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越南传统药用植物的抗氧化和细胞增殖特性。

Antioxidant and Cell Proliferation Properties of the Vietnamese Traditional Medicinal Plant .

机构信息

Department of Pharmacy, College of Pharmacy, Kangwon National University, 1 Gangwondaegakgil Chuncheon-si, Gangwon-do 24341, Korea.

Faculty of Pharmacy, Phenikaa University, Yen Nghia, Ha Dong district, Hanoi 12116, Vietnam.

出版信息

Molecules. 2020 Oct 19;25(20):4800. doi: 10.3390/molecules25204800.

DOI:10.3390/molecules25204800
PMID:33086647
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7587549/
Abstract

is regarded as one of the most important medicinal plants in the traditional medicine system of Vietnam. However, scientific evidence for the antioxidant effects against lipid peroxidation and the potential effects in cancer of this plant are lacking. In our experiments, 70% ethanolic extracts of leaves (LPP) and stem bark (SPP) were evaluated for their low-density lipoprotein (LDL) oxidation and cytotoxic activity against cancer cell lines. Both LPP and SPP inhibited Cu-mediated LDL by increasing the lag time of conjugated diene formation and inhibiting the generation of thiobarbituric acid reactive substances (TBARS) in a dose-dependent manner. In cancer cells, LPP and SPP triggered the most potent cytotoxic effects against human leukemia cells, CRF-SBA and HL-60, with half-maximal inhibitory concentration (IC) values ranging from 118.5 to 157.2 µg/mL. SPP exhibited significant cytotoxicity against MIA PACA2, A549, and KG cell lines with IC values of 167.5, 244.1 and 255.0 µg/mL, respectively. Meanwhile, LPP showed cytotoxic activity against KG with an IC value of 228.1 µg/mL. SPP mediated cytotoxicity in HL-60 and CCRF-SBA cells through the activation of the apoptosis pathway, including the activation of caspases 3, and 9 and poly (ADP-ribose) polymerase (PARP). These results suggested that SPP may prevent the development and progression of atherosclerosis and leukemia in humans.

摘要

被认为是越南传统医学体系中最重要的药用植物之一。然而,目前缺乏关于该植物抗氧化作用对抗脂质过氧化和潜在抗癌作用的科学证据。在我们的实验中,评估了叶(LPP)和茎皮(SPP)的 70%乙醇提取物对低密度脂蛋白(LDL)氧化和抗癌细胞系的细胞毒性作用。LPP 和 SPP 均通过增加共轭二烯形成的滞后时间和抑制硫代巴比妥酸反应物质(TBARS)的生成,以剂量依赖的方式抑制 Cu 介导的 LDL 氧化。在癌细胞中,LPP 和 SPP 对人白血病细胞 CRF-SBA 和 HL-60 触发了最强的细胞毒性作用,半最大抑制浓度(IC)值范围为 118.5 至 157.2µg/mL。SPP 对 MIA PACA2、A549 和 KG 细胞系的细胞毒性作用显著,IC 值分别为 167.5、244.1 和 255.0µg/mL。同时,LPP 对 KG 的细胞毒性作用的 IC 值为 228.1µg/mL。SPP 通过激活凋亡途径,包括激活半胱天冬酶 3 和 9 以及多聚(ADP-核糖)聚合酶(PARP),介导 HL-60 和 CCRF-SBA 细胞的细胞毒性。这些结果表明,SPP 可能预防人类动脉粥样硬化和白血病的发生和发展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebdd/7587549/2a9c06b1305d/molecules-25-04800-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebdd/7587549/e42ab4c6fe50/molecules-25-04800-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebdd/7587549/d2b3eb5eb95c/molecules-25-04800-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebdd/7587549/c04c90b4d450/molecules-25-04800-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebdd/7587549/2a9c06b1305d/molecules-25-04800-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebdd/7587549/e42ab4c6fe50/molecules-25-04800-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebdd/7587549/d2b3eb5eb95c/molecules-25-04800-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebdd/7587549/c04c90b4d450/molecules-25-04800-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebdd/7587549/2a9c06b1305d/molecules-25-04800-g004.jpg

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