紫外线-328 的前瞻性肝毒性作用以及二甲氧基姜黄素对斑马鱼肝毒性的肯定性解救作用

S. Senthilmurugan, R. Prinitha, S. Miltonprabu
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摘要

由于 BUV-328(苯并三唑紫外线稳定剂)即使在低浓度下也具有毒性,因此在许多生物和环境基质中的空前使用对环境具有重要意义。为了更好地了解 DiMC 对暴露于亚致死浓度 BUV-328 的斑马鱼肝脏组织的保护功能,本研究对 DiMC 进行了评估。成年斑马鱼接触亚致死浓度为 55µg/l 的 BUV-328。另一组斑马鱼补充 DiMC,以研究 DiMC 对 BUV-328 诱导的肝毒性的改善潜力。对暴露组的氧化应激生化指标、组织病理学变化和抗氧化酶进行了测定。本研究的结果表明,暴露于 BUV-328 会增加氧化应激标记物,降低抗氧化酶的活性,改变肝脏中的生化成分。研究发现,BUV-328 暴露组肝组织病理学损伤增加,如肥大、细胞和核增大、细胞质和核变性、细胞核坏死和萎缩、脂质和细胞质空泡化、核向周边移位。BUV-328 诱导的氧化、生化和组织学改变在添加 DiMC 的组中几乎得到恢复,这表明 DiMC 对 BUV-328 诱导的肝毒性具有保护作用。
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Prospective hepatotoxic effect of UV-328 and its affirmable rescue by Dimethoxy curcumin in Zebrafish
The unprecedented usage of BUV-328 (Benzotriazole Ultraviolet Stabilizer) in many biological and environmental matrices is of acute environmental importance because of its toxicity even at low concentrations. To better understand the protective function of DiMC on the liver tissues of zebrafish exposed to sublethal concentration of BUV-328 was assessed in the present investigation. Adult zebrafish were exposed to BUV-328 at sublethal concentrations of 55µg/l. The responses were assessed in the liver tissues at 28 days and another group was supplemented with DiMC to investigate its ameliorative potential against BUV-328 induced hepatotoxicity. Biochemical markers of oxidative stress, histopathological changes, and antioxidant enzymes were measured in the exposed groups. The outcomes of our present study revealed that BUV-328 exposure upregulated the oxidative stress markers and diminished the activities of the antioxidant enzymes, altered the biochemical constituents in liver. Histopathological abrasions such as hypertrophy, cellular and nuclear enlargement, cytoplasmic and nuclear degeneration, necrosis with pyknotic nuclei, lipid and cytoplasmic vacuolization and nuclear displacement to the periphery were found to be increased in BUV-328 exposure group. The oxidative, biochemical and histological alterations induced by BUV-328 were almost recuperated in DiMC supplemented group which signifies its protective influence against BUV-328 incited hepatotoxicity.
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