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. Author manuscript; available in PMC: 2009 Dec 23.
Published in final edited form as: J Membr Biol. 2008 Nov 18;226(1-3):43–55. doi: 10.1007/s00232-008-9138-0

Figure 1. Spontaneous and voltage activated Ca2 release events in skinned and intact skeletal muscle fibers, respectively.

Figure 1

A, B, strips of fluo-3 fluorescence line-scan images taken from a chemically skinned skeletal muscle fiber isolated from a mouse and from a frog, respectively. The frog image was from measurements performed in the Department of Physiology at University of Debrecen under the conditions described in Szentesi et al. (2004). C, D, strips of line-scan images from a voltage-clamped intact mouse skeletal muscle fiber depolarized by a 500 ms long pulse to −45 and −40 mV, respectively. E, F strips of line-scan images from a voltage-clamped intact frog skeletal muscle fiber depolarized by a 500 ms long pulse to −55 and −50 mV, respectively.