2016
DOI: 10.1016/j.yexcr.2016.08.002
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Effects of oxidative stress on hyperglycaemia-induced brain malformations in a diabetes mouse model

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Cited by 13 publications
(13 citation statements)
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“…Hyperglycemia has been shown to negatively affect embryo development 32 . Here, through comparing the development of gastrula chick embryos exposed to 50 mM glucose (high glucose (HG)) and/or 3 or 6 μM Baicalin for 26, 39 and 48 h (Fig.…”
Section: Resultsmentioning
confidence: 99%
“…Hyperglycemia has been shown to negatively affect embryo development 32 . Here, through comparing the development of gastrula chick embryos exposed to 50 mM glucose (high glucose (HG)) and/or 3 or 6 μM Baicalin for 26, 39 and 48 h (Fig.…”
Section: Resultsmentioning
confidence: 99%
“…Circle plot displayed the gene associated with peaks that were upregulated or downregulated within each GO term (Supplemental Figure 8, B and C). For example, peaks associated with the genes in the BMP, FoxP1, and Wnt cardiac morphogenetic signaling pathways were identified, and they have been linked to increased risk of fetal neurologic and cardiac developmental defects in matDM-exposed embryos (61)(62)(63)(64)(65). HG stress resulted in dysregulation of chromatin accessibility of genes important for reorganizing actin cytoskeleton, cell polarity, and alignment during tissue morphogenesis (66,67).…”
Section: Discussionmentioning
confidence: 99%
“…In a diabetic mouse model that mimicking pregestational DM, abnormal morphogenesis, and histological structure of brain in mouse fetuses were identified. [ 37 ] Enhanced cell apoptosis and activated oxidative stress were detected in mouse fetal brains, where Nrf2 signaling played a crucial role. [ 37 ] The role of oxidative stress on pathogenesis of autism was further supported by idiopathic autism mouse model.…”
Section: Discussionmentioning
confidence: 99%
“…[ 37 ] Enhanced cell apoptosis and activated oxidative stress were detected in mouse fetal brains, where Nrf2 signaling played a crucial role. [ 37 ] The role of oxidative stress on pathogenesis of autism was further supported by idiopathic autism mouse model. [ 38 , 39 ] It was demonstrated that gestational exposure to chemical trigger of oxidative stress strengthened some of the autistic-like traits, including delayed motor maturation and increased vocalization rate.…”
Section: Discussionmentioning
confidence: 99%