Abstract
The aim of this study was to evaluate a multi-endpoint cytotoxicity screening method using V79 cells based on four different endpoints of cytotoxicity: trypan blue exclusion, reduction of XTT, neutral red uptake and total protein content. In addition, cell morphology was routinely observed after each treatment. Seven compounds were studied, which can be divided into five classes: protein synthesis inhibitors (cycloheximide, actinomycin D); inhibitors of cell division (bleomycin, vincristine); membrane-active compounds (Triton X-100); lysosomotropic agents (ammonium chloride); and general toxicants (sodium chloride). We obtained a variety of different toxicity profiles, which may be useful in defining the mechanisms of toxic action of these compounds. The multi-endpoint screening system proved to be readily applicable, robust and rapid, and gave reliable toxicity results over a wide range of chemical concentrations.
Get full access to this article
View all access options for this article.