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 50 条
  • [1] Neuritogenesis of herbal (+)- and (-)-syringaresinols separated by chiral HPLC in PC12h and neuro2a cells
    Chiba, K
    Yamazaki, M
    Umegaki, E
    Li, MR
    Xu, ZW
    Terada, S
    Taka, M
    Naoi, N
    Mohri, T
    [J]. BIOLOGICAL & PHARMACEUTICAL BULLETIN, 2002, 25 (06) : 791 - 793
  • [2] Fundamental role of nitric oxide in neuritogenesis of PC12h cells
    Yamazaki, M
    Chiba, K
    Mohri, T
    [J]. BRITISH JOURNAL OF PHARMACOLOGY, 2005, 146 (05) : 662 - 669
  • [3] Expression of functional nitric oxide synthase for neuritogenesis in PC12h cells
    Yamazaki, Matsumi
    Chiba, Kenzo
    [J]. JOURNAL OF HEALTH SCIENCE, 2006, 52 (06) : 769 - 773
  • [4] Proteasome in PC12h cells
    Ohtani-Kaneko, R
    Yamashita, K
    Iigo, M
    Hara, M
    Hirata, K
    Kumai, T
    Onodera, Y
    [J]. ADVANCES IN COMPARATIVE ENDOCRINOLOGY, TOMES 1 AND 2, 1997, : 1183 - 1187
  • [5] EFFECT OF NATURAL IRIDOID COMPOUNDS ON DIFFERENTIATION OF PC12H CELLS
    YAMAZAKI, M
    IMAKURA, K
    CHIBA, K
    MOHRI, T
    [J]. JOURNAL OF NEUROCHEMISTRY, 1995, 65 : S80 - S80
  • [6] Characterization of Exocytotic Events From Single PC12 Cells: Amperometric Studies in Native PC12h, DA-Loaded PC12h and Bovine Adrenal Chromaffin Cells
    Nobuyuki Sasakawa
    Norie Murayama
    Konosuke Kumakura
    [J]. Cellular and Molecular Neurobiology, 2005, 25 : 777 - 787
  • [7] Differences in neuritogenic response to nitric oxide in PC12 and PC12h cells
    Yamazaki, M
    Chiba, K
    Mohri, T
    [J]. NEUROSCIENCE LETTERS, 2006, 393 (2-3) : 222 - 225
  • [8] Characterization of exocytotic events from single PC12 cells: Amperometric studies in native PC12h, DA-loaded PC12h and bovine adrenal chromaffin cells
    Sasakawa, N
    Murayama, N
    Kumakura, K
    [J]. CELLULAR AND MOLECULAR NEUROBIOLOGY, 2005, 25 (3-4) : 777 - 787
  • [9] DEPOLARIZATION-INDUCED TYROSINE PHOSPHORYLATION IN PC12H CELLS
    OKUMURA, N
    OKADA, M
    NAKAGAWA, H
    [J]. JOURNAL OF BIOCHEMISTRY, 1994, 116 (02): : 346 - 350
  • [10] ENHANCEMENT OF NEURITE OUTGROWTH IN PC12H CELLS BY A PROTEASE INHIBITOR
    SAITO, Y
    KAWASHIMA, S
    [J]. NEUROSCIENCE LETTERS, 1988, 89 (01) : 102 - 107