Oxidative stress gene expression profile in inbred mouse after ischemia/reperfusion small bowel injury

被引:14
作者
Bertoletto, Paulo Roberto [1 ]
Ikejiri, Adauto Tsutomu [1 ,2 ]
Neto, Frederico Somaio [1 ,2 ]
Chaves, Jose Carlos [1 ,2 ]
Teruya, Roberto [2 ,3 ]
Bertoletto, Eduardo Rodrigues [4 ]
Taha, Murched Omar [5 ]
Fagundes, Djalma Jose [5 ]
机构
[1] UFGD, Sch Med, Dourados, MS, Brazil
[2] UNIFESP, Postgrad Program Interdisciplinary Surg Sci, Dourados, MS, Brazil
[3] Fed Univ Mato Grosso Sul UFMS, Dept Surg, Campo Grande, MS, Brazil
[4] Sao Camilo Univ Ctr, Sao Paulo, Brazil
[5] Univ Fed Sao Paulo, Dept Surg, Surg Tech & Expt Surg Div, Sao Paulo, Brazil
关键词
Oxidative Stress; Antioxidants; Gene expression; Ischemia; Reperfusion; Real-Time Polymerase Chain Reaction; Mice; ISCHEMIA-REPERFUSION INJURY; NITRIC-OXIDE BIOSYNTHESIS; MODULATION; OXYGEN; PATHOPHYSIOLOGY; ERYTHROCYTE; METABOLISM; MYOGLOBIN; ARGININE; RABBITS;
D O I
10.1590/S0102-86502012001100006
中图分类号
R61 [外科手术学];
学科分类号
摘要
PURPOSE: To determine the profile of gene expressions associated with oxidative stress and thereby contribute to establish parameters about the role of enzyme clusters related to the ischemia/reperfusion intestinal injury. METHODS: Twelve male inbred mice (C57BL/6) were randomly assigned: Control Group (CG) submitted to anesthesia, laparotomy and observed by 120min; Ischemia/reperfusion Group (IRG) submitted to anesthesia, laparotomy, 60min of small bowel ischemia and 60min of reperfusion. A pool of six samples was submitted to the qPCR-RT protocol (six clusters) for mouse oxidative stress and antioxidant defense pathways. RESULTS: On the 84 genes investigated, 64 (76.2%) had statistic significant expression and 20 (23.8%) showed no statistical difference to the control group. From these 64 significantly expressed genes, 60 (93.7%) were up-regulated and 04 (6.3%) were down-regulated. From the group with no statistical significantly expression, 12 genes were up-regulated and 8 genes were down-regulated. Surprisingly, 37 (44.04%) showed a higher than threefold up-regulation and then arbitrarily the values was considered as a very significant. Thus, 37 genes (44.04%) were expressed very significantly up-regulated. The remained 47 (55.9%) genes were up-regulated less than three folds (35 genes - 41.6%) or down-regulated less than three folds (12 genes - 14.3%). CONCLUSION: The intestinal ischemia and reperfusion promote a global hyper-expression profile of six different clusters genes related to antioxidant defense and oxidative stress.
引用
收藏
页码:773 / 782
页数:10
相关论文
共 35 条
[21]   Cytoskeletons in prokaryotes [J].
Mayer, F .
CELL BIOLOGY INTERNATIONAL, 2003, 27 (05) :429-438
[22]   Regulation of gene expression by oxygen:: NF-κB and HIF-1, two extremes [J].
Michiels, C ;
Minet, E ;
Mottet, D ;
Raes, M .
FREE RADICAL BIOLOGY AND MEDICINE, 2002, 33 (09) :1231-1242
[23]   Cytoglobin, a Novel Member of the Globin Family, Protects Kidney Fibroblasts against Oxidative Stress under lschemic Conditions [J].
Nishi, Hiroshi ;
Inagi, Reiko ;
Kawada, Norifumi ;
Yoshizato, Katsutoshi ;
Mimura, Imari ;
Fujita, Toshiro ;
Nangaku, Masaomi .
AMERICAN JOURNAL OF PATHOLOGY, 2011, 178 (01) :128-139
[24]   Reduced Liver Injury and Cytokine Release After Transplantation of Preconditioned Intestines [J].
Oltean, Mihai ;
Zhu, Changlian ;
Mera, Simona ;
Pullerits, Rille ;
Mattsby-Baltzer, Inger ;
Molne, Johan ;
Hallberg, Eva ;
Blomgren, Klas ;
Olausson, Michael .
JOURNAL OF SURGICAL RESEARCH, 2009, 154 (01) :30-37
[25]   The Fanconi anemia complementation group C gene product: structural evidence of multifunctionality [J].
Pang, QS ;
Christianson, TA ;
Keeble, W ;
Diaz, J ;
Faulkner, GR ;
Reifsteck, C ;
Olson, S ;
Bagby, GC .
BLOOD, 2001, 98 (05) :1392-1401
[26]   Molecular diagnosis of inherited disorders: Lessons from hemoglobinopathies [J].
Patrinos, GR ;
Kollia, P ;
Papadakis, MN .
HUMAN MUTATION, 2005, 26 (05) :399-412
[27]   Assigning protein functions by comparative genome analysis: Protein phylogenetic profiles [J].
Pellegrini, M ;
Marcotte, EM ;
Thompson, MJ ;
Eisenberg, D ;
Yeates, TO .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (08) :4285-4288
[28]   Damaging effects of ischemia/reperfusion on intestinal muscle [J].
Pontell, Louise ;
Sharma, Purnima ;
Rivera, Leni R. ;
Thacker, Michelle ;
Tan, Yan Hong ;
Brock, James A. ;
Furness, John B. .
CELL AND TISSUE RESEARCH, 2011, 343 (02) :411-419
[29]   Identification of the α-aminoadipic semialdehyde synthase gene, which is defective in familial hyperlysinemia [J].
Sacksteder, KA ;
Biery, BJ ;
Morrell, JC ;
Goodman, BK ;
Geisbrecht, BV ;
Cox, RP ;
Gould, SJ ;
Geraghty, MT .
AMERICAN JOURNAL OF HUMAN GENETICS, 2000, 66 (06) :1736-1743
[30]   The eosinophil peroxidase gene forms a cluster with the genes for myeloperoxidase and lactoperoxidase on human chromosome 17 [J].
Sakamaki, K ;
Kanda, N ;
Ueda, T ;
Aikawa, E ;
Nagata, S .
CYTOGENETICS AND CELL GENETICS, 2000, 88 (3-4) :246-248