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从鹅掌楸茎中提取的生物功能成分。

Bio-functional constituents from the stems of Liriodendron tulipifera.

机构信息

Department of Biotechnology, College of Life Science, Kaohsiung Medical University, 100, Shih-Chuan 1st Road, San-Ming District, Kaohsiung 80708, Taiwan.

出版信息

Molecules. 2012 Apr 10;17(4):4357-72. doi: 10.3390/molecules17044357.

Abstract

Four known compounds have been isolated from the stems of Liriodendron tulipifera, and the structures of these pure constituents were determined using spectroscopic analysis. Isolated compounds were screened for free radical scavenging ability, metal chelating power assay and ferric reducing antioxidant power assay (FRAP). The anti-tyrosinase effects of L. tulipifera compounds were calculated the inhibition of hydroxylation of L-tyrosine to L-dopa according to an in vitro mushroom tyrosinase assay. The study also examined the bio-effects of the four compounds on the human melanoma A375.S2, and showed that liriodenine (1) and (-)-norglaucine (4) significantly inhibited the proliferation of melanoma cells in the cell viability assay. Wound healing results indicated that liriodenine (1), (-)-glaucine (3) and (-)-norglaucine (4) exerted anti-migration potential. Interestingly, (-)-glaucine (3), neither liriodenine (1) nor (-)-norglaucine (4) showed promising anti-migration potential without inducing significant cytotoxicity. Furthermore, a dramatically increased level of intracellular reactive oxygen species (ROS) was detected from (-)-glaucine (3). The cell cycle assessment demonstrated a moderate G2/M accumulation by (-)-glaucine (3). The above results revealed the anti-cancer effects of L. tulipifera compounds, especially on the anti-migration ability indicating the promising chemopreventive agents to human skin melanoma cells.

摘要

从鹅掌楸的茎中分离得到了 4 种已知化合物,并通过光谱分析确定了这些纯成分的结构。对分离得到的化合物进行了自由基清除能力、金属螯合能力测定和铁还原抗氧化能力测定(FRAP)。根据体外蘑菇酪氨酸酶测定,计算了鹅掌楸化合物对酪氨酸酶的抑制作用,即抑制 L-酪氨酸羟化为 L-多巴的作用。该研究还检测了这四种化合物对人黑色素瘤 A375.S2 的生物效应,结果表明,里氧啶(1)和(-)-去甲北美黄连碱(4)显著抑制了细胞活力测定中黑色素瘤细胞的增殖。划痕愈合结果表明,里氧啶(1)、(-)-小檗碱(3)和(-)-去甲北美黄连碱(4)均具有抗迁移潜力。有趣的是,(-)-小檗碱(3)既没有抑制黑色素瘤细胞的迁移,也没有诱导明显的细胞毒性。此外,还从(-)-小檗碱(3)中检测到细胞内活性氧(ROS)水平显著增加。细胞周期评估显示(-)-小檗碱(3)可使细胞适度积累于 G2/M 期。上述结果揭示了鹅掌楸化合物的抗癌作用,尤其是对迁移能力的抑制作用,表明其具有开发为人皮肤黑色素瘤细胞化学预防剂的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ff9/6268983/bb87d6576a5d/molecules-17-04357-g001.jpg

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