Suppression of NLRP3 inflammasome orchestrates the protective efficacy of tiron against isoprenaline-induced myocardial injury

The major contribution of myocardial damage to global mortalities raises debate regarding the exploration of new therapeutic strategies for its treatment. Therefore, our study investigated the counteracting effect of tiron against isoprenaline (ISO)-mediated cardiac infarction in mice. Tiron was administered to mice for 7 days prior to two consecutive injections of ISO on days 8 and 9 of the treatment protocol. Tiron significantly reduced the levels of CK-MB, LDH, and AST in serum samples of ISO-challenged mice. A considerable increase in the cardiac antioxidant response was observed in tiron-treated mice, as indicated by depletion of MDA and enhancement of antioxidant activities. Furthermore, tiron induced a marked decrease in NLRP3, ASC, and caspase-1 levels accompanied by weak immune reactions of IL-1β, NF-κB, TLR4, and iNOS in the infarct cardiac tissues. Histopathological screening validated these variations observed in the cardiac specimens. Thus, tiron clearly mitigated the oxidative and inflammatory stress by repressing the NLRP3 inflammasome and the TLR4/NF-κB/iNOS signaling cascade.

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Publication Details

Journal
Frontiers in Pharmacology
Published
2024-08-15
DOI
https://doi.org/10.3389/fphar.2024.1379908
Citations
7
Primary Topic
Inflammasome and immune disorders
Type
article
Field-Weighted Citation Impact
1.64

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article

Suppression of NLRP3 inflammasome orchestrates the protective efficacy of tiron against isoprenaline-induced myocardial injury

Mohamed El‐Sherbiny, Eman S. El‐Ashry, Rasha Hamed Al‐Serwi, Dalia H. El‐Kashef et al.
7 citations
Frontiers in Pharmacology
Inflammasome and immune disorders
1.64
article

Suppression of NLRP3 inflammasome orchestrates the protective efficacy of tiron against isoprenaline-induced myocardial injury

Mohamed El‐Sherbiny, Eman S. El‐Ashry, Rasha Hamed Al‐Serwi, Dalia H. El‐Kashef, Iman Ibrahim, Doaa Abdelrahaman, Ola A. Habotta, Ateya Megahed Ibrahim, Safwa M. Sorour, Hala Magdy Anwer, Ehab S. Taher, Rada Olga, Ostan Mihaela, Khairiah M. Alwutayed, Reham M. Ibrahim, Ahmed Abdeen
article en
7 citations

Abstract

The major contribution of myocardial damage to global mortalities raises debate regarding the exploration of new therapeutic strategies for its treatment. Therefore, our study investigated the counteracting effect of tiron against isoprenaline (ISO)-mediated cardiac infarction in mice. Tiron was administered to mice for 7 days prior to two consecutive injections of ISO on days 8 and 9 of the treatment protocol. Tiron significantly reduced the levels of CK-MB, LDH, and AST in serum samples of ISO-challenged mice. A considerable increase in the cardiac antioxidant response was observed in tiron-treated mice, as indicated by depletion of MDA and enhancement of antioxidant activities. Furthermore, tiron induced a marked decrease in NLRP3, ASC, and caspase-1 levels accompanied by weak immune reactions of IL-1β, NF-κB, TLR4, and iNOS in the infarct cardiac tissues. Histopathological screening validated these variations observed in the cardiac specimens. Thus, tiron clearly mitigated the oxidative and inflammatory stress by repressing the NLRP3 inflammasome and the TLR4/NF-κB/iNOS signaling cascade.

Frontiers in PharmacologyVol. 15
Princess Nourah bint Abdulrahman University (SA), Alfaisal University (SA), Prince Sattam Bin Abdulaziz University (SA), Zarqa University (JO), Mansoura University (EG), Benha University (EG), Almaarefa University, Port Said University (EG)
Prince Sattam bin Abdulaziz University, AlMaarefa University, Princess Nourah Bint Abdulrahman University, Zarqa University, College of Veterinary Medicine and Biomedical Sciences, Texas A and M University
Good health and well-being
Openalex Percentile: Top 16%
Inflammasome and immune disorders
1.64
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