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Publication
Featured researches published by Osamu Iida.
Journal of Agricultural and Food Chemistry | 2008
Kaori Yoshida; Atsuyuki Hishida; Osamu Iida; Keizo Hosokawa; Jun Kawabata
In the screening experiments for rat intestinal alpha-glucosidase inhibitors in 218 plants cultivated in the Japanese temperate region, potent maltase-inhibiting activity was found in the extract of flowers of Spiraea cantoniensis. The enzyme assay guided fractionation of the extract led to the isolation of three flavonol caffeoylglycosides, quercetin 3- O-(6- O-caffeoyl)-beta-galactoside ( 1), kaempferol 3- O-(6- O-caffeoyl)-beta-galactoside ( 2), and kaempferol 3- O-(6- O-caffeoyl)-beta-glucoside ( 3), as rat intestinal maltase inhibitors. This is the first report on the alpha-glucosidase-inhibitory activity of those flavonol caffeoylglycosides. Comparison in the activity of the isolates indicated the importance of caffeoyl substructures in the molecule for the alpha-glucosidase-inhibiting activity. The relatively high contents of the active isolates in the plant suggest that S. cantoniensis could be physiologically useful for treatment of diabetes.
Bioscience, Biotechnology, and Biochemistry | 2010
Keisuke Takahashi; Yasuyuki Yoshioka; Eisuke Kato; Shigeki Katsuki; Osamu Iida; Keizo Hosokawa; Jun Kawabata
In screening experiments for rat intestinal α-glucosidase (sucrase and maltase) inhibitors in 325 plants cultivated in Japan’s southern island, of Tanegashima, marked inhibition against both sucrase and maltase was found in the extract of the fruit of Solanum torvum. Enzyme-assay guided fractionation of the extract led to the isolation of methyl caffeate (1) as a rat intestinal sucrase and maltase inhibitor. We examined 13 caffeoyl derivatives for sucrase- and maltase-inhibitory activities. The results showed that methyl caffeate (1) had a most favorable structure for both sucrase and maltase inhibition, except for a higher activity of methyl 3,4,5-trihydroxycinnamate (14) against sucrase. Its moderate inhibitory action against α-glucosidase provides a prospect for antidiabetic usage of S. torvum fruit.
Journal of Natural Products | 2010
Kaori Yoshida; Atsuyuki Hishida; Osamu Iida; Keizo Hosokawa; Jun Kawabata
Six new monoterpene acylglucosides named kodemariosides A-F (1-6) were isolated from the leaves and flowers of Spiraea cantoniensis. Their absolute structures including a highly oxygenated monoterpene aglycon part were determined by NMR experiments and chemical derivatization.
Journal of Agricultural and Food Chemistry | 2017
Taichi Yoshitomi; Naohiro Oshima; Yuto Goto; Shunsuke Nakamori; Daigo Wakana; Naoko Anjiki; Koji Sugimura; Noriaki Kawano; Hiroyuki Fuchino; Osamu Iida; Toshiko Kagawa; Hideto Jinno; Nobuo Kawahara; Yoshinori Kobayashi; Takuro Maruyama
To construct a model formula to evaluate the thermogenetic effect of ginger (Zingiber officinale Roscoe) from the ingredient information, we established transient receptor potential vanilloid subtype 1 (TRPV1)-stimulating activity prediction models by using a partial least-squares projections to latent structures (PLS) regression analysis in which the ingredient data from liquid chromatography-high-resolution mass spectrometry (LC-HRMS) and the stimulating activity values for TRPV1 receptor were used as explanatory and objective variables, respectively. By optimizing the peak extraction condition of the LC-HRMS data and the data preprocessing parameters of the PLS regression analysis, we succeeded in the construction of a TRPV1-stimulating activity prediction model with high precision ability. We then searched for the components responsible for the TRPV1-stimulating activity by analyzing the loading plot and s-plot of the model, and we identified [6]-gingerol (1) and hexahydrocurcumin (3) as TRPV1-stimulating activity components.
Journal of Natural Medicines | 2015
Masashi Matsumoto; Manabu Hirayama; Norihiro Ohtomi; Takeshi Ohno; Yukihiro Nomura; Osamu Iida; Koji Sugimura; Nobuo Kawahara; Takashi Tsuchida; Masayuki Mikage
We investigated the ephedrine alkaloid [(−)-ephedrine and (+)-pseudoephedrine] composition ratio of a crude Chinese herbal drug described in the Japanese Pharmacopoeia ‘Ephedra herb (Chinese name: Mahuang)’. There were marked changes in the alkaloid composition ratio of wild plants in areas where both male and female clusters coexisted. However, in genetically homogeneous areas with the growth of male or female clusters alone, all of the coefficients of the regression lines were positive, but each gradient varied. This suggests that the alkaloid composition ratio has a clear tendency in each individual. Based on this, we cultivated individuals for vegetative propagation, and evaluated the alkaloid content ratio. Those propagated by separating the roots showed a specific tendency regardless of the cultivation area (Wakayama, Tanegashima). Those propagated by separating the herbaceous stem showed a specific tendency regardless of the soil or harvest time. In addition, we surveyed the (−)-ephedrine content ratio of 3- to 6-year-old strains. There was a high positive correlation coefficient between the previous and subsequent years. These findings suggest that the ephedrine alkaloid composition ratio of Ephedra herb depends on genetic factors, but not on environmental factors or the growth period.
Phytochemistry Letters | 2015
Hitoshi Tanaka; Yoshiaki Takaya; Junya Toyoda; Tadashi Yasuda; Masaru Sato; Jin Murata; Hiroko Murata; Koichi Kaburagi; Osamu Iida; Koji Sugimura; Eiji Sakai
Asian Pacific Journal of Cancer Prevention | 2006
Shin Nishiumi; Keizo Hosokawa; Rie Mukai; Itsuko Fukuda; Atsuyuki Hishida; Osamu Iida; Kenichi Yoshida; Hitoshi Ashida
Tetrahedron | 2018
Mariko Kitajima; Tomomi Yanagisawa; Mari Tsukahara; Yasuka Yamaguchi; Noriyuki Kogure; Ruri Kikura-Hanajiri; Yukihiro Goda; Osamu Iida; Yasushi Sugimura; Nobuo Kawahara; Hiromitsu Takayama
The Japanese journal of pharmacognosy | 2015
Eiji Sakai; Osamu Iida; Nobuo Kawahara; Jin Murata; Takahiro Sasaki
The Japanese journal of pharmacognosy | 2014
Koji Sugimura; Sachio Shiga; Fumihiro Kamada; Shigeki Katsuki; Osamu Iida