Hosoda Kouichi, Shimomura Hirofumi, Wanibuchi Kiyofumi, Masui Hisashi, Amgalanbaatar Avarzed, Hayashi Shunji, Takahashi Takashi, Hirai Yoshikazu
Division of Bacteriology, Department of Infection and Immunity, Jichi Medical University, 3311-1, Yakushiji, Shimotsuke-shi, Tochigi. 329-0498, Japan.
Faculty of Pharmaceutical Sciences, Yokohama College of Pharmacy, 601, Matano-cho, Totsuka-ku, Yokohama, Kanagawa. 245-0066, Japan.
Sci Rep. 2015 Mar 9;5:8860. doi: 10.1038/srep08860.
This study demonstrated that the vitamin D₃ decomposition product VDP1 exerts an antibacterial action against Helicobacter pylori but not against other bacteria. Treatment with VDP1 induced a collapse of cell membrane structures of H. pylori and ultimately lysed the bacterial cells. A unique dimyristoyl phosphatidylethanolamine in the membrane lipid compositions contributed to the interaction of VDP1 with H. pylori cells. In separate experiments, VDP1 had no influence on the viability of the human cancer cell lines MKN45 and T47D and lacked any vitamin D₃-like hormonal action against the latter. In both (1)H and (13)C NMR analyses, the spectra patterns of VDP1 corresponded with those of Grundmann's ketone. These results suggest that VDP1 (or Grundmann's ketone-type indene compound) may become a fundamental structure for the development of new antibacterial substances with selective bactericidal action against H. pylori.
本研究表明,维生素D₃分解产物VDP1对幽门螺杆菌具有抗菌作用,但对其他细菌无此作用。用VDP1处理会导致幽门螺杆菌细胞膜结构崩溃,最终使细菌细胞裂解。膜脂成分中一种独特的二肉豆蔻酰磷脂酰乙醇胺促成了VDP1与幽门螺杆菌细胞的相互作用。在单独的实验中,VDP1对人癌细胞系MKN45和T47D的活力没有影响,且对后者缺乏任何维生素D₃样激素作用。在¹H和¹³C NMR分析中,VDP1的光谱模式与格伦德曼酮的光谱模式一致。这些结果表明,VDP1(或格伦德曼酮型茚化合物)可能成为开发对幽门螺杆菌具有选择性杀菌作用的新型抗菌物质的基本结构。