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Article 2024 · 2 atıf

Atrazine-Induced Toxicity and Biochemical Changes in Mus musculus: the Ameliorative Efficacy of Nigella sativa L. (Ranunculaceae) Oil

Malik, Sumera Yasmeen, Arshad, Muhammad, Batool, Sajida, Batool, Saira, Iram, Fatima, Batool, Tahira, Ali, Baber, Wahab, Sana, Khan, Muhammad Nauman, Kaplan, Alevcan, Bibi, Maryam, Assad, Nasir, Alnemar, Shikhah K., Elsadek, Mohamed Farouk, Ercisli, Sezai, Iqbal, Majid

Özet

The study aimed to evaluate the ameliorative potential of Nigella sativa oil (N.s) against the adverse effects induced by atrazine (ATZ) in mice. Four groups were divided into: Control group (untreated); N.s group ( N. sativa oil, 2 mL/kg/BW); ATZ group (atrazine 200 mg/kg/BW); ATZ+N.s group (atrazine 200 mL/kg/BW; and N. sativa oil, 2 mL/kg/BW). All doses were administered by gavage once daily for 4 weeks. The atrazine-administered group showed a significant increase in total leukocytes, granulocytes, and agranulocytes and a decrease in red blood cells, hemoglobin, mean corpuscular volume, and packed cell volume. Serum concentrations of aspartate aminotransferase, alanine transaminase, and alkaline phosphatase were high in the ATZ group. Atrazine exposure reduced serum albumin and total protein levels in the blood. A significantly higher concentration of bilirubin, urea, and creatinine was also found in the ATZ group. The simultaneous administration of atrazine and N. sativa led to improvements in all the parameters studied above. Thus, this study revealed that atrazine exposure has toxic effects on hematological parameters, liver, and kidney function, and that N. sativa oil reduces these toxic effects of atrazine in male mice.

Anahtar Kelimeler
Nigella sativa oil atrazine mice hematological parameters liver function test kidney function test black seed oil OXIDATIVE STRESS LIVER EXTRACTS ENZYMES KIDNEY DAMAGE SEEDS
WoS Kategorileri
Environmental Sciences
Sürdürülebilir Kalkınma Amaçları
Künye
Dergi
POLISH JOURNAL OF ENVIRONMENTAL STUDIES
Yıl
2024
Cilt
33
Sayı
5
Sayfa
5211-5220
ISSN
1230-1485
eISSN
2083-5906
DOI
10.15244/pjoes/183076
WoS UID
WOS:001260338900017
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