Arachidonic acid mediates dual effect of TNF-α on Ca2+ transients and contraction of adult rat cardiomyocytes

被引:58
作者
Amadou, A [1 ]
Nawrocki, A [1 ]
Best-Belpomme, M [1 ]
Pavoine, C [1 ]
Pecker, F [1 ]
机构
[1] Hop Henri Mondor, INSERM, U99, F-94010 Creteil, France
来源
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY | 2002年 / 282卷 / 06期
关键词
heart; cytosolic Ca2+-dependent phospholipase A(2); ceramidase; sphingosine;
D O I
10.1152/ajpcell.00471.2001
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Tumor necrosis factor (TNF)-alpha has a biphasic effect on heart contractility and stimulates phospholipase A(2) (PLA(2)) in cardiomyocytes. Because arachidonic acid (AA) exerts a dual effect on intracellular Ca2+ concentration ([Ca2+](i)) transients, we investigated the possible role of AA as a mediator of TNF-alpha on [Ca2+](i) transients and contraction with electrically stimulated adult rat cardiac myocytes. At a low concentration (10 ng/ml) TNF-alpha produced a 40% increase in the amplitude of both [Ca2+](i) transients and contraction within 40 min. At a high concentration (50 ng/ml) TNF-alpha evoked a biphasic effect comprising an initial positive effect peaking at 5 min, followed by a sustained negative effect leading to 50-40% decreases in [Ca2+](i) transients and contraction after 30 min. Both the positive and negative effects of TNF-alpha were reproduced by AA and blocked by arachidonyltrifluoromethyl ketone (AACOCF3), an inhibitor of cytosolic PLA(2). Lipoxygenase and cyclooxygenase inhibitors reproduced the high-dose effects of TNF-alpha and AA. The negative effects of TNF-alpha and AA were also reproduced by sphingosine and were abrogated by the ceramidase inhibitor n-oleoylethanolamine. These results point out the key role of the cytosolic PLA(2)/AA pathway in mediating the contractile effects of TNF-alpha.
引用
收藏
页码:C1339 / C1347
页数:9
相关论文
共 42 条
[11]   INTERLEUKIN-1 AND TUMOR NECROSIS FACTOR INHIBIT CARDIAC MYOCYTE BETA-ADRENERGIC RESPONSIVENESS [J].
GULICK, T ;
CHUNG, MK ;
PIEPER, SJ ;
LANGE, LG ;
SCHREINER, GF .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (17) :6753-6757
[12]   TNF-INDUCED CARDIOMYOPATHY [J].
HEGEWISCH, S ;
WEH, HJ ;
HOSSFELD, DK .
LANCET, 1990, 335 (8684) :294-295
[13]  
Hoffmann P, 1995, CARDIOVASC RES, V30, P889, DOI 10.1016/S0008-6363(95)00133-6
[14]  
JAYADEV S, 1994, J BIOL CHEM, V269, P5757
[15]   EFFECTS OF LONG-CHAIN POLYUNSATURATED FATTY-ACIDS ON THE CONTRACTION OF NEONATAL RAT CARDIAC MYOCYTES [J].
KANG, JX ;
LEAF, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (21) :9886-9890
[16]   TUMOR-NECROSIS-FACTOR-ALPHA GENE AND PROTEIN EXPRESSION IN ADULT FELINE MYOCARDIUM AFTER ENDOTOXIN ADMINISTRATION [J].
KAPADIA, S ;
LEE, J ;
TORREAMIONE, G ;
BIRDSALL, HH ;
MA, TS ;
MANN, DL .
JOURNAL OF CLINICAL INVESTIGATION, 1995, 96 (02) :1042-1052
[17]   Tumor necrosis factor alpha-induced apoptosis in cardiac myocytes - Involvement of the sphingolipid signaling cascade in cardiac cell death [J].
Krown, KA ;
Page, MT ;
Nguyen, C ;
Zechner, D ;
Gutierrez, V ;
Comstock, KL ;
Glembotski, CC ;
Quintana, PJE ;
Sabbadini, RA .
JOURNAL OF CLINICAL INVESTIGATION, 1996, 98 (12) :2854-2865
[18]   Dilated cardiomyopathy in transgenic mice with cardiac-specific overexpression of tumor necrosis factor-alpha [J].
Kubota, T ;
McTiernan, CF ;
Frye, CS ;
Slawson, SE ;
Lemster, BH ;
Koretsky, AP ;
Demetris, AJ ;
Feldman, AM .
CIRCULATION RESEARCH, 1997, 81 (04) :627-635
[19]   ELEVATED CIRCULATING LEVELS OF TUMOR-NECROSIS-FACTOR IN SEVERE CHRONIC HEART-FAILURE [J].
LEVINE, B ;
KALMAN, J ;
MAYER, L ;
FILLIT, HM ;
PACKER, M .
NEW ENGLAND JOURNAL OF MEDICINE, 1990, 323 (04) :236-241
[20]   Inhibition of the neutral magnesium-dependent sphingomyelinase by glutathione [J].
Liu, B ;
Hannun, YA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (26) :16281-16287