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Impact of Perinatal Hypoxia on the Developing Brain

Overview
Journal Physiol Res
Specialty Physiology
Date 2020 Mar 22
PMID 32199007
Citations 24
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Abstract

Perinatal hypoxia is still one of the greatest threats to the newborn child, even in developed countries. However, there is a lack of works which summarize up-to-date information about that huge topic. Our review covers a broader spectrum of recent results from studies on mechanisms leading to hypoxia-induced injury. It also resumes possible primary causes and observed behavioral outcomes of perinatal hypoxia. In this review, we recognize two types of hypoxia, according to the localization of its primary cause: environmental and placental. Later we analyze possible pathways of prenatal hypoxia-induced injury including gene expression changes, glutaminergic excitatory damage (and a role of NMDA receptors in it), oxidative stress with ROS and RNS production, inflammation and apoptosis. Moreover, we focus on the impact of these pathophysiological changes on the structure and development of the brain, especially on its regions: corpus striatum and hippocampus. These brain changes of the offspring lead to impairments in their postnatal growth and sensorimotor development, and in their motor functions, activity, emotionality and learning ability in adulthood. Later we compare various animal models used to investigate the impact of prenatal and postnatal injury (hypoxic, ischemic or combinatory) on living organisms, and show their advantages and limitations.

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References
1.
Vlassaks E, Gavilanes A, Vles J, Deville S, Kramer B, Strackx E . The effects of fetal and perinatal asphyxia on neuronal cytokine levels and ceramide metabolism in adulthood. J Neuroimmunol. 2012; 255(1-2):97-101. DOI: 10.1016/j.jneuroim.2012.09.011. View

2.
Raman L, Tkac I, Ennis K, Georgieff M, Gruetter R, Rao R . In vivo effect of chronic hypoxia on the neurochemical profile of the developing rat hippocampus. Brain Res Dev Brain Res. 2005; 156(2):202-9. DOI: 10.1016/j.devbrainres.2005.02.013. View

3.
Weitzdoerfer R, Gerstl N, Pollak D, Hoeger H, Dreher W, Lubec G . Long-term influence of perinatal asphyxia on the social behavior in aging rats. Gerontology. 2004; 50(4):200-5. DOI: 10.1159/000078348. View

4.
Patterson A, Zhang L . Hypoxia and fetal heart development. Curr Mol Med. 2010; 10(7):653-66. PMC: 3075953. DOI: 10.2174/156652410792630643. View

5.
Kimball R, Wayment M, Merrill D, Wahlquist T, Reynolds P, Arroyo J . Hypoxia reduces placental mTOR activation in a hypoxia-induced model of intrauterine growth restriction (IUGR). Physiol Rep. 2015; 3(12). PMC: 4760431. DOI: 10.14814/phy2.12651. View