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The turnover of ECM proteins is enzymatically regulated by ECM proteases, degrading enzymes belonging to the metzincin family, including matrix metalloproteinases (MMPs), \(\alpha\)-disintegrin and metalloproteinases (ADAMs) and \(\alpha\)-disintegrin and metalloproteinases with thrombospondin motifs (ADAMTSs) [23]

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In both PHH and PRH the in vitro comet assay response was recognizably higher for NFluo than for the other three NAs, but for PRH, NMIPA, NDMA, NDELA might be assumed to be equipotent under the given model assumptions

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