Sakuranetin counteracts polyethylene microplastics induced nephrotoxic effects via modulation of Nrf2/Keap1 pathway

被引:1
|
作者
Akbar, Ali [1 ]
Amin, Fatima [1 ]
Batool, Moazama [2 ]
Khatoon, Aisha [3 ]
Ahmad, Zubair [4 ]
Atique, Usman [5 ]
机构
[1] Univ Agr Faisalabad, Dept Zool Wildlife & Fisheries, Faisalabad, Pakistan
[2] Govt Coll Women Univ, Dept Zool, Sialkot, Pakistan
[3] Univ Agr Faisalabad, Dept Pathol, Faisalabad, Pakistan
[4] King Saud Univ, Dept Zool, Coll Sci, POB 2455, Riyadh 11451, Saudi Arabia
[5] Chungnam Natl Univ, Dept Biosci & Biotechnol, Daejeon, South Korea
关键词
Sakuranetin; Polyethylene microplastics; Toxicity; Kidney damage; Oxidative stress; SPECTROPHOTOMETRIC ASSAY; OXIDATIVE STRESS; GLUTATHIONE; INFLAMMATION; APOPTOSIS;
D O I
10.1016/j.jksus.2024.103343
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Polyethylene microplastics (PEMPs) are widely distributed in environment and exerts deleterious effects on animal as well as human health. Sakuranetin (SKN) is a natural flavonoid that manifests profound therapeutic potential. Albino rats (n = 24) were partitioned into 4 groups i.e., Control, PEMPs 1.5 mg/kg, PEMPs 1.5 mg/kg + SKN 10 mg/kg and SKN 10 mg/kg administered group. After 30 days of treatment, our results revealed that PEMPs exposure reduced nuclear factor erythroid 2-related factor 2 (Nrf-2) and antioxidant genes while enhancing the expression of kelch-like ECH-associated protein 1(Keap-1). Besides, PEMPs intoxication reduced the level of renal biomarkers i.e., creatinine clearance and increased the level of creatinine, urea, neutrophil gelatinase-associated lipocalin (NGAL) and kidney injury molecule-1 (KIM-1). Additionally, it lessened the activities of glutathione S-transferase (GST), superoxide dismutase (SOD), glutathione reductase (GSR), catalase (CAT), glutathione peroxidase (GPx) and heme oxygenase-1 (HO-1) whereas the levels of malondialdehyde (MDA) and reactive oxygen species (ROS) were increased. Conversely, it increased the levels of nuclear factorkappa B (NF-kB), tumor necrosis factor-alpha (TNF-a), interleukin-1beta (IL-1b) and IL-6 as well as escalated the activity of cyclooxygenase-2 (COX-2). Furthermore, the expression of bcl-2-associated X protein (Bax) and caspase-3 were elevated, while the expression of B-cell lymphoma 2 (Bcl-2) was lowered. However, SKN treatment significantly (P < 0.05) restored aforementioned renal impairments. Therefore, it is proposed that SKN may be applied as a nephroprotective agent against the PEMPs-prompted renal toxicity.
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页数:6
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