Cardioprotective effects of co-administration of thymoquinone and ischemic postconditioning in diabetic rats

Objective(s): Ischemia/reperfusion (I/R) is a leading cause of myocardial infarction (MI) injury, contributing to excess injury to cardiac tissues involved in inflammation, apoptosis, and oxidative stress. The present study was conducted to examine the effects of combined thymoquinone (TQ) with isch...

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Main Authors: Junchuan Ran, Huanglin Xu, Wenyuan Li
Format: Article
Language:English
Published: Mashhad University of Medical Sciences 2021-07-01
Series:Iranian Journal of Basic Medical Sciences
Subjects:
Online Access:https://ijbms.mums.ac.ir/article_18395_5776f1d2a749f8e59c3a909cd9b1319d.pdf
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author Junchuan Ran
Huanglin Xu
Wenyuan Li
author_facet Junchuan Ran
Huanglin Xu
Wenyuan Li
author_sort Junchuan Ran
collection DOAJ
description Objective(s): Ischemia/reperfusion (I/R) is a leading cause of myocardial infarction (MI) injury, contributing to excess injury to cardiac tissues involved in inflammation, apoptosis, and oxidative stress. The present study was conducted to examine the effects of combined thymoquinone (TQ) with ischemic postconditioning (IPostC) therapy on apoptosis and inflammation due to I/R injury in diabetic rat hearts. Materials and Methods: A single dose injection of streptozotocin (STZ; 60 mg/kg) was administered to thirty-two Wistar male rats to induce diabetes. Hearts were fixed on a Langendorff setting and exposed to a 30 min regional ischemia subsequently to 60 min reperfusion. IPostC was induced at the onset of reperfusion by 3 cycles of 30 sec R/I. ELISA, Western blotting assay, and TUNEL staining were applied to assess the cardioprotective effect of IPostC and TQ against I/R injury in diabetic and non-diabetic rats.Results: Administration of TQ alone in non-diabetic isolated hearts significantly diminished CK-MB, TNF-α, IL-1β, and apoptosis and enhanced p-GSK-3β and Bcl-2 (p <0.05). Following administration of TQ, the cardioprotective effects of IPostC by elevating p-GSK-3β and Bcl-2 and alleviating apoptosis and inflammation were reestablished compared with non-IPostC diabetic hearts. Conclusion: These results provide substantial evidence that co-administration of TQ plus IPostC can exert cardioprotective effects on diabetic myocardium during I/R damage by attenuating the inflammatory response and apoptosis.
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spelling doaj.art-f076eef9f6e547e491cb409f2693286c2022-12-21T19:34:13ZengMashhad University of Medical SciencesIranian Journal of Basic Medical Sciences2008-38662008-38742021-07-0124789289910.22038/ijbms.2021.47670.1098118395Cardioprotective effects of co-administration of thymoquinone and ischemic postconditioning in diabetic ratsJunchuan Ran0Huanglin Xu1Wenyuan Li2Department of Cardiology, Gansu Gem Flower Hospital, Lanzhou, Gansu, 730060, ChinaDepartment of Cardiology, Xigu People’s Hospital,Lanzhou, Gansu, 730060, ChinaDepartment of Cardiology, Gansu Gem Flower Hospital, Lanzhou, Gansu, 730060, ChinaObjective(s): Ischemia/reperfusion (I/R) is a leading cause of myocardial infarction (MI) injury, contributing to excess injury to cardiac tissues involved in inflammation, apoptosis, and oxidative stress. The present study was conducted to examine the effects of combined thymoquinone (TQ) with ischemic postconditioning (IPostC) therapy on apoptosis and inflammation due to I/R injury in diabetic rat hearts. Materials and Methods: A single dose injection of streptozotocin (STZ; 60 mg/kg) was administered to thirty-two Wistar male rats to induce diabetes. Hearts were fixed on a Langendorff setting and exposed to a 30 min regional ischemia subsequently to 60 min reperfusion. IPostC was induced at the onset of reperfusion by 3 cycles of 30 sec R/I. ELISA, Western blotting assay, and TUNEL staining were applied to assess the cardioprotective effect of IPostC and TQ against I/R injury in diabetic and non-diabetic rats.Results: Administration of TQ alone in non-diabetic isolated hearts significantly diminished CK-MB, TNF-α, IL-1β, and apoptosis and enhanced p-GSK-3β and Bcl-2 (p <0.05). Following administration of TQ, the cardioprotective effects of IPostC by elevating p-GSK-3β and Bcl-2 and alleviating apoptosis and inflammation were reestablished compared with non-IPostC diabetic hearts. Conclusion: These results provide substantial evidence that co-administration of TQ plus IPostC can exert cardioprotective effects on diabetic myocardium during I/R damage by attenuating the inflammatory response and apoptosis.https://ijbms.mums.ac.ir/article_18395_5776f1d2a749f8e59c3a909cd9b1319d.pdfapoptosisdiabetesinflammationischemic postconditioningpolyphenols
spellingShingle Junchuan Ran
Huanglin Xu
Wenyuan Li
Cardioprotective effects of co-administration of thymoquinone and ischemic postconditioning in diabetic rats
Iranian Journal of Basic Medical Sciences
apoptosis
diabetes
inflammation
ischemic postconditioning
polyphenols
title Cardioprotective effects of co-administration of thymoquinone and ischemic postconditioning in diabetic rats
title_full Cardioprotective effects of co-administration of thymoquinone and ischemic postconditioning in diabetic rats
title_fullStr Cardioprotective effects of co-administration of thymoquinone and ischemic postconditioning in diabetic rats
title_full_unstemmed Cardioprotective effects of co-administration of thymoquinone and ischemic postconditioning in diabetic rats
title_short Cardioprotective effects of co-administration of thymoquinone and ischemic postconditioning in diabetic rats
title_sort cardioprotective effects of co administration of thymoquinone and ischemic postconditioning in diabetic rats
topic apoptosis
diabetes
inflammation
ischemic postconditioning
polyphenols
url https://ijbms.mums.ac.ir/article_18395_5776f1d2a749f8e59c3a909cd9b1319d.pdf
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AT huanglinxu cardioprotectiveeffectsofcoadministrationofthymoquinoneandischemicpostconditioningindiabeticrats
AT wenyuanli cardioprotectiveeffectsofcoadministrationofthymoquinoneandischemicpostconditioningindiabeticrats