Hypoxia/reoxygenation alters essential fatty acids metabolism in cultured rat cardiomyocytes: Protection by antioxidants

被引:12
作者
Bordoni, A [1 ]
Angeloni, C [1 ]
Leoncini, E [1 ]
Danesi, F [1 ]
Maranesi, M [1 ]
Biagi, PL [1 ]
Hrelia, S [1 ]
机构
[1] Ctr Ric Nutr, Dipartimento Biochim G Moruzzi, I-40126 Bologna, Italy
关键词
hypoxia/reoxygenation; cultured cardiomyocytes; HUFA biosynthesis; green tea;
D O I
10.1016/j.numecd.2004.04.003
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background and aims: Peroxidation of membrane lipids, altering cell integrity and function, plays an important part in the onset and development of cardiac damage following ischemia and reperfusion. Celts maintain their membrane lipid homeostasis by substituting peroxidized lipids with new polyunsaturated fatty acids. The microsomal enzymatic system converting essential fatty acids to highly unsaturated fatty acids (HUFAs) contributes to this repairing mechanism. The membrane of the endoplasmic reticulum could be one of the potential targets of free radicals generated in ischemia/reperfusion, thus causing a reduced efficacy of the system required for HUFA biosynthesis. To verify this hypothesis, and the consequent modification in fatty acid composition, we exposed cultured rat cardionnyocytes to different periods of hypoxia (H), eventually followed by reoxygenation (R). Furthermore, the effectiveness of antioxidants like alpha-tocopherot and a green tea extract in counteracting H/R damage towards HUFA biosynthesis was tested. Methods and results: Linoteic (LA) and alpha-linotenic acid (ALA) conversion was measured by pre-labelling cells with [1-C-14]LA or [1-C-14]ALA for 1 h; total lipid fatty acid composition was determined by gas chromatographic analysis. H profoundly affected HUFA biosynthesis, and this effect was much more evident on LA than on ALA. Conversion of both substrates was partially restored during R due to the readmission of the final acceptor of the desaturating complex. Fatty acid composition data were in agreement with the modifications observed in essential fatty acid conversion. Antioxidant protection appeared to be related to the duration of H, and to be more effective during H than during R. Conclusion: This study points out the importance of possessing good antioxidant defenses not only after, but mainly prior to the onset of H. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:166 / 173
页数:8
相关论文
共 28 条
[1]   Heart and blood pressure adaptations in Wistar rats fed with different high-fat diets for 18 months [J].
Aguila, MB ;
Mandarim-de-Lacerda, CA .
NUTRITION, 2003, 19 (04) :347-352
[2]   Adaptation to high altitude hypoxia protects the rat heart against ischemia-induced arrhythmias.: Involvement of mitochondrial KATP channel [J].
Asemu, G ;
Papousek, F ;
Ostádal, B ;
Kolár, F .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 1999, 31 (10) :1821-1831
[3]   ALPHA-1-STIMULATED PHOSPHOINOSITIDE BREAKDOWN IN CULTURED CARDIOMYOCYTES - DIACYLGLYCEROL PRODUCTION AND COMPOSITION IN DOCOSAHEXAENOIC ACID SUPPLEMENTED CELLS [J].
BORDONI, A ;
BIAGI, PL ;
ROSSI, CA ;
HRELIA, S .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1991, 174 (02) :869-877
[4]   Green tea protection of hypoxia/reoxygenation injury in cultured cardiac cells [J].
Bordoni, A ;
Hrelia, S ;
Angeloni, C ;
Giordano, E ;
Guarnieri, C ;
Caldarera, CM ;
Biagi, PL .
JOURNAL OF NUTRITIONAL BIOCHEMISTRY, 2002, 13 (02) :103-111
[5]   The impairment of essential fatty acid metabolism as a key factor in doxorubicin-induced damage in cultured rat cardiomyocytes [J].
Bordoni, A ;
Biagi, PL ;
Hrelia, S .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS, 1999, 1440 (01) :100-106
[6]   DESATURATION STEP IN ANIMAL BIOSYNTHESIS OF POLYUNSATURATED FATTY ACIDS [J].
BRENNER, RR .
LIPIDS, 1971, 6 (08) :567-&
[7]   BIOLOGICAL ANTIOXIDANTS [J].
BURTON, GW ;
FOSTER, DO ;
PERLY, B ;
SLATER, TF ;
SMITH, ICP ;
INGOLD, KU .
PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES, 1985, 311 (1152) :565-578
[8]  
Cook H.W., 1996, New Comprehensive Biochemistry, V31, P129, DOI 10.1016/S0167-7306(08)60512-8
[9]  
FERRARI R, 1985, ACTA VITAMINOL ENZYM, V5, P11
[10]  
FOLCH J, 1957, J BIOL CHEM, V226, P497