The effect of arachidonic acid on junctional conductance in isolated murine hepatocytes

Arachidonic acid (AA) is known to inhibit intercellular conductance in normal and tumour cells. We showed that junctional conductance (Gj) in isolated murine hepatocytes was relatively tolerant to the uncoupling effect of AA. Extracellular application of 100 microM AA decreased Gj in less than 50% of hepatocytes, and the effect was much slower in other cells (10-15 min vs. 2-5 min, respectively). The uncoupling effect of AA did not depend on the intracellular [Ca2+] within the pCa(i) range 7.7-9.0. Similar results were obtained using the pipette-filling solutions with low (1 mM) and high (10 mM) concentrations of a Ca-chelating agent (EGTA). To verify whether the resistance of the hepatocyte Gj to AA may result from the "wash-out" of the intracellular intermediates during the intracellular dialysis, Gj was measured 10-45 min after the preincubation of hepatocytes with AA. After such a treatment, in 62% of cell pairs the Gj values recorded did not differ from the control. Extracellular or intracellular acidification (pHo 6.0 or pHi 5.0-6.0) did not markedly affect the AA action. However, in some cases AA induced the recovery of Gj blocked after intracellular acidification, the phenomenon suggesting the activation of the H+ transport in the presence of AA. Possible mechanisms of the observed resistance of junctional conductance of mouse hepatocytes in primary culture are discussed.