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The Role of the Jak-Stat Signaling Pathway in the Protective Effects of Hepatic Ischemia Post-Conditioning Against the Injury Induced by Ischemia/Reperfusion in the Rat Liver Publisher



Afshar NGP1 ; Ali Arab H1 ; Vatannejad A1 ; Ashabi G2 ; Golabchifar AA1
Authors
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Authors Affiliations
  1. 1. Department of Comparative Biosciences, Faculty of Veterinary Medicine, University of Tehran, Tehran, Iran
  2. 2. Department of Physiology, Faculty of Medicine, Tehran University of Medical Sciences, Tehran, Iran

Source: Advanced Pharmaceutical Bulletin Published:2024


Abstract

Purpose: Hepatic ischemic post-conditioning (IPOC) is shown to protect the liver from injury induced by ischemia/reperfusion (IR). However, the mechanism underlying this protection has remained elusive. The present study aimed to investigate the role of the interleukin 6-Janus kinase-signal transducers and activators of transcription (IL-6-JAK-STAT) pathway in the protective effect of hepatic IPOC against the IR-induced injury in the liver. Methods: Twenty-five rats were randomly divided into 5 groups of (1) sham-operated, (2) IR, (3) IR + hepatic IPOC, (4) IR + tofacitinib (TOFA), and (5) IR +TOFA + hepatic IPOC. The changes induced by IR and the effects of different treatments were assessed by enzyme release, histopathological observations, the serum level of IL-6, and the occurrence of apoptosis detected via the expression of the Bax/Bcl-2 ratio. Results: The hepatic IPOC improved the liver injury induced by IR as shown by histological changes, reduction of IL-6 level, aspartate aminotransferase (AST), and alanine aminotransferase (ALT) compared to the IR group (P< 0.001, P< 0.05, P< 0.05, respectively). There was also downregulation of the Bax/Bcl2 ratio in the rats exposed to IR + hepatic IPOC compared with those in the IR group (P< 0.05). However, TOFA, an inhibitor of JAK-STAT activity, inhibited the protective effect of hepatic IPOC. Conclusion: It suggests that the protective effect of hepatic IPOC against IR-induced injury may be mediated by activating the IL-6-JAK-STAT pathway. © 2024 The Author (s).