Expression Pattern of MicroRNA-21 during the Liver Ischemia/Reperfusion

Ischemia/reperfusion (I/R) injury in cadaveric liver transplantation is not avoidable. Liver I/R injury is an important phenomenon in hepatic damage. MicroRNA-21 (miR-21) plays an important role in I/R injury. The present study aimed to determine the expression pattern of miR-21 in liver I/R injury/...

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Main Authors: Alireza Salah, Mohammad Hossein Karimi, Javad Sajedianfard, Saeed Nazifi, Ramin Yaghobi
Format: Article
Language:English
Published: Tehran University of Medical Sciences 2021-02-01
Series:Iranian Journal of Allergy, Asthma and Immunology
Subjects:
Online Access:https://ijaai.tums.ac.ir/index.php/ijaai/article/view/2828
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author Alireza Salah
Mohammad Hossein Karimi
Javad Sajedianfard
Saeed Nazifi
Ramin Yaghobi
author_facet Alireza Salah
Mohammad Hossein Karimi
Javad Sajedianfard
Saeed Nazifi
Ramin Yaghobi
author_sort Alireza Salah
collection DOAJ
description Ischemia/reperfusion (I/R) injury in cadaveric liver transplantation is not avoidable. Liver I/R injury is an important phenomenon in hepatic damage. MicroRNA-21 (miR-21) plays an important role in I/R injury. The present study aimed to determine the expression pattern of miR-21 in liver I/R injury/recovery and its correlation with the immunologic transmission signals pathways several days post-reperfusion. In an animal model for I/R in the liver, 40 male Balb/c mice were divided into 3 groups. The animals were monitored for 3 and 24 hours, and also for 4, 7, 14, and 28 days post-reperfusion. Liver tissue damage was assessed by histopathology. The plasma alanine aminotransferase (ALT), aspartate aminotransferase (AST), alkaline phosphatase (ALP), and total antioxidant capacity (TAC) levels were measured with enzymatic assays. MiR-21, programmed cell death 4 (PDCD4) mRNA, T-cell-restricted intracellular antigen 1 (TIA1) mRNA, and fas ligand (FASL) mRNA expression levels were measured; using reverse transcription-polymerase chain reaction (RT-PCR) at different times after the reperfusion in liver tissue and blood. Histopathology and plasma ALT, AST, ALP, and TAC levels confirmed liver damage induced by I/R injury. MiR-21 increased by twofold in the liver tissue and on the inflammatory phase after 24 hours of reperfusion; it then continued to decrease up to day 7 post-reperfusion. Afterward, it continued to rise slightly up to day 14 post-reperfusion. This trend was in parallel with the recovery of the liver damage. MiR-21 expression level in the liver and blood is a predictor of the extent of I/R injury.
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spelling doaj.art-2f27a33aa8104a90b64a2b8544c289182022-12-21T23:14:13ZengTehran University of Medical SciencesIranian Journal of Allergy, Asthma and Immunology1735-15021735-52492021-02-0120110.18502/ijaai.v20i1.5415Expression Pattern of MicroRNA-21 during the Liver Ischemia/ReperfusionAlireza Salah0Mohammad Hossein Karimi1Javad Sajedianfard2Saeed Nazifi3Ramin Yaghobi4Department of Basic Sciences, School of Veterinary Medicine, Shiraz University, Shiraz, IranOrgan Transplant Research Center, Shiraz University of Medical Sciences, Shiraz, IranDepartment of Basic Sciences, School of Veterinary Medicine, Shiraz University, Shiraz, IranDepartment of Clinical Studies, School of Veterinary Medicine, Shiraz University, Shiraz, IranOrgan Transplant Research Center, Shiraz University of Medical Sciences, Shiraz, IranIschemia/reperfusion (I/R) injury in cadaveric liver transplantation is not avoidable. Liver I/R injury is an important phenomenon in hepatic damage. MicroRNA-21 (miR-21) plays an important role in I/R injury. The present study aimed to determine the expression pattern of miR-21 in liver I/R injury/recovery and its correlation with the immunologic transmission signals pathways several days post-reperfusion. In an animal model for I/R in the liver, 40 male Balb/c mice were divided into 3 groups. The animals were monitored for 3 and 24 hours, and also for 4, 7, 14, and 28 days post-reperfusion. Liver tissue damage was assessed by histopathology. The plasma alanine aminotransferase (ALT), aspartate aminotransferase (AST), alkaline phosphatase (ALP), and total antioxidant capacity (TAC) levels were measured with enzymatic assays. MiR-21, programmed cell death 4 (PDCD4) mRNA, T-cell-restricted intracellular antigen 1 (TIA1) mRNA, and fas ligand (FASL) mRNA expression levels were measured; using reverse transcription-polymerase chain reaction (RT-PCR) at different times after the reperfusion in liver tissue and blood. Histopathology and plasma ALT, AST, ALP, and TAC levels confirmed liver damage induced by I/R injury. MiR-21 increased by twofold in the liver tissue and on the inflammatory phase after 24 hours of reperfusion; it then continued to decrease up to day 7 post-reperfusion. Afterward, it continued to rise slightly up to day 14 post-reperfusion. This trend was in parallel with the recovery of the liver damage. MiR-21 expression level in the liver and blood is a predictor of the extent of I/R injury.https://ijaai.tums.ac.ir/index.php/ijaai/article/view/2828IschemiaLiverMiceMicroRNA-21Reperfusion
spellingShingle Alireza Salah
Mohammad Hossein Karimi
Javad Sajedianfard
Saeed Nazifi
Ramin Yaghobi
Expression Pattern of MicroRNA-21 during the Liver Ischemia/Reperfusion
Iranian Journal of Allergy, Asthma and Immunology
Ischemia
Liver
Mice
MicroRNA-21
Reperfusion
title Expression Pattern of MicroRNA-21 during the Liver Ischemia/Reperfusion
title_full Expression Pattern of MicroRNA-21 during the Liver Ischemia/Reperfusion
title_fullStr Expression Pattern of MicroRNA-21 during the Liver Ischemia/Reperfusion
title_full_unstemmed Expression Pattern of MicroRNA-21 during the Liver Ischemia/Reperfusion
title_short Expression Pattern of MicroRNA-21 during the Liver Ischemia/Reperfusion
title_sort expression pattern of microrna 21 during the liver ischemia reperfusion
topic Ischemia
Liver
Mice
MicroRNA-21
Reperfusion
url https://ijaai.tums.ac.ir/index.php/ijaai/article/view/2828
work_keys_str_mv AT alirezasalah expressionpatternofmicrorna21duringtheliverischemiareperfusion
AT mohammadhosseinkarimi expressionpatternofmicrorna21duringtheliverischemiareperfusion
AT javadsajedianfard expressionpatternofmicrorna21duringtheliverischemiareperfusion
AT saeednazifi expressionpatternofmicrorna21duringtheliverischemiareperfusion
AT raminyaghobi expressionpatternofmicrorna21duringtheliverischemiareperfusion