The inhibitory effect of proanthocyanidin on soluble and collagen-bound proteases

AbstractObjective tudy evaluated the inhibitory effect of proanthocyanidin (PA), a natural collagen cross-linker, on soluble and matrix-bound proteases, which are responsible for progressive degradation of exposed collagen fibrils within the hybrid layer and resin–dentine bond failure over time. s hibitory effects of PA (1%, 2%, 3%, 4.5% and 6%) on soluble recombinant matrix metalloproteinases (MMP-2, -8 and -9) and cysteine cathepsins (cathepsin B and K) were evaluated using MMP and cysteine cathepsins fluorometric assay kits. Chlorhexidine (CHX) was used as an inhibitor control. The effect of PA on endogenous matrix-bound proteases was examined by determining the change in dry mass of demineralized dentine beams and solubilized collagen peptides over 30 days. Two-way ANOVA and Tukey multiple comparison tests were used to analyze the effect of PA and proteases on the percentage inhibition of soluble proteases (α = 0.05). Kruskal–Wallis one-way ANOVA and Dunnʹs multiple comparison tests were used to analyse the effect of PA on loss of dry mass and hydroxyproline content over time (α = 0.05). s hocyanidin inactivated more than 90% of soluble recombinant MMP-2, -8 and -9 and around 75–90% of cysteine cathepsin B and K, which was significantly higher than CHX (P < 0.05). The inhibition of endogenous proteases by PA increased in a dose-dependent manner. The loss of dry mass and hydroxyproline release in the medium over time was the lowest in dentine beams pretreated with PA < CHX < control (P < 0.05). sion hocyanidin exhibited both dentine MMP and cysteine cathepsins inhibition, which was higher than chlorhexidine.