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. 2010 May 5;299(2):C264–C278. doi: 10.1152/ajpcell.00318.2009

Fig. 7.

Fig. 7.

Caffeine applied to the bilayer cis side increases the NPo of reconstituted SR ryanodine-sensitive channels. A: unitary current recordings of SR Ca2+- and ryanodine-sensitive channels in absence (top) and presence of 0.1 (2nd trace) or 1 mM (3rd trace) caffeine added to the cis solution. Further application of 80 μM ruthenium red (4th trace) drastically suppresses channel activity (see main text); V = +35 mV. NPo was obtained as described for Fig. 2. B: averaged NPo in response to caffeine added to the cis solution. *Different from control, P < 0.05; ***different from control, P < 0.001 (n = 8).