Didymin protects against polystyrene nanoplastic-induced hepatic damage in male albino rats by modulation of Nrf-2/Keap-1 pathway

被引:0
|
作者
Ijaz, M. U. [1 ]
Nadeem, N. [1 ]
Hamza, A. [1 ]
Almutairi, M. H. [2 ]
Atique, U. [3 ]
机构
[1] Univ Agr Faisalabad, Dept Zool Wildlife & Fisheries, Faisalabad, Pakistan
[2] King Saud Univ, Coll Sci, Dept Zool, Riyadh, Saudi Arabia
[3] Chungnam Natl Univ, Coll Biol Syst, Daejeon, South Korea
关键词
Polystyrene nanoplastics; Didymin; Antioxidant; Liver damage; Inflammation; Apoptosis; SPECTROPHOTOMETRIC ASSAY; OXIDATIVE STRESS; GLUTATHIONE;
D O I
10.1590/1414-431X2023e13173
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Polystyrene nanoplastics (PS-NPs) are ubiquitous environmental pollutants that can cause oxidative stress in various organs, including the liver. Didymin is a dietary flavanone that displays multiple pharmacological activities. Therefore, the present study evaluated the palliative role of didymin against PS-NPs-induced hepatic damage in rats. Albino rats (n=48) were randomly distributed into 4 groups: control, PS-NPs treated group, PS-NPs + didymin co-administered group, and didymin supplemented group. After 30 days, PS-NPs intoxication lowered the expression of Nrf-2 and anti-oxidant genes [catalase (CAT), superoxide dismutase (SOD), glutathione peroxidase (GPx), glutathione reductase (GSR), glutathione-S-transferase (GST), and heme oxygenase-1 (HO-1)], whereas the expression of KEAP1 kelch like ECH associated protein 1 (Keap-1) was increased. PS-NPs exposure also reduced the activities of anti-oxidants enzymes (CAT, SOD, GPx, GSR, GST, GSH, and OH-1), while malondialdehyde (MDA) and reactive oxygen species (ROS) levels were increased. The levels of alanine transaminase (ALT), aspartate aminotransferase (AST), and alkaline phosphatase (ALP) were increased in PS-NPs-exposed rats. Moreover, inflammatory indices [interleukin-1 beta (IL-1 beta), tumor necrosis factor alpha (TNF-alpha), interleukin-6 (IL-6), nuclear factor-kappa B (NF-kappa B), and cyclooxygenase-2 (COX-2)] were increased in PS-NPs-exposed rats. Furthermore, PS-NPs intoxication increased the expressions of apoptotic markers including Bax and Caspase-3, as well as reducing Bcl-2 expression. The histopathological analysis showed significant damage in PS-NPs-treated rats. However, didymin supplementation ameliorated all the PS-NPs-induced damage in the liver of rats. Therefore, it was concluded that didymin can act as a remedy against PS-NPs-induced liver toxicity due to its anti-apoptotic, anti-oxidant, and anti-inflammatory activities.
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页数:8
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