D-galactose induced inflammation lipid peroxidation and platelet activation in rats

被引:12
|
作者
Hadzi-Petrushev, Nikola [1 ]
Stojkovski, Velimir [2 ]
Mitrov, Dine [2 ]
Mladenov, Mitko [1 ]
机构
[1] Ss Cyril & Methodius Univ, Inst Biol, Fac Nat Sci & Math, Skopje 1000, Macedonia
[2] Ss Cyril & Methodius Univ, Fac Med Vet, Skopje 1000, Macedonia
关键词
D-galactose induced senescence; Lipid peroxidation; Inflammation; Platelet activation; Rats; IN-VIVO FORMATION; ADVANCED GLYCATION; F-2; ALPHA; RECEPTOR; F2-ALPHA; URINARY;
D O I
10.1016/j.cyto.2014.05.006
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
Background: To investigate events possibly related to the development of D-galactose induced senescence, we examined whether 8-iso PGF(2 alpha), formation, a marker of in vivo lipid peroxidation is altered and whether its biosynthesis is associated with 11-dehydro-TXB2 excretion rate, as a marker of in vivo platelet activation. In this setting, we also investigated the relationship between proinflammatory mediators (IL-6 and TNF-alpha from one, and lipid peroxidation and platelet activation, from another aspect. Methods and results: Forty animals were divided, depending on treatment with D-galactose into: placebo and D-galactose treated rats. 8-iso-PGF(2 alpha), IL-6 and TNF-alpha were measured in plasma, while 11-dehydro-TXB2 was determined in the urine after a six week treatment with D-galactose. Compared to placebo, D-galactose treated animals showed significantly higher levels of all measured parameters. Conclusions: D-galactose induced changes in the rate of F-2-isoprostane formation are associated with the changes in the excretion rate of 11-dehydro-TXB2. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:150 / 153
页数:4
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