Riichiro Ohba
Sojo University
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Publication
Featured researches published by Riichiro Ohba.
Comparative Biochemistry and Physiology C-toxicology & Pharmacology | 2001
Hiroshi Yoshii; Norihide Tachi; Riichiro Ohba; Osamu Sakamura; Hidemaro Takeyama; Toru Itani
Oligopeptides of 1 KDa or less were obtained by hydrolysis of chicken egg yolks with a crude enzyme, and by dialysis with a semipermeable membrane filter. Since the extracted peptides had an inhibitory action on the activity of angiotensin I-converting enzyme (ACE) in vitro, they were orally administered at 20, 100 and 500 mg/kg body weight to spontaneously hypertensive rats (SHR) for 12 weeks to analyze the physiological role on cardiovascular functions. The administered oligopeptides suppressed the development of hypertension at all dosages. After 12 weeks at 500 mg/kg body weight, the values for systolic, mean, and diastolic blood pressure were approximately 10% less in SHRs administered than controls. Furthermore, serum ACE activity of the peptide-administered groups was significantly lower than that of the control group in a dose-related manner. Our results imply that oligopeptides extracted from hens egg yolks could potentially suppress the development of hypertension in SHR, and this effect might be induced by the inhibition of ACE activity.
Phytochemistry | 2001
Norihiko Terahara; Alfons Callebaut; Riichiro Ohba; Tadahiro Nagata; Mayumi Ohnishi-Kameyama; Masahiro Suzuki
Four anthocyanins from Ajuga reptans flowers and its cell cultures were isolated, and a fifth was also characterized by HPLC-mass spectrometry. By means of chemical and spectroscopic analyses, their structures were identified as delphinidin 3-(p-coumaroyl-feruloyl)sophoroside-5-malonylglucoside, delphinidin 3-(diferuloyl)sophoroside-5-malonylglucoside, and cyanidin 3-(di-p-coumaroyl)sophoroside-5-glucoside, respectively. The other two were tentatively identified as delphinidin 3-(diferuloyl)sophoroside-5-glucoside and cyanidin 3-(feruloyl-p-coumaroyl)sophoroside-5-malonylglucoside. In neutral aqueous solution, the crude extract from A. reptans flower cell cultures and the major anthocyanin cyanidin 3-(di-p-coumaroyl)sophoroside-5-malonylglucoside were more stable than cyanidin 3-glucoside, and also prevented more efficiently peroxidation than did the latter. A. reptans flower cell culture anthocyanins may have a potential as natural colorants for food utilities or other purposes.
Food Science and Technology Research | 2003
Riichiro Ohba; Tomoaki Deguchi; Minekazu Kishikawa; Fahmi Arsyad; Shigeru Morimura; Kenji Kida
Food Science and Technology Research | 2005
Noriaki Saigusa; Norihiko Terahara; Riichiro Ohba
Food Science and Technology Research | 2007
Noriaki Saigusa; Riichiro Ohba
Food Science and Technology Research | 2004
Yoshiharu Sasaki; Riichiro Ohba
Food Science and Technology Research | 2003
Riichiro Ohba; Tomoaki Deguchi; Minekazu Kishikawa; Shigeru Morimura; Isao Suzuki
Journal of The Japanese Society for Food Science and Technology-nippon Shokuhin Kagaku Kogaku Kaishi | 1999
Hiroshi Yoshii; Norihide Tachi; Osamu Sakamura; Hidemaro Takeyama; Riichiro Ohba; Toru Itani
Food Science and Technology Research | 2007
Noriaki Saigusa; Noritomo Kawashima; Riichiro Ohba
Journal of The Japanese Society for Food Science and Technology-nippon Shokuhin Kagaku Kogaku Kaishi | 2000
Riichiro Ohba; Masaki Iio