7 results on '"Ishigo S"'
Search Results
2. Kinetic analysis of D-Alanine upon oral intake in humans.
- Author
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Kimura T, Sakai S, Horio M, Takahara S, Ishigo S, Nakane M, Negishi E, Imoto H, Mita M, Hamase K, Higa-Maekawa Y, Kakuta Y, Mizui M, and Isaka Y
- Subjects
- Humans, Administration, Oral, Male, Adult, Kinetics, Half-Life, Female, Healthy Volunteers, Stereoisomerism, Young Adult, Alanine blood, Alanine pharmacokinetics
- Abstract
D-Alanine, a rare enantiomer of alanine, can potentially alleviate the worsening of viral infections and maintain circadian rhythm. This study aimed to analyze the kinetics of D-Alanine upon oral intake. Five healthy volunteers were administered D-Alanine as a single oral dose at 11,236 or 33,708 µmoL (1-3 g). Upon intake of the lower dose, the plasma level of D-Alanine reached its peak concentration of 588.4 ± 40.9 µM with a peak time of 0.60 ± 0.06 h. The compartment model estimated the clearance of D-Alanine at 12.5 ± 0.3 L/h, or 208 ± 5 mL/min, distribution volume of 8.3 ± 0.7 L and half-life of 0.46 ± 0.04 h, suggesting a rapid clearance of D-Alanine. The peak concentration and area under the curve increased proportionally upon intake of the higher dose, while the clearance, distribution volume and half-life did not. The urinary ratio of D-Alanine per sum of D- and L-Alanine reached its peak of nearly 100%, followed by a slow decline. The peak time of the urinary ratio was 1.15 ± 0.15 h, showing a time lag of blood to urine excretion. Fractional excretion, a ratio of the clearance of a substance per a standard molecule in kidney, of D-Alanine increased from 14.0 ± 5.8% to 64.5 ± 10.3%; the latter corresponded to the urinary clearance of D-Alanine as about 77 mL/min for an adult, with a peak time of 1.90 ± 0.56 h. D-Alanine was quickly absorbed and appeared in blood, followed by urinary excretion. This kinetic analysis increases our fundamental knowledge of the oral intake of D-Alanine for the chronic dosing. Trial number: #UMIN000050865. Date of registration: 2023/6/30., (© 2024. The Author(s).)
- Published
- 2024
- Full Text
- View/download PDF
3. Chiral amino acid analysis of Japanese traditional Kurozu and the developmental changes during earthenware jar fermentation processes.
- Author
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Miyoshi Y, Nagano M, Ishigo S, Ito Y, Hashiguchi K, Hishida N, Mita M, Lindner W, and Hamase K
- Subjects
- Fermentation, Food Handling methods, Metabolomics, Stereoisomerism, Acetic Acid chemistry, Amino Acids analysis, Amino Acids chemistry, Chromatography, High Pressure Liquid methods
- Abstract
Enantioselective amino acid metabolome analysis of the Japanese traditional black vinegars (amber rice vinegar, Kurozu) was performed using two-dimensional high-performance liquid chromatography combining a microbore-monolithic ODS column and narrowbore-enantioselective columns. d-Amino acids, the enantiomers of widely observed l-amino acids, are currently paid attention as novel physiologically active substances, and the foodstuffs and beverages containing high amounts of d-amino acids are the subjects of interest. In the present study, the amino acid enantiomers were determined by two-dimensional HPLC techniques after pre-column fluorescence derivatization with 4-fluoro-7-nitro-2,1,3-benzoxadiazole. In the first dimension, the amino acid enantiomers are separated as their d plus l mixtures by the reversed-phase mode, then the d-amino acids and their l-counterparts are separately determined in the second dimension by the enantioselective columns. As a result, large amounts of d-Ala (800-4000nmol/mL), d-Asp (200-400nmol/mL) and d-Glu (150-500nmol/mL) were observed in some of the traditionally produced Kurozu vinegars. Relatively large or small amounts of d-Ser (50-100nmol/mL), d-Leu (10-50nmol/mL) and d-allo-Ile (less than 20nmol/mL) were also present in these samples. Developmental changes in the d-amino acid amounts during the fermentation and aging processes have also been investigated., (Copyright © 2014 Elsevier B.V. All rights reserved.)
- Published
- 2014
- Full Text
- View/download PDF
4. Distribution of an antifungal drug, itraconazole, in pathological and non-pathological tissues.
- Author
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Seishima M, Oyama Z, Oda M, and Ishigo S
- Subjects
- Administration, Oral, Biological Availability, Biopsy, Needle, Dose-Response Relationship, Drug, Drug Administration Schedule, Follow-Up Studies, Humans, Immunohistochemistry, Male, Middle Aged, Treatment Outcome, Chromoblastomycosis drug therapy, Chromoblastomycosis pathology, Itraconazole administration & dosage, Itraconazole pharmacokinetics, Trichophyton isolation & purification
- Abstract
An antifungal drug, itraconazole (ITZ) is effective for chromomycosis patients, but the distribution of ITZ and its metabolite, hydroxy-intraconazole (OH-ITZ) is unclear in pathological tissues. This study investigated how much ITZ and OH-ITZ accumulated in the lesional tissues of chromomycosis and non-lesional skin after oral treatment with ITZ. We determined the concentrations of ITZ and OH-ITZ in the lesional tissues of chromomycosis by Foncecaea pedrosoi and non-lesional skin after oral treatment with a total dose of 2.3g of ITZ. ITZ concentration was significantly higher in pathological skin than non-pathological skin. The ITZ concentration in the lesional tissues was higher in the central site than in the marginal site. No difference was seen in the OH-ITZ concentrations among three skin parts, the center and the margin in lesional skin, and non-lesional skin adjacent to the lesion. This study showed higher concentrations of ITZ in pathological tissues than in non-pathological tissues., (Copyright John Libbey Eurotext 2003.)
- Published
- 2004
5. Analysis of Clostridium difficile isolates from nosocomial outbreaks at three hospitals in diverse areas of Japan.
- Author
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Kato H, Kato N, Watanabe K, Yamamoto T, Suzuki K, Ishigo S, Kunihiro S, Nakamura I, Killgore GE, and Nakamura S
- Subjects
- Bacterial Typing Techniques, Blotting, Western methods, Clostridioides difficile genetics, Clostridioides difficile isolation & purification, Electrophoresis, Gel, Pulsed-Field, Hospitals, Humans, Japan, Polymerase Chain Reaction methods, Ribotyping, Clostridioides difficile classification, Cross Infection microbiology, Disease Outbreaks, Enterocolitis, Pseudomembranous microbiology
- Abstract
Clostridium difficile isolates recovered from patients with C. difficile-associated diarrhea (CDAD) at three hospitals located in diverse areas of Japan were analyzed by three typing systems, PCR ribotyping, pulsed-field gel electrophoresis (PFGE), and Western immunoblotting. At the three hospitals examined, a single PCR ribotype strain (type smz) was predominant and accounted for 22 (65%) of 34, 18 (64%) of 28, and 11 (44%) of 25 isolates, respectively. All of the 51 isolates that represented PCR ribotype smz were nontypeable by PFGE because of DNA degradation. Since the type smz strain did not react with any of the antisera against 10 different serogroups (A, B, C, D, F, G, H, I, K, and X), we prepared a new antiserum against a type smz isolate. All 51 type smz isolates presented identical banding patterns, reacting with the newly prepared antiserum (designated subserogroup JP-0 of serogroup JP). These results were compared with those of a strain from a hospital outbreak that occurred in New York, which has been identified as type J9 by restriction enzyme analysis and type 01/A by arbitrarily primed PCR but was nontypeable by PFGE because of DNA degradation. This strain was reported to be epidemic at multiple hospitals in the United States. The J9 strain represented a PCR ribotype pattern different from that of a type smz strain and was typed as subserogroup G-1 of serogroup G by immunoblot analysis. A single outbreak type causing nosocomial CDAD in Japan was found to be different from the strain causing multiple outbreaks in the United States, even though the outbreak strains from the two countries were nontypeable by PFGE because of DNA degradation.
- Published
- 2001
- Full Text
- View/download PDF
6. The antiseptic effect of a quick drying rubbing type povidone-iodine alcoholic disinfectant solution.
- Author
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Minakuchi K, Yamamoto Y, Matsunaga K, Hayata M, Yasuda T, Katsuno Y, Takada H, Iriyama J, Ishigo S, and Asano Y
- Subjects
- Bacteria drug effects, Benzalkonium Compounds adverse effects, Benzalkonium Compounds therapeutic use, Dermatitis, Occupational etiology, Ethanol, Hand microbiology, Humans, Medical Staff, Hospital, Povidone-Iodine adverse effects, Antisepsis methods, Hand Disinfection methods, Povidone-Iodine therapeutic use
- Abstract
A quick drying rubbing type disinfectant of non-water non-towel type is an antiseptic method suitable for practical use in intensive care units where emergency situations are common. We determined the antiseptic efficacy and safety of a quick drying rubbing type povidone-iodine alcoholic disinfectant solution (HAD Hand Wash) in comparison with benzalkonium chloride alcoholic lotion. The bacterial reduction rate obtained by hand washing with a single 3 ml application was 93.8% for HAD Hand Wash and 94.1% for benzalkonium chloride alcoholic lotion. Thus, excellent antiseptic efficacy was obtained with both disinfectants. Roughening of hand skin which appeared in association with HAD Hand Wash solution was transient and mild in nature in all of the cases, indicating the high safety of this disinfectant. It is justified to say from these findings that HAD Hand Wash is useful as a hand and finger disinfectant.
- Published
- 1993
7. Comparison of bactericidal activities of various disinfectants against methicillin-sensitive Staphylococcus aureus and methicillin-resistant Staphylococcus aureus.
- Author
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Yasuda T, Yoshimura S, Katsuno Y, Takada H, Ito M, Takahashi M, Yahazaki F, Iriyama J, Ishigo S, and Asano Y
- Subjects
- Benzalkonium Compounds pharmacology, Chlorhexidine analogs & derivatives, Chlorhexidine pharmacology, Dose-Response Relationship, Drug, Glycine analogs & derivatives, Glycine pharmacology, Humans, In Vitro Techniques, Povidone-Iodine pharmacology, Time Factors, Disinfectants pharmacology, Methicillin pharmacology, Methicillin Resistance, Staphylococcus aureus drug effects
- Abstract
Various disinfectants were compared in terms of the duration of bactericidal activity against methicillin-sensitive Staphylococcus aureus (MSSA), and methicillin-resistant Staphylococcus aureus (MRSA), among S. aureus isolated in our hospital. Strains of S. aureus which showed minimum inhibitory concentrations of cloxacillin of less than 1.56 micrograms/ml and of 3.13 micrograms/ml or higher were designated MSSA and MRSA respectively. There was no difference in sensitivity to disinfectants between MSSA and MRSA. There was a great variation in the duration of bactericidal activity of chlorhexidine gluconate against these species with the majority requiring contact times of between 2 minutes and over 20 minutes. All strains except for one strain of MRSA were killed within 20 seconds after disinfection with benzalkonium chloride. All strains were killed within 20 seconds after disinfection with alkyldiaminoethylglycine hydrochloride or povidone-iodine.
- Published
- 1993
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