HIGHLIGHTS
- What: In view of this, the authors focused on SECs and hypothesized that FXa inhibition might protect SECs and ameliorate hepatic IRI by suppressing FXa-PAR-2 signaling-induced inflammation. The authors focused on FXa, a protease-activated upstream of thrombin in the coagulation cascade and a selective inhibitor of edoxaban. The authors focused on ERK 1/2 and revealed that its activation was induced in the liver after hepatic IRI in_vivo and in the SECs after H/R stress.
- Who: Koki Maeda and colleagues from the Department of Hepatobiliary Pancreatic and Transplant Surgery, Mie . . .

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