Salivary leucocytes as suitable biomatrix for the comet assay in human biomonitoring studies.


Journal

Archives of toxicology
ISSN: 1432-0738
Titre abrégé: Arch Toxicol
Pays: Germany
ID NLM: 0417615

Informations de publication

Date de publication:
06 2021
Historique:
received: 23 02 2021
accepted: 25 03 2021
pubmed: 1 4 2021
medline: 8 1 2022
entrez: 31 3 2021
Statut: ppublish

Résumé

Peripheral blood leucocytes (PBL) have been traditionally used to investigate DNA damage by the comet assay in population studies, but validating alternative non-invasive samples would expand the application of this assay in human biomonitoring. The objectives of this study were (i) to test the validity of salivary leucocytes as a proper biomatrix for the comet assay, (ii) to evaluate the ability of this approach to detect different types of primary and oxidative DNA damage, and (iii) to determine whether frozen salivary leucocytes are still suitable for displaying those types of DNA damage. Fresh and frozen leucocytes isolated from saliva samples (six healthy non-smoking volunteers), were exposed to four genotoxic agents inducing different types of DNA damage, both primary (methyl methanesulfonate, actinomycin-D, ultraviolet radiation) and oxidative (potassium bromate), and standard or enzyme-modified comet assay was conducted. Results were compared with those obtained from PBL. Cells exposed to the four genotoxic agents showed dose-dependent increases of primary and oxidative DNA damage, demonstrating the suitability of all these samples to detect genetic damage from different origin. When comparing baseline levels of DNA damage, just a slight significant increase in primary DNA damage was observed in frozen salivary leucocytes regarding the other biomatrices, but similar results were obtained regarding sensitivity to DNA damage induction by all agents tested. This study demonstrates that salivary leucocytes can be employed in comet assay as an alternative or complement to blood samples. Frozen salivary leucocytes were proved to be a very convenient sample in large biomonitoring studies.

Identifiants

pubmed: 33787950
doi: 10.1007/s00204-021-03038-8
pii: 10.1007/s00204-021-03038-8
pmc: PMC8009925
doi:

Types de publication

Comparative Study Journal Article Research Support, Non-U.S. Gov't Validation Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

2179-2187

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Auteurs

Natalia Fernández-Bertólez (N)

Centro de Investigaciones Científicas Avanzadas (CICA), Departamento de Psicología, Facultad de Ciencias de la Educación, Universidade da Coruña, Grupo DICOMOSA, Campus Elviña s/n, 15071, A Coruña, Spain.
Instituto de Investigación Biomédica de A Coruña (INIBIC), AE CICA-INIBIC, Oza, 15071, A Coruña, Spain.

Amaya Azqueta (A)

Department of Pharmacology and Toxicology, University of Navarra, c/ Irunlarrea 1, 31009, Pamplona, Spain.
IdiSNA, Navarra Institute for Health Research, Pamplona, Spain.

Eduardo Pásaro (E)

Centro de Investigaciones Científicas Avanzadas (CICA), Departamento de Psicología, Facultad de Ciencias de la Educación, Universidade da Coruña, Grupo DICOMOSA, Campus Elviña s/n, 15071, A Coruña, Spain.
Instituto de Investigación Biomédica de A Coruña (INIBIC), AE CICA-INIBIC, Oza, 15071, A Coruña, Spain.

Blanca Laffon (B)

Centro de Investigaciones Científicas Avanzadas (CICA), Departamento de Psicología, Facultad de Ciencias de la Educación, Universidade da Coruña, Grupo DICOMOSA, Campus Elviña s/n, 15071, A Coruña, Spain. blaffon@udc.es.
Instituto de Investigación Biomédica de A Coruña (INIBIC), AE CICA-INIBIC, Oza, 15071, A Coruña, Spain. blaffon@udc.es.

Vanessa Valdiglesias (V)

Instituto de Investigación Biomédica de A Coruña (INIBIC), AE CICA-INIBIC, Oza, 15071, A Coruña, Spain.
Centro de Investigaciones Científicas Avanzadas (CICA), Departamento de Biología, Facultad de Ciencias, Universidade da Coruña, Grupo DICOMOSA, Campus A Zapateira s/n, 15071, A Coruña, Spain.

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