Toshimi Matsuno
Takeda Pharmaceutical Company
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Featured researches published by Toshimi Matsuno.
Experimental Parasitology | 1984
Toshimi Matsuno; Nobuo Kobayashi; Fumio Hariguchi; Toshiyuki Yamazaki; Kinichi Imai; Hiroshi Onaga
The anticoccidial activity of an orotic acid analog, 1,6-dihydro-6-oxo-2-pyrazinecarboxylic acid 4-oxide (carboxyemimycin), was tested in battery experiments, utilizing 9-day-old Single-Comb White Leghorn cockerels. Carboxyemimycin, at 125 ppm and more in feed, exhibited marked anticoccidial activities against Eimeria tenella, E. necatrix, E. acervulina, and E. maxima. High doses of carboxyemimycin--up to 1000 ppm--did not cause any reduction in weight gains. The battery and in vitro studies with delayed and restricted medications revealed that carboxyemimycin affected the development of E. tenella in first and second generation schizogony and in gametogony.
Experimental Parasitology | 1986
Nobuo Kobayashi; Toshimi Matsuno; Fumio Hariguchi; Toshiyuki Yamazaki; Kinichi Imai; Hiroshi Onaga; Toshio Ishii
The anticoccidial activity of an uridine analog, 1-(beta-D-ribofuranosyl)-2(1H)-pyrazinone 4-oxide (emimycin riboside), against five species of chicken Eimeria was tested individually in battery experiments. With 16 ppm of the compound in feed, marked anticoccidial activity was obtained against Eimeria tenella, E. necatrix, E. acervulina, E. maxima, and E. brunetti. The last named species was more drug-sensitive than the others--dietary levels of at least 8 ppm of the drug exhibited good protection and eliminated practically all clinical signs. The battery tests with delayed and restricted medications showed that emimycin riboside affected the development of parasites in first and second generation schizogony of the life cycle of E. tenella.
Veterinary Parasitology | 1986
Toshimi Matsuno
In a series of battery experiments utilizing 9-day-old White Leghorn male chicks, 9-(2-chloro-6-fluorobenzyl)-6-methylaminopurine (VM 6387) and 9-(2-chloro-6-fluorobenzyl)-6-dimethylaminopurine (VM 6736) showed remarkable anticoccidial activity against Eimeria tenella, E. acervulina, and E. maxima. The effective dose range was estimated from the results of the efficacy test against E. tenella on the basis of improvement of body weight gain and clinical signs of infection. The tests included dietary levels of 60-100 ppm of VM 6387 and 70-110 ppm of VM 6736. Both compounds gave good protection against E. acervulina and E. maxima at the same dose range. The sporulation of oocysts obtained from cecal contents of birds fed lower levels of VM 6387 was inhibited. Studies of the effects of VM 6387 on stages of the E. tenella life cycle demonstrated that the compound possesses remarkable activity at 1-5 days post-infection corresponding to the period of schizogony, as well as prolonged activity thereafter, when the parasite was undergoing gametogenesis.
Chemical & Pharmaceutical Bulletin | 1976
Mitsuhiko Mano; Takuji Seo; Toshimi Matsuno; Kinichi Imai
Archive | 1990
Toshimi Matsuno; Fumio Hariguchi; Tsutomu Okamoto
Archive | 1999
Hideki Miki; Koichi Iwanaga; Toshimi Matsuno; Isao Aoki
Chemical & Pharmaceutical Bulletin | 1981
Kinichi Imai; Mitsuhiko Mano; Takuji Seo; Toshimi Matsuno
Journal of Veterinary Medical Science | 1991
Toshimi Matsuno; Fumio Hariguchi; Tsutomu Okamoto
Archive | 1997
Hideki Miki; Koichi Iwanaga; Toshimi Matsuno; Isao Aoki
Journal of Veterinary Medical Science | 1996
Nobuo Kobayashi; Fumio Hariguchi; Tsutomu Okamoto; Yukitaka Okada; Toshikatsu Hayashi; Toshimi Matsuno