菊花素纳米晶对毒死蜱暴露大鼠甲状腺的影响。

Tahereh Farkhondeh, Fatemeh Ahrari, Shahnaz Rajabi, Effat Alemzadeh, Behzad Mesbahzadeh, Maryam Rezaei, Sara Ziafati Majidi, Saeed Samarghandian
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引用次数: 0

摘要

背景:毒死蜱(Chlorpyrifos, CPF)是一种有机磷杀虫剂,主要用于农业害虫防治。目的:探讨菊花素纳米晶对高剂量毒死蜱暴露后雄性大鼠甲状腺激素和甲状腺组织的保护作用。方法:将大鼠随机分为6组,每组6只大鼠;健康对照组2例。用金菊素纳米晶(5 mg/kg)处理,3。金菊素纳米晶(10 mg/kg)处理,4。用金菊素纳米晶(5 mg/kg) +毒死蜱处理,5。用金菊素纳米晶(10 mg/kg) +毒死蜱处理,6。毒死蜱(30 mg/kg)处理。干预15天后,对大鼠进行麻醉,并从心脏取血测量甲状腺激素。然后,将甲状腺分离并保存在10%福尔马林中进行组织病理学研究。甲状腺样品也保存在-80°C,用于测量氧化应激参数。结果:各治疗组血清T3、T4浓度均较对照组显著降低(p < 0.01)。此外,激素水平检查显示,各组血浆TSH浓度变化无统计学意义(p > 0.05)。CPF和菊花素纳米晶体处理不影响甲状腺氧化生物标志物(MDA、GSH和NO)的水平。甲状腺组织切片的显微照片显示,所有组的甲状腺组织切片均可见空泡变性的滤泡上皮和缺失的胶体。结论:口服金菊素纳米晶不能抑制大剂量CPF对大鼠甲状腺的毒性作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Effect of Chrysin Nanocrystal on the Thyroid Gland of Rats Exposed to Chlorpyrifos.

Background: Chlorpyrifos (CPF) is an organophosphate insecticide that is mostly used in agriculture for pest control.

Aim: This investigation aimed to evaluate the possible protective role of chrysin nanocrystals on thyroid gland hormones and histology in male rats after exposure to a high dose of chlorpyrifos.

Method: Rats were randomly divided into 6 groups (6 rats in each group): 1. healthy control group, 2. treated with chrysin nanocrystal (5 mg/kg), 3. treated with chrysin nanocrystal (10 mg/kg), 4. treated with chrysin nanocrystal (5 mg/kg) + chlorpyrifos, 5. treated with chrysin nanocrystal (10 mg/kg) + chlorpyrifos, and 6. treated with chlorpyrifos (30 mg/kg). After 15 days of intervention, rats were anesthetized, and blood samples were taken from the heart to measure thyroid hormones. Then, the thyroid gland was isolated and stored in 10% formalin for histopathological studies. Thyroid samples were also stored at -80 ° C for measuring oxidative stress parameters.

Result: A significant reduction was observed in the serum concentrations of T3 and T4 in all treated groups compared with the control group (p < 0.01). In addition, hormone level examination revealed no statistically significant (p ˃ 0.05) changes in plasma TSH concentration in any of the groups. The treatment with CPF and chrysin nanocrystal did not affect the levels of oxidative biomarkers (MDA, GSH, and NO) in thyroid glands. Photomicrographs of a histological section of the thyroid gland showed vacuolar degenerated follicle epithelium and missing colloids in the histological section of the thyroid gland of all groups.

Conclusion: Our findings demonstrated that the oral administration of chrysin nanocrystals could not inhibit the toxic effect of a high dose of CPF on the thyroid gland in the rats.

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