Literature DB >> 23547745

N-acetyl-L-cysteine protects against inhaled sulfur mustard poisoning in the large swine.

B Jugg1, S Fairhall, A Smith, S Rutter, T Mann, R Perrott, J Jenner, J Salguero, J Shute, A M Sciuto.   

Abstract

CONTEXT: Sulfur mustard is a blister agent that can cause death by pulmonary damage. There is currently no effective treatment. N-acetyl-L-cysteine (NAC) has mucolytic and antioxidant actions and is an important pre-cursor of cellular glutathione synthesis. These actions may have potential to reduce mustard-induced lung injury.
OBJECTIVE: Evaluate the effect of nebulised NAC as a post-exposure treatment for inhaled sulfur mustard in a large animal model.
MATERIALS AND METHODS: Fourteen anesthetized, surgically prepared pigs were exposed to sulfur mustard vapor (100 μg.kg⁻¹), 10 min) and monitored, spontaneously breathing, to 12 h. Control animals had no further intervention (n = 6). Animals in the treatment group were administered multiple inhaled doses of NAC (1 ml of 200 mg.ml⁻¹ Mucomyst™ at + 30 min, 2, 4, 6, 8, and 10 h post-exposure, n = 8). Cardiovascular and respiratory parameters were recorded. Arterial blood was collected for blood gas analysis while blood and bronchoalveolar lavage fluid were collected for hematology and inflammatory cell analysis. Urine was collected to detect a sulfur mustard breakdown product. Lung tissue samples were taken for histopathological and post-experimental analyses.
RESULTS: Five of six sulfur mustard-exposed animals survived to 12 h. Arterial blood oxygenation (PaO₂) and saturation levels were significantly decreased at 12 h. Arterial blood carbon dioxide (PaCO₂) significantly increased, and arterial blood pH and bicarbonate (HCO₃⁻) significantly decreased at 12 h. Shunt fraction was significantly increased at 12 h. In the NAC-treated group all animals survived to 12 h (n = 8). There was significantly improved arterial blood oxygen saturation, HCO₃⁻ levels, and shunt fraction compared to those of the sulfur mustard controls. There were significantly fewer neutrophils and lower concentrations of protein in lavage compared to sulfur mustard controls. DISCUSSION: NAC's mucolytic and antioxidant properties may be responsible for the beneficial effects seen, improving clinically relevant physiological indices affected by sulfur mustard exposure.
CONCLUSION: Beneficial effects of nebulized NAC were apparent following inhaled sulfur mustard exposure. Further therapeutic benefit may result from a combination therapy approach.

Entities:  

Mesh:

Substances:

Year:  2013        PMID: 23547745     DOI: 10.3109/15563650.2013.780208

Source DB:  PubMed          Journal:  Clin Toxicol (Phila)        ISSN: 1556-3650            Impact factor:   4.467


  11 in total

1.  TRPA1 and CGRP antagonists counteract vesicant-induced skin injury and inflammation.

Authors:  Satyanarayana Achanta; Narendranath Reddy Chintagari; Marian Brackmann; Shrilatha Balakrishna; Sven-Eric Jordt
Journal:  Toxicol Lett       Date:  2018-03-10       Impact factor: 4.372

2.  Airway tissue plasminogen activator prevents acute mortality due to lethal sulfur mustard inhalation.

Authors:  Livia A Veress; Dana R Anderson; Tara B Hendry-Hofer; Paul R Houin; Jacqueline S Rioux; Rhonda B Garlick; Joan E Loader; Danielle C Paradiso; Russell W Smith; Raymond C Rancourt; Wesley W Holmes; Carl W White
Journal:  Toxicol Sci       Date:  2014-10-20       Impact factor: 4.849

3.  A novel sulfur mustard (HD) vapor inhalation exposure system for accurate inhaled dose delivery.

Authors:  Mark R Perry; Eric M Benson; Jonathon W Kohne; Jennifer L Plahovinsak; Michael C Babin; Gennady E Platoff; David T Yeung
Journal:  J Pharmacol Toxicol Methods       Date:  2014-10-05       Impact factor: 1.950

Review 4.  Sulfur mustard inhalation: mechanisms of injury, alteration of coagulation, and fibrinolytic therapy.

Authors:  Carl W White; Raymond C Rancourt; Livia A Veress
Journal:  Ann N Y Acad Sci       Date:  2016-07-06       Impact factor: 5.691

5.  A novel sulfur mustard (HD) vapor inhalation exposure model of pulmonary toxicity for the efficacy evaluation of candidate medical countermeasures.

Authors:  Mark R Perry; Matthew Neal; Roger Hawks; David Pressburger; Jan Satola; Cheryl Triplett; Beth Reed; Meredith Andrews; Jill A Harvilchuck; Michael S Nealy; Gennady E Platoff; David T Yeung
Journal:  Inhal Toxicol       Date:  2021-08-15       Impact factor: 2.724

Review 6.  Emerging targets for treating sulfur mustard-induced injuries.

Authors:  Shama Ahmad; Aftab Ahmad
Journal:  Ann N Y Acad Sci       Date:  2016-06-10       Impact factor: 5.691

Review 7.  Mustard vesicant-induced lung injury: Advances in therapy.

Authors:  Barry Weinberger; Rama Malaviya; Vasanthi R Sunil; Alessandro Venosa; Diane E Heck; Jeffrey D Laskin; Debra L Laskin
Journal:  Toxicol Appl Pharmacol       Date:  2016-05-19       Impact factor: 4.219

8.  Effects of collagen-derived bioactive peptides and natural antioxidant compounds on proliferation and matrix protein synthesis by cultured normal human dermal fibroblasts.

Authors:  Suzanne Edgar; Blake Hopley; Licia Genovese; Sara Sibilla; David Laight; Janis Shute
Journal:  Sci Rep       Date:  2018-07-11       Impact factor: 4.379

Review 9.  N-Acetylcysteine as a treatment for sulphur mustard poisoning.

Authors:  Thomas W Sawyer
Journal:  Free Radic Biol Med       Date:  2020-09-25       Impact factor: 7.376

Review 10.  Friend or Foe? The Roles of Antioxidants in Acute Lung Injury.

Authors:  Yang Liu; Shujun Zhou; Du Xiang; Lingao Ju; Dexin Shen; Xinghuan Wang; Yanfeng Wang
Journal:  Antioxidants (Basel)       Date:  2021-12-07
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.