Effect of hypermethioninemia on some parameters of oxidative stress and on Na+,K+-ATPase activity in hippocampus of rats

被引:19
作者
Stefanello, Francieli M. [1 ]
Scherer, Emilene B. S. [1 ]
Kurek, Andrea G. [1 ]
Mattos, Cristiane B. [1 ]
Wyse, Angela T. S. [1 ]
机构
[1] Univ Fed Rio Grande do Sul, ICBS, Dept Bioquim, BR-90035003 Porto Alegre, RS, Brazil
关键词
hypermethioninemia; lipid peroxidation; Na+; K+-ATPase; hippocampus; K+-ATPASE ACTIVITY; SYNAPTIC PLASMA-MEMBRANE; ENERGY-METABOLISM; CEREBRAL-CORTEX; NA+; INHIBITION; BRAIN; METHIONINE; INVOLVEMENT; DYSFUNCTION;
D O I
10.1007/s11011-007-9052-7
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
In the present study we investigated the effect of chronic administration of methionine, a metabolite accumulated in many inherited pathological conditions such as methionine adenosyltransferase deficiency and homocystinuria, on some parameters of oxidative stress, namely thiobarbituric acid reactive substances (TBARS), catalase activity and total thiol content, as well as on Na+, K+- ATPase activity in rat hippocampus. For chronic treatment, rats received subcutaneous injections of methionine (1.34 - 2.68 mu mol/g of body weight), twice a day, from the 6th to the 28th day of age and controls received saline. Animals were killed 12 h after the last injection. Results showed that chronic hypermethioninemia significantly increased TBARS, decreased Na+, K+- ATPase activity but did not alter catalase and total thiol content. Since chronic hypermethioninemia altered TBARS and Na+, K+- ATPase activity at 12 h after methionine administration, we also investigated the effect of acute administration of this amino acid on the same parameters studied after chronic methionine administration. For acute treatment, 29-day-old rats received one single injection of methionine (2.68 mu mol/ g of body weight) or saline and were killed 1, 3 or 12 h later. Results showed that rats subjected to acute hypermethioninemia presented a reduction of Na+, K+- ATPase activity and an increase in TBARS when the animals were killed at 3 and 12 h, but not at 1 h, after methionine administration. These data indicate that hypermethioninemia increases lipid peroxidation which may, at least partially, explain the effect of methionine on the reduction in Na+, K+- ATPase activity. If confirmed in human beings, our findings could suggest that the induction of oxidative stress and the inhibition of Na+, K+- ATPase activity caused by methionine might contribute to the neurophysiopathology observed in patients with severe hypermethioninemia.
引用
收藏
页码:172 / 182
页数:11
相关论文
共 51 条
  • [1] AEBI H, 1984, METHOD ENZYMOL, V105, P121
  • [2] Changes in thiol content and expression of glutathione redox system genes in the hippocampus and cerebellum in Alzheimer's disease
    Aksenov, MY
    Markesbery, WR
    [J]. NEUROSCIENCE LETTERS, 2001, 302 (2-3) : 141 - 145
  • [3] Glycine N-methyltransferase deficiency:: A new patient with a novel mutation
    Augoustides-Savvopoulou, P
    Luka, Z
    Karyda, S
    Stabler, SP
    Allen, RH
    Patsiaoura, K
    Wagner, C
    Mudd, SH
    [J]. JOURNAL OF INHERITED METABOLIC DISEASE, 2003, 26 (08) : 745 - 759
  • [4] BENEVENGA NJ, 1984, ANNU REV NUTR, V4, P157, DOI 10.1146/annurev.nu.04.070184.001105
  • [5] Chemistry, physiology and pathology of free radicals
    Bergendi, L
    Benes, L
    Duracková, Z
    Ferencik, M
    [J]. LIFE SCIENCES, 1999, 65 (18-19) : 1865 - 1874
  • [6] BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
  • [7] A DIRECT COLORIMETRIC ASSAY FOR CA-2+-STIMULATED ATPASE ACTIVITY
    CHAN, KM
    DELFERT, D
    JUNGER, KD
    [J]. ANALYTICAL BIOCHEMISTRY, 1986, 157 (02) : 375 - 380
  • [8] DEVELOPMENT OF ENZYMES OF ENERGY-METABOLISM IN THE NEONATAL MAMMALIAN BRAIN
    CLARK, JB
    BATES, TE
    CULLINGFORD, T
    LAND, JM
    [J]. DEVELOPMENTAL NEUROSCIENCE, 1993, 15 (3-5) : 174 - 180
  • [9] COUSIN MA, 1995, J NEUROCHEM, V64, P2097
  • [10] PROTEIN-SYNTHESIS AND MEMORY - A REVIEW
    DAVIS, HP
    SQUIRE, LR
    [J]. PSYCHOLOGICAL BULLETIN, 1984, 96 (03) : 518 - 559