Preconditioning protects the heart in a prolonged uremic condition

被引:39
作者
Kocsis, Gabriella F. [1 ]
Sarkoezy, Marta [1 ]
Bencsik, Peter [2 ]
Pipicz, Marton [1 ]
Varga, Zoltan V. [1 ]
Paloczi, Janos [1 ]
Csonka, Csaba [1 ,2 ]
Ferdinandy, Peter [2 ,3 ]
Csont, Tamas [1 ,2 ]
机构
[1] Univ Szeged, Dept Biochem, Cardiovasc Res Grp, Fac Med, H-6720 Szeged, Hungary
[2] Pharmahungary Grp, Szeged, Hungary
[3] Semmelweis Univ, Dept Pharmacol & Pharmacotherapy, H-1085 Budapest, Hungary
来源
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY | 2012年 / 303卷 / 10期
基金
匈牙利科学研究基金会;
关键词
chronic renal failure; myocardium; ischemic preconditioning; infarct size; myocardial function; INFARCT SIZE-REDUCTION; CHRONIC KIDNEY-DISEASE; CHRONIC-RENAL-FAILURE; LONG-TERM SURVIVAL; ANGIOTENSIN-II; RECEPTOR BLOCKERS; NITRIC-OXIDE; CARDIOVASCULAR-DISEASE; MYOCARDIAL-INFARCTION; AT(1) RECEPTOR;
D O I
10.1152/ajpheart.00379.2012
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Kocsis GF, Sarkozy M, Bencsik P, Pipicz M, Varga ZV, Paloczi J, Csonka C, Ferdinandy P, Csont T. Preconditioning protects the heart in a prolonged uremic condition. Am J Physiol Heart Circ Physiol 303: H1229-H1236, 2012. First published September 14, 2012; doi:10.1152/ajpheart.00379.2012.-Metabolic diseases such as hyperlipidemia and diabetes attenuate the cardioprotective effect of ischemic preconditioning. In the present study, we examined whether another metabolic disease, prolonged uremia, affects ischemia/reperfusion injury and cardioprotection by ischemic preconditioning. Uremia was induced by partial nephrectomy in male Wistar rats. The development of uremia was verified 29 wk after surgery. Transthoracic echocardiography was performed to monitor cardiac function. At week 30, hearts of nephrectomized and sham-operated rats were isolated and subjected to a 30-min coronary occlusion followed by 120 min reperfusion with or without preceding preconditioning induced by three intermittent cycles of brief ischemia and reperfusion. In nephrectomized rats, plasma uric acid, carbamide, and creatinine as well as urine protein levels were increased as compared with sham-operated controls. Systolic anterior and septal wall thicknesses were increased in nephrectomized rats, suggesting the development of a minimal cardiac hypertrophy. Ejection fraction was decreased and isovolumic relaxation time was shortened in nephrectomized rats demonstrating a mild systolic and diastolic dysfunction. Infarct size was not affected significantly by nephrectomy itself. Ischemic preconditioning significantly decreased infarct size from 24.8 +/- 5.2% to 6.6 +/- 1.3% in the sham-operated group and also in the uremic group from 35.4 +/- 9.5% to 11.9 +/- 3.1% of the area at risk. Plasma ANG II and nitrotyrosine were significantly increased in the uremic rats. We conclude that although prolonged experimental uremia leads to severe metabolic changes and the development of a mild myocardial dysfunction, the cardioprotective effect of ischemic preconditioning is still preserved.
引用
收藏
页码:H1229 / H1236
页数:8
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