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Evaluation of the Protective Effects of Lugol's Solution in Rats Poisoned with Aluminum Phosphide (Rice Tablets).
- Source :
-
Cardiovascular toxicology [Cardiovasc Toxicol] 2024 Sep; Vol. 24 (9), pp. 955-967. Date of Electronic Publication: 2024 Jul 11. - Publication Year :
- 2024
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Abstract
- Aluminum phosphide (AlP) is the main component of rice tablets (a pesticide), which produces phosphine gas (PH3) when exposed to stomach acid. The most important symptoms of PH3 toxicity include, lethargy, tachycardia, hypotension, and cardiac shock. It was shown that Iodine can chemically react with PH3, and the purpose of this study is to investigate the protective effects of Lugol solution in poisoning with rice tablets. Five doses (12, 15, 21, 23, and 25 mg/kg) of AlP were selected, for calculating its lethal dose (LD50). Then, the rats were divided into 4 groups: AlP, Lugol, AlP + Lugol, and Almond oil (as a control). After 4 h, the blood pressure and electrocardiogram (ECG) were recorded, and blood samples were obtained for biochemical tests, then liver, lung, kidney, heart, and brain tissues were removed for histopathological examination. The results of the blood pressure showed no significant changes (P > 0.05). In ECG, the PR interval showed a significant decrease in the AlP + Lugol group (P < 0.05). In biochemical tests, LDH, Ca <superscript>2+</superscript> , Creatinine, ALP, Mg <superscript>2+</superscript> , and K <superscript>+</superscript> represented significant decreases in AlP + Lugol compared to the AlP group (P < 0.05). Also, the administration of Lugol's solution to AlP-poisoned rats resulted in a significant decrease in malondialdehyde levels and a significant increase in catalase activity (P < 0.05). Histopathological evaluation indicates that Lugol improves changes in the lungs, kidneys, brain, and heart. Our results showed that the Lugol solution could reduce tissue damage and oxidative stress in AlP-poisoned rats. We assume that the positive effects of Lugol on pulmonary and cardiac tissues are due to its ability to react directly with PH3.<br /> (© 2024. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.)
- Subjects :
- Animals
Male
Oxidative Stress drug effects
Biomarkers blood
Disease Models, Animal
Blood Pressure drug effects
Antidotes pharmacology
Kidney drug effects
Kidney pathology
Kidney metabolism
Heart Rate drug effects
Lung drug effects
Lung pathology
Lung metabolism
Electrocardiography
Poisoning prevention & control
Antioxidants pharmacology
Pesticides toxicity
Tablets
Liver drug effects
Liver pathology
Liver metabolism
Rats
Lethal Dose 50
Myocardium pathology
Myocardium metabolism
Iodides
Phosphines toxicity
Aluminum Compounds toxicity
Rats, Wistar
Subjects
Details
- Language :
- English
- ISSN :
- 1559-0259
- Volume :
- 24
- Issue :
- 9
- Database :
- MEDLINE
- Journal :
- Cardiovascular toxicology
- Publication Type :
- Academic Journal
- Accession number :
- 38990500
- Full Text :
- https://doi.org/10.1007/s12012-024-09890-1