Analysis of the cytotoxic properties of linoleic acid metabolites produced by renal and hepatic P450s

被引:76
作者
Moran, JH
Mitchell, LA
Bradbury, JA
Qu, W
Zeldin, DC
Schnellmann, RG
Grant, DF
机构
[1] Univ Arkansas Med Sci, Dept Pharmacol & Toxicol, Little Rock, AR 72205 USA
[2] NIEHS, Div Intramural Res, NIH, Res Triangle Pk, NC 27709 USA
关键词
D O I
10.1006/taap.2000.9053
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Cytochrome P450 epoxidation of linoleic acid produces biologically active metabolites which have been associated with many pathological conditions that often lead to acute renal failure. In the present study, we evaluated the ability of specific cytochrome P450s to produce linoleic acid monoepoxides. We then tested the cytotoxic properties of linoleic acid, linoleic acid monoepoxides, and corresponding diols in a rabbit renal proximal tubule model. CYP1A2, CYP2E1, CYP2J2, CYP2J3, CYP2J5, and CYP2J9 metabolized linoleic acid at rates comparable to arachidonic acid and produced linoleic acid monoepoxides as major products. Cytotoxicity studies showed that linoleic acid, linoleic acid monoepoxides, and corresponding diols are toxic at pathologically relevant concentrations (100-500 muM). Concentration-dependent studies showed that linoleic acid and linoleic acid monoepoxides are the most toxic and induce mitochondrial dysfunction prior to cell death. Cytoprotectants known to block cell death associated with mitochondrial dysfunction and oxidative stress did not prevent cell death induced by linoleic acid and linoleic acid monoepoxides. This study shows that P450s in the CYP1 and CYP2 gene families metabolize linoleic acid to linoleic acid monoepoxides and that the monoepoxides, as well as linoleic acid, disrupt mitochondrial function without causing oxidative stress. (C) 2000 Academic Press.
引用
收藏
页码:268 / 279
页数:12
相关论文
共 58 条
[11]  
HANAKI Y, 1991, JPN J MED, V30, P224
[12]   EPOXYEICOSATRIENOIC ACIDS ACTIVATE NA+/H+ EXCHANGE AND ARE MITOGENIC IN CULTURED RAT GLOMERULAR MESANGIAL CELLS [J].
HARRIS, RC ;
HOMMA, T ;
JACOBSON, HR ;
CAPDEVILA, J .
JOURNAL OF CELLULAR PHYSIOLOGY, 1990, 144 (03) :429-437
[13]  
HAYAKAWA M, 1990, BIOCHEM INT, V21, P573
[14]   INHIBITION OF RENIN RELEASE BY 14,15-EPOXYEICOSATRIENOIC ACID IN RENAL CORTICAL SLICES [J].
HENRICH, WL ;
FALCK, JR ;
CAMPBELL, WB .
AMERICAN JOURNAL OF PHYSIOLOGY, 1990, 258 (02) :E269-E274
[15]   CYTOCHROME P450 METABOLITES OF ARACHIDONIC-ACID ARE POTENT INHIBITORS OF VASOPRESSIN ACTION ON RABBIT CORTICAL COLLECTING DUCT [J].
HIRT, DL ;
CAPDEVILA, J ;
FALCK, JR ;
BREYER, MD ;
JACOBSON, HR .
JOURNAL OF CLINICAL INVESTIGATION, 1989, 84 (06) :1805-1812
[16]   Structural determination of the substrate specificities and regioselectivities of the rat and human fatty acid ω-hydroxylases [J].
Hoch, U ;
Zhang, ZP ;
Kroetz, DL ;
de Montellano, PRO .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 2000, 373 (01) :63-71
[17]   Origin and function of epoxyeicosatrienoic acids in vascular endothelial cells: More than just endothelium-derived hyperpolarizing factor? [J].
Hoebel, BG ;
Steyrer, E ;
Graier, WF .
CLINICAL AND EXPERIMENTAL PHARMACOLOGY AND PHYSIOLOGY, 1998, 25 (10) :826-830
[18]   COMPLETE CDNA SEQUENCE AND CDNA-DIRECTED EXPRESSION OF CYP4A11, A FATTY-ACID OMEGA-HYDROXYLASE EXPRESSED IN HUMAN KIDNEY [J].
IMAOKA, S ;
OGAWA, H ;
KIMURA, S ;
GONZALEZ, FJ .
DNA AND CELL BIOLOGY, 1993, 12 (10) :893-899
[19]   LEUKOTOXIN, 9,10-EPOXY-12-OCTADECENOATE CAUSES PULMONARY VASODILATION IN RATS [J].
ISHIZAKI, T ;
TAKAHASHI, H ;
OZAWA, T ;
CHANG, SW ;
VOELKEL, NF .
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 1995, 268 (01) :L123-L128
[20]   Proton re-uptake partitioning between uncoupling protein and ATP synthase during benzohydroxamic acid-resistant state 3 respiration in tomato fruit mitochondria [J].
Jarmuszkiewicz, W ;
Almeida, AM ;
Vercesi, AE ;
Sluse, FE ;
Sluse-Goffart, CM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (18) :13315-13320