A metabolomic analysis on the toxicological effects of the universal solvent, dimethyl sulfoxide

Dimethyl sulfoxide (DMSO) is a solvent used to dissolve a variety of organic compounds. It is presumed to be non-toxic at concentrations below 1 % v/v, although several studies have demonstrated that low dose DMSO exposure can alter cellular biochemistry. This study evaluated the toxicity of DMSO at 0.0002 % v/v to the Sydney Rock oyster, Saccostrea glomerata, following 7d of exposure. Metabolites were chosen as the toxicity endpoints because they can be used as energy sources and counteract contaminant-induced stress. Relative to seawater controls, exposure to DMSO caused a 74 % significant change in metabolites in the female digestive gland, including decreases in most amino acids, carbohydrates, nicotinamides, and lipids. The female gonad showed a 43 % significant change in metabolites, with decreases in amino acids and carbohydrates, but increases in lipids. The male digestive gland showed a 29 % significant change in metabolites, with increases in lipids. The decline in metabolites in the female digestive gland, but not in the male digestive gland, may be due to their differential metabolic demands. Furthermore, pathway impact analysis revealed that DMSO exposure altered energy metabolism, disturbed osmotic balance, and induced oxidative stress in oysters. Because the effects of DMSO are not uniform across gender and tissue, use of DMSO as a solvent will confound metabolomic experimental results when comparisons among sexes and/or tissues are integral to the experimental design. There is a risk of incomplete dissolution of contaminants unless carrier solvents are used. Therefore, in practice, a solvent control along with a water control is recommended for experimentation.

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Publication Details

Journal
Comparative Biochemistry and Physiology Part C Toxicology & Pharmacology
Published
2024-11-08
DOI
https://doi.org/10.1016/j.cbpc.2024.110073
Citations
6
Primary Topic
Chemistry and Chemical Engineering
Type
article
Field-Weighted Citation Impact
1.50

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article

A metabolomic analysis on the toxicological effects of the universal solvent, dimethyl sulfoxide

Steven D. Melvin, Wayne A. O’Connor, Rafiquel Islam, Sazal Kumar et al.
6 citations
Comparative Biochemistry and Physiology Part C Toxicology & Pharmacology
Chemistry and Chemical Engineering
1.50
article

A metabolomic analysis on the toxicological effects of the universal solvent, dimethyl sulfoxide

Steven D. Melvin, Wayne A. O’Connor, Rafiquel Islam, Sazal Kumar, Frédéric D.L. Leusch, Geoff R. MacFarlane, Allison Luengen
article en
6 citations

Abstract

Dimethyl sulfoxide (DMSO) is a solvent used to dissolve a variety of organic compounds. It is presumed to be non-toxic at concentrations below 1 % v/v, although several studies have demonstrated that low dose DMSO exposure can alter cellular biochemistry. This study evaluated the toxicity of DMSO at 0.0002 % v/v to the Sydney Rock oyster, Saccostrea glomerata, following 7d of exposure. Metabolites were chosen as the toxicity endpoints because they can be used as energy sources and counteract contaminant-induced stress. Relative to seawater controls, exposure to DMSO caused a 74 % significant change in metabolites in the female digestive gland, including decreases in most amino acids, carbohydrates, nicotinamides, and lipids. The female gonad showed a 43 % significant change in metabolites, with decreases in amino acids and carbohydrates, but increases in lipids. The male digestive gland showed a 29 % significant change in metabolites, with increases in lipids. The decline in metabolites in the female digestive gland, but not in the male digestive gland, may be due to their differential metabolic demands. Furthermore, pathway impact analysis revealed that DMSO exposure altered energy metabolism, disturbed osmotic balance, and induced oxidative stress in oysters. Because the effects of DMSO are not uniform across gender and tissue, use of DMSO as a solvent will confound metabolomic experimental results when comparisons among sexes and/or tissues are integral to the experimental design. There is a risk of incomplete dissolution of contaminants unless carrier solvents are used. Therefore, in practice, a solvent control along with a water control is recommended for experimentation.

Comparative Biochemistry and Physiology Part C Toxicology & PharmacologyVol. 287
Griffith University (AU), New South Wales Department of Primary Industries (AU), University of San Francisco (US), University of Newcastle Australia (AU)
Australian Research Council
Openalex Percentile: Top 19%
Chemistry and Chemical Engineering
1.50
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