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Epigallocatechin-3-gallate, a green tea catechin, protects the heart against regional ischemia-reperfusion injuries through activation of RISK survival pathways in rats

Epigallocatechin-3-gallate (EGCG), the major catechin derived from green tea, has been shown to modulate numerous molecular targets in the setting of inflammation. This study aimed to determine whether EGCG protects against regional myocardial ischemia/reperfusion (I/R) injuries and its underlying m...

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Published in:Archives of pharmacal research 2014, Vol.37 (8), p.1079-1085
Main Authors: Kim, Seok Jai, Li, Mei, Jeong, Cheol Won, Bae, Hong Beom, Kwak, Sang Hyun, Lee, Seong Heon, Lee, Hyun Jung, Heo, Bong Ha, Yook, Keun Bae, Yoo, Kyung Yeon
Format: Article
Language:Korean
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Summary:Epigallocatechin-3-gallate (EGCG), the major catechin derived from green tea, has been shown to modulate numerous molecular targets in the setting of inflammation. This study aimed to determine whether EGCG protects against regional myocardial ischemia/reperfusion (I/R) injuries and its underlying mechanisms involving the role of reperfusion injury salvage kinase (RISK) pathways (PI3K-Akt and ERK 1/2) and $GSK-3{\beta}$ or apoptotic kinases (p38 and JNK). The rats were subjected to I/R injuries consisting of 30 min ischemia followed by 2 h reperfusion. EGCG (10 mg/kg, intravenously) was administered alone or along with wortmannin (PI3K inhibitor, 0.6 mg/kg, intravenously) 5 min before the onset of reperfusion. Wortmannin was administered 10 min before the reperfusion. Infarct size was measured at the end of the reperfusion. The phosphorylation of Akt, $GSK-3{\beta}$, and MAPK kinases (ERK1/2, P38 and JNK) was determined by Western blotting after 10 min of reperfusion. EGCG reduced the infarct size compared with the control ($25.4{\pm}9.2$ versus $43.2{\pm}8.2$ %, p
ISSN:0253-6269
1976-3786