Isoflurane inhibits cardiac myocyte apoptosis during oxidative and inflammatory stress by activating Akt and enhancing Bcl-2 expression

被引:89
作者
Jamnicki-Abegg, M
Weihrauch, D
Pagel, PS
Kersten, JR
Bosnjak, ZJ
Warltier, DC
Bienengraeber, MW
机构
[1] Med Coll Wisconsin, Dept Anesthesiol, Clement J Zablocki Vet Affairs Med Ctr, Milwaukee, WI 53226 USA
[2] Med Coll Wisconsin, Dept Pharmacol & Toxicol, Clement J Zablocki Vet Affairs Med Ctr, Milwaukee, WI 53226 USA
[3] Med Coll Wisconsin, Dept Med, Clement J Zablocki Vet Affairs Med Ctr, Div Cardiovasc Dis, Milwaukee, WI 53226 USA
[4] Med Coll Wisconsin, Dept Physiol, Clement J Zablocki Vet Affairs Med Ctr, Milwaukee, WI 53226 USA
[5] Marquette Univ, Dept Biomed Engn, Milwaukee, WI 53233 USA
关键词
D O I
10.1097/00000542-200511000-00015
中图分类号
R614 [麻醉学];
学科分类号
100217 [麻醉学];
摘要
Background: Volatile anesthetics attenuate apoptosis. The underlying mechanisms remain undefined. The authors tested whether isoflurane reduces apoptosis in cardiomyocytes subjected to oxidative or inflammatory stress by enhancing Akt and B-cell lymphoma-2 (Bcl-2). Methods: Adult and neonatal rat ventricular myocytes and atrial HL-1 myocytes were exposed to hypoxia, hydrogen peroxide, or neutrophils with or without isoflurane pretreatment. The authors assessed cell damage and investigated apoptosis using mitochondrial cytochrome c release, caspase activity, and TUNEL assay. They determined expression of phospho-Akt and Bcl-2 and tested their involvement by blocking phospho-Akt with wortmannin and Bcl-2 with HA14-1. Results: Isoflurane significantly reduced the cell damage andapoptosis induced by hypoxia, H2O2, and neutrophils. Isoflurane reduced hypoxia-induced mitochondrial cytochrome c release in HL-1 cells by 45 :L 12% and caspase activity by 28 +/- 4%; in neonatal cells, it reduced caspase activity by 43 +/- 5% and TUNEL-posifive cells by 50 +/- 2%. Isoflurane attenuated H2O2-induced caspase activity in HL-1 cells by 48 +/- 16% and TUNEL-positive cells by 78 +/- 3%; in neonatal cells, it reduced caspase activity by 30 +/- 3% and TUNEL-positive cells by 32 +/- 7%. In adult cardiomyocytes exposed to neutrophils, isoflurane decreased both mitochondrial cytochrome c and caspase activity by 47 +/- 3% and TUNEL-positive cells by 25 +/- 4%. Isoflurane enhanced phospho-Akt and Bcl-2 expression. Wortmannin and HA14-1 prevented the action of isofluranc (53 +/- 8% and 54 +/- 7% apoptotic cells vs. 18 +/- 1% without blockers). Conclusions. Isoflurane protects cardiomyocytes against apoptosis induced by hypoxia, H2O2, or activated neutrophils through Akt activation and increased Bcl-2 expression. This suggests that a reduction in apoptosis contributes to the cardioprotective effects of isoflurane.
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收藏
页码:1006 / 1014
页数:9
相关论文
共 54 条
[1]
AlMohanna F, 1997, AM J PATHOL, V151, P111
[2]
Hypoxia induces the activation of the phosphatidylinositol 3-kinase/Akt cell survival pathway in PC12 cells -: Protective role in apoptosis [J].
Alvarez-Tejado, M ;
Naranjo-Suárez, S ;
Jiménez, C ;
Carrera, AC ;
Landázuri, MO ;
del Peso, L .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (25) :22368-22374
[3]
THE ROLE OF OXYGEN-FREE RADICALS IN PRECONDITIONING [J].
AMBROSIO, G ;
TRITTO, I ;
CHIARIELLO, M .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 1995, 27 (04) :1035-1039
[4]
Mitochondria and the Bcl-2 family proteins in apoptosis signaling pathways [J].
Antonsson, B .
MOLECULAR AND CELLULAR BIOCHEMISTRY, 2004, 256 (1-2) :141-155
[5]
Attenuation of ischemia and/or reperfusion injury during myocardial infarction using mild hypothermia in rats: An immunohistochemical study of Bcl-2, Bax, Bak and TUNEL [J].
Babu, PP ;
Suzuki, G ;
Ono, Y ;
Yoshida, Y .
PATHOLOGY INTERNATIONAL, 2004, 54 (12) :896-903
[6]
Morphine mimics the antiapoptotic effect of preconditioning via an Ins(1,4,5)P3 signaling pathway in rat ventricular myocytes [J].
Barrère-Lemaire, S ;
Combes, N ;
Sportouch-Dukhan, C ;
Richard, S ;
Nargeot, J ;
Piot, C .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2005, 288 (01) :H83-H88
[7]
Isoflurane protects against myocardial infarction during early reperfusion by activation of phosphatidylinositol-3-kinase signal transduction: Evidence for anesthetic-induced postconditioning in rabbits [J].
Chiari, PC ;
Bienengraeber, MW ;
Pagel, PS ;
Krolikowski, JG ;
Kersten, JR ;
Warltier, DC .
ANESTHESIOLOGY, 2005, 102 (01) :102-109
[8]
The mitochondrial death pathway and cardiac myocyte apoptosis [J].
Crow, MT ;
Mani, K ;
Nam, YJ ;
Kitsis, RN .
CIRCULATION RESEARCH, 2004, 95 (10) :957-970
[9]
Cuisnier O, 2003, INT J ONCOL, V23, P1033
[10]
Intermittent hypoxia attenuates ischemia/reperfusion induced apoptosis in cardiac myocytes via regulating Bcl-2/Bax expression [J].
Dong, JW ;
Zhu, HF ;
Zhu, WZ ;
Ding, HL ;
Ma, TM ;
Zhou, ZN .
CELL RESEARCH, 2003, 13 (05) :385-391