服用啶虫脒对肝脏中 Bcl-2 免疫活性的影响

Gökhan Nur
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摘要

本研究旨在显示新烟碱类杀虫剂啶虫脒对 B 细胞淋巴瘤 2(Bcl-2)基因表达的影响,Bcl-2 基因在肝组织凋亡机制中发挥着重要作用。研究共分为四组,分别施用三种剂量的啶虫脒(5、10 和 15 毫克/千克),以及不施用任何物质的阴性组。小鼠灌胃啶虫脒 14 天后颈椎脱臼处死,切除的肝组织在 10%的甲醛溶液中固定,用于组织学和免疫组化分析,并在常规组织随访后用石蜡封片,切片经血涂片和免疫染色。组织学分析表明,对照组肝组织正常;而啶虫脒处理组肝窦扩张、血管舒张、肝实质坏死和脂肪变性,且随剂量的增加而增加。肝组织中的 Bcl-2 免疫反应出现在窦状上皮细胞中。在对照组和 5 mg kg-1 组中观察到严重的 Bcl-2 免疫反应,在 10 mg kg-1 和 15 mg kg-1 啶虫脒处理组中观察到中度的 Bcl-2 免疫反应。从中央静脉到基尔南间隙的区域均可观察到 Bcl-2 免疫反应。据观察,研究中使用的啶虫脒对肝组织有毒性作用,影响了凋亡途径中重要的生物标志物 bcl-2 的表达,并导致 bcl-2 免疫活性呈剂量依赖性下降。
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The Effect of Acetamiprid Administration on Bcl-2 Immunoreactivity in the Liver
This study aimed to show the effect of acetamiprid, a neonicotinoid insecticide, on B-cell lymphoma 2 (Bcl-2) gene expression, which plays an important role in apoptotic mechanisms in liver tissue. The study consisted of four groups in total, in which three doses of acetamiprid (5, 10, and 15 mg kg-1) were administered, together with the negative group, in which no substance was administered. Liver tissues resected from mice sacrificed by cervical dislocation after 14 days of acetamiprid administration by gavage were fixed in a 10% formaldehyde solution for histological and immunohistochemical analyses and blocked in paraffin after routine tissue follow-up, and sections were stained with haematoxylin-eosin and immunostaining. Histological analysis revealed normal liver tissue in the control group; whereas, sinusoidal dilatation, vasodilatation, and necrosis and steatosis in the parenchyma were found in the acetamiprid-treated group at an increasing rate depending on the dose amount. The immunoreactivity of Bcl-2 in liver tissue was observed in the sinusoidal epithelium. Bcl-2 immunoreactivity was observed severely in the control and 5 mg kg-1 groups and moderately in the 10 mg kg-1 and 15 mg kg-1 acetamiprid-treated groups. Bcl-2 immunoreactivity was observed homogenously in the region from the central vein to the Kiernan’s space. It was observed that acetamiprid used in the study showed a toxic effect on liver tissue, affected bcl-2 expression, an important biomarker in apoptotic pathways, and induced a dose-dependent decrease in bcl-2 immunoreactivity.
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