Taurine-mediated cardioprotection is greater when administered upon reperfusion than prior to ischemia.

作者: Tadaomi-Alfonso Miyamoto , Takayuki Ueno , Yoshihumi Iguro , Goichi Yotsumoto , Yoshihiro Fukumoto

DOI: 10.1007/978-0-387-75681-3_3

关键词:

摘要: Taurine (TA) administered exogenously before the induction of myocardial ischemia decreases lactic acid production and increases pyruvic during ischemia. It also preserves activity GOT, GPT, LDH CPK enhances recovery CKMB synthesis as early 5 minutes after onset reperfusion. The aim study was to determine optimal conditions for administering TA in order reduce ischemia-reperfusion injury. Left ventricular (LV) function, creatine kinase (CK) lipid peroxide products (LPOP=oxidant stress), well area at risk (AAR), infarct size (IS) reperfusion were studied 3 groups isolated rat hearts perfused with Krebs Henseleit Buffer (KHB)-stabilized that subjected 20 minutes(’) global 37o followed by 60′ KHB: Hearts containing KHB 10′ just prior or first 10’ Conclusion:Taurine equally effective preventing infarction; however, when reperfusion, taurine reduced peroxidation injury more, thereby providing improved function.

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