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J Am Coll Cardiol, 2007; 50:1272-1278, doi:10.1016/j.jacc.2007.05.039 (Published online 9 September 2007).
© 2007 by the American College of Cardiology Foundation
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Important Role of Endogenous Hydrogen Peroxide in Pacing-Induced Metabolic Coronary Vasodilation in Dogs In Vivo

Toyotaka Yada, MD, PhD*,*, Hiroaki Shimokawa, MD, PhD{dagger}, Osamu Hiramatsu, PhD*, Yoshiro Shinozaki, BS{ddagger}, Hidezo Mori, MD, PhD§, Masami Goto, MD, PhD*, Yasuo Ogasawara, PhD* and Fumihiko Kajiya, MD, PhD*

* Department of Medical Engineering and Systems Cardiology, Kawasaki Medical School, Kurashiki, Japan
{dagger} Department of Cardiovascular Medicine, Tohoku University Graduate School of Medicine, Sendai, Japan
{ddagger} Department of Physiology, Tokai University School of Medicine, Isehara, Japan
§ Department of Cardiac Physiology, National Cardiovascular Center Research Institute, Suita, Japan


Figure 1
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Figure 1 Experimental Protocols

CCD = charge-coupled device; L-NMMA = NG-monomethyl-L-arginine; SPT = sulfophenyltheophylline; TEA = tetraethylammonium.

 

Figure 2
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Figure 2 Coronary Vascular Responses to Cardiac Pacing

The coronary vasodilating responses of both-sized coronary arteries were significantly inhibited in all experimental conditions except L-NMMA alone. **p < 0.01. Abbreviations as in Figure 1.

 

Figure 3
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Figure 3 Detection of H2O2 Production With DCF Fluorescent Method

Hydrogen peroxide (H2O2) production was unaltered after NG-monomethyl-L-arginine (L-NMMA) but was markedly suppressed by catalase. Number of arterioles/animals used was 5/5 for each group. *p < 0.05, **p < 0.01. DCF = 2',7'-dichlorodihydrofluorescein diacetate.

 

Figure 4
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Figure 4 Detection of NO Production With DAR Fluorescent Method

Nitric oxide (NO) production was unaltered after catalase but was markedly suppressed by NG-monomethyl-L-arginine (L-NMMA). Number of arterioles/animals used was 5/5 for each group. *p < 0.05, **p < 0.01. DAR = diaminorhodamine-4M AM.

 




 
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