Zobrazeno 1 - 10
of 36
pro vyhledávání: '"Kenji Mizojiri"'
Autor:
Kazuo Kitamura, Tanenao Eto, Mitsuru Notoya, Hiroshi Hasegawa, Kenji Mizojiri, Kazuhiro Inazawa, Vinci Mizuhira, Kenji Kangawa
Publikováno v:
ACTA HISTOCHEMICA ET CYTOCHEMICA. 31:335-343
Adrenomedullin (AM) is a novel hypotensive peptide isolated from the human pheochromocytoma. In the present study, 125I-AM was intravenously administered to rats and its distribution was examined by autoradiographic (ARG) techniques using wholebody,
Autor:
Vinci Mizuhira, Tsuneyuki Ebara, Hiroshi Iwao, Shokei Kim, Tokihito Yukimura, Takeshi Matsuura, Kenji Mizojiri, Mitsuru Notoya, Keifu Song, Katsuyuki Miura
Publikováno v:
Kidney International. 50:135-147
High resolution localization of endothelin receptors in rat renal medulla. The cellular localization of endothelin receptors in the inner medulla of the rat kidney was investigated by using high resolution light and electron microscopic autoradiograp
Publikováno v:
Hypertension. 27:364-370
Abstract We investigated the effect of long-term administration of the angiotensin-converting enzyme inhibitor lisinopril on renal arterioles in spontaneously hypertensive rats (SHR) and Wistar-Kyoto rats (WKY) using a morphometric method and vascula
Autor:
Kenji Mizojiri, Ryo Norikura
Publikováno v:
Drug Metabolism and Pharmacokinetics. 11:147-159
The present study used the published data to examine the relationship between accumulation factor (predicted value) and accumulation ratio (observed value) of a compound as a ratio of tissue concentration at 24 hr after single administration to that
Publikováno v:
The Journal of Toxicological Sciences. 21:523-527
Autor:
Yuzo Nakagawa, Junko Kikuchi, Yoshihiro Terui, Kouji Iwatani, Takeo Yoshimori, Ryo Norikura, Kenji Mizojiri, Machiko Nakanishi
Publikováno v:
Drug Metabolism and Pharmacokinetics. 8:67-81
The metabolism of S-1452, calcium (5Z)-7-[(1R, 2S, 3S, 4S)-3-phenylsulfonylaminobicyclo[2.2.1]hept-2-yl]-5-heptenoate hydrate, a new TXA2 receptor antagonist, in rats was studied. Twelve unconjugated metabolites including the unchanged free acid of S
Autor:
Machiko Nakanishi, Shinya Futaguchi, Hiroshi Okabe, Yuka Iwamoto, Ryo Norikura, Kenji Mizojiri, Hideo Tanaka, Takeo Yoshimori
Publikováno v:
Drug Metabolism and Pharmacokinetics. 8:97-105
The tissue distribution and excretion of S-1452 were studied in rats after a single and repeated oral administration of 14C-S-1452 at a dose of 5mg/kg or 5mg/kg/day for 10 days. 1. The level of radioactivity in the liver was markedly higher than thos
Publikováno v:
Drug Metabolism and Pharmacokinetics. 8:107-112
Transfer of radioactivity into the fetus and milk were studied after a single oral administration of 14C-S-1452 at a dose of 5mg/kg in pregnant rats on 19 days of gestation and in lactating rats. 1. In whole body autoradiography, distribution pattern
Publikováno v:
Drug Metabolism and Pharmacokinetics. 8:83-96
The absorption, distribution, metabolism and excretion of S-1452, a new thromboxane A2 receptor antagonist, were studied after a single oral or intravenous administration of 14C-labelled compounds at a dose of 5mg/kg to fasted and non-fasted rats. Al
Publikováno v:
Drug Metabolism and Pharmacokinetics. 8:113-125