壳聚糖纳米绿茶提取物对CCl4和乙醇对肝纤维化的修复作用:定量和超微结构研究

A. Safer
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引用次数: 1

摘要

通过超微结构研究了壳聚糖纳米绿茶对肝纤维化的抗氧化作用,定量比较了CCl4和乙醇作用对肝纤维化损伤的百分比差异以及壳聚糖纳米绿茶的抗氧化作用对肝纤维化的修复作用。特别是在消除CCl4和乙醇对细胞质和ECM的破坏作用方面。壳聚糖纳米绿茶具有多种有益活性。之前,我们简要报道了壳聚糖纳米绿茶在实验模型中完全破坏肝纤维化,但这是一个简短的描述和一个选定的领域。然而,在本报告中,我们试图对这种作用进行广泛的阐述,并对细胞质和细胞器的各个方面以及ECM部分进行一些详细的阐述。用200 ~ 250 nm大小的壳聚糖包封GTE颗粒,在CCl4和乙醇剂量作用3周后靶向大鼠肝纤维化。我们的数据表明,壳聚糖纳米gte诱导了ECM蛋白纤维材料的巨大变化,并使该区域变得非常光滑和清洁。受损细胞器恢复正常外观和功能,细胞质损伤部位高度愈合,实质ECM接近正常化,蛋白纤维温和去除,使视场光滑。这一鉴定可能解释了纳米gte的多重治疗和抗纤维化活性。
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Remediation of Hepatic Fibrosis as a Result of the use of CCl4 and Ethanol by Chitosan Nano-Green Tea Extract: Quantification and Ultrastructural Studies
Antioxidant effects of Chitosan nano-green tea on hepatic fibrosis was studies ultrastrucutrally with detailed quantification comparing the percentage differences between the damaged done by CCl4 and ethanol effects and the rehabilitation by the use of Chitosan nano-green tea’s antioxidant effect. Especially in demolishing the damaging effects of CCl4 and ethanol on both the cell cytoplasm and the ECM. Chitosan nano-green tea exhibited several beneficial activities. Previously, we briefly reported that Chitosan nano-green tea completely demolishes hepatofibrosis in experimental models, but it was a short account and on one selected area. However, in this report we try to give an extensive elaboration on such effect and some details regarding the various aspects of cytoplasm and organelles as well as the ECM part. The 200 to 250 nm sized chitosan encapsulated GTE particles were used targeting rat liver fibrosis after being treated with CCl4 and ethanol doses for three weeks. Our data indicates that chitosan nano-GTE-induced a great change in demolishing the ECM protein fibrous materials and had left the area extremely smooth and clean. Damaged cell organelles were back to normal appearance and functions, cell cytoplasm damaged parts were highly healed up, parenchyma ECM were close to normalization with gentle removal of protein fibers which led to the smoothness of the field. This identification may explain the multiple therapeutic and anti-fibrotic activities of the nano-GTE.
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