SwePub
Sök i LIBRIS databas

  Extended search

id:"swepub:oai:DiVA.org:umu-11164"
 

Search: id:"swepub:oai:DiVA.org:umu-11164" > In vitro profiling ...

  • 1 of 1
  • Previous record
  • Next record
  •    To hitlist
  • Hamers, Timo (author)

In vitro profiling of the endocrine-disrupting potency of brominated flame retardants

  • Article/chapterEnglish2006

Publisher, publication year, extent ...

  • 2006-04-06
  • Oxford University Press (OUP),2006
  • printrdacarrier

Numbers

  • LIBRIS-ID:oai:DiVA.org:umu-11164
  • https://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-11164URI
  • https://doi.org/10.1093/toxsci/kfj187DOI

Supplementary language notes

  • Language:English
  • Summary in:English

Part of subdatabase

Classification

  • Subject category:vet swepub-contenttype
  • Subject category:art swepub-publicationtype

Notes

  • Over the last few years, increasing evidence has become available that some brominated flame retardants (BFRs) may have endocrine-disrupting (ED) potencies. The goal of the current study was to perform a systematic in vitro screening of the ED potencies of BFRs (1) to elucidate possible modes of action of BFRs in man and wildlife and (2) to classify BFRs with similar profiles of ED potencies. A test set of 27 individual BFRs were selected, consisting of 19 polybrominated diphenyl ether congeners, tetrabromobisphenol-A, hexabromocyclododecane, 2,4,6-tribromophenol, ortho-hydroxylated brominated diphenyl ether 47, and tetrabromobisphenol-A–bis(2,3)dibromopropyl ether. All BFRs were tested for their potency to interact with the arylhydrocarbon receptor, androgen receptor (AR), progesterone receptor (PR), and estrogen receptor. In addition, all BFRs were tested for their potency to inhibit estradiol (sulfation by estradiol sulfotransferase (E2SULT), to interfere with thyroid hormone 3,3',5-triiodothyronine (T3)–mediated cell proliferation, and to compete with T3-precursor thyroxine for binding to the plasma transport protein transthyretin (TTR). The results of the in vitro screening indicated that BFRs have ED potencies, some of which had not or only marginally been described before (AR antagonism, PR antagonism, E2SULT inhibition, and potentiation of T3-mediated effects). For some BFRs, the potency to induce AR antagonism, E2SULT inhibition, and TTR competition was higher than for natural ligands or clinical drugs used as positive controls. Based on their similarity in ED profiles, BFRs were classified into five different clusters. These findings support further investigation of the potential ED effects of these environmentally relevant BFRs in man and wildlife.

Subject headings and genre

  • toxicity profiling
  • brominated flame retardants
  • endocrine disruption
  • hierarchical cluster analysis
  • principal component analysis

Added entries (persons, corporate bodies, meetings, titles ...)

  • Kamstra, Jorke H. (author)
  • Sonneveld, Edwin (author)
  • Murk, Albertinka J. (author)
  • Kester, Monique H. A. (author)
  • Andersson, Patrik L.Umeå universitet,Kemiska institutionen (author)
  • Legler, Juliette (author)
  • Brouwer, Abraham (author)
  • Umeå universitetKemiska institutionen (creator_code:org_t)

Related titles

  • In:Toxicological Sciences: Oxford University Press (OUP)92:1, s. 157-731096-60801096-0929

Internet link

Find in a library

To the university's database

  • 1 of 1
  • Previous record
  • Next record
  •    To hitlist

Kungliga biblioteket hanterar dina personuppgifter i enlighet med EU:s dataskyddsförordning (2018), GDPR. Läs mer om hur det funkar här.
Så här hanterar KB dina uppgifter vid användning av denna tjänst.

 
pil uppåt Close

Copy and save the link in order to return to this view