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Environmental toxicology and chemistry2014; 33(9); 2062-2069; doi: 10.1002/etc.2656

Identification of interspecific differences in phase II reactions: determination of metabolites in the urine of 16 mammalian species exposed to environmental pyrene.

Abstract: Interspecific differences in xenobiotic metabolism are a key to determining relative sensitivities of animals to xenobiotics. However, information on domesticated livestock, companion animals, and captive and free-ranging wildlife is incomplete. The present study evaluated interspecific differences in phase II conjugation using pyrene as a nondestructive biomarker of polycyclic aromatic hydrocarbon (PAH) exposure. Polycyclic aromatic hydrocarbons and their metabolites have carcinogenic and endocrine-disrupting effects in humans and wildlife and can have serious consequences. The authors collected urine from 16 mammalian species and analyzed pyrene metabolites. Interspecific differences in urinary pyrene metabolites, especially in the concentration and composition of phase II conjugated metabolites, were apparent. Glucuronide conjugates are dominant metabolites in the urine of many species, including deer, cattle, pigs, horses, and humans. However, they could not be detected in ferret urine even though the gene for ferret Uridine 5'-diphospho-glucuronosyltransferase (UDP-glucuronosyltransferase, UGT) 1A6 is not a pseudogene. Sulfate conjugates were detected mainly in the urine of cats, ferrets, and rabbits. Interestingly, sulfate conjugates were detected in pig urine. Although pigs are known to have limited aryl sulfotransferase activity, the present study demonstrated that pig liver was active in 1-hydroxypyrene sulfation. The findings have some application for biomonitoring environmental pollution.
Publication Date: 2014-07-30 PubMed ID: 24899081DOI: 10.1002/etc.2656Google Scholar: Lookup
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

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The research investigates how different mammal species metabolize pyrene, a potentially harmful environmental compound. This study identified certain species-specific metabolic patterns, with implications for monitoring environmental pollution.

Objective of the research

  • This research aimed to identify the interspecific metabolic differences across 16 mammal species in their response to the environmental pollutant, pyrene. Pyrene is a polycyclic aromatic hydrocarbon (PAH) with potential for carcinogenic and endocrine-disruptive effects, necessitating the study of its metabolism in various animals, including livestock, pets, and wildlife.

Methods

  • The authors collected urine samples from a variety of mammals, including deer, cattle, pigs, horses, humans, cats, ferrets, and rabbits. The urine was analyzed for metabolites of pyrene, particularly focusing on phase II conjugated metabolites to show how different species metabolize the compound.

Key Findings

  • Significant interspecies differences were identified in the concentration and composition of urinary pyrene metabolites.
  • Glucuronide conjugates were the dominant metabolites found in many species, such as deer, cattle, pigs, horses, and humans – indicating that these species metabolize pyrene in a similar manner.
  • Contrarily, glucuronide conjugates were not present in ferret urine, which was surprising given that the gene responsible for this metabolic pathway in ferrets (UGT 1A6) is not a pseudogene.
  • The urine of cats, ferrets, and rabbits primarily contained sulfate conjugates, suggesting they metabolize pyrene differently. Additionally, pigs, known to have limited aryl sulfotransferase activity, were found to have sulfate conjugates in their urine, showing an active capability to sulfate 1-hydroxypyrene in pig liver.

Implications

  • The observed interspecific differences in the metabolism of an environmental pollutant has implications for assessing species-specific sensitivities and responses to xenobiotics or foreign substances in the body.
  • The research carries significant potential for biomonitoring environmental pollution, meaning that by understanding how different species metabolize pollutants, we may identify the species that are more sensitive to certain pollutants, and better design and monitor interventions.

Cite This Article

APA
Saengtienchai A, Ikenaka Y, Nakayama SM, Mizukawa H, Kakehi M, Bortey-Sam N, Darwish WS, Tsubota T, Terasaki M, Poapolathep A, Ishizuka M. (2014). Identification of interspecific differences in phase II reactions: determination of metabolites in the urine of 16 mammalian species exposed to environmental pyrene. Environ Toxicol Chem, 33(9), 2062-2069. https://doi.org/10.1002/etc.2656

Publication

ISSN: 1552-8618
NlmUniqueID: 8308958
Country: United States
Language: English
Volume: 33
Issue: 9
Pages: 2062-2069

Researcher Affiliations

Saengtienchai, Aksorn
  • Laboratory of Toxicology, Department of Environmental Veterinary Science, Graduate, School of Veterinary Medicine, Hokkaido University, Sapporo, Japan; Department of Pharmacology, Faculty of Veterinary Medicine, Kasetsart University, Bangkok, Thailand.
Ikenaka, Yoshinori
    Nakayama, Shouta M M
      Mizukawa, Hazuki
        Kakehi, Mayu
          Bortey-Sam, Nesta
            Darwish, Wageh Sobhy
              Tsubota, Toshio
                Terasaki, Masanori
                  Poapolathep, Amnart
                    Ishizuka, Mayumi

                      MeSH Terms

                      • Animals
                      • Carcinogens / metabolism
                      • Cats
                      • Cattle
                      • Endocrine Disruptors / metabolism
                      • Environmental Monitoring
                      • Horses
                      • Humans
                      • Mammals / metabolism
                      • Mammals / urine
                      • Polycyclic Aromatic Hydrocarbons / metabolism
                      • Polycyclic Aromatic Hydrocarbons / urine
                      • Pyrenes / metabolism
                      • Pyrenes / urine
                      • Swine

                      Citations

                      This article has been cited 5 times.
                      1. Li X, Duan X, Zhang H, Ding M, Wang Y, Yang Y, Yao W, Zhou X, Wang W. Genetic polymorphisms of metabolic enzyme genes associated with leukocyte mitochondrial DNA copy number in PAHs exposure workers.. Cancer Rep (Hoboken) 2021 Aug;4(4):e1361.
                        doi: 10.1002/cnr2.1361pubmed: 33788425google scholar: lookup
                      2. Rietz Liljedahl E, Johanson G, Korres de Paula H, Faniband M, Assarsson E, Littorin M, Engfeldt M, Lidén C, Julander A, Wahlberg K, Lindh C, Broberg K. Filaggrin Polymorphisms and the Uptake of Chemicals through the Skin-A Human Experimental Study.. Environ Health Perspect 2021 Jan;129(1):17002.
                        doi: 10.1289/EHP7310pubmed: 33439052google scholar: lookup
                      3. Bortey-Sam N, Ikenaka Y, Akoto O, Nakayama SMM, Marfo JT, Saengtienchai A, Mizukawa H, Ishizuka M. Sex and site differences in urinary excretion of conjugated pyrene metabolites in the West African Shorthorn cattle.. J Vet Med Sci 2018 Mar 2;80(2):375-381.
                        doi: 10.1292/jvms.17-0410pubmed: 29279463google scholar: lookup
                      4. Jacobson GA, Raidal S, Robson K, Narkowicz CK, Nichols DS, Haydn Walters E. Bronchopulmonary pharmacokinetics of (R)-salbutamol and (S)-salbutamol enantiomers in pulmonary epithelial lining fluid and lung tissue of horses.. Br J Clin Pharmacol 2017 Jul;83(7):1436-1445.
                        doi: 10.1111/bcp.13228pubmed: 28061018google scholar: lookup
                      5. Moorthy B, Chu C, Carlin DJ. Polycyclic aromatic hydrocarbons: from metabolism to lung cancer.. Toxicol Sci 2015 May;145(1):5-15.
                        doi: 10.1093/toxsci/kfv040pubmed: 25911656google scholar: lookup