洋甘菊提取物对2,4 -二氯苯氧乙酸致大鼠肝脏超微结构改变的潜在保护作用

Dalal A. Al-Baroudi, Thanaa. A. El-kholy, Reham A. Arafat, A. Ali
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引用次数: 2

摘要

本研究旨在通过电镜验证洋甘菊提取物的保肝作用及其对2,4 -二氯苯氧基乙酸(2,4 - d)引起的肝组织超薄结构变化的缓解作用。实验选用12 ~ 14周龄雄性Wistar大鼠,分为6组,每组6只。第一组作为对照。第二组和第三组分别口服累积剂量75和150 mg/kg体重(b.wt.) 2,4 - D。第四组只口服洋甘菊提取物(500 mg/kg b.wt)。最后两组服用洋甘菊提取物,剂量为2,4 - d(75或150毫克/公斤体重)。实验结束(4周),解剖大鼠肝脏,电镜观察。给药2,4 - d75 mg/kg的大鼠肝脏切片组织病理学检查显示,细胞核形状和大小、包膜和异染色质团块增加。给药2,4 - d150mg /kg后,线粒体、内质网、库普弗细胞固缩、改变,溶酶体和脂滴增加。洋甘菊组小鼠肝脏超微结构正常。洋甘菊和2,4 - d75治疗组,2,4 - d75诱导的所有退行性改变均有改善。洋甘菊和2,4 - d150组对细胞核和线粒体均有部分改善。由于其抗氧化特性,洋甘菊减少了2,4 - d引起的氧化损伤。建议服用洋甘菊提取物来改善肝毒性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Potential Protective Role of Chamomile Extract on Rat Liver Ultrastructural Changes Induced by 2, 4-Dichlorophenoxyacetic Acid
The current study aimed to demonstrate the hepatoprotective effect of chamomile extract and its role in relieving the ultrathin structure changes in liver tissue caused by 2, 4-Dichlorophenoxy acetic acid (2, 4-D) using electron microscopy.This experiment was performed on 12 -14 weeks old male Wistar rats divided into six groups (six animals each). The first group was kept as control. The second and third groups received orally accumulative doses of 75 and 150 mg/kg body weight (b.wt.), of 2, 4- D respectively. The forth group received orally Chamomile extract (500 mg/kg b.wt.) alone. The last two groups received Chamomile extract with either doses of 2, 4-D (75 or 150 mg/kg b.wt). At the end of the experimental period (4 weeks), the liver was dissected and examined by electron microscope. Histopathological examination of liver sections of rats administered 2, 4-D75 mg/kg showed differences in nuclear shapes and size, envelope and increase in heterochromatin masses. Adminstration of 2, 4-D150mg/kg showed pyknosis and changes inmitochondria, endoplasmic reticulum, Kupffer cells, increases in lysosomes and lipid droplets. Chamomile group showed the normal control ultra structure of the liver. In group treated with chamomile and 2, 4-D75,there was improvements in all degenerative changes induced by 2, 4-D75. Chamomile and 2, 4-D150 groupshowed partial improvement in both nucleus and the mitochondria. Chamomile reduces the oxidative damage induced by 2, 4-D due to its antioxidant properties. It is recommended that Chamomile extract can be taken to ameliorate hepatotoxicity.
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