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The mechanisms of volume regulation by cardiac cells in response to hyposmotic conditions was investigated. The study protocol involved optical, biochemical and nuclear magnetic resonance studies of regulatory volume decrease (RVD) by chick heart cells exposed to hyposmotic solution. The results showed that RVD following exposure to hyposmotic solution was due to a substantial loss of the ions Na+ and K+ and the amino acids taurine, glutamate, glycine and aspartate. RVD was also accompanied by production of glutamate and aspartate. The RVD-associated release and production of amino acids could have significant metabolic effects for cardiac muscle cells.

The integrity of F-actin and its association with the activation of a Cl- current (I(Cl)) in cultured chick cardiac myocytes subjected to hyposmotic challenge were monitored by whole cell patch clamp and fluorescence confocal microscopy. Disruption of F-actin by 25 microM cytochalasin B augmented hyposmotic cell swelling by 51% (from a relative volume of 1.54 +/- 0.10 in control to 2.33 +/- 0.21), whereas stabilization of F-actin by 20 microM phalloidin attenuated swelling by 15% (relative volume of 1.31 +/- 0.05). Trace fluorochrome-labeled (fluorescein isothiocyanate or tetramethylrhodamine isothiocyanate) phalloidin revealed an intact F-actin conformation in control cells under hyposmotic conditions despite the considerable changes in cell volume. Sarcoplasmic F-actin was very disorganized and occurred only randomly beneath the sarcolemma in cells treated with cytochalasin B, whereas no changes in F-actin distribution occurred under either isosmotic or hyposmotic conditions in cells treated with phalloidin. Swelling-activated I(Cl) (68.0 +/- 6.0 pA/pF at +60 mV) was suppressed by both cytochalasin B (22.7 +/- 5.1 pA/pF) and phalloidin (22.5 +/- 3.5 pA/pF). On the basis of these results, we suggest that swelling of cardiac myocytes initiates dynamic changes in the cytoarchitecture of F-actin, which may be involved in the volume transduction processes associated with activation of I(Cl).