Research Topics
| Toshiki SudoSummaryAffiliation: Otsuka Pharmaceutical Co Country: Japan Publications
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Detail Information
Publications
Potent effects of novel anti-platelet aggregatory cilostamide analogues on recombinant cyclic nucleotide phosphodiesterase isozyme activityT Sudo
Thrombosis and Vascular Research Laboratory, Otsuka Pharmaceutical Co, Ltd, Tokushima, Japan
Biochem Pharmacol 59:347-56. 2000..998). These data demonstrated that OPC-33540 is a highly selective and potent PDE3 inhibitor and a useful probe for identification of the intracellular functions of PDE3...
Estimation of anti-platelet drugs on human platelet aggregation with a novel whole blood aggregometer by a screen filtration pressure methodT Sudo
Thrombosis and Vascular Research Laboratory, Otsuka Pharmaceutical Co, Ltd, 463 10 Kagasuno, Kawauchi cho, Tokushima 771 0192, Japan
Br J Pharmacol 133:1396-404. 2001..4. These results demonstrate that the SFP aggregometer can sensitively detect anti-platelet aggregatory effects of various kinds of drugs. So that it is a useful tool for evaluation of anti-platelet drugs...
Characterization of platelet aggregation in whole blood of laboratory animals by a screen filtration pressure methodToshiki Sudo
First Institute of New Drug Research, Otsuka Pharmaceutical Co, Ltd 463 10, Kagasuno, Kawauchi cho, Tokushima 771 0192, Japan
Platelets 14:239-46. 2003..These results demonstrated that species differences in laboratory animals exist for whole blood aggregation, and that the SFP aggregometer may be useful to evaluate platelet function in various animal species...
Phosphorylation of the vasodilator-stimulated phosphoprotein (VASP) by the anti-platelet drug, cilostazol, in plateletsToshiki Sudo
First Institute of New Drug Research, Otsuka Pharmaceutical Co, Ltd, Tokushima, Japan
Platelets 14:381-90. 2003..The PKA/PKG inhibitor, H-89, inhibited VASP phosphorylation by cilostazol. These results demonstrated that cilostazol phosphorylates VASP through the PDE3 inhibition, increase of cAMP level, and PKA activation in platelets...
Genetic strain differences in platelet aggregation of laboratory miceToshiki Sudo
First Institute of New Drug Discovery, Otsuka Pharmaceutical Co, Ltd, Kawauchi cho, Tokushima 771 0192, Japan
Thromb Haemost 95:159-65. 2006..The present study demonstrated that there is considerable strain difference in platelet aggregation among laboratory mice, which should be taken into account in backcrossing knockout strains...
Genetic strain differences in platelet aggregation and thrombus formation of laboratory ratsToshiki Sudo
First Institute of New Drug Discovery, Otsuka Pharmaceutical Co Ltd, 463 10 Kagasuno, Tokushima, Japan
Thromb Haemost 97:665-72. 2007..The present study demonstrates that there are considerable strain differences in platelet aggregation among laboratory rats, which reflect thrombus formation...
Effects of the cAMP-elevating agents cilostamide, cilostazol and forskolin on the phosphorylation of Akt and GSK-3beta in plateletsHideki Hayashi
First Institute of New Drug Discovery, Otsuka Pharmaceutical Co, Ltd, Kawauchi cho, Tokushima, 771 0192, Japan
Thromb Haemost 102:327-35. 2009..Our results provide new insights into the inhibitory effect of cAMP-elevating agents on platelet function...
Identification of the active region responsible for the anti-thrombotic activity of anopheline anti-platelet protein from a malaria vector mosquitoHideki Hayashi
First Institute of New Drug Discovery, Otsuka Pharmaceutical Company Limited, Tokushima, Japan
Platelets 24:324-32. 2013..These results indicated that the essential moiety of AAPP for collagen binding and anti-thrombotic activity was in the region encoded by exon 3-4, which is highly conserved among the counterpart regions of other mosquito species...
Anopheline anti-platelet protein from a malaria vector mosquito has anti-thrombotic effects in vivo without compromising hemostasisHideki Hayashi
First Institute of New Drug Discovery, Otsuka Pharmaceutical Company Limited, Tokushima, Japan
Thromb Res 129:169-75. 2012..To examine the potential of AAPP as a therapeutic agent, we investigated the in vivo anti-thrombotic effects of AAPP...
Lactoferrin inhibits platelet production from human megakaryocytes in vitroKuniko Matsumura-Takeda
Department of Pharmacokinetics and Biopharmaceutics, Subdivision of Biopharmaceutical Sciences, Institute of Health Biosciences, The University of Tokushima, 1 78 1 Sho machi, Tokushima 770 8505, Japan
Biol Pharm Bull 31:569-73. 2008..In addition, it did not inhibit MK progenitors. These results suggest that LF directly inhibits PLT production from matured MKs, but does not inhibit megakaryopoiesis, including proliferation/maturation processes...
Characterization of STZ-Induced Type 2 Diabetes in Zucker Fatty RatsTakashi Okamoto
First Institute of New Drug Discovery, Otsuka Pharmaceutical Co, Ltd, Tokushima, Japan
Exp Anim 57:335-45. 2008..Metformin lowered the blood glucose levels of STZ-ZF rats in a dose-dependent manner. These results suggest that STZ-ZF rats are useful for studies of T2DM and for the evaluation of the efficacy of anti-diabetic drugs...
Strain-dependent embryonic lethality and exaggerated vascular remodeling in heparin cofactor II-deficient miceKen ichi Aihara
Department of Medicine and Bioregulatory Sciences and 21st Century Center of Excellence Program, The University of Tokushima Graduate School of Health Biosciences, Tokushima, Japan
J Clin Invest 117:1514-26. 2007....
Inhibition of collagen-induced platelet aggregation by anopheline antiplatelet protein, a saliva protein from a malaria vector mosquitoShigeto Yoshida
Division of Medical Zoology, Department of Infection and Immunity, Jichi Medical University, Tochigi, Japan
Blood 111:2007-14. 2008..Our study may provide important insights for elucidating the effects of mosquito blood feeding against host hemostasis...
Disruption of nuclear vitamin D receptor gene causes enhanced thrombogenicity in miceKen ichi Aihara
Department of Medicine and Bioregulatory Sciences, University of Tokushima Graduate School of Medicine, Japan
J Biol Chem 279:35798-802. 2004..These results demonstrate that activation of nuclear VDR elicits antithrombotic effects in vivo, and suggest that the VDR system may play a physiological role in the maintenance of antithrombotic homeostasis...
