Electrolyte Transport Through a Cation-Selective ion Channel in Large Intestinal Enterocytes of Xenopus Laevis
Author(s) -
Rolf Krattenmacher,
Rosita Voigt,
Meike V. F. Heinz,
Wolfgang Clauss
Publication year - 1991
Publication title -
journal of experimental biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.367
H-Index - 185
eISSN - 1477-9145
pISSN - 0022-0949
DOI - 10.1242/jeb.155.1.275
Subject(s) - xenopus , divalent , chemistry , extracellular , biophysics , ion channel , ion transporter , toad , sodium , niflumic acid , electrolyte , quinidine , selectivity , electrophysiology , channel blocker , ligand gated ion channel , ion , calcium , biochemistry , membrane , biology , endocrinology , pharmacology , receptor , gene , catalysis , organic chemistry , electrode , neuroscience
Electrogenic ion transport through the colon epithelium of the African clawed toad (Xenopus laevis) was investigated with electrophysiological methods in vitro. Interest was focused on a previously described phenomenon, that removal of Ca2+ from the mucosal Ringer's solution increases electrogenic sodium absorption. Our results clearly show that Ca2+ removal reveals an apical ion channel that is not a specific Na+ channel, but a non-selective cation channel with an ‘apparent’ ion selectivity of the order K+ greater than Na+ = Rb+ greater than Cs+ greater than Li+. This Ca2(+)-sensitive current increased linearly with the mucosal pH, and could be inhibited by other divalent cations (Mg2+, Ba2+) and the organic ion channel blockers quinidine and verapamil. The mucosal Ca2+ concentration that induced a half-maximal inhibition of the Ca2(+)-sensitive current was about 1 mumol l-1 and was independent of the mucosal pH. Owing to the high Ca2+ sensitivity, a regulation of the channel conductivity by extracellular Ca2+ is ruled out. It is concluded that this channel, which is almost identical to similar channels found in amphibian skin and bladder, acts as a pathway for cation absorbing or secreting processes. Possibly the binding of extracellular Ca2+ is related to selectivity changes of the Ca2(+)-sensitive ion channel.
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