Chemical Constituents of Lycoris albiflora and their Cytotoxic Activities

被引:0
作者
Jitsuno, Maki [1 ]
Yokosuka, Akihito [1 ]
Hashimoto, Ken [2 ]
Amano, Osamu [3 ]
Sakagami, Hiroshi [2 ]
Mimaki, Yoshihiro [1 ]
机构
[1] Tokyo Univ Pharm & Life Sci, Sch Pharm, Tokyo 1920392, Japan
[2] Meikai Univ, Sch Dent, Dept Diagnost & Therapeut Sci, Div Pharmacol, Sakado, Saitama 3500283, Japan
[3] Meikai Univ, Sch Dent, Dept Human Dev & Fostering, Div Anat, Sakado, Saitama 3500283, Japan
关键词
Lycoris albiflora; Amaryllidaceae; alkaloids; HL-60; cells; HSC-2; cytotoxic activity; apoptosis; autophagy; AMARYLLIDACEAE ALKALOIDS; CELL-DEATH; BULBS; AUTOPHAGY; HERB;
D O I
暂无
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
An alcoholic extract of Lycoris albiflora (Amaryllidaceae) showed potent cytotoxic activity against HL-60 cells with an IC50 value of 1.7 mu g/mL. Phytochemical examination of the extract resulted in the isolation of 15 alkaloids, including two phenanthridine-type alkaloids (1, 2), one benzylphenethylamine-type alkaloid (3), two crinane-type alkaloids (4, 5), one pyrrolophenanthridine-type alkaloid (6), six lycorenan-type alkaloids (7-12), and three galanthamine-type alkaloids (13-15), together with three neolignans (16-18), two flavans (19, 20), and two acetophenone derivatives (21, 22). Compound 3 (hostasinine A) has not been isolated from Amaryllidaceae plants, and 1, 2, 4, 5, 7-9, 11, 12 and 14-22 are the first isolation and identification from L. albiflora. The phenanthridine-type alkaloids (1, 2), as well as the alkaloids (3-5); exhibited potent cytotoxic activities against not only HL-60 cells but also HSC-2 cells, thus leading to the conclusion that these alkaloids are mainly responsible for the cytotoxicity of the L. albiflora extract. Compound 1 (lycoricidinol), with the most potent cytotoxic activities, induced apoptosis in both HL-60 cells and HSC-2 cells. It is notable that 1 induced transient autophagy and morphological changes in mitochondria in the early stages of the apoptotic cell death process in HSC-2 cells.
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页码:187 / 192
页数:6
相关论文
共 23 条
[1]   Alkaloids from Narcissus cv Salome [J].
Almanza, GR ;
Fernandez, JM ;
Wakori, EWT ;
Viladomat, F ;
Codina, C ;
Bastida, J .
PHYTOCHEMISTRY, 1996, 43 (06) :1375-1378
[2]   A short synthesis of (+)-narciclasine via a strategy derived from stereocontrolled epoxide formation and SnCl4-catalyzed arene-epoxide coupling [J].
Elango, S ;
Yan, TH .
JOURNAL OF ORGANIC CHEMISTRY, 2002, 67 (20) :6954-6959
[3]   H-1 AND C-13 NMR ANALYSIS OF LYCORINE AND ALPHA-DIHYDROLYCORINE [J].
EVIDENTE, A ;
CICALA, MR ;
GIUDICIANNI, I ;
RANDAZZO, G ;
RICCIO, R .
PHYTOCHEMISTRY, 1983, 22 (02) :581-584
[4]   FREE AND GLUCOSYLOXY ACETOPHENONES FROM PANCRATIUM-BIFLORUM .31. [J].
GHOSAL, S ;
MITTAL, P ;
KUMAR, Y ;
SINGH, SK .
PHYTOCHEMISTRY, 1989, 28 (11) :3193-3196
[5]  
GONZALEZ GA, 2004, BIOCHEM SYST ECOL, V32, P179
[6]   ABSOLUTE-CONFIGURATION OF DEHYDRODICONIFERYL ALCOHOL [J].
HIRAI, N ;
OKAMOTO, M ;
UDAGAWA, H ;
YAMAMURO, M ;
KATO, M ;
KOSHIMIZU, K .
BIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY, 1994, 58 (09) :1679-1684
[7]   Antiproliferative Amaryllidaceae alkaloids isolated from the bulbs of Sprekelia formosissima and Hymenocallis x festalis [J].
Hohmann, J ;
Forgo, P ;
Molnár, J ;
Wolfard, K ;
Molnár, A ;
Thalhammer, T ;
Máthé, I ;
Sharples, D .
PLANTA MEDICA, 2002, 68 (05) :454-457
[8]   Total synthesis and biological evaluation of Amaryllidaceae alkaloids:: Narciclasine, ent-7-deoxypancratistatin, regioisomer of 7-deoxypancratistatin, 10b-epi-deoxypancratistatin, and truncated derivatives [J].
Hudlicky, T ;
Rinner, U ;
Gonzalez, D ;
Akgun, H ;
Schilling, S ;
Siengalewicz, P ;
Martinot, TA ;
Pettit, GR .
JOURNAL OF ORGANIC CHEMISTRY, 2002, 67 (25) :8726-8743
[9]  
Ito H, 2005, INT J ONCOL, V26, P1401
[10]  
JEFFS WP, 1985, J ORG CHEM, V50, P1732