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1 Physiological Laboratory, Downing Street, Cambridge CB2 3EG, UK
The influence of extracellular hypotonicity on the relationship between cell volume (Vc) and resting membrane potential (Em) was investigated in Rana temporaria skeletal muscle. Vc was measured by confocal microscope imaging of fibres through their transverse (xz) planes, and Em was determined using standard microelectrode techniques. Hypotonic solutions first elicited a rapid increase in fibre volume,
VR+ that fulfilled expectations of simple osmotic behaviour described in earlier reports. However, this was consistently followed by a slow increase in Vc (
VS+) to 1015% above osmotic predictions. Longer (>1 h) exposures to hypotonic solutions permitted a subsequent slow decrease in Vc (
VS), the eventual magnitude of which exceeded that of the preceding
VS+. Restoration of isotonic conditions elicited a prompt recovery in Vc that matched simple osmotic predictions and thus left a net change in Vc. Such alterations in Vc attributable to
VS+ then gradually reversed, while those due to
VS persisted. Both
VS+ and
VS persisted under conditions of Cl deprivation. The depolarization of Em that accompanied
VR+ was consistent with dilution of intracellular [K+]. Em did not significantly alter during the subsequent
VS transients. These empirical features of
VS+ and
VS were analysed using the quantitative charge-difference model of Fraser and Huang, published in 2004. This attributed the
VS+ to an electroneutral increase in the effective osmotic activity of normally membrane-impermeant intracellular anions. In contrast, the
VS could only be explained by an efflux of such anions and was accordingly comparable to organic anion-dependent regulatory volume decreases reported in other cell types.
(Received 9 December 2004;
accepted after revision 10 January 2005;
first published online 13 January 2005)
Corresponding author J. A Fraser: Physiological Laboratory, University of Cambridge, Downing Street, Cambridge CB2 3EG, UK. Email: jaf21{at}cam.ac.uk
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