The liver injury following ischemia and reperfusion is worse in experimental knockout heterozygote mouse model for expression of connexin 43

dataset

posted on 2019-12-18, 03:30 authored by Alexandre Maximiliano Trevisan, Bruno Cogliati, Adriana Ribeiro Homem, Thiago Pinheiro Arrais Aloiav, Nelson de Aquino Neto, Jairo Marques Moreira, Leonardo da Cruz Reno, Alexandre Moulin Naumann, Flavio Henrique Ferreira Galvão, Wellington Andraus, Luiz Augusto Carneiro D'Albuquerque

Abstract Purpose: To evaluate that Connexin (Cx43) plays a role in lesions after hepatic ischemia/reperfusion (IR) injury. Methods: We use Cx43 deficient model (heterozygotes mice) and compared to a wild group. The groups underwent 1 hour ischemia and 24 hours reperfusion. The heterozygote genotype was confirmed by PCR. We analyzed the hepatic enzymes (AST, ALT, GGT) and histology. Results: The mice with Cx43 deficiency showed an ALT mean value of 4166 vs. 307 in the control group (p<0.001); AST mean value of 7231 vs. 471 in the control group (p<0.001); GGT mean value of 9.4 vs. 1.7 in the control group (p=0.001); histology showed necrosis and inflammation in the knockout group. Conclusions: This research demonstrated that the deficiency of Cx43 worses the prognosis for liver injury. The topic is a promising target for therapeutics advancements in liver diseases and procedures.