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. 2002 Dec 6;546(Pt 2):501–509. doi: 10.1113/jphysiol.2002.027573

Figure 3. Stretch-activated membrane currents in guinea-pig ventricular myocytes under action potential clamp.

Figure 3

A, upper panel, free action potentials were recorded then used as the waveform to voltage clamp each myocyte. Lower panel, compensation currents (which have a reverse polarity to ionic currents) recorded under action potential clamp before (○) and after (•) a stretch that increased sarcomere length from 1.77 to 2.00 μm. Following decay of large capacitive currents, compensation currents at short sarcomere length are very small. B, stretch-induced current. C, mean current-voltage relationship for the stretch-activated current from 10 cells, having a current of greater than 5 pA at +30 mV. Stretch increased sarcomere length from 1.82 ± 0.01 to 1.98 ± 0.01 μm. The current-voltage relationship was achieved by plotting current (B) against clamp voltage (A, upper panel).