LIVIVO - The Search Portal for Life Sciences

zur deutschen Oberfläche wechseln
Advanced search

Search results

Result 1 - 10 of total 83

Search options

  1. Article ; Online: Agonistic and potentiating effects of perfluoroalkyl substances (PFAS) on the Atlantic cod (Gadus morhua) peroxisome proliferator-activated receptors (Ppars).

    Søderstrøm, Sofie / Lille-Langøy, Roger / Yadetie, Fekadu / Rauch, Mateusz / Milinski, Ana / Dejaegere, Annick / Stote, Roland H / Goksøyr, Anders / Karlsen, Odd André

    Environment international

    2022  Volume 163, Page(s) 107203

    Abstract: Toxicity mediated by per- and polyfluoroalkyl substances (PFAS), and especially perfluoroalkyl acids (PFAAs), has been linked to activation of peroxisome proliferator-activated receptors (Ppar) in many vertebrates. Here, we present the primary structures, ...

    Abstract Toxicity mediated by per- and polyfluoroalkyl substances (PFAS), and especially perfluoroalkyl acids (PFAAs), has been linked to activation of peroxisome proliferator-activated receptors (Ppar) in many vertebrates. Here, we present the primary structures, phylogeny, and tissue-specific distributions of the Atlantic cod (Gadus morhua) gmPpara1, gmPpara2, gmPparb, and gmPparg, and demonstrate that the carboxylic acids PFHxA, PFOA, PFNA, as well as the sulfonic acid PFHxS, activate gmPpara1 in vitro, which was also supported by in silico analyses. Intriguingly, a binary mixture of PFOA and the non-activating PFOS produced a higher activation of gmPpara1 compared to PFOA alone, suggesting that PFOS has a potentiating effect on receptor activation. Supporting the experimental data, docking and molecular dynamics simulations of single and double-ligand complexes led to the identification of a putative allosteric binding site, which upon binding of PFOS stabilizes an active conformation of gmPpara1. Notably, binary exposures of gmPpara1, gmPpara2, and gmPparb to model-agonists and PFAAs produced similar potentiating effects. This study provides novel mechanistic insights into how PFAAs may modulate the Ppar signaling pathway by either binding the canonical ligand-binding pocket or by interacting with an allosteric binding site. Thus, individual PFAAs, or mixtures, could potentially modulate the Ppar-signaling pathway in Atlantic cod by interfering with at least one gmPpar subtype.
    MeSH term(s) Alkanesulfonic Acids/toxicity ; Animals ; Environmental Pollutants ; Fluorocarbons/analysis ; Gadus morhua ; Gonadal Steroid Hormones ; Ligands ; Peroxisome Proliferator-Activated Receptors
    Chemical Substances Alkanesulfonic Acids ; Environmental Pollutants ; Fluorocarbons ; Gonadal Steroid Hormones ; Ligands ; Peroxisome Proliferator-Activated Receptors
    Language English
    Publishing date 2022-03-29
    Publishing country Netherlands
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 554791-x
    ISSN 1873-6750 ; 0160-4120
    ISSN (online) 1873-6750
    ISSN 0160-4120
    DOI 10.1016/j.envint.2022.107203
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  2. Article: Polycyclic aromatic hydrocarbons modulate the activity of Atlantic cod (Gadus morhua) vitamin D receptor paralogs in vitro

    Goksøyr, S. Ø. / Goldstone, J. / Lille-Langøy, R. / Lock, E.-J. / Olsvik, P. A. / Goksøyr, A. / Karlsen, O. A.

    Aquatic toxicology

    2021  Volume 238, Issue -, Page(s) 105914

    Language English
    Document type Article
    ZDB-ID 782699-0
    ISSN 0166-445x
    Database Current Contents Nutrition, Environment, Agriculture

    More links

    Kategorien

  3. Article: Substituted Two- to Five-Ring Polycyclic Aromatic Compounds Are Potent Agonists of Atlantic Cod (Gadus morhua) Aryl Hydrocarbon Receptors Ahr1a and Ahr2a

    Lille-Langøy, Roger / Jørgensen, Kåre Bredeli / Goksøyr, Anders / Pampanin, Daniela M. / Sydnes, Magne O. / Karlsen, Odd André

    Environmental science & technology. 2021 Nov. 05, v. 55, no. 22

    2021  

    Abstract: Polycyclic aromatic hydrocarbons (PAHs) are among the most toxic and bioavailable components found in petroleum and represent a high risk to aquatic organisms. The aryl hydrocarbon receptor (Ahr) is a ligand-activated transcription factor that mediates ... ...

    Abstract Polycyclic aromatic hydrocarbons (PAHs) are among the most toxic and bioavailable components found in petroleum and represent a high risk to aquatic organisms. The aryl hydrocarbon receptor (Ahr) is a ligand-activated transcription factor that mediates the toxicity of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) and other planar aromatic hydrocarbons, including certain PAHs. Ahr acts as a xenosensor and modulates the transcription of biotransformation genes in vertebrates, such as cytochrome P450 1A (cyp1a). Atlantic cod (Gadus morhua) possesses two Ahr proteins, Ahr1a and Ahr2a, which diverge in their primary structure, tissue-specific expression, ligand affinities, and transactivation profiles. Here, a luciferase reporter gene assay was used to assess the sensitivity of the Atlantic cod Ahrs to 31 polycyclic aromatic compounds (PACs), including two- to five-ring native PAHs, a sulfur-containing heterocyclic PAC, as well as several methylated, methoxylated, and hydroxylated congeners. Notably, most parent compounds, including naphthalene, phenanthrene, and partly, chrysene, did not act as agonists for the Ahrs, while hydroxylated and/or alkylated versions of these PAHs were potent agonists. Importantly, the greater potencies of substituted PAH derivatives and their ubiquitous occurrence in nature emphasize that more knowledge on the toxicity of these environmentally and toxicologically relevant compounds is imperative.
    Keywords Gadus morhua ; aryl hydrocarbon receptors ; bioavailability ; biotransformation ; cytochrome P-450 ; environmental science ; hydroxylation ; ligands ; luciferase ; methylation ; naphthalene ; petroleum ; phenanthrenes ; reporter genes ; risk ; technology ; tetrachlorodibenzo-p-dioxin ; toxicity ; transcriptional activation
    Language English
    Dates of publication 2021-1105
    Size p. 15123-15135.
    Publishing place American Chemical Society
    Document type Article
    ISSN 1520-5851
    DOI 10.1021/acs.est.1c02946
    Database NAL-Catalogue (AGRICOLA)

    More links

    Kategorien

  4. Article ; Online: Polycyclic aromatic hydrocarbons modulate the activity of Atlantic cod (Gadus morhua) vitamin D receptor paralogs in vitro.

    Goksøyr, Siri Øfsthus / Goldstone, Jed / Lille-Langøy, Roger / Lock, Erik-Jan / Olsvik, Pål A / Goksøyr, Anders / Karlsen, Odd André

    Aquatic toxicology (Amsterdam, Netherlands)

    2021  Volume 238, Page(s) 105914

    Abstract: Vitamin D receptor (VDR) mediates the biological function of the steroid hormone calcitriol, which is the metabolically active version of vitamin D. Calcitriol is important for a wide array of physiological functions, including calcium and phosphate ... ...

    Abstract Vitamin D receptor (VDR) mediates the biological function of the steroid hormone calcitriol, which is the metabolically active version of vitamin D. Calcitriol is important for a wide array of physiological functions, including calcium and phosphate homeostasis. In contrast to mammals, which harbor one VDR encoding gene, teleosts possess two orthologous vdr genes encoding Vdr alpha (Vdra) and Vdr beta (Vdrb). Genome mining identified the vdra and vdrb paralogs in the Atlantic cod (Gadus morhua) genome, which were further characterized regarding their phylogeny, tissue-specific expression, and transactivational properties induced by calcitriol. In addition, a selected set of polycyclic aromatic hydrocarbons (PAHs), including naphthalene, phenanthrene, fluorene, pyrene, chrysene, benzo[a]pyrene (BaP), and 7-methylbenzo[a]pyrene, were assessed for their ability to modulate the transcriptional activity of gmVdra and gmVdrb in vitro. Both gmVdra and gmVdrb were activated by calcitriol with similar potencies, but gmVdra produced significantly higher maximal fold activation. Notably, none of the tested PAHs showed agonistic properties towards the Atlantic cod Vdrs. However, binary exposures of calcitriol together with phenanthrene, fluorene, or pyrene, antagonized the activation of gmVdra, while chrysene and BaP significantly potentiated the calcitriol-mediated activity of both receptors. Homology modeling, solvent mapping, and docking analyses complemented the experimental data, and revealed a putative secondary binding site in addition to the canonical ligand-binding pocket (LBP). Calcitriol was predicted to interact with both binding sites, whereas PAHs docked primarily to the LBP. Importantly, our in vitro data suggest that PAHs can interact with the paralogous gmVdrs and interfere with their transcriptional activities, and thus potentially modulate the vitamin D signaling pathway and contribute to adverse effects of crude oil and PAH exposures on cardiac development and bone deformities in fish.
    Language English
    Publishing date 2021-07-16
    Publishing country Netherlands
    Document type Journal Article
    ZDB-ID 782699-0
    ISSN 1879-1514 ; 0166-445X
    ISSN (online) 1879-1514
    ISSN 0166-445X
    DOI 10.1016/j.aquatox.2021.105914
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  5. Article: Xenobiotic metabolism and its physiological consequences in high-Antarctic Notothenioid fishes.

    Strobel, Anneli / Lille-Langøy, Roger / Segner, Helmut / Burkhardt-Holm, Patricia / Goksøyr, Anders / Karlsen, Odd André

    Polar biology

    2021  Volume 45, Issue 2, Page(s) 345–358

    Abstract: The Antarctic ecosystem is progressively exposed to anthropogenic contaminants, such as polycyclic aromatic hydrocarbons (PAHs). So far, it is largely unknown if PAHs leave a mark in the physiology of high-Antarctic fish. We approached this issue via two ...

    Abstract The Antarctic ecosystem is progressively exposed to anthropogenic contaminants, such as polycyclic aromatic hydrocarbons (PAHs). So far, it is largely unknown if PAHs leave a mark in the physiology of high-Antarctic fish. We approached this issue via two avenues: first, we examined the functional response of the aryl hydrocarbon receptor (Ahr), which is a molecular initiating event of many toxic effects of PAHs in biota.
    Supplementary information: The online version contains supplementary material available at 10.1007/s00300-021-02992-4.
    Language English
    Publishing date 2021-12-26
    Publishing country Germany
    Document type Journal Article
    ZDB-ID 1478942-5
    ISSN 1432-2056 ; 0722-4060
    ISSN (online) 1432-2056
    ISSN 0722-4060
    DOI 10.1007/s00300-021-02992-4
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  6. Article ; Online: Substituted Two- to Five-Ring Polycyclic Aromatic Compounds Are Potent Agonists of Atlantic Cod (

    Lille-Langøy, Roger / Jørgensen, Kåre Bredeli / Goksøyr, Anders / Pampanin, Daniela M / Sydnes, Magne O / Karlsen, Odd André

    Environmental science & technology

    2021  Volume 55, Issue 22, Page(s) 15123–15135

    Abstract: Polycyclic aromatic hydrocarbons (PAHs) are among the most toxic and bioavailable components found in petroleum and represent a high risk to aquatic organisms. The aryl hydrocarbon receptor (Ahr) is a ligand-activated transcription factor that mediates ... ...

    Abstract Polycyclic aromatic hydrocarbons (PAHs) are among the most toxic and bioavailable components found in petroleum and represent a high risk to aquatic organisms. The aryl hydrocarbon receptor (Ahr) is a ligand-activated transcription factor that mediates the toxicity of 2,3,7,8-tetrachlorodibenzo-
    MeSH term(s) Animals ; Gadus morhua ; Polychlorinated Dibenzodioxins ; Polycyclic Aromatic Hydrocarbons/toxicity ; Polycyclic Compounds ; Receptors, Aryl Hydrocarbon/genetics
    Chemical Substances Polychlorinated Dibenzodioxins ; Polycyclic Aromatic Hydrocarbons ; Polycyclic Compounds ; Receptors, Aryl Hydrocarbon
    Language English
    Publishing date 2021-11-05
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ISSN 1520-5851
    ISSN (online) 1520-5851
    DOI 10.1021/acs.est.1c02946
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  7. Article ; Online: Environmental Pollutants Modulate Transcriptional Activity of Nuclear Receptors of Whales

    Lühmann, Katharina / Lille-Langøy, Roger / Øygarden, Lene / Kovacs, Kit M / Lydersen, Christian / Goksøyr, Anders / Routti, Heli

    Environmental science & technology

    2020  Volume 54, Issue 9, Page(s) 5629–5639

    Abstract: This study reports the transcriptional activity of fin ( ...

    Abstract This study reports the transcriptional activity of fin (
    MeSH term(s) Animals ; Environmental Pollutants/analysis ; Fin Whale ; Humans ; Polychlorinated Biphenyls/analysis ; Receptors, Cytoplasmic and Nuclear ; Water Pollutants, Chemical/analysis
    Chemical Substances Environmental Pollutants ; Receptors, Cytoplasmic and Nuclear ; Water Pollutants, Chemical ; Polychlorinated Biphenyls (DFC2HB4I0K)
    Language English
    Publishing date 2020-04-13
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ISSN 1520-5851
    ISSN (online) 1520-5851
    DOI 10.1021/acs.est.9b06952
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  8. Article ; Online: Environmental contaminants modulate the transcriptional activity of polar bear (Ursus maritimus) and human peroxisome proliferator-activated receptor alpha (PPARA).

    Routti, Heli / Berg, Mari K / Lille-Langøy, Roger / Øygarden, Lene / Harju, Mikael / Dietz, Rune / Sonne, Christian / Goksøyr, Anders

    Scientific reports

    2019  Volume 9, Issue 1, Page(s) 6918

    Abstract: Peroxisome proliferator-activated receptor alfa (PPARA/NR1C1) is a ligand activated nuclear receptor that is a key regulator of lipid metabolism in tissues with high fatty acid catabolism such as the liver. Here, we cloned PPARA from polar bear liver ... ...

    Abstract Peroxisome proliferator-activated receptor alfa (PPARA/NR1C1) is a ligand activated nuclear receptor that is a key regulator of lipid metabolism in tissues with high fatty acid catabolism such as the liver. Here, we cloned PPARA from polar bear liver tissue and studied in vitro transactivation of polar bear and human PPARA by environmental contaminants using a luciferase reporter assay. Six hinge and ligand-binding domain amino acids have been substituted in polar bear PPARA compared to human PPARA. Perfluorocarboxylic acids (PFCA) and perfluorosulfonic acids induced the transcriptional activity of both human and polar bear PPARA. The most abundant PFCA in polar bear tissue, perfluorononanoate, increased polar bear PPARA-mediated luciferase activity to a level comparable to that of the potent PPARA agonist WY-14643 (~8-fold, 25 μM). Several brominated flame retardants were weak agonists of human and polar bear PPARA. While single exposures to polychlorinated biphenyls did not, or only slightly, increase the transcriptional activity of PPARA, a technical mixture of PCBs (Aroclor 1254) strongly induced the transcriptional activity of human (~8-fold) and polar bear PPARA (~22-fold). Polar bear PPARA was both quantitatively and qualitatively more susceptible than human PPARA to transactivation by less lipophilic compounds.
    MeSH term(s) Amino Acid Sequence ; Animals ; COS Cells ; Chlorocebus aethiops ; Environmental Pollutants/toxicity ; Evolution, Molecular ; Humans ; Models, Molecular ; PPAR alpha/chemistry ; PPAR alpha/genetics ; Polychlorinated Biphenyls/toxicity ; Protein Conformation ; Sequence Alignment ; Species Specificity ; Transcription, Genetic/drug effects ; Ursidae
    Chemical Substances Environmental Pollutants ; PPAR alpha ; Polychlorinated Biphenyls (DFC2HB4I0K)
    Language English
    Publishing date 2019-05-06
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2615211-3
    ISSN 2045-2322 ; 2045-2322
    ISSN (online) 2045-2322
    ISSN 2045-2322
    DOI 10.1038/s41598-019-43337-w
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  9. Article: Proteomics and lipidomics analyses reveal modulation of lipid metabolism by perfluoroalkyl substances in liver of Atlantic cod (Gadus morhua)

    Dale, K. / Yadetie, F. / Müller, M. B. / Pampanin, M. D. / Gilabert, A. / Zhang, X. / Tairova, Z. / Haarr, A. / Lille-Langøy, R. / Lyche, J. L. / Porte, C. / Karlsen, O. A. / Goksøyr, A.

    Aquatic toxicology

    2020  Volume 227, Issue -, Page(s) 105590

    Language English
    Document type Article
    ZDB-ID 782699-0
    ISSN 0166-445x
    Database Current Contents Nutrition, Environment, Agriculture

    More links

    Kategorien

  10. Article ; Online: Molecular and Functional Properties of the Atlantic Cod (

    Aranguren-Abadía, Libe / Lille-Langøy, Roger / Madsen, Alexander K / Karchner, Sibel I / Franks, Diana G / Yadetie, Fekadu / Hahn, Mark E / Goksøyr, Anders / Karlsen, Odd André

    Environmental science & technology

    2020  Volume 54, Issue 2, Page(s) 1033–1044

    Abstract: The aryl hydrocarbon receptor (Ahr) is a ligand-activated transcription factor that mediates the toxicity of halogenated and polycyclic aromatic hydrocarbons in vertebrates. Atlantic cod ( ...

    Abstract The aryl hydrocarbon receptor (Ahr) is a ligand-activated transcription factor that mediates the toxicity of halogenated and polycyclic aromatic hydrocarbons in vertebrates. Atlantic cod (
    MeSH term(s) Animals ; Gadus morhua ; Phylogeny ; Polychlorinated Dibenzodioxins ; Polycyclic Aromatic Hydrocarbons ; Receptors, Aryl Hydrocarbon
    Chemical Substances Polychlorinated Dibenzodioxins ; Polycyclic Aromatic Hydrocarbons ; Receptors, Aryl Hydrocarbon
    Language English
    Publishing date 2020-01-03
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Research Support, U.S. Gov't, Non-P.H.S.
    ISSN 1520-5851
    ISSN (online) 1520-5851
    DOI 10.1021/acs.est.9b05312
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

To top