Ephedra sinica mitigates hepatic oxidative stress and inflammation via suppressing the TLR4/MyD88/NF-κB pathway in fipronil-treated rats

被引:26
|
作者
Seif, Mohamed [1 ,2 ]
Deabes, Mohamed [2 ]
El-Askary, Ahmad [3 ]
El-Kott, Attalla F. [4 ,5 ]
Albadrani, Ghadeer M. [6 ]
Seif, Amr [7 ]
Wang, Zaizhao [1 ]
机构
[1] Northwest A&F Univ, Coll Anim Sci & Technol, 22 Xinong Rd, Yangling 712100, Shaanxi, Peoples R China
[2] Natl Res Ctr, Toxicol & Food Contaminants Dept, Food Ind & Nutr Res Div, PO 12622, Giza, Egypt
[3] Taif Univ, Coll Appl Med Sci, Dept Clin Lab Sci, POB 11099, At Taif 21944, Saudi Arabia
[4] King Khalid Univ, Fac Sci, Biol Dept, Abha 61421, Saudi Arabia
[5] Damanhour Univ, Coll Sci, Zool Dept, Damanhour 22511, Egypt
[6] Princess Nourah Bint Abdulrahman Univ, Coll Sci, Dept Biol, Riyadh 11474, Saudi Arabia
[7] Assiut Univ, Fac Med, Asyut 71516, Egypt
关键词
Anti-inflammation; Ephedra sinica; Liver injury; Rats; TLR4; MyD88; NF-kappa B; KAPPA-B ACTIVATION; LIPID-PEROXIDATION; ANTIOXIDANT ACTIVITY; SUBCHRONIC EXPOSURE; COLORIMETRIC METHOD; INSULIN-RESISTANCE; GENE-EXPRESSION; DOWN-REGULATION; VITAMIN-E; LIVER;
D O I
10.1007/s11356-021-15142-4
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Ephedra sinica (ES) is a promising medicinal plant with a wide range of pharmacological aspects, including antioxidant and anti-inflammatory properties. Fipronil (FN) is a popularly used systemic insecticide in agriculture and veterinary applications. FN exposure can result in a variety of negative health consequences. The study aimed to explore the prophylactic effects of Ephedra sinica extract (ESE) against hepatotoxicity in FN-treated rats by following the TLR4/ MyD88/ NF-kappa B pathway. ESE was tested for polyphenolic and antioxidant activity. Forty rats were separated into four groups and given orally by FN (10 mg/kg B.W.) and/or ESE (150 mg/kg B.W.). Blood and tissue samples were collected at the end of the experiment and prepared for pathophysiological, gene expression, and pathological analysis. ESE showed strong antioxidant activity, as well as reduced levels of hepatic MDA and oxidative stress markers (H2O2, NO). Hepatic SOD and CAT activities were increased even further. Furthermore, in FN-treated rats, ESE improved liver functions (ALT, AST, ALP, and LDH) and recovered the lipid profile (Cho, TriG, HDL, and LDL). Moreover, by inhibiting TLR4/ MyD88/ NF-kappa B induction, ESE alleviated hepatic pathological changes and decreased FN-induced elevations of TNF-alpha, IL-6, and IL-1 beta mRNA/protein levels. These findings suggested that ESE mitigated FN-induced hepatotoxicity via combating oxidative stress and relieving inflammation.
引用
收藏
页码:62943 / 62958
页数:16
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