| Literature DB >> 28489470 |
Adam V Wisnewski1, Jean Kanyo2, Jennifer Asher3, James A Goodrich3, Grace Barnett3, Lyn Patrylak3, Jian Liu1, Carrie A Redlich1, Ala F Nassar1.
Abstract
1. Hexamethylenediisocyanate (HDI) is a widely used aliphatic diisocyanate and a well-recognized cause of occupational asthma. 2. "Self" molecules (peptides/proteins) in the lower airways, susceptible to chemical reactivity with HDI, have been hypothesized to play a role in asthma pathogenesis and/or chemical metabolism, but remain poorly characterized. 3. This study employed unique approaches to identify and characterize "self" targets of HDI reactivity in the lower airways. Anesthetized rabbits free breathed through a tracheostomy tube connected to chambers containing either, O2, or O2 plus ∼200 ppb HDI vapors. Following 60 minutes of exposure, the airways were lavaged and the fluid was analyzed by LC-MS and LC-MS/MS. 4. The low-molecular weight (<3 kDa) fraction of HDI exposed, but not control rabbit bronchoalveolar lavage (BAL) fluid identified 783.26 and 476.18 m/z [M+H]+ ions with high energy collision-induced dissociation (HCD) fragmentation patterns consistent with bis glutathione (GSH)-HDI and mono(GSH)-HDI. Proteomic analyses of the high molecular weight (>3 kDa) fraction of exposed rabbit BAL fluid identified HDI modification of specific lysines in uteroglobin (aka clara cell protein) and albumin. 5. In summary, this study utilized a unique approach to chemical vapor exposure in rabbits, to identify HDI reaction products with "self" molecules in the lower airways.Entities:
Keywords: Exposure; glutathione; hexamethylene diisocyanate; tracheostomy
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Year: 2017 PMID: 28489470 PMCID: PMC5863241 DOI: 10.1080/00498254.2017.1329569
Source DB: PubMed Journal: Xenobiotica ISSN: 0049-8254 Impact factor: 1.908