Protective effect of dietary squalene supplementation on mitochondrial function in liver of aged rats

被引:30
作者
Buddhan, S.
Sivakumar, R.
Dhandapani, N.
Ganesan, B.
Anandan, R.
机构
[1] Cent Inst Fisheries Technol, Biochem & Nutr Div, Cochin 682029, Kerala, India
[2] RVS Coll Pharmaceut Sci, Dept Pharmaceut Chem, Coimbatore 641402, Tamil Nadu, India
[3] Vinayaka Missions Res Fdn Deemed Univ, Dept Biochem, Salem 636308, Tamil Nadu, India
来源
PROSTAGLANDINS LEUKOTRIENES AND ESSENTIAL FATTY ACIDS | 2007年 / 76卷 / 06期
关键词
D O I
10.1016/j.plefa.2007.05.001
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
Mitochondria are an important intracellular source and target of reactive oxygen species. The life span of a species is thought to be determined, in part, by the rate of mitochondrial damage inflicted by oxygen free radicals during the course of normal cellular metabolism. In the present study, we have investigated the protective effect of squalene supplementation for 15 days and 30 days on energy status and antioxidant defense system in liver mitochondria of 18 young and IS aged rats. The dietary supplementation of 2% squalene significantly minimized aging associated alterations in mitochondrial energy status by maintaining the activities of TCA cycle enzymes (isocitrate dehydrogenase, a-ketoglutarate dehydrogenase, succinate dehydrogenase and malate dehydrogenase) and respiratory marker enzymes (NADH dehydrogenase and cytochrome-c-oxidase) at higher level in the liver mitochondria of aged rats compared with unsupplemented controls. It exerted an antioxidant effect by inhibiting mitochondrial lipid peroxidation (malondialdehyde) in liver of young and aged rats. Supplementation with squalene also maintained the mitochondrial antioxidant defense system at higher rate by increasing the level of reduced glutathione and the activities of glutathione-dependent antioxidant enzymes (glutathione peroxidase and glutathione-S-transferase) and antiperoxidative enzymes (superoxide dismutase and catalase) in the liver of young and aged rats. The results of this study provide evidence that dietary supplementation with squalene can improve liver mitochondrial function during aging and minimize the age-associated disorders in which reactive oxygen species are a major cause. (c) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:349 / 355
页数:7
相关论文
共 41 条
[1]   Neurochemical changes related to ageing in the rat brain and the effect of DL-α-lipoic acid [J].
Arivazhagan, P ;
Panneerselvam, C .
EXPERIMENTAL GERONTOLOGY, 2002, 37 (12) :1489-1494
[2]   Effect of DL-α-lipoic acid on the status of lipid peroxidation and antioxidants in mitochondria of aged rats [J].
Arivazhagan, P ;
Ramanathan, K ;
Panneerselvam, C .
JOURNAL OF NUTRITIONAL BIOCHEMISTRY, 2001, 12 (01) :2-6
[3]  
ARNES BN, 1993, P NATL ACAD SCI USA, V90, P7915
[4]   INVESTIGATION OF ANTIOXIDANT STATUS, DNA-REPAIR CAPACITY AND MUTATION AS A FUNCTION OF AGE IN HUMANS [J].
BARNETT, YA ;
KING, CM .
MUTATION RESEARCH-DNAGING GENETIC INSTABILITY AND AGING, 1995, 338 (1-6) :115-128
[5]   A COLORIMETRIC METHOD FOR DETERMINATION OF ISOCITRIC DEHYDROGENASE [J].
BELL, JL ;
BARON, DN .
CLINICA CHIMICA ACTA, 1960, 5 (05) :740-747
[6]   Effectiveness and safety of low-dose pravastatin and squalene, alone and in combination, in elderly patients with hypercholesterolemia [J].
Chan, P ;
Tomlinson, B ;
Lee, CB ;
Lee, YS .
JOURNAL OF CLINICAL PHARMACOLOGY, 1996, 36 (05) :422-427
[7]   ALTERATIONS IN MITOCHONDRIAL-MEMBRANE FLUIDITY BY LIPID-PEROXIDATION PRODUCTS [J].
CHEN, JJ ;
YU, BP .
FREE RADICAL BIOLOGY AND MEDICINE, 1994, 17 (05) :411-418
[8]   The preventive and therapeutic potential of the squalene-containing compound, Roidex, on tumor promotion and regression [J].
Desai, KN ;
Wei, H ;
Lamartiniere, CA .
CANCER LETTERS, 1996, 101 (01) :93-96
[9]   TISSUE SULFHYDRYL GROUPS [J].
ELLMAN, GL .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1959, 82 (01) :70-77
[10]   Squalene inhibits sodium arsenite-induced sister chromatid exchanges and micronuclei in Chinese hamster ovary-K1 cells [J].
Fan, SR ;
Ho, IC ;
Yeoh, FLF ;
Lin, CJ ;
Lee, TC .
MUTATION RESEARCH-GENETIC TOXICOLOGY, 1996, 368 (3-4) :165-169