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Effect of moringa seed extract in chlorpyrifos-induced cerebral and ocular toxicity in mice.
Alanazi, Ibtesam S; Altyar, Ahmed E; Zaazouee, Mohamed Sayed; Elshanbary, Alaa Ahmed; Abdel-Fattah, Abdel-Fattah M; Kamel, Mohamed; Albaik, Mai; Ghaboura, Nehmat.
Affiliation
  • Alanazi IS; Department of Biology, Faculty of Sciences, University of Hafr Al Batin, Hafr Al Batin, Saudi Arabia.
  • Altyar AE; Department of Pharmacy Practice, Faculty of Pharmacy, King Abdulaziz University, Jeddah, Saudi Arabia.
  • Zaazouee MS; Pharmacy Program, Batterjee Medical College, Jeddah, Saudi Arabia.
  • Elshanbary AA; Faculty of Medicine, Al-Azhar University, Assiut, Egypt.
  • Abdel-Fattah AM; Faculty of Medicine, Alexandria University, Alexandria, Egypt.
  • Kamel M; Pharmacology Department, Faculty of Veterinary Medicine, Suez Canal University, Ismailia, Egypt.
  • Albaik M; Department of Medicine and Infectious Diseases, Faculty of Veterinary Medicine, Cairo University, Giza, Egypt.
  • Ghaboura N; Department of Chemistry, Preparatory Year Program, Batterjee Medical College, Jeddah, Saudi Arabia.
Front Vet Sci ; 11: 1381428, 2024.
Article in En | MEDLINE | ID: mdl-38659447
ABSTRACT
Chlorpyrifos (CPF) is one of the most commonly used organophosphosphate-based (OP) insecticides. Its wide use has led to higher morbidity and mortality, especially in developing countries. Moringa seed extracts (MSE) have shown neuroprotective activity, antioxidant, anti-inflammatory, and antibacterial features. The literature lacks data investigating the role of MSE against CPF-induced cerebral and ocular toxicity in mice. Therefore, we aim to investigate this concern. A total of 40 mature male Wistar Albino mice were randomly distributed to five groups. Initially, they underwent a one-week adaptation period, followed by a one-week treatment regimen. The groups included a control group that received saline, MSE 100 mg/kg, CPF 12 mg/kg, CPF-MSE 50 mg/kg, and CPF-MSE 100 mg/kg. After the treatment phase, analyses were conducted on serum, ocular, and cerebral tissues. MSE100 and CPF-MSE100 normalized the pro-inflammatory markers (interleukin-1ß (IL-1ß), interleukin-6 (IL-6), and tumor necrosis factor-alpha (TNF-α)) and AChE serum levels. CPF-MSE50 significantly enhanced these serum levels compared to CPF; however, it showed higher levels compared to the control. Moreover, the tissue analysis showed a significant decrease in oxidative stress (malondialdehyde (MDA) and nitric oxide (NO)) and an increase in antioxidant markers (glutathione (GSH), glutathione peroxidase (GSH-PX)), superoxide dismutase (SOD), and catalase (CAT) in the treated groups compared to CPF. Importantly, the significance of these effects was found to be dose-dependent, particularly evident in the CPF-MSE100 group. We conclude that MSE has a promising therapeutic effect in the cerebral and ocular tissues of CPF-intoxicated mice, providing a potential solution for OP public health issues.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Front Vet Sci Year: 2024 Document type: Article Affiliation country: Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Front Vet Sci Year: 2024 Document type: Article Affiliation country: Country of publication: