Author:
Chan Karen Y. T.,Yong Alyssa S. M.,Wang Xu,Ringgold Kristyn M.,St. John Alexander E.,Baylis James R.,White Nathan J.,Kastrup Christian J.
Abstract
AbstractThe adhesion of blood clots to wounds is necessary to seal injured vasculature and achieve hemostasis. However, it has not been specifically tested if adhesive failure of clots is a major contributor to rebleeding and what mechanisms prevent clot delamination. Here, we quantified the contribution of adhesive and cohesive failure to rebleeding in a rat model of femoral artery injury, and identified mechanisms that contribute to the adhesive strength of bulk clots in a lap-shear test in vitro. In the rat bleeding model, the frequency of clot failures correlated positively with blood loss (R = 0.81,p = 0.014) and negatively with survival time (R = − 0.89,p = 0.0030), with adhesive failures accounting for 51 ± 14% of rebleeds. In vitro, adhesion depended on fibrinogen and coagulation factor XIII (FXIII), and supraphysiological FXIII improved adhesive strength. Furthermore, when exogenous FXIII was topically applied into the wound pocket of rats, eleven adhesive failures occurred between eight rats, compared to seventeen adhesive failures between eight untreated rats, whereas the number of cohesive failures remained the same at sixteen in both groups. In conclusion, rebleeding from both adhesive and cohesive failure of clots decreases survival from hemorrhage in vivo. Both endogenous and exogenous FXIII improves the adhesive strength of clots.
Funder
Natural Sciences and Engineering Research Council
Canadian Institutes of Health Research
Canadian Foundation for Innovation
British Columbia Knowledge Development Fund
Michael Smith Foundation for Health Research
Publisher
Springer Science and Business Media LLC
Cited by
11 articles.
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