THE EFFECT OF Na+ AND Cl- REMOVAL AND OF LOOP DIURETICS ON ACETYLCHOLINE‐EVOKED MEMBRANE POTENTIAL CHANGES IN MOUSE LACRIMAL ACINAR CELLS
- 16 July 1985
- journal article
- research article
- Published by Wiley in Quarterly Journal of Experimental Physiology
- Vol. 70 (3) , 437-445
- https://doi.org/10.1113/expphysiol.1985.sp002927
Abstract
Intracellular micro‐electrode recordings were made from acinar units in mouse lacrimal gland segments superfused with physiological saline solutions. Two micro‐electrodes were used: one for recording the membrane potential and the other for current injection. A third extracellular micropipette was used for local ionophoretic acetylcholine (ACh) application. The ACh‐evoked membrane potential change was recorded at the spontaneous resting potential and after the resting potential had been increased or decreased by direct current injection. The membrane potential at which ACh did not evoke any change in potential (null potential, reversal potential) (EACh) was determined. EACh was about ‐53 mV under normal ionic conditions. When all Cl− in the superfusion fluid was replaced by NO3− or all Na+ replaced by N‐methyl‐D‐glucamine+ (NMDG+) or Tris+, EACh was shifted to more negative values. During exposure to Cl−‐free NO3− solution or Na+‐free NMDG+ solution EACh was about ‐72 mV. These effects on EACh were fully reversible. Inclusion of the loop diuretics piretanide (2 x 10−4 M) or furosemide (l0−3 M) also shifted EACh towards more negative values. In these cases EACh was the same as during exposure to Na+‐free Tris+ solution with a value of about ‐62 mV. Replacement of extracellular Cl− by Br− had no effect on EACh whereas replacement of Na+ by Li+ shifted EACh towards less negative values. The results can most easily be understood in terms of a cellular transport model in which Ca2+‐activated Cl− channels are present in the luminal membrane whereas the basolateral membrane contains three transport proteins: the Na+‐K+‐pump, the Na+‐K+‐2Cl− co‐transporter and the Ca2+‐activated K+ channel. These three transport proteins function together as a Cl− pump. ACh acts to open both Cl− and K+ channels via an increase in the free [Ca2+]i. When the Na+‐K+‐2Cl− co‐transporter is blocked by Na+ removal or by the loop diuretics, [Cl−]i drops and ECl (the Cl− equilibrium potential) becomes more negative. The permeability of the Cl− pathway may also decrease.This publication has 18 references indexed in Scilit:
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