. Alkaline media diminished this acidification but had no effect on the [Ca2+]i response. 4. FCCP and DNP also depolarized type I cell mitochondria. The onset of mitochondrial depolarization preceded changes in cell membrane conductance by 3-4 s. 5. We conclude that uncouplers excite the carotid body by inhibiting a background K+ conductance and inducing a small inward current, both of which lead to membrane depolarization and voltage-gated Ca2+ entry. These effects are unlikely to be caused by cell acidification. The inhibition of background K+ current may be related to the uncoupling of oxidative phosphorylation.

Original publication

DOI

10.1111/j.1469-7793.1998.819ba.x

Type

Journal article

Journal

J Physiol

Publication Date

15/12/1998

Volume

513 ( Pt 3)

Pages

819 - 833

Keywords

2,4-Dinitrophenol, Animals, Animals, Newborn, Carbonyl Cyanide p-Trifluoromethoxyphenylhydrazone, Carotid Body, Cell Membrane, Electric Stimulation, Electrophysiology, Gallopamil, Hydrogen-Ion Concentration, Ion Channel Gating, Membrane Potentials, Mitochondria, Oxidative Phosphorylation, Patch-Clamp Techniques, Potassium Channels, Rats, Uncoupling Agents