荆刺草对DMBA诱导大鼠肝癌的体内硅片研究

Heni Ratnasari, A. Rahma, Rifki Febriansah
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引用次数: 0

摘要

肝癌是全球癌症死亡的第二大常见原因。目前的治疗方法是化疗,但有很多缺点。以含黄酮类化合物的板多坦为化学预防剂。本研究是通过分子对接试验,与5氟尿嘧啶比较诺毕尔素化合物对VEGF、COX-2和C-Myc的抑制作用。致癌性试验将20只小鼠尾巴分为5个喂养组。以CMC-Na 0.5% 1 ml/200 g、DMBA 20 mg/kg BW和BHCF分别为750 mg/kg BW和1500 mg/kg BW对小鼠进行诱导。DMBA每周注射2次,连续5周。采用免疫组织化学和红木精-伊红进行组织学观察。薄层色谱显示BHCF中含有黄酮类化合物作为次生代谢产物。分子对接证实,诺比列素对VEGF的抑制作用较好,亲和值为-7.6 kcal/mol。诱导DMBA引起VEGF对肝组织的中度过度表达。组织学上,引入1500 mg/kg BW的BHCF比750 mg/kg BW的BHCF改善组织学程度更好。体外和体内实验结果表明,黄酮类化合物的存在可作为肝癌的化学预防药物。关键词:菊苣,DMBA,肝细胞癌,硅,体内
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Effect of Ageratum conyzoides L on Hepatocellular Carcinoma Rats Induced by DMBA based on In Vivo-In Silico Study
Liver cancer is the second most common cause of cancer deaths worldwide. Treatment that has been carried out was chemotherapy which has many disadvantages. Bandotan Herb (Ageratum conyzoides L.) containing flavonoid compounds was used as chemopreventive agents. This research was experimental study using molecular docking test of nobiletin compounds against VEGF, COX-2 and C-Myc compared to 5Fluorouracil. Carcinogenic test required 20 mice tails to be divided into 5 feeding groups. Induction was conducted on a peroral using CMC-Na 0.5% 1 ml/200 gram, DMBA 20 mg/kg BW and BHCF at a dose of 750 mg/kg BW and 1500 mg/kg BW. DMBA was injected 2 times a week for 5 weeks. Histological observation was carried out using Immunohistochemistry and Haematoxylin-Eosin. TLC stated that BHCF contained flavonoid as a secondary metabolites. Molecular docking proved that nobiletin was better in inhibiting the expression of VEGF with an affinity value -7.6 kcal/mol. Induction of DMBA caused moderate over-expression of VEGF against liver tissue. Histologically, the introduction of BHCF at a dose of 1500 mg/kg BW provides better improvement degrees of histology than 750 mg/kg BW. The presence of flavonoid can be used as chemopreventive agents for liver cancer based on in silico and in vivo assay. Keywords—Ageratum comyzoides L., DMBA, hepatocellular carcinoma, in silico, in vivo
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