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Functional distinction between two transport mechanisms in rabbit gall‐bladder epithelium by use of ouabain, ethacrynic acid and metabolic inhibitors.
Author(s) -
Frederiksen O
Publication year - 1978
Publication title -
the journal of physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.802
H-Index - 240
eISSN - 1469-7793
pISSN - 0022-3751
DOI - 10.1113/jphysiol.1978.sp012389
Subject(s) - ouabain , chemistry , bicarbonate , conductance , hyperpolarization (physics) , metabolism , in vitro , strophanthin , endocrinology , medicine , biophysics , biochemistry , sodium , stereochemistry , biology , nuclear magnetic resonance spectroscopy , mathematics , organic chemistry , combinatorics
1. Net fluid transport rate, transepithelial p.d. and resistance, and unidirectional Na+‐fluxes were measured in rabbit gall‐bladder preparations exposed on both sides to bicarbonate‐Ringer solution in vitro. 2. Both ouabain and ethacrynic acid (ETCA) caused dose‐dependent decreases of net fluid transport rate; ouabain inhibited fluid transport predominantly from the serosal side, whereas the inhibitory effect of ETCA was elicited mainly from the mucosal (luminal) side. Applied bilaterally, the ID50 for ouabain was 2.5 X 10(‐6) M, and for ETCA 2.3 X 10(‐4) M. After maximal inhibition at each concentration level of the two inhibitors fluid transport could not be reversed. 3. 2,4‐Dinitrophenol (2,4‐DNP) (2 X 10(‐4) M) or substitution of O2 by N2 caused an 80% reversible decrease of net fluid transport. 4. The spontaneous p.d. across the rabbit gall‐bladder was about 2.7 mV, mucosal side positive. 2,4‐DNP, N2 and serosal application of ouabain depressed the p.d. after an initial hyperpolarization. This decrease was reversible during recovery from 2,4‐DNP and N2, but irreversible after removal of ouabain at concentrations greater than or equal to 10(‐4) M. Mucosal application of ETCA (10(‐3) M) caused no decrease in p.d., which actually increased slightly. 5. Calculated passive serosal‐to‐mucosal Na+‐fluxes changed in the same direction as did changes in conductance. 6. It is concluded that ETCA does not interfere primarily with the Na‐K‐ATPase or cellular oxidative metabolism. The data support the proposal that the pump responsible for isosmotic transepithelial fluid transfer is located in the luminal end of the cells. This pump is ETCA‐sensitive. The ATPase‐dependent Na‐K pump, which can be inhibited by ouabain, is localized in the serosa‐facing cell membrane. The data suggest that the inhibition of net fluid transport by ouabain is indirect and mediated by changes in intracellular ion concentrations. 7. The results support the concept that the transepithelial fluid transport mechanism is electroneutral, and suggest that the mucosa positive transepithelial p.d. is due to differences in electromotive forces arising from ion (mainly K+) diffusion across the mucosal and serosal cell membranes.