Elevated airway GSH resynthesis confers protection to Clara cells from naphthalene injury in mice made tolerant by repeated exposures

Citation
Jaa. West et al., Elevated airway GSH resynthesis confers protection to Clara cells from naphthalene injury in mice made tolerant by repeated exposures, J PHARM EXP, 294(2), 2000, pp. 516-523
Citations number
27
Categorie Soggetti
Pharmacology & Toxicology
Journal title
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS
ISSN journal
00223565 → ACNP
Volume
294
Issue
2
Year of publication
2000
Pages
516 - 523
Database
ISI
SICI code
0022-3565(200008)294:2<516:EAGRCP>2.0.ZU;2-P
Abstract
Repeated exposures to Clara cell cytotoxicants, such as naphthalene (NA), r ender target cell populations resistant to further acute injury. Previous s tudies suggest that alterations in bioactivation enzymes in target sites (b ronchioles) of tolerant mice are insufficient to account for the marked red uction in susceptibility. Mice were made tolerant by seven daily injections of NA. GSH in the terminal airways was 2.7-fold greater in tolerant mice t han in vehicle controls and a NA (300 mg/kg) challenge dose did not produce injury. Tolerant mice, allowed to recuperate for 96 h after the seventh NA injection, were again susceptible to NA injury, and terminal airway GSH le vels had declined to control levels. To determine whether alterations in GS H resynthesis account for tolerance, the activity of gamma-glutamylcysteine synthetase (gamma-GCS) was measured or mice were treated with a combinatio n of buthionine sulfoximine (BSO), a gamma-GCS inhibitor, and NA. gamma-GCS activity was elevated in resistant airways of tolerant mice. Tolerant mice treated with both BSO and NA appeared as susceptible to injury as NA-chall enged controls. We conclude that GSH is critical for Clara cell resistance to NA injury in tolerant mice because: 1) GSH levels in target airways from NA-tolerant animals are elevated; 2) after a 96-h recuperation period, tol erant mice had lower GSH levels and are again susceptible to NA injury; 3) alterations in the activity of gamma-GCS correspond with changes in suscept ibility to NA injury; and 4) inhibition of gamma-GCS with BSO increases sus ceptibility to NA injury in tolerant mice.