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
[1]   Combination effect of systemic hypothermia and caspase inhibitor administration against hypoxic-ischemic brain damage in neonatal rats [J].
Adachi, M ;
Sohma, O ;
Tsuneishi, S ;
Takada, S ;
Nakamura, H .
PEDIATRIC RESEARCH, 2001, 50 (05) :590-595
[2]   Unilateral hypoxic-ischemic injury in the neonatal rat brain evaluated by in vivo MRI - Correlation with histopathology and neuroprotection by MK-801 [J].
Albensi, BC ;
Schweizer, MP ;
Rarick, TM ;
Filloux, F .
INVESTIGATIVE RADIOLOGY, 1999, 34 (04) :249-261
[3]  
Alkan T., 2001, Archives of Physiology and Biochemistry, V109, P135, DOI 10.1076/apab.109.2.135.4271
[4]   BDNF protects against spatial memory deficits following neonatal hypoxia-ischemia [J].
Almli, CR ;
Levy, TJ ;
Han, BH ;
Shah, AR ;
Gidday, JM ;
Holtzman, DM .
EXPERIMENTAL NEUROLOGY, 2000, 166 (01) :99-114
[5]   Age-related effects of interleukin-1 beta on polymorphonuclear neutrophil-dependent increases in blood-brain barrier permeability in rats [J].
Anthony, DC ;
Bolton, SJ ;
Fearn, S ;
Perry, VH .
BRAIN, 1997, 120 :435-444
[6]   Minocycline markedly protects the neonatal brain against hypoxic-ischemic injury [J].
Arvin, KL ;
Han, BH ;
Du, YS ;
Lin, SZ ;
Paul, SM ;
Holtzman, DM .
ANNALS OF NEUROLOGY, 2002, 52 (01) :54-61
[7]  
Ashamalla HL, 1996, CANCER, V77, P2407, DOI 10.1002/(SICI)1097-0142(19960601)77:11<2407::AID-CNCR33>3.0.CO
[8]  
2-Z
[9]  
Atochin D N, 2001, Ross Fiziol Zh Im I M Sechenova, V87, P1118
[10]  
Atochin DN, 2000, UNDERSEA HYPERBAR M, V27, P185