Evaluation of the Protective Effects of Lugol's Solution in Rats Poisoned with Aluminum Phosphide (Rice Tablets).
Zeinab VafaeipourMohsen ImenshahidiAmir Hooshang MohammadpourSeyed Mohammad TaghdisiNoor Mohammad DaneshMohammad MoshiriAmir Hossein JafarianKhalil AbnousPublished in: Cardiovascular toxicology (2024)
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 2+ , Creatinine, ALP, Mg 2+ , and K + 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.
Keyphrases
- blood pressure
- oxidative stress
- heart rate
- gene expression
- heart failure
- white matter
- left ventricular
- type diabetes
- atrial fibrillation
- metabolic syndrome
- skeletal muscle
- cerebral ischemia
- physical activity
- room temperature
- multiple sclerosis
- solid state
- brain injury
- uric acid
- insulin resistance
- functional connectivity
- glycemic control
- heat stress
- weight loss