芦竹树皮的生物活性和植物化学研究

H. El-Rafie, A. Zeid, A. Sleem, Rs Mohammed
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引用次数: 7

摘要

牛角豆属是豆科开花植物的一个属,是一个经济上重要的大科。本研究旨在首次对芦笋树皮总乙醇和连续提取物进行生物活性筛选。研究的生物活性包括四氧嘧啶诱导的糖尿病大鼠的糖尿病管理,对四种人类肿瘤细胞系的细胞毒活性和对ccl4诱导的大鼠肝毒性的肝保护活性,并通过测定血清标记酶如AST, ALT和ALP来研究其活性。其中,石油醚提取物(PEE)的生物活性最高,100mg的PEE提取物的抗糖尿病活性为二甲双胍的74.38%。与对照药物阿霉素相比,其对MCF-7 (IC50=2.35µg)、Hela (IC50=3.85µg)和HEPG-2 (IC50=9.54µg)的抗增殖活性显著。以水飞蓟素为参比药物,PEE的肝功能酶AST、ALT和ALP浓度较未治疗的CCl - 4肝损伤组分别下降29.18%、28.26%和34.11%,证明PEE具有保肝活性。基于以上结果,我们对其进行了进一步的植物化学研究,包括对其组分进行GC/MS分析,对其甾醇组分进行GLC分析,对PEE进行柱层析和TLC分离,以分离其生物活性成分。
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Bioactivities and Phytochemical Studies of Acrocarpus fraxinifolius Bark Wight Arn
Acrocarpus is a genus of flowering plants in the legume family Fabaceae which considered as a large and economically important family. This study aimed to carry out the biological activity screening on the total ethanol and successive extracts of Acrocarpus fraxinofolius (A. fraxinofolius) bark, for the first time. The biological activity studied embraced, management of diabetes in alloxan induced diabetic rats, cytotoxic activity against four human tumor cell lines and hepatoprotective activity against CCl4-induced hepatotoxicity in rats and the activity was studied by assaying the serum marker enzymes like AST, ALT, and ALP. Concerning this, the petroleum ether extract (PEE) showed the most bioactive extract where, the anti-diabetic activity exhibited by 100mg of PEE extract was 74.38% relative to metformin. It also showed a significant anti-proliferative activity against MCF-7 (IC50=2.35µg), Hela (IC50=3.85µg) and HEPG-2 (IC50=9.54µg) compared with Doxorubicin as reference drug. The hepatoprotective activity of the PEE was evidenced by a significant decrease in the liver function enzymes, i.e. AST, ALT and ALP by 29.18%, 28.26%, and 34.11%, respectively, using silymarin as the reference drug, compared to their concentration levels in an untreated group with liver damage induced by CCl₄. Based on the above outcomes, further phytochemical investigation including GC/MS analysis of its fractions, GLC analysis of its sterol fraction, column chromatography and TLC fractionation of PEE to separate its bioactive compounds were conducted.
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