Metabolomics Analysis of Rabbit Plasma after Ocular Exposure to Vapors of Sulfur Mustard

Author:

Bouhlel Jihéne1,Caffin Fanny2ORCID,Gros-Désormeaux Fanny2ORCID,Douki Thierry3,Benoist Jean-François14ORCID,Castelli Florence A.1ORCID,Chu-Van Emeline1,Piérard Christophe2,Junot Christophe1ORCID,Fenaille François1ORCID

Affiliation:

1. CEA, INRAE, Département Médicaments et Technologies pour la Santé (DMTS), SPI, MetaboHUB-IDF, Université Paris-Saclay, 91191 Gif-sur-Yvette, France

2. Institut de Recherche Biomédicale des Armées (IRBA), 91223 Brétigny-sur-Orge, France

3. CEA, CNRS, IRIG, SyMMES, Université Grenoble Alpes, 38000 Grenoble, France

4. Biochemistry Laboratory, APHP, Hôpital Universitaire Necker Enfants Malades, 75015 Paris, France

Abstract

Sulfur mustard (SM) is a highly potent alkylating vesicant agent and remains a relevant threat to both civilians and military personnel. The eyes are the most sensitive organ after airborne SM exposure, causing ocular injuries with no antidote or specific therapeutics available. In order to identify relevant biomarkers and to obtain a deeper understanding of the underlying biochemical events, we performed an untargeted metabolomics analysis using liquid chromatography coupled to high-resolution mass spectrometry of plasma samples from New Zealand white rabbits ocularly exposed to vapors of SM. Metabolic profiles (332 unique metabolites) from SM-exposed (n = 16) and unexposed rabbits (n = 8) were compared at different time intervals from 1 to 28 days. The observed time-dependent changes in metabolic profiles highlighted the profound dysregulation of the sulfur amino acids, the phenylalanine, the tyrosine and tryptophan pathway, and the polyamine and purine biosynthesis, which could reflect antioxidant and anti-inflammatory activities. Taurine and 3,4-dihydroxy-phenylalanine (Dopa) seem to be specifically related to SM exposure and correspond well with the different phases of ocular damage, while the dysregulation of adenosine, polyamines, and acylcarnitines might be related to ocular neovascularization. Additionally, neither cysteine, N-acetylcysteine, or guanine SM adducts were detected in the plasma of exposed rabbits at any time point. Overall, our study provides an unprecedented view of the plasma metabolic changes post-SM ocular exposure, which may open up the development of potential new treatment strategies.

Publisher

MDPI AG

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