Apoptotic Cell Death Correlates With ROS Overproduction and Early Cytokine Expression After Hypoxia-Ischemia in Fetal Lambs

被引:14
作者
Alonso-Alconada, Daniel [1 ]
Hilario, Enrique [1 ]
Jose Alvarez, Francisco [2 ]
Alvarez, Antonia [1 ]
机构
[1] Univ Basque Country, Sch Med & Dent, Dept Cell Biol & Histol, Leioa 48940, Vizcaya, Spain
[2] Hosp Cruces, Res Unit Expt Perinatal Physiopathol, Baracaldo, Vizcaya, Spain
关键词
hypoxia-ischemia; fetal lamb; cytokines; oxidative damage; apoptosis; CEREBRAL-ARTERY OCCLUSION; NECROSIS-FACTOR-ALPHA; BRAIN-INJURY; TERM NEWBORN; GENE-EXPRESSION; PRETERM LAMBS; MESSENGER-RNA; FREE-RADICALS; RAT; DAMAGE;
D O I
10.1177/1933719111432868
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Despite advances in neonatology, the hypoxic-ischemic injury in the perinatal period remains the single most important cause of brain injury in the newborn, leading to death or lifelong sequelae. Using a sheep model of intrauterine asphyxia, we evaluated the correlation between reactive oxygen species (ROS) overproduction, cytokine expression, and apoptotic cell death. Fetal lambs were assigned to sham group, nonasphyctic animals; and hypoxia-ischemia (HI) group, lambs subjected to 60 minutes of HI) by partial cord occlusion and sacrificed 3 hours later. Different brain regions were separated to quantify the number of apoptotic cells and the same territories were dissociated for flow cytometry studies. Our results suggest that the overproduction of ROS and the early increase in cytokine production after HI in fetal lambs correlate in a significant manner with the apoptotic index, as well as with each brain region evaluated.
引用
收藏
页码:754 / 763
页数:10
相关论文
共 39 条
[11]   Cerebral blood flow and morphological changes after hypoxic-ischaemic injury in preterm lambs [J].
Hilario, E ;
Rey-Santano, MC ;
Goñi-de-Cerio, F ;
Alvarez, FJ ;
Gastiasoro, E ;
Mielgo, VE ;
Caballero, A ;
Valls-I-Soler, A ;
Gómez-Urquijo, S ;
Alvarez, A .
ACTA PAEDIATRICA, 2005, 94 (07) :903-911
[12]   Physiologic and histologic changes in near-term fetal lambs exposed to asphyxia by partial umbilical cord occlusion [J].
Ikeda, T ;
Murata, Y ;
Quilligan, EJ ;
Choi, BH ;
Parer, JT ;
Doi, S ;
Park, SD .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1998, 178 (01) :24-32
[13]   Oxidative stress, brain white matter damage and intrauterine asphyxia in fetal lambs [J].
Ikeda, T ;
Choi, BH ;
Yee, S ;
Murata, Y ;
Quilligan, EJ .
INTERNATIONAL JOURNAL OF DEVELOPMENTAL NEUROSCIENCE, 1999, 17 (01) :1-14
[14]   Tumour necrosis factor-induced death of adult human oligodendrocytes is mediated by apoptosis inducing factor [J].
Jurewicz, A ;
Matysiak, M ;
Tybor, K ;
Kilianek, L ;
Raine, CS ;
Selmaj, K .
BRAIN, 2005, 128 :2675-2688
[15]   Free radical injury and blood-brain barrier permeability in hypoxic-ischemic encephalopathy [J].
Kumar, Ashok ;
Mittal, Roopali ;
Khanna, Hari Dev ;
Basu, Sriparna .
PEDIATRICS, 2008, 122 (03) :E722-E727
[16]   Neonatal survival 1 - 4 million neonatal deaths: When? where? why? [J].
Lawn, JE ;
Cousens, S ;
Zupan, J .
LANCET, 2005, 365 (9462) :891-900
[17]   TUMOR-NECROSIS-FACTOR-ALPHA EXPRESSION IN ISCHEMIC NEURONS [J].
LIU, T ;
CLARK, RK ;
MCDONNELL, PC ;
YOUNG, PR ;
WHITE, RF ;
BARONE, FC ;
FEUERSTEIN, GZ .
STROKE, 1994, 25 (07) :1481-1488
[18]   THE INTERLEUKIN-1 RECEPTOR ANTAGONIST (RHIL-1RA) PROTECTS AGAINST CEREBRAL INFARCTION IN A RAT MODEL OF HYPOXIA-ISCHEMIA [J].
MARTIN, D ;
CHINOOKOSWONG, N ;
MILLER, G .
EXPERIMENTAL NEUROLOGY, 1994, 130 (02) :362-367
[19]   Mechanisms of hypoxic-ischemic injury in the term infant [J].
McLean, C ;
Ferriero, D .
SEMINARS IN PERINATOLOGY, 2004, 28 (06) :425-432
[20]   Experimental stroke induces massive, rapid activation of the peripheral immune system [J].
Offner, Halina ;
Subramanian, Sandhya ;
Parker, Susan M. ;
Afentoulis, Michael E. ;
Vandenbark, Arthur A. ;
D Hurn, Patricia .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 2006, 26 (05) :654-665