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. Author manuscript; available in PMC: 2014 May 1.
Published in final edited form as: J Mol Cell Cardiol. 2012 Dec 6;58:172–181. doi: 10.1016/j.yjmcc.2012.11.011

Figure 2. Summary of X-ROS signaling in heart.

Figure 2

A, Average DCF fluorescence signal (black) from ventricular myocytes stretched 8% of cell length (n = 36 rat cells). The pre and post stretch intervals are well fit by a linear function, while the stretched interval is better fit by a polynomial function. Taking the derivative of these DCF fits gives the rate of ROS production (green). There is a rapid and transient increase in the rate of ROS production upon stretch. B, Histogram of Ca2+ sparks (n = 3,233 sparks) from 52 myocytes stretched as above. There is a rapid increase in the frequency of Ca2+ sparks (500ms bins) upon stretch. C, Histogram of Ca2+ sparks (n = 1,715 sparks) from 29 myocytes pre-treated with 10mM of the general anti-oxidant N-acetylcysteine and stretched as above. NAC blocks any statistically significant change in Ca2+ spark frequency; the question mark denotes a possible initial stretch-dependent increase in spark rate that is not blocked by NAC (Modified from [1]).