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On the Mechanisms of Taurine in Alleviating Electrocardiographic, Hemodynamic, and Biochemical Parameters Following Aluminum Phosphide Cardiotoxicity Publisher Pubmed



Samadi M1, 3 ; Baeeri M3 ; Haghiaminjan H2 ; Rahimifard M3 ; Gholami M3 ; Hassani S3 ; Sattari M1 ; Azarmi Y1 ; Bameri B3 ; Armandeh M3 ; Hooshangi Shayesteh MR3 ; Eghbal MA1, 4 ; Abdollahi M3
Authors
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Authors Affiliations
  1. 1. Department of Toxicology and Pharmacology, Faculty of Pharmacy, Tabriz University of Medical Sciences, Tabriz, Iran
  2. 2. Pharmaceutical Sciences Research Center, Ardabil University of Medical Sciences, Ardabil, Iran
  3. 3. Department of Toxicology and Pharmacology, School of Pharmacy, and Toxicology and Diseases Group, Pharmaceutical Sciences Research Center (PSRC), The Institute of Pharmaceutical Sciences (TIPS), Tehran University of Medical Sciences, Tehran, Iran
  4. 4. Drug Applied Research Center, Tabriz University of Medical Sciences, Tabriz, Iran

Source: Food and Chemical Toxicology Published:2021


Abstract

Background: Aluminum phosphide (AlP) causes severe cardiotoxicity. Taurine has been chosen for the present study because of its positive known effects on cardiac injuries. Method: To evaluate AlP-induced cardiotoxicity, the animals were divided into seven groups, including the control group, the taurine group (500 mg/kg), AlP with LD50 dose, AlP + taurine 20, 50, 100, and 200 mg/kg group. To assess cardiac hemodynamic parameters, Wistar rats received taurine intraperitoneally 60 min after AlP gavage. Cardiac hemodynamic parameters were evaluated for 180 min. To study biochemical parameters, 24 h after AlP treatment, the animals were sacrificed, and heart tissues were collected. Result: ECG, BP, and HR abnormalities of AlP poisoning were improved by taurine treatment. AlP induced biochemical alterations including complexes I and IV activities, the ADP/ATP ratio, mitochondrial membrane potential, cytochrome C release, and oxidative stress biomarkers ameliorated by taurine. Moreover, taurine improved apoptosis, as well as lessened CK-MB and troponin I levels. Also, there were no significant changes between taurine 500 mg/kg and the control group in tests. Conclusion: The present findings showed that taurine could be a possible candidate for AlP cardiotoxicity treatment via the effect on mitochondrial electron transfer chain and maintaining intracellular ATP balance. © 2021 Elsevier Ltd
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