Non-enzymatic lipid peroxidation of microsomes and mitochondria isolated from liver and heart of pigeon and rat

被引:15
作者
Gutiérrez, AM
Reboredo, GR
Arcemis, CJ
Catalá, A
机构
[1] Univ Nacl La Plata, Fac Ciencias Vet, Catedra Bioquim, RA-1900 La Plata, Buenos Aires, Argentina
[2] Univ Nacl La Plata, Fac Ciencias Nat & Museo, Catedra Fisiol Anim, RA-1900 La Plata, Buenos Aires, Argentina
关键词
lipid peroxidation; microsomes; mitochondria; pigeon; rat;
D O I
10.1016/S1357-2725(99)00105-3
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Studies were carried out to determine the level of ascorbate-Fe2+ dependent lipid peroxidation of mitochondria and microsomes isolated from liver and heart of rat and pigeon. Measurements of chemiluminescence indicate that the lipid peroxidation process was more effective in mitochondria and microsomes from rat liver than in the same organelles obtained from pigeon, In both mitochondria and microsomes from liver of both species a significant decrease of arachidonic acid was observed during peroxidation; The rate C18,2 n6/C20:4 n6 was 4.5 times higher in pigeon than in rat liver. This observation can explain the differences noted when light emission and unsaturation index of both species were analysed. A significant decrease of C18,2 n6 and C20,4 n6 in pigeon liver mitochondria was observed when compared with native organelles whereas in pigeon liver microsomes only C20,4 n6 diminished. In rat liver mitochondria only arachidonic acid C20:4 n6 showed a: significant decrease whereas in rat liver microsomes C20:4 n6 and C22:6 n3 decreased significantly, However changes were not observed in the fatty acid profile of:mitochondria and microsomes isolated from pigeon heart. In the heart under our peroxidation conditions the fatty acid profile does not appear to be responsible for thr:different susceptibility to the lipid peroxidation process; The lack of a relationship between fatty acid unsaturation and sensitivity to peroxidation observed in heart suggest that other factor/s may be involved in the protection to lipid peroxidation in microsomes and mitochondria isolated from heart. (C) 1999 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:73 / 79
页数:7
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