Structure-activity relationship of a neurite outgrowth-promoting substance purified from the brown alga, Sargassum macrocarpum, and its analogues on PC12D cells

被引:16
作者
Tsang, CK [1 ]
Sagara, A [1 ]
Kamei, Y [1 ]
机构
[1] Saga Univ, Marine & Highland Biosci Ctr, Saga 8470021, Japan
关键词
carotenoids; nerve growth factor; neurite outgrowth; quinones; Sargassum macrocarpum; structure-activity;
D O I
10.1023/A:1017540620106
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The structure-activity relationship of a neurite outgrowth-promoting substance (designated as MC14) from the brown alga, Sargassum macrocarpum, was analysed. Eight synthetic carotenoids and 1,4-benzoquinone were used to determine the moiety of the MC14 molecule structurally responsible for the nerve growth factor (NGF)-mediated neurite outgrowth-promoting activity on PC12D cells. The bioassays showed that none of these carotenoids exhibited NGF-potentiating activity. In contrast, 1,4-benzoquinone enhanced significantly NGF-mediated neurite outgrowth from PC12D cells, there being a 260% increase over the activity of negative control (10 ng mL(-1) NGF). The effect of quinone structure on NGF-potentiating activity, when examined using 12 naturally occurring quinones, demonstrated that lawsone, alizarin and lapachol significantly enhanced NGF-mediated neurite outgrowth by 329%, 325% and 265%, respectively, of that in the negative control. These results show that quinone is the structural moiety of MC14 molecule responsible for the neurite outgrowth-promoting activity. In addition, the hydroxyl group bonded to quinone had a significant effect on neuritogenic activity. The bearing of a hydroxyl group at the 1'-position of benzoquinone, and the bearing of two hydroxyl groups at the 1' and 2'-positions of anthraquinone, played a crucial role in enhancing the neurite outgrowth-promoting action of NGF.
引用
收藏
页码:349 / 357
页数:9
相关论文
共 19 条
[1]  
BARDE YA, 1994, MOL NEUROBIOLOGY MEC, P45
[2]   Advances and challenges in the prevention and treatment of Alzheimer's disease [J].
Brinton, RD ;
Yamazaki, RS .
PHARMACEUTICAL RESEARCH, 1998, 15 (03) :386-398
[3]   The role of neuronal growth factors in neurodegenerative disorders of the human brain [J].
Connor, B ;
Dragunow, M .
BRAIN RESEARCH REVIEWS, 1998, 27 (01) :1-39
[4]  
EBENDAL T, 1991, PLASTICITY REGENERAT, P164
[5]   SOMATOSTATIN ENHANCES NERVE GROWTH FACTOR-INDUCED NEURITE OUTGROWTH IN PC12 CELLS [J].
FERRIERO, DM ;
SHELDON, RA ;
MESSING, RO .
DEVELOPMENTAL BRAIN RESEARCH, 1994, 80 (1-2) :13-18
[6]   AMELIORATION OF CHOLINERGIC NEURON ATROPHY AND SPATIAL MEMORY IMPAIRMENT IN AGED RATS BY NERVE GROWTH-FACTOR [J].
FISCHER, W ;
WICTORIN, K ;
BJORKLUND, A ;
WILLIAMS, LR ;
VARON, S ;
GAGE, FH .
NATURE, 1987, 329 (6134) :65-68
[7]  
GUNNING PW, 1981, J NEUROSCI, V1, P1085
[8]  
HEFTI F, 1986, J NEUROSCI, V6, P2155
[9]   A novel fungal metabolite NG-061 enhances and mimics neurotrophic effect of nerve growth factor (NGF) on neurite outgrowth in PC12 cells [J].
Ito, M ;
Sakai, N ;
Ito, K ;
Mizobe, F ;
Bhandari, R ;
Eguchi, T ;
Kakinuma, K ;
Hanada, K ;
Mizoue, K .
JOURNAL OF ANTIBIOTICS, 1999, 52 (03) :224-230
[10]   Nardosinone, a novel enhancer of nerve growth factor in neurite outgrowth from PC12D cells [J].
Li, P ;
Matsunaga, K ;
Yamamoto, K ;
Yoshikawa, R ;
Kawashima, K ;
Ohizumi, Y .
NEUROSCIENCE LETTERS, 1999, 273 (01) :53-56