Key result
A time-dependent outward rectifying anion conductance (Iovt) in rat inner medullary collecting duct cells exhibits similar conductivity to Cl- and HCO3- and is blocked by DIDS, DPC, and furosemide.
This study identifies a novel ClC-K channel-mediated Cl- and HCO3- conductance in rat inner medullary collecting duct cells, representing the first report of a channel-mediated HCO3- current in kidney tubular cells.
Suggests novel HCO3- pathway in rat collecting duct; leaves open its role in human renal physiology.
The anion conductance in primary cultures of rat inner medullary collecting duct cells was studied using perforated-patch whole-cell clamp technique. Depolarizations above 0 mv induced an outward anionic current with a time-dependent activation (Iovt) exhibiting a similar conductivity to Cl- and HCO3-. Iovt showed half-maximal activation around 32 mV with a slope factor of 23 mV, and showed a voltage-dependent activation time course that was well fitted by a sum of two exponential functions. Iovt was potentiated when external pH or external Ca2+ was increased and was blocked by external DIDS, DPC and furosemide. These characteristics of Iovt resemble that of the ClC-K1 channels mediated currents; however, anion substitution studies showed that Iovt exhibits a Br->Cl->I->NO3- conductivity sequence, different from that observed in the ClC-K1 channels-mediated conductance. We suggest that, in inner medullary collecting duct cells, ClC-K channels of an unidentified type give rise to this Cl- and HCO3- conductance. This is the first study of a channel-mediated HCO3- current in kidney tubular cells.
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Bolívar et al. (2014) studied Normal physiology (rat inner medullary collecting duct cells). Electrophysiological characterization (patch clamp) and ion substitution vs. Control bath solutions was evaluated on Characterization of time-dependent outward rectifying anion conductance (Iovt). A time-dependent outward rectifying anion conductance (Iovt) in rat inner medullary collecting duct cells exhibits similar conductivity to Cl- and HCO3- and is blocked by DIDS, DPC, and furosemide.
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