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Assessment of agonistic and antagonistic properties of widely used oral care antimicrobial substances toward steroid estrogenic and androgenic receptors

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388971%3A_____%2F19%3A00504291" target="_blank" >RIV/61388971:_____/19:00504291 - isvavai.cz</a>

  • Alternative codes found

    RIV/00216208:11310/19:10395523

  • Result on the web

    <a href="https://www.sciencedirect.com/science/article/pii/S0045653518321039?via%3Dihub" target="_blank" >https://www.sciencedirect.com/science/article/pii/S0045653518321039?via%3Dihub</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.chemosphere.2018.11.006" target="_blank" >10.1016/j.chemosphere.2018.11.006</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Assessment of agonistic and antagonistic properties of widely used oral care antimicrobial substances toward steroid estrogenic and androgenic receptors

  • Original language description

    Personal care product consumption has increased in the last decades. A typical representative ingredient, i.e., triclosan, was identified in the scientific literature as an endocrine disruptor, and its use is restricted in several applications. Oral hygiene formulations contain various compounds, including synthetic phenol derivatives, quaternary ammonium compounds (QAC5), various amides and amines, or natural essential oils containing terpenes. The aim of this paper was to explore possible endocrine-disrupting effects of these most-used compounds. For this purpose, two different assays based on recombinant yeast (BMAEREluc/ER alpha, BMAEREIuc/AR) and human cell lines (T47D, AIZ-AR) were employed to investigate the agonistic and antagonistic properties of these compounds on human estrogen and androgen receptors. The results showed that none of the compounds were indicated as agonists of the steroid receptors. However, octenidine (00', QAC-like) and hexadecylpyridinium (HOP, QAC) were able to completely inhibit both androgenic (IC50 OCT = 0.84 mu M, IC50 HDP = 1.66 mu M) and estrogenic (IC50 OCT = 0.50 mu M, IC50 HDP = 1.64 mu M) signaling pathways in a dose-dependent manner. Additionally, chlorhexidine was found to inhibit the 17 beta-estradiol response, with a similar IC50 (2.9 mu M). In contrast, the natural terpenes thymol and menthol were found to be competitive antagonists of the receptors, however, their IC50 values were higher (by orders of magnitude). We tried to estimate the risk associated with the presence of these compounds in environmental matrices by calculating hazard quotients (HQs), and the calculated HQs were found to be close to or greater than 1 only when predicted environmental concentrations were used for surface waters.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    30108 - Toxicology

Result continuities

  • Project

    <a href="/en/project/GJ17-15678Y" target="_blank" >GJ17-15678Y: Potential of microorganisms to biodegrade antimicrobial compounds</a><br>

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2019

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Chemosphere

  • ISSN

    0045-6535

  • e-ISSN

  • Volume of the periodical

    217

  • Issue of the periodical within the volume

    FEB 2019

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    8

  • Pages from-to

    534-541

  • UT code for WoS article

    000456223500058

  • EID of the result in the Scopus database

    2-s2.0-85057193460