2019
DOI: 10.1016/j.braindev.2018.10.009
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Correlation between human nervous system development and acquisition of fetal skills: An overview

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Cited by 53 publications
(58 citation statements)
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References 79 publications
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“…We used piglet models of excitotoxic brain injury from stereotaxic QA injection (Lee, Liu, et al, 2020) and global HI (Lee et al, 2016; 1997; Santos et al, 2018; Wang et al, 2015; Wang et al, 2016). Brain development at term gestation, perinatal growth, connectivity, and prenatal and extended postnatal myelination are analogous in humans and piglets (Borsani, Della Vedova, Rezzani, Rodella, & Cristini, 2019; Bozek et al, 2018; de Graaf‐Peters & Hadders‐Algra, 2006; Dobbing & Sands, 1979; Ishibashi et al, 2012; Lee, Santos, et al, 2020; Mudd & Dilger, 2017; Oishi, Faria, & Mori, 2012; Sheng, Kerlero de Rosbo, Carnegie, & Bernard, 1989; Simchick et al, 2019; Siu, Balsor, Jones, & Murphy, 2015; Sweasey, Patterson, & Glancy, 1976). We created the piglet model of QA‐induced excitotoxicity (Lee, Liu, et al, 2020) because excitotoxicity is a key mechanism of HI brain injury (Johnston, 2005).…”
Section: Discussionmentioning
confidence: 99%
“…We used piglet models of excitotoxic brain injury from stereotaxic QA injection (Lee, Liu, et al, 2020) and global HI (Lee et al, 2016; 1997; Santos et al, 2018; Wang et al, 2015; Wang et al, 2016). Brain development at term gestation, perinatal growth, connectivity, and prenatal and extended postnatal myelination are analogous in humans and piglets (Borsani, Della Vedova, Rezzani, Rodella, & Cristini, 2019; Bozek et al, 2018; de Graaf‐Peters & Hadders‐Algra, 2006; Dobbing & Sands, 1979; Ishibashi et al, 2012; Lee, Santos, et al, 2020; Mudd & Dilger, 2017; Oishi, Faria, & Mori, 2012; Sheng, Kerlero de Rosbo, Carnegie, & Bernard, 1989; Simchick et al, 2019; Siu, Balsor, Jones, & Murphy, 2015; Sweasey, Patterson, & Glancy, 1976). We created the piglet model of QA‐induced excitotoxicity (Lee, Liu, et al, 2020) because excitotoxicity is a key mechanism of HI brain injury (Johnston, 2005).…”
Section: Discussionmentioning
confidence: 99%
“…Additionally, while AA contributes to Type II immune responses, its oxidative metabolites such as downstream P450 metabolites including epoxyeicosatrienoic acids, contribute to the resolution of inflammation [23,24]. Given the prolonged period of development, intrauterine augmentation of AA transfer to the fetus may be beneficial to support critical neonatal development [25,26]. Since AA has a proven benefit to nervous system function, augmentation of intrauterine transfer may be necessary given the longevity and cruciality of fetal nervous system development throughout pregnancy.…”
Section: Discussionmentioning
confidence: 99%
“…However, it is only in recent decades that the influence of prenatal vitamin D levels on brain development has been understood. The early stages of gestation (first and second trimesters) are a critical period in the development of the foetal nervous system due to the beginning of neurogenesis and the myelination process [ 29 ] and, as we know, foetuses are utterly dependent on their mothers’ vitamin D status. This could be why low levels of this vitamin during this period may be closely related to the children’s neurodevelopment [ 30 , 31 ] and why this effect on cognitive and language skills is not observed when the vitamin D deficiency occurs at the end of gestation.…”
Section: Discussionmentioning
confidence: 99%