Literature DB >> 18402468

Xenobiotic geometry and media pH determine cytotoxicity through solubility.

Gregor Luthe1, Regine Garcia Boy, James Jacobus, Bryan J Smith, Asif Rahaman, Larry W Robertson, Gabriele Ludewig.   

Abstract

Polychlorinated biphenyls (PCBs), a class of 209 individual congeners, have become persistent and ubiquitous environmental contaminants. The health impacts of PCBs, such as cancer, cardiovascular disease, developmental toxicity, and neurotoxicity, have been widely reported, but for many of these, the mechanisms of toxicity are still poorly understood. Many mechanistic studies involve cultured cells where the biological activity is dependent upon the solubility of the xenobiotic. In the present study, we investigated the factors that determine solubility as measured by diffraction spectroscopy and have modeled, with semiempirical and ab initio molecular orbital methods, the dihedral angle and calculated the dipole moment of a series of monofluorinated analogues (F-PCBs 3) of 4-chlorobiphenyl (PCB 3) as model compounds in vacuum and in water. We found a strong positive correlation between the dihedral angle, the rotation energy, the cavitation energy, the solubility, and the cytotoxicity in three human cell lines. The dipole moment was of minor influence. We also determined the influence of pH changes in a medium containing 10% fetal bovine serum (FBS), changes that could be expected when cells in culture are removed from a CO 2 incubator even for a short time. We found that the solubility is strongly affected by the pH and that this effect is not reversed by subsequent pH readjustment. In a study examining cytotoxicity, we showed that the actual pH and the pH history of a medium containing FBS were of major influence. We suggest that pH-driven changes in the tertiary and quaternary structure of albumin are responsible. These observations have implications for studies of the biological activity of semisoluble compounds, like PCBs and related compounds.

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Year:  2008        PMID: 18402468     DOI: 10.1021/tx700214p

Source DB:  PubMed          Journal:  Chem Res Toxicol        ISSN: 0893-228X            Impact factor:   3.739


  4 in total

1.  Polyploidy-induction by dihydroxylated monochlorobiphenyls: structure-activity-relationships.

Authors:  Susanne Flor; Gabriele Ludewig
Journal:  Environ Int       Date:  2010-05-14       Impact factor: 9.621

2.  Observation of an unusual electronically distorted semiquinone radical of PCB metabolites in the active site of prostaglandin H synthase-2.

Authors:  Orarat Wangpradit; Edelmiro Moman; Kevin B Nolan; Garry R Buettner; Larry W Robertson; Gregor Luthe
Journal:  Chemosphere       Date:  2010-09-16       Impact factor: 7.086

3.  Mechanistic insights into the specificity of human cytosolic sulfotransferase 2A1 (hSULT2A1) for hydroxylated polychlorinated biphenyls through the use of fluoro-tagged probes.

Authors:  E J Ekuase; T J van 't Erve; A Rahaman; L W Robertson; M W Duffel; G Luthe
Journal:  Environ Sci Pollut Res Int       Date:  2015-07-14       Impact factor: 4.223

4.  Oxidation of 4-chlorobiphenyl metabolites to electrophilic species by prostaglandin H synthase.

Authors:  Orarat Wangpradit; Lynn M Teesch; S V Santhana Mariappan; Michael W Duffel; Karin Norstrom; Larry W Robertson; Gregor Luthe
Journal:  Chem Res Toxicol       Date:  2009-01       Impact factor: 3.739

  4 in total

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