A Possible Anti-Inflammatory Effect of Proline in the Brain Cortex and Cerebellum of Rats

被引:26
作者
Andrade, Vivian Strassburger [1 ]
Rojas, Denise Bertin [1 ]
de Andrade, Rodrigo Binkowski [1 ]
Kim, Tomas Duk Hwa [1 ]
Vizuete, Adriana Fernanda [1 ]
Zanatta, Angela [1 ]
Wajner, Moacir [1 ]
Saraiva Goncalves, Carlos-Alberto [1 ]
Duval Wannmacher, Clovis Milton [1 ]
机构
[1] Univ Fed Rio Grande do Sul, Inst Ciencias Basicas Saude, Dept Bioquim, Rua Ramiro Barcelos 2600, BR-90035003 Porto Alegre, RS, Brazil
关键词
Lipopolysaccharide; Oxidative stress; Proline; Phosphoryl transfer network; Hyperprolinemia; FIBRILLARY ACIDIC PROTEIN; OXIDATIVE STRESS; LIPOPOLYSACCHARIDE; S100B; DAMAGE; PHOSPHOTRANSFER; ASTROCYTES; EXPRESSION; CYTOKINES; KINASE;
D O I
10.1007/s12035-017-0626-z
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
ght fr Although many studies show the toxic effects of proline, recently it has been reported some anti-inflammatory effect of this amino acid. Our principal objective was to investigate the effects of proline on the alterations caused by LPS (lipopolysaccharide) administration in the cerebral cortex and cerebellum of young Wistar rats. The animals were divided into four groups: control (0.85% saline); proline, (12.8 mu mol of proline/g body weiom day 7 to 13; 14.6 mu mol of proline/g body weight from day 14 to 17 and 16.4 mu mol of proline/g body weight from day 18 to 21); LPS (1 mg/g body weight); LPS plus proline. The animals were killed at 22 days of age, 12 h after the last injection, by decapitation without anesthesia. The brain cortex and cerebellum were separated for chemical determinations. The effects of proline and LPS in the cerebral cortex and cerebellum on the expression of S100B and GFAP, oxidative stress parameters, enzymes of phosphoryl transfer network activity, and mitochondrial respiration chain complexes were investigated. Two-way ANOVA showed that the administration of proline did not alter the analyzed parameter in cerebral cortex and cerebellum. On the other hand, LPS administration caused a change in these parameters. Besides, the co-administration of proline and LPS showed the ability of Pro in preventing the effects of LPS. These results indicated that LPS induces inflammation, oxidative stress, and alters energy parameters in cerebral cortex and cerebellum of the rats. Moreover, co-administration of Pro was able to prevent these harmful effects of LPS.
引用
收藏
页码:4068 / 4077
页数:10
相关论文
共 56 条
  • [1] Adams E, 1970, Int Rev Connect Tissue Res, V5, P1
  • [2] Aebi H, 1984, Methods Enzymol, V105, P121
  • [3] 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
  • [4] Mitochondrial Complex I Activity and Oxidative Damage to Mitochondrial Proteins in the Prefrontal Cortex of Patients With Bipolar Disorder
    Andreazza, Ana C.
    Shao, Li
    Wang, Jun-Feng
    Young, L. Trevor
    [J]. ARCHIVES OF GENERAL PSYCHIATRY, 2010, 67 (04) : 360 - 368
  • [5] Diversity of endotoxin-induced nitrotyrosine formation in macrophage-endothelium-rich organs
    Bian, K
    Murad, F
    [J]. FREE RADICAL BIOLOGY AND MEDICINE, 2001, 31 (04) : 421 - 429
  • [6] Induction of glial fibrillary acidic protein expression in astrocytes by nitric oxide
    Brahmachari, S
    Fung, YK
    Pahan, K
    [J]. JOURNAL OF NEUROSCIENCE, 2006, 26 (18) : 4930 - 4939
  • [7] Phagocytosis and LPS-stimulated production of cytokines and prostaglandin E2 is different in Kupffer cells isolated from the periportal or perivenous liver region
    Bykov, I
    Ylipaasto, P
    Eerola, L
    Lindros, KO
    [J]. SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY, 2003, 38 (12) : 1256 - 1261
  • [8] Synergistic drug-cytokine induction of hepatocellular death as an in vitro approach for the study of inflammation-associated idiosyncratic drug hepatotoxicity
    Cosgrove, Benjamin D.
    King, Bracken M.
    Hasan, Maya A.
    Alexopoulos, Leonidas G.
    Farazi, Paraskevi A.
    Hendriks, Bart S.
    Griffith, Linda G.
    Sorger, Peter K.
    Tidor, Bruce
    Xu, Jinghai J.
    Lauffenburger, Douglas A.
    [J]. TOXICOLOGY AND APPLIED PHARMACOLOGY, 2009, 237 (03) : 317 - 330
  • [9] Diplock A.T., 1994, NEW COMPR BIOCH, V28, P113
  • [10] Adenylate kinase-catalyzed phosphotransfer in the myocardium - Increased contribution in heart failure
    Dzeja, PP
    Vitkevicius, KT
    Redfield, MM
    Burnett, JC
    Terzic, A
    [J]. CIRCULATION RESEARCH, 1999, 84 (10) : 1137 - 1143