Pathophysiology of an hypoxic-ischemic insult during the perinatal period

被引:82
作者
Calvert, JW
Zhang, JH
机构
[1] Loma Linda Univ, Med Ctr, Div Neurosurg, Dept Neurosurg, Loma Linda, CA 92354 USA
[2] Loma Linda Univ, Med Ctr, Dept Cellular & Mol Physiol, Loma Linda, CA USA
[3] Louisiana State Univ, Hlth Sci Ctr, Shreveport, LA USA
关键词
hypoxia; ischemia; perinatal; white matter; hypothermia; hyperbaric oxygen; apoptosis; inflammation; treatment outcome;
D O I
10.1179/016164105X25216
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Hypoxia-ischemia is a leading cause of morbidity and mortality in the perinatal period with an incidence of similar to 1/4000 live births. Biochemical events such as energy failure, membrane depolarization, brain edema, an increase of neurotransmitter release and inhibition of uptake, an increase of intracellular Ca2+, production of oxygen-free radicals, lipid peroxidation, and a decrease of blood flow are triggered by hypoxia-ischemia and may lead to brain dysfunction and neuronal death. These abnormalities can result in mental impairments, seizures, and permanent motor deficits, such as cerebral palsy. The physical and emotional strain that is placed on the children affected and their families is enormous. The care that these individuals nosed is not only confined to childhood, but rather extends throughout their entire life span, so it is very important to understand the pathophysiology that follows a hypoxic-ischemic insult. This review hill highlight many of the mechanisms that lead to neuronal death and include the emerging area of white matter injury as well as the role of inflammation and will provide a summary of therapeutic strategies. Hypothermia and oxygen will also be discussed as treatments that currently lack a specific target in the hypoxic/ischemic cascade.
引用
收藏
页码:246 / 260
页数:15
相关论文
共 220 条
[11]  
Back SA, 2001, J NEUROSCI, V21, P1302
[12]   Selective vulnerability of late oligodendrocyte progenitors to hypoxia-ischemia [J].
Back, SA ;
Han, BH ;
Luo, NL ;
Chricton, CA ;
Xanthoudakis, S ;
Tam, J ;
Arvin, KL ;
Holtzman, DM .
JOURNAL OF NEUROSCIENCE, 2002, 22 (02) :455-463
[13]   Effect of hyperbaric oxygen on striatal metabolites: a microdialysis study in awake freely moving rats after MCA occlusion [J].
Badr, AE ;
Yin, W ;
Mychaskiw, G ;
Zhang, JH .
BRAIN RESEARCH, 2001, 916 (1-2) :85-90
[14]   Formation of free radicals in hypoxic ischemic brain damage in the neonatal rat, assessed by an endogenous spin trap and lipid peroxidation [J].
Bagenholm, R ;
Nilsson, UA ;
Kjellmer, I .
BRAIN RESEARCH, 1997, 773 (1-2) :132-138
[15]   Free radicals are formed in the brain of fetal sheep during reperfusion after cerebral ischemia [J].
Bågenholm, R ;
Nilsson, UA ;
Götborg, CW ;
Kjellmer, I .
PEDIATRIC RESEARCH, 1998, 43 (02) :271-275
[16]   Prophylactic but not delayed administration of simvastatin protects against long-lasting cognitive and morphological consequences of neonatal hypoxic-ischemic brain injury, reduces interleukin-1β and tumor necrosis factor-α mRNA induction, and does not affect endothelial nitric oxide synthase expression [J].
Balduini, W ;
Mazzoni, E ;
Carloni, S ;
De Simoni, MG ;
Perego, C ;
Sironi, L ;
Cimino, M .
STROKE, 2003, 34 (08) :2007-2012
[17]   Mechanisms underlying hypoxia-induced neuronal apoptosis [J].
Banasiak, KJ ;
Xia, Y ;
Haddad, GG .
PROGRESS IN NEUROBIOLOGY, 2000, 62 (03) :215-249
[18]   Treatment of term infants with head cooling and mild systemic hypothermia (35.0°C and 34.5°C) after perinatal asphyxia [J].
Battin, MR ;
Penrice, J ;
Gunn, TR ;
Gunn, AJ .
PEDIATRICS, 2003, 111 (02) :244-251
[19]   Neurodevelopmental outcome of infants treated with head cooling and mild hypothermia after perinatal asphyxia [J].
Battin, MR ;
Dezoete, JA ;
Gunn, TR ;
Gluckman, PD ;
Gunn, AJ .
PEDIATRICS, 2001, 107 (03) :480-484
[20]   Perinatal brain injury [J].
Berger, R ;
Garnier, Y .
JOURNAL OF PERINATAL MEDICINE, 2000, 28 (04) :261-285