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Pyrethroid-Induced Organ Toxicity and Anti-Oxidant-Supplemented Amelioration of Toxicity and Organ Damage

The Protective Roles of Ascorbic Acid and α-Tocopherol

Bibliographic Data

ID15513994
AuthorsMohsen S Al-Omar (0000-0001-8134-9623, Qassim University), Mamuna Naz (Prince Sattam Bin Abdulaziz University), Salman A A Mohammed (0000-0002-9250-100X, Qassim University, corresponding author), Momina Mansha (Quaid-i-Azam University), Mohd Nazam Ansari (0000-0001-8580-3002, Prince Sattam Bin Abdulaziz University), Najeeb Ur Rehman (0000-0001-6925-7697, Prince Sattam Bin Abdulaziz University), Mehnaz Kamal (0000-0002-3585-0828, Prince Sattam Bin Abdulaziz University), Hamdoon A Mohammed (0000-0003-2896-6790, Qassim University), Mohammad Yusuf (0000-0003-1417-7774, Taif University), Abubaker M Hamad (0000-0002-2410-7916, Prince Sattam Bin Abdulaziz University), Naseem Akhtar (0000-0003-3607-3992, Buraydah Colleges), Riaz A Khan (0000-0003-0185-0149, Qassim University, corresponding author)
Year2020
Volume17
Issue17
Pages6177-6177
Publication date2020-08-25
Peer ReviewedYes
Open AccessYes
TypeARTICLE
VenueInternational Journal of Environmental Research and Public Health (JOURNAL)
Journal identifiersISSN: 1661-7827 • E-ISSN: 1660-4601
PublisherMultidisciplinary Digital Publishing Institute (PUBLISHER • CH)
DOI10.3390/ijerph17176177
PMID32854455
OpenAlexW3080626286
LanguageEN
References cited52

The pyrethroid toxicants, fatal at high doses, are found as remnants of crop pesticides and ingredients of commercially available insecticides. The toxic effects of high-content insecticidal pyrethroid formulations are available in 0.05 g, 1.17 g, and 0.04 g pyrethroid-instilled products, namely burning coils, pyrethroid-soaked mats, and liquid formulations of pyrethroids that release pyrethroid vapor/smoke upon heating. They provided 5.46 g/kg, 21.15 g/kg, and 4.24 g/kg of toxicants to the experimental animals over a total of 3 weeks/5 h per os (p.o.) administration, producing necrosis, hyperemia, and fatty changes in the liver; fiber separation in cardiac muscles; atrophy, lymphatic infiltration, blood vessel congestion, and hyperemia in the heart tissues of the experimental animals. The glomerular tuft necrosis, cytoplasmic degeneration of renal tubular cells, necrotic tubules, congestion, and dilatation of blood vessels were observed in the kidney tissue of intoxicated animals. Air-space enlargement, interstitial inflammation, lymphocyte infiltration aggregates, connective tissue infiltration by inflammatory cells, and hyperemia were found in the lung tissues. The pyrethroid toxicants also produced nervous tissue degeneration and decreased neurons in the brain, which were observed through histopathological examinations of the brain, lungs, heart, kidneys, and liver. The protective effects of ascorbic acid (AA/vitamin C) and α-tocopherol (E307/vitamin E) at 100 mg/kg oral doses administered daily for the entire period of the toxicant exposure of three weeks to the experimental mice, aged between 3-4 months and weighing ≈30 g, ameliorated the tissue damage, as observed through the histopathological examinations. The ascorbic acid caused recovery of the liver, kidney, brain, and heart tissue damage, while α-tocopherol was effective at ameliorating the damage in the kidneys and lung tissue compared with the control groups. The high levels of tissue damage recovery suggested a prophylactic effect of the concurrent use of ascorbic acid and α-tocopherol for the subjects under the exposure of pyrethroids

Ascorbic acid · Atrophy · Biology · Kidney · Lung · Lymphatic system · Necrosis · Pathology · Pesticide · Pyrethroid · Toxicity · Chemistry · Environmental Toxicology and Ecotoxicology · Medicine · Pesticide Exposure and Toxicity · Vitamin C and Antioxidants Research · Endocrinology · Internal Medicine · Pharmacology

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