We have investigated the change in SerpinB3 during hepatic ischemia and the potential role of its antiprotease activity in cell protection by the administration of wild-type SerpinB3 (SerpinB3-WT) or active loop-deleted recombinant SerpinB3 protein (SerpinB3-D) in a rat model of ischemia (60 min)/reperfusion (60 min) (I/R). A time-dependent increase of SerpinB3, both at transcription and protein level, was found in ischemic livers after 60, 120 and 180 min. SerpinB3-WT decreased polymorphonuclear cell infiltration and serum enzymes, and increased ATP when compared with I/R group. These events were not obtained using SerpinB3-D. No signifi-cant changes in both liver SerpinB3 mRNA and protein were found in all I/R groups considered. The present data show that the administration of SerpinB3-WT reduced the I/R injury and this effect appears to be depen-dent on its anti-protease activity.

SerpinB3 administration protects liver against ischemia-reperfusion injury

Turato C.
;
Vairetti M.;Cagna M.;Ferrigno A.;De Siervi S.;Di Pasqua L. G.
2022-01-01

Abstract

We have investigated the change in SerpinB3 during hepatic ischemia and the potential role of its antiprotease activity in cell protection by the administration of wild-type SerpinB3 (SerpinB3-WT) or active loop-deleted recombinant SerpinB3 protein (SerpinB3-D) in a rat model of ischemia (60 min)/reperfusion (60 min) (I/R). A time-dependent increase of SerpinB3, both at transcription and protein level, was found in ischemic livers after 60, 120 and 180 min. SerpinB3-WT decreased polymorphonuclear cell infiltration and serum enzymes, and increased ATP when compared with I/R group. These events were not obtained using SerpinB3-D. No signifi-cant changes in both liver SerpinB3 mRNA and protein were found in all I/R groups considered. The present data show that the administration of SerpinB3-WT reduced the I/R injury and this effect appears to be depen-dent on its anti-protease activity.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11571/1477133
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