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Cyanobufalins: Cardioactive Toxins from Cyanobacterial Blooms

He, Haiyin, Bertin, Matthew J., Wu, ShiBiao, Wahome, Paul G., Beauchesne, Kevin R., Youngs, Ross O., Zimba, Paul V., Moeller, Peter D. R., Sauri, Josep, Carter, Guy T.
Journal of natural products 2018 v.81 no.11 pp. 2576-2581
aquatic environment, biosynthesis, cardiomyocytes, cardiotoxicity, cell lines, chemical bonding, chlorine, cytotoxicity, humans, lakes, microorganisms, moieties, quantitative analysis, steroids, tissue culture, toxins, Ohio
Cyanobufalins A–C (1–3), a new series of cardiotoxic steroids, have been discovered from cyanobacterial blooms in Buckeye Lake and Grand Lake St. Marys in Ohio. Compounds 1–3 contain distinctive structural features, including geminal methyl groups at C-4, a 7,8 double bond, and a C-16 chlorine substituent that distinguish them from plant- or animal-derived congeners. Despite these structural differences, the compounds are qualitatively identical to bufalin in their cytotoxic profiles versus cell lines in tissue culture and cardiac activity, as demonstrated in an impedance-based cellular assay conducted with IPSC-derived cardiomyocytes. Cyanobufalins are nonselectively toxic to human cells in the single-digit nanomolar range and show stimulation of contractility in cardiomyocytes at sub-nanomolar concentrations. The estimated combined concentration of 1–3 in the environment is in the same nanomolar range, and consequently more precise quantitative analyses are recommended along with more detailed cardiotoxicity studies. This is the first time that cardioactive steroid toxins have been found associated with microorganisms in an aquatic environment. Several factors point to a microbial biosynthetic origin for the cyanobufalins.