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Am J Physiol Heart Circ Physiol 290: H2136-H2145, 2006. First published December 22, 2005; doi:10.1152/ajpheart.01072.2005
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C-phycocyanin protects against ischemia-reperfusion injury of heart through involvement of p38 MAPK and ERK signaling

Mahmood Khan,1 Saradhadevi Varadharaj,1 Latha P. Ganesan,1 Jagdish C. Shobha,2 Madireddi U. Naidu,2 Narasimham L. Parinandi,1 Susheela Tridandapani,1 Vijay Kumar Kutala,1,2 and Periannan Kuppusamy1

1Davis Heart and Lung Research Institute, Division of Cardiovascular Medicine, Department of Internal Medicine, The Ohio State University, Columbus, Ohio; and 2Department of Clinical Pharmacology and Therapeutics, Nizam's Institute of Medical Sciences, Hyderabad, India

Submitted 11 October 2005 ; accepted in final form 6 December 2005

We previously showed that C-phycocyanin (PC), an antioxidant biliprotein pigment of Spirulina platensis (a blue-green alga), effectively inhibited doxorubicin-induced oxidative stress and apoptosis in cardiomyocytes. Here we investigated the cardioprotective effect of PC against ischemia-reperfusion (I/R)-induced myocardial injury in an isolated perfused Langendorff heart model. Rat hearts were subjected to 30 min of global ischemia at 37°C followed by 45 min of reperfusion. Hearts were perfused with PC (10 µM) or Spirulina preparation (SP, 50 mg/l) for 15 min before the onset of ischemia and throughout reperfusion. After 45 min of reperfusion, untreated (control) hearts showed a significant decrease in recovery of coronary flow (44%), left ventricular developed pressure (21%), and rate-pressure product (24%), an increase in release of lactate dehydrogenase and creatine kinase in coronary effluent, significant myocardial infarction (44% of risk area), and TdT-mediated dUTP nick end label-positive apoptotic cells compared with the preischemic state. PC or SP significantly enhanced recovery of heart function and decreased infarct size, attenuated lactate dehydrogenase and creatine kinase release, and suppressed I/R-induced free radical generation. PC reversed I/R-induced activation of p38 MAPK, Bax, and caspase-3, suppression of Bcl-2, and increase in TdT-mediated dUTP nick end label-positive apoptotic cells. However, I/R also induced activation of ERK1/2, which was enhanced by PC treatment. Overall, these results for the first time showed that PC attenuated I/R-induced cardiac dysfunction through its antioxidant and antiapoptotic actions and modulation of p38 MAPK and ERK1/2.

oxidative stress; apoptosis; Spirulina; antioxidant; reactive oxygen species; free radicals



Address for reprint requests and other correspondence: P. Kuppusamy, Davis Heart and Lung Research Institute, The Ohio State Univ., 420 West 12th Ave., Rm. 114, Columbus, OH 43210 (e-mail: kuppusamy.1{at}osu.edu)




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