Ketogenic diet increases glutathione peroxidase activity in rat hippocampus

被引:116
作者
Ziegler, DR
Ribeiro, LC
Hagenn, M
Siqueira, IR
Araújo, E
Torres, ILS
Gottfried, C
Netto, CA
Gonaalves, CA
机构
[1] Univ Vale Rio dos Sinos, Ctr Ciencias Saude, BR-93022000 Sao Leopoldo, RS, Brazil
[2] Univ Fed Rio Grande do Sul, ICBS, Dept Bioquim, Porto Alegre, RS, Brazil
[3] Univ Fed Rio Grande do Sul, ICBS, Dept Fisiol, Porto Alegre, RS, Brazil
关键词
Ketogenic diet; oxidative stress; glutathione peroxidase; lipoperoxidation; hippocampus;
D O I
10.1023/A:1026107405399
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Ketogenic diets have been used in the treatment of refractory childhood epilepsy for almost 80 years; however, we know little about the underlying biochemical basis of their action. In this study, we evaluate oxidative stress in different brain regions from Wistar rats fed a ketogenic diet. Cerebral cortex appears to have not been affected by this diet, and cerebellum presented a decrease in antioxidant capacity measured by a luminol oxidation assay without changes in antioxidant enzyme activities - glutathione peroxidase, catalase, and superoxide dismutase. In the hippocampus, however, we observed an increase in antioxidant activity accompanied by an increase of glutathione peroxidase ( about 4 times) and no changes in lipoperoxidation levels. We suggest that the higher activity of this enzyme induced by ketogenic diet in hippocampus might contribute to protect this structure from neurodegenerative sequelae of convulsive disorders.
引用
收藏
页码:1793 / 1797
页数:5
相关论文
共 30 条
[1]
AEBI H, 1984, METHOD ENZYMOL, V105, P121
[2]
Regional vulnerability to oxidative stress in a model of experimental epilepsy [J].
Arnaiz, SL ;
Travacio, M ;
Llesuy, S ;
Arnaiz, GRD .
NEUROCHEMICAL RESEARCH, 1998, 23 (12) :1477-1483
[3]
Superoxide dismutase, glutathione peroxidase activities and the hydroperoxide concentration are modified in the hippocampus of epileptic rats [J].
Bellissimo, MI ;
Amado, D ;
Abdalla, DSP ;
Ferreira, EC ;
Cavalheiro, EA ;
Naffah-Mazzacoratti, MD .
EPILEPSY RESEARCH, 2001, 46 (02) :121-128
[4]
Tissue-specific functions of individual glutathione peroxidases [J].
Brigelius-Flohé, R .
FREE RADICAL BIOLOGY AND MEDICINE, 1999, 27 (9-10) :951-965
[5]
Selective vulnerability to kainate-induced oxidative damage in different rat brain regions [J].
Candelario-Jalil, E ;
Al-Dalain, SM ;
Castillo, R ;
Martínez, G ;
Fernández, OSL .
JOURNAL OF APPLIED TOXICOLOGY, 2001, 21 (05) :403-407
[6]
Relationships between neuronal death and the cellular redox status. Focus on the developing nervous system [J].
Castagne, V ;
Gautschi, M ;
Lefevre, K ;
Posada, A ;
Clarke, PGH .
PROGRESS IN NEUROBIOLOGY, 1999, 59 (04) :397-423
[7]
Choi Byung Ho, 1993, Yonsei Medical Journal, V34, P1
[8]
OXIDATIVE STRESS, GLUTAMATE, AND NEURODEGENERATIVE DISORDERS [J].
COYLE, JT ;
PUTTFARCKEN, P .
SCIENCE, 1993, 262 (5134) :689-695
[9]
4-nerolidylcatechol from Pothomorphe spp. scavenges peroxyl radicals and inhibits Fe(II)-dependent DNA damage [J].
Desmarchelier, C ;
Barros, S ;
Repetto, M ;
Latorre, LR ;
Kato, M ;
Coussio, J ;
Ciccia, G .
PLANTA MEDICA, 1997, 63 (06) :561-563
[10]
Metabolism and functions of glutathione in brain [J].
Dringen, R .
PROGRESS IN NEUROBIOLOGY, 2000, 62 (06) :649-671