Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
9018422 | Toxicology and Applied Pharmacology | 2005 | 12 Pages |
Abstract
Pulmonary antioxidants and their therapeutic implications have been extensively studied during past decades. The purpose of this review is to briefly summarize the key findings of these studies as well as to elaborate on some novel approaches with respect to potential preventive treatments for neonatal chronic lung disease bronchopulmonary dysplasia (BPD). Such new ideas include, for example, modification of transcription factors governing the hypoxic response pathways, important in angiogenesis, cell survival, and glycolytic responses. The fundamental strategy behind that approach is that fetal lung normally develops under hypoxic conditions and that this hypoxic, growth-favoring environment is interrupted by a premature birth. Importantly, during fetal lung development, alveolar development appears to be dependent on vascular development. Therefore, enhancement of signaling factors that occur during hypoxic fetal life ('continued fetal life ex utero'), including angiogenic responses, could potentially lead to improved lung growth and thereby alleviate the alveolar and vascular hypoplasia characteristic of BPD.
Keywords
extracellular SODDMOGFlt-1pVHLG6PDHManganese SODPECAM-1DeferoxamineHREPDGFARNTγ-GTHK-IINOS-2MnSODET-1BPDCATDFOγ-GCLGSHGPXFMS-like tyrosine kinase 1EPOdimethyloxaloylglycineCuZnSODGLUT-1IGF-1ecSODaryl hydrocarbon nuclear translocatorerythropoietinendothelin 1Bronchopulmonary dysplasiaFIHfactor inhibiting HIFhypoxia response elementplatelet derived growth factorinsulin-like growth factor 1platelet endothelial cell adhesion molecule 1nitric oxide synthase 2heme oxygenasehexokinase IICatalaseGamma glutamyl transpeptidaseGlutathioneglutathione reductaseglutathione peroxidaseglucose transporter 1glucose 6-phosphate dehydrogenase
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Authors
Tiina M. Asikainen, Carl W. White,