Zobrazeno 1 - 10
of 202
pro vyhledávání: '"M Kiyoki"'
Publikováno v:
Calcified Tissue International. 63:143-147
We compared the cytotoxic effects of alendronate (ALN) and incadronate (YM175) on isolated rabbit osteoclasts in vitro and on rats in vivo. In the in vitro experiment, each bisphosphonate was added to the culture of isolated osteoclasts at the final
Autor:
I. Nakamura, M. Kiyoki, K. Shiobara, Y. Nishijima, T. Ohta, M. Shimizu, T. Takehara, R. Nemoto
Publikováno v:
BJU International. 80:274-280
Objective To assess serum pyridinoline (Py) and deoxypyridinoline (dPy), using a new high-performance liquid chromatography (HPLC) method, as a serum marker to determine the incidence of metastatic bone disease in an animal model and in the monitorin
Publikováno v:
Advanced Drug Delivery Reviews. 20:181-187
Prostacyclin is one of the most potent vasoactive autacoids, and is now clinically used as an anti-platelet agent, but with limited indications due to its chemical instability, as well as side effects. A chemically stable prostacyclin derivative (Cli
Publikováno v:
Endocrinology. 137:2586-2592
In normal rats given alendronate (0.01-6.25 mg/kg) or elcatonin (synthetic eel calcitonin; 0.32-8.0 U/kg), changes in urinary calcium (Ca), pyridinoline (Pyr), and deoxypyridinoline (D-Pyr) excretion during the hypocalcemic response were assessed. Al
Publikováno v:
Dermatology. 192:233-238
Background: The 1,24(R)(OH)2D3 (tacalcitol) ointment (2 μg/g) is available commercially as an antipsoriatic drug in Japan, but the cream preparation of tacalci
Publikováno v:
Bone. 16:235-245
Alendronate is an aminobisphosphonate that acts as a potent inhibitor of osteoclastic bone resorption. To understand the mechanism of action of alendronate in vivo, in this study we investigated the relationship between distribution of [14C]-alendron
Autor:
H Honda, M Kiyoki, T Nakamoto, R Hasegawa, S Jindai, H. Eguchi, T Kubota, M Shiraki, T Yamaji, K. Hosoda
Publikováno v:
Clinical Chemistry. 38:2233-2238
To overcome the problems of limited-region specificity associated with conventional radioimmunoassay (RIA), we developed a sandwich enzyme immunoassay (EIA) for intact human osteocalcin (hOC). For this EIA we used antibodies to the N- and C-terminal
Publikováno v:
Skin pharmacology and applied skin physiology. 14(4)
The human epidermal keratinocyte cell line K-TL-1, developed from a benign epidermal tumor, was cultured in the presence of the synthetic vitamin D3 analogue tacalcitol [1alpha,24(R)-dihydroxyvitamin D3] to assess the effects on the production of ner
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 282(2)
We evaluated the potency of truncated secretory leukoprotease inhibitor (truncated SLPI) in a human sputum elastase (HSE)-induced lung injury model and in a specific neutrophil-mediated acute lung injury model in hamsters. Intratracheal administratio
Autor:
Toshitaka Nakamura, Y. Tsukamoto, H. Eguchi, Y. Azuma, K. Hosoda, M. Arita, M. Kiyoki, T. Ohta
Publikováno v:
Calcified tissue international. 59(4)
We developed a sandwich enzyme immunoassay system for intact rat osteocalcin to improve the region specificity for the detection of this molecule. We synthesized two peptides of N-terminal 20 residues and C-terminal 10 residues of rat osteocalcin. Af