Neuritogenesis of herbal geniposide-related compounds in PC12h cells

被引:5
作者
Chiba, Kenzo
Yamazaki, Matsumi
Kikuchi, Masafumi
Machida, Koichi
Kikuchi, Masao
机构
[1] Hokuriku Univ, Fac Pharmaceut Sci, Dept Biochem, Kanazawa, Ishikawa 9201181, Japan
[2] Hokuriku Univ, Org Frontier Res Prevent Pharmaceut Sci, Kanazawa, Ishikawa 9201181, Japan
[3] Tohoku Pharmaceut Univ, Aoba Ku, Sendai, Miyagi 9818558, Japan
关键词
iridoid compounds; optical isomer; neuritogenic activity; PC12h cells;
D O I
10.1248/jhs.52.743
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Previously, we have reported that geniposide, a compound isolated from an extract of Gardenia fructus, has neuritogenic activity in PC12h cells, a subclone of the rat pheochromocytoma cell. In this study, we have examined the effects of seven geniposide-related compounds (S-1, 6 alpha-hydroxygeniposide; S-2, 6 beta-hydroxygeniposide; S-3, 6 alpha-methoxygeniposide; S-4, 6 beta-methoxygeniposide; S-5, loganin; S-6, 7-ketologanin; and S-7, syringopicroside) isolated from various medicinal herbs. The geniposide-type iridoids S-1, S-2, S-3, and S-4, and S-7 induced neurite outgrowth that was similar or more potent to that of geniposide. S-2 and S-4, which are optical isomers of S-1 and S-3, respectively, were particularly potent. The 2 loganin-type iridoids, S-5 and S-6, showed less activity than geniposide. The neuritogenic activity of geniposide-type iridoids appears to be not necessarily correlated directly to their hydrophobicity. These results suggest that geniposide-type iridoids have potent neuritogenic activity and that specific configurations for the interactions between iridoid compounds and the target molecule are necessary for neuritogenic function.
引用
收藏
页码:743 / 747
页数:5
相关论文
共 15 条
[1]  
Chang IM, 1998, RES COMMUN MOL PATH, V102, P189
[2]   A DRUG USED IN TRADITIONAL MEDICINE - HARPAGOPHYTUM-PROCUMBENS DC .2. CARDIOVASCULAR ACTIVITY [J].
CIRCOSTA, C ;
OCCHIUTO, F ;
RAGUSA, S ;
TROVATO, A ;
TUMINO, G ;
BRIGUGLIO, F ;
DEPASQUALE, A .
JOURNAL OF ETHNOPHARMACOLOGY, 1984, 11 (03) :259-274
[3]   NATURALLY OCCURRING OXYGEN HETEROCYCLICS .9. ISOLATION AND CHARACTERIZATION OF GENIPIN [J].
DJERASSI, C ;
GRAY, JD ;
KINCL, FA .
JOURNAL OF ORGANIC CHEMISTRY, 1960, 25 (12) :2174-2177
[5]   Comparisons of geniposidic acid and geniposide on antitumor and radioprotection after sublethal irradiation [J].
Hsu, HY ;
Yang, JJ ;
Lin, SY ;
Lin, CC .
CANCER LETTERS, 1997, 113 (1-2) :31-37
[6]   STUDIES ON IRIDOID-RELATED COMPOUNDS .2. THE STRUCTURE AND ANTI-MICROBIAL ACTIVITY OF AGLUCONES OF GALIOSIDE AND GARDENOSIDE [J].
ISHIGURO, K ;
YAMAKI, M ;
TAKAGI, S .
JOURNAL OF NATURAL PRODUCTS, 1983, 46 (04) :532-536
[7]   Studies on the constituents of Gardenia species.: III.: New iridoid glycosides from the leaves of Gardenia jasminoides cv.fortuneana HARA [J].
Machida, K ;
Takehara, E ;
Kobayashi, H ;
Kikuchi, M .
CHEMICAL & PHARMACEUTICAL BULLETIN, 2003, 51 (12) :1417-1419
[8]   Studies on the constituents of Syringa species.: X.: Five new iridoid glycosides from the leaves of Syringa reticulata (BLUME) HARA [J].
Machida, K ;
Kaneko, A ;
Hosogai, T ;
Kakuda, R ;
Yaoita, Y ;
Kikuchi, M .
CHEMICAL & PHARMACEUTICAL BULLETIN, 2002, 50 (04) :493-497
[9]   ANALYSIS OF THE COMPONENTS OF LONICERA SPECIES .3. CAERULEOSIDE-A AND CAERULEOSIDE-B, BIS-IRIDOID GLUCOSIDES FROM LONICERA-CAERULEA [J].
MACHIDA, K ;
ASANO, J ;
KIKUCHI, M .
PHYTOCHEMISTRY, 1995, 39 (01) :111-114
[10]  
Machida K., 1993, TOHOKU YOKKA DAIGAKU, V40, P105