马尾草提取物表达Caspase-3抑制伯氏疟原虫感染小鼠肝细胞凋亡

A. M. Ukratalo
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引用次数: 0

摘要

细胞凋亡过程是一个内外因素综合作用的过程,涉及多种酶(Caspase-9、-8、-7、-6、-3)在细胞凋亡过程中起主要作用。本研究旨在通过表达caspase-3,研究褐藻甲醇提取物马尾藻对感染伯氏疟原虫小鼠肝细胞凋亡的抑制作用。体重20-30克的小鼠每头感染伯氏疟原虫可达0.1毫升,直至寄生虫率达到1-5%。小鼠(小家鼠)分别以1、10、100、100、200、100克/ 100毫升剂量给予重复马尾藻甲醇提取物,连续4 d观察至第6天。免疫组化染色观察caspase-3的表达。观察结果将作描述性分析。结果表明,马尾藻甲醇提取物能抑制伯氏疟原虫感染小鼠肝细胞凋亡。本研究中Caspase-3表达的减少被认为是由于褐藻中含有黄酮类化合物、单宁和皂苷,这些化合物可以通过NF-kB的作用降低促炎细胞因子Caspase-3, NF-kB是一种转录因子,在刺激和协调先天和适应性免疫反应中起作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Inhibition of Apoptosis of Liver Cells of Mice Infected With Plasmodium berghei Through The Expression of Caspase-3 Using Sargassum duplicatum Extract
The process of apoptosis is an integrated process between external and internal factors involving several enzymes (Caspase-9, -8, -7, -6, -3) that act as major players in the process of apoptosis. This research aims to determine the potential of brown algae methanol extract Sargassum duplicatum against inhibition of apoptosis of liver cells of mice infected with Plasmodium berghei through the expression of caspase-3. Mice weighing 20–30 grams in Plasmodium berghei infection as much as 0.1 ml per head and left until the percent of parasitemia reaches 1-5%. Then mice (Mus musculus) were given methanol extract of Sargassum duplicatum seaweed at a dose of 1 gr / 100 ml, 10 gr / 100 ml, 100, gr / 100 ml, and 200 gr / 100 ml for 4 consecutive days and observed until day 6. After that, a histological preparation was made with immunohistochemistry staining to see the expression of caspase-3. The results of the observations will be analyzed descriptively. The results showed that Sargassum duplicatum methanol extract was able to inhibit liver cell apoptosis in mice infected with Plasmodium berghei. The decrease in Caspase-3 expression in this study is thought to be caused because the brown algae Sargassum duplicatum contains flavonoid compounds, tannins, and saponins which can reduce the pro-inflammatory cytokine caspase-3 through the role of NF-kB which is a transcription factor that plays a role in stimulating and coordinating innate and adaptive immune responses.
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