首页> 外文期刊>Journal of applied toxicology >Comparison of the effects of erdosteine and N-acetylcysteine on apoptosis regulation in endotoxin-induced acute lung injury.
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Comparison of the effects of erdosteine and N-acetylcysteine on apoptosis regulation in endotoxin-induced acute lung injury.

机译:内啡肽和N-乙酰半胱氨酸对内毒素诱导的急性肺损伤中细胞凋亡调节作用的比较。

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摘要

This study was carried out to investigate comparatively the frequency of apoptosis in lung epithelial cells after intratracheal instillation of endotoxin [lipopolysaccharide (LPS)] in rats and the role of tumor necrosis factor alpha (TNF-alpha) on apoptosis, and the effects of erdosteine and N-acetylcysteine on the regulation of apoptosis. Female Wistar rats were given oral erdosteine (10-500 mg kg(-1)) or N-acetylcysteine (10-500 mg kg(-1)) once a day for 3 consecutive days. Then the rats were intratracheally instilled with LPS (5 mg kg(-1)) to induce acute lung injury. The rats were killed at 24 h after LPS administration. Lung tissue samples were stained with hematoxylin-eosin for histopathological assessments. The apoptosis level in the lung bronchial and bronchiolar epithelium was determined using the TUNEL (terminal deoxynucleotidyl transferase-mediated dUTP nick endlabelling) method. Cytoplasmic TNF-alpha was evaluated by immunohistochemistry. Pretreatment with erdosteine and pretreatment with N-acetylcysteine at a dose of 10 mg kg(-1) had no protective effect on LPS-induced lung injury. When the doses of drugs increased, the severity of the lung damage caused by LPS decreased. It was found that as the pretreatment dose of erdosteine was increased, the rate of apoptosis induced by LPS in lung epithelial cells decreased and this decrease was statistically significant in doses of 300 mg kg(-1) and 500 mg kg(-1). Pretreatment with N-acetylcysteine up to a dose of 500 mg kg(-1) did not show any significant effect on apoptosis regulation. It was noticed that both antioxidants had no significant effect on the local production level of TNF-alpha. These findings suggest that erdosteine could be a possible therapeutic agent for acute lethal lung injury and its mortality.
机译:本研究旨在比较气管内滴注大鼠内毒素[脂多糖(LPS)]后肺上皮细胞凋亡的频率,以及肿瘤坏死因子α(TNF-α)对细胞凋亡的作用以及厄多司坦的作用。和N-乙酰半胱氨酸对细胞凋亡的调节。雌性Wistar大鼠连续3天每天口服一次口服鄂多斯汀(10-500 mg kg(-1))或N-乙酰半胱氨酸(10-500 mg kg(-1))。然后将大鼠气管内滴注LPS(5 mg kg(-1))诱导急性肺损伤。 LPS给药后24小时处死大鼠。肺组织样品用苏木精-伊红染色以进行组织病理学评估。使用TUNEL(末端脱氧核苷酸转移酶介导的dUTP缺口末端标记)方法确定肺支气管和支气管上皮中的细胞凋亡水平。通过免疫组织化学评估细胞质的TNF-α。剂量为10 mg kg(-1)的Erdosteine预处理和N-乙酰半胱氨酸预处理对LPS诱导的肺损伤没有保护作用。当药物剂量增加时,由LPS引起的肺部损害的严重程度降低。发现随着鄂尔多斯汀预处理剂量的增加,LPS诱导的肺上皮细胞凋亡率降低,并且这种降低在300 mg kg(-1)和500 mg kg(-1)剂量下具有统计学意义。剂量达500 mg kg(-1)的N-乙酰半胱氨酸预处理未对细胞凋亡调节产生明显影响。注意到两种抗氧化剂对TNF-α的局部生产水平没有显着影响。这些发现表明,厄多半胱氨酸可能是急性致死性肺损伤及其死亡率的治疗剂。

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