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印苦楝种子中的柠檬苦素的细胞毒性和诱导细胞凋亡活性。

Cytotoxic and apoptosis-inducing activities of limonoids from the seeds of Azadirachta indica (neem).

机构信息

College of Science and Technology, Nihon University, 1-8-14 Kanda Surugadai, Chiyoda-ku, Tokyo 101-8308, Japan.

出版信息

J Nat Prod. 2011 Apr 25;74(4):866-70. doi: 10.1021/np100783k. Epub 2011 Mar 7.

Abstract

Thirty-five limonoids, including 15 of the azadiradione type (1-15), five of the gedunin type (16-20), four of the azadirachtin type (21-24), nine of the nimbin type (25-33), and two degraded limonoids (34, 35), isolated from Azadirachta indica seed extracts, were evaluated for their cytotoxic activities against five human cancer cell lines. Seven compounds (3, 6, 7, 16, 18, 28, and 29) exhibited cytotoxic activity against one or more cell lines. Among these compounds, 7-deacetyl-7-benzoylepoxyazadiradione (7), 7-deacetyl-7-benzoylgeduin (18), and 28-deoxonimbolide (28) exhibited potent cytotoxic activity against HL60 leukemia cells with IC(50) values in the range 2.7-3.1 μM. Compounds 7, 18, and 28 induced early apoptosis in HL60 cells, observed by flow cytometry. Western blot analysis showed that compounds 7, 18, and 28 activated caspases-3, -8, and -9 in HL60 cells. This suggested that compounds 7, 18, and 28 induced apoptotic cell death in HL60 cells via both the mitochondrial- and the death receptor-mediated pathways. Futhermore, compound 7 was shown to possess high selective cytotoxicity for leukemia cells since it exhibited only weak cytotoxicity against a normal lymphocyte cell line (RPMI 1788).

摘要

从印楝种子提取物中分离得到的 35 种柠檬苦素类化合物,包括 15 种阿扎迪定酮型(1-15)、5 种吉德宁型(16-20)、4 种阿扎特金型(21-24)、9 种尼宾型(25-33)和 2 种降解柠檬苦素(34、35),对 5 个人类癌细胞系进行了细胞毒性活性评价。有 7 种化合物(3、6、7、16、18、28 和 29)对一种或多种细胞系表现出细胞毒性活性。在这些化合物中,7-脱乙酰基-7-苯甲酰氧基阿扎定酮(7)、7-脱乙酰基-7-苯甲酰吉德宁(18)和 28-脱氧化南美藤烯内酯(28)对 HL60 白血病细胞表现出很强的细胞毒性活性,IC50 值在 2.7-3.1 μM 范围内。化合物 7、18 和 28 通过流式细胞术观察到诱导 HL60 细胞早期凋亡。Western blot 分析表明,化合物 7、18 和 28 在 HL60 细胞中激活了 caspase-3、-8 和 -9。这表明化合物 7、18 和 28 通过线粒体和死亡受体介导的途径诱导 HL60 细胞凋亡性细胞死亡。此外,化合物 7 对白血病细胞具有高选择性细胞毒性,因为它对正常淋巴细胞系(RPMI 1788)仅表现出较弱的细胞毒性。

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