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A role for CFTR in the elevation of glutathione levels in the lung by oral glutathione administration
The cystic fibrosis transmembrane conductance regulator (CFTR) protein is the only known apical glutathione (GSH) transporter in the lung. The purpose of these studies was to determine whether oral GSH or glutathione disulfide (GSSG) treatment could increase lung epithelial lining fluid (ELF) GSH le...
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| Main Authors: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2007
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3983954/ https://ncbi.nlm.nih.gov/pubmed/17369290 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1152/ajplung.00365.2006 |
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