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The Protective Effect of Sonneratia apetala Fruit Extract on Acetaminophen-Induced Liver Injury in Mice

机译:无瓣樱子果实提取物对乙酰氨基酚诱发的小鼠肝损伤的保护作用

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摘要

Acute liver injury is a common consequence of taking overdose of acetaminophen (APAP). The aim of this study was to evaluate the antioxidant activity and hepatoprotective effect of a mangrove plant Sonneratia apetala fruit extract (SAFE) on APAP-induced liver injury in mice. Mice were orally pretreated with SAFE (100, 200, and 400 mg/kg) daily for one week. The control and APAP groups were intragastrically administered with distilled water, and NAC group was treated with N-Acetyl-L-cysteine (NAC) before APAP exposure. The results manifested that SAFE significantly improved survival rates, attenuated hepatic histological damage, and decreased the alanine aminotransferase (ALT) and aspartate aminotransferase (AST) levels in serum in APAP-exposed mice. SAFE treatment also increased glutathione (GSH) level and glutathione peroxidase (GSH-Px) activity, enhanced catalase (CAT), and total antioxidant capacity (T-AOC), as well as reducing malondialdehyde (MDA) level in liver. In addition, the formation of tumor necrosis factor-alpha (TNF-α), interleukin 6 (IL-6), and elevation of myeloperoxidase (MPO) in APAP-exposed mice were inhibited after SAFE treatment. And SAFE also displayed high DPPH radical scavenging activity and reducing power in vitro. The main bioactive components of SAFE such as total phenol, flavonoid, condensed tannin, and carbohydrate were determined. The current study proved that SAFE exerted potential protective effect against APAP-induced acute liver injury, which might be associated with the antioxidant and anti-inflammatory activities of SAFE.
机译:服用过量对乙酰氨基酚(APAP)会导致急性肝损伤。这项研究的目的是评估红树林植物桑那拉无瓣果提取物(SAFE)对APAP诱导的小鼠肝损伤的抗氧化活性和保肝作用。每天用SAFE(100、200和400 mg / kg)口服对小鼠进行一周的预处理。对照组和APAP组在腹腔内注射蒸馏水,NAC组在暴露于APAP之前接受N-乙酰-L-半胱氨酸(NAC)处理。结果表明,SAFE可显着提高暴露于APAP的小鼠血清中的存活率,减轻肝脏组织学损伤并降低血清丙氨酸氨基转移酶(ALT)和天冬氨酸氨基转移酶(AST)的水平。 SAFE治疗还可以提高肝脏中的谷胱甘肽(GSH)和谷胱甘肽过氧化物酶(GSH-Px)活性,增强过氧化氢酶(CAT)和总抗氧化能力(T-AOC),并降低丙二醛(MDA)含量。此外,在SAFE处理后,可抑制暴露于APAP的小鼠中的肿瘤坏死因子-α(TNF-α),白介素6(IL-6)的形成和髓过氧化物酶(MPO)的升高。 SAFE还显示出较高的DPPH自由基清除活性,并在体外降低了功率。确定了SAFE的主要生物活性成分,例如总酚,类黄酮,缩合单宁和碳水化合物。目前的研究证明,SAFE对APAP引起的急性肝损伤具有潜在的保护作用,这可能与SAFE的抗氧化和抗炎活性有关。

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