Ukai M - Search Results

1

Pharmacological characterization of a new antimuscarinic agent, solifenacin succinate, in comparison with other antimuscarinic agents.

Ohtake A, Saitoh C, Yuyama H, Ukai M, Okutsu H, Noguchi Y, Hatanaka T, Suzuki M, Sato S, Sasamata M, Miyata K. Ohtake A, et al. Among authors: ukai m. Biol Pharm Bull. 2007 Jan;30(1):54-8. doi: 10.1248/bpb.30.54. Biol Pharm Bull. 2007. PMID: 17202659 Free article.

2

In vitro and in vivo tissue selectivity profile of solifenacin succinate (YM905) for urinary bladder over salivary gland in rats.

Ohtake A, Ukai M, Hatanaka T, Kobayashi S, Ikeda K, Sato S, Miyata K, Sasamata M. Ohtake A, et al. Among authors: ukai m. Eur J Pharmacol. 2004 May 25;492(2-3):243-50. doi: 10.1016/j.ejphar.2004.03.044. Eur J Pharmacol. 2004. PMID: 15178371

3

Effects of solifenacin succinate (YM905) on detrusor overactivity in conscious cerebral infarcted rats.

Suzuki M, Ohtake A, Yoshino T, Yuyama H, Hayashi A, Ukai M, Okutsu H, Noguchi Y, Sato S, Sasamata M. Suzuki M, et al. Among authors: ukai m. Eur J Pharmacol. 2005 Apr 4;512(1):61-6. doi: 10.1016/j.ejphar.2005.02.023. Eur J Pharmacol. 2005. PMID: 15814091

4

Pharmacological characterization of YM598, a selective endothelin-A receptor antagonist.

Sudoh K, Yuyama H, Noguchi Y, Fujimori A, Ukai M, Ohtake A, Sato S, Sasamata M, Miyata K. Sudoh K, et al. Among authors: ukai m. J Cardiovasc Pharmacol. 2004 Nov;44 Suppl 1:S390-3. doi: 10.1097/01.fjc.0000166296.25690.ca. J Cardiovasc Pharmacol. 2004. PMID: 15838329

5

Effect of tamsulosin on spontaneous bladder contraction in conscious rats with bladder outlet obstruction: comparison with effect on intraurethral pressure.

Ohtake A, Ukai M, Saitoh C, Sonoda R, Noguchi Y, Okutsu H, Yuyama H, Sato S, Sasamata M, Miyata K. Ohtake A, et al. Among authors: ukai m. Eur J Pharmacol. 2006 Sep 18;545(2-3):185-91. doi: 10.1016/j.ejphar.2006.06.054. Epub 2006 Jun 29. Eur J Pharmacol. 2006. PMID: 16887117

6

Tamsulosin potently and selectively antagonizes human recombinant α(1A/1D)-adrenoceptors: slow dissociation from the α(1A)-adrenoceptor may account for selectivity for α(1A)-adrenoceptor over α(1B)-adrenoceptor subtype.

Sato S, Hatanaka T, Yuyama H, Ukai M, Noguchi Y, Ohtake A, Taguchi K, Sasamata M, Miyata K. Sato S, et al. Among authors: ukai m. Biol Pharm Bull. 2012;35(1):72-7. doi: 10.1248/bpb.35.72. Biol Pharm Bull. 2012. PMID: 22223340 Free article.

7

In vitro and in vivo pharmacological profile of the selective β3-adrenoceptor agonist mirabegron in rats.

Hatanaka T, Ukai M, Watanabe M, Someya A, Ohtake A, Suzuki M, Ueshima K, Sato S, Sasamata M. Hatanaka T, et al. Among authors: ukai m. Naunyn Schmiedebergs Arch Pharmacol. 2013 Mar;386(3):247-53. doi: 10.1007/s00210-012-0821-4. Epub 2012 Dec 14. Naunyn Schmiedebergs Arch Pharmacol. 2013. PMID: 23239087

8

Superiority of YM598 over atrasentan as a selective endothelin ETA receptor antagonist.

Yuyama H, Noguchi Y, Fujimori A, Ukai M, Fujiyasu N, Ohtake A, Sato S, Sudoh K, Sasamata M, Miyata K. Yuyama H, et al. Among authors: ukai m. Eur J Pharmacol. 2004 Sep 13;498(1-3):171-7. doi: 10.1016/j.ejphar.2004.07.003. Eur J Pharmacol. 2004. PMID: 15363992

9

Participation of endogenous endothelin and ETA receptor in premicturition contractions in rats with bladder outlet obstruction.

Ukai M, Yuyama H, Noguchi Y, Someya A, Okutsu H, Watanabe M, Yoshino T, Ohtake A, Suzuki M, Sato S, Sasamata M. Ukai M, et al. Naunyn Schmiedebergs Arch Pharmacol. 2006 Jun;373(3):197-203. doi: 10.1007/s00210-006-0064-3. Epub 2006 May 17. Naunyn Schmiedebergs Arch Pharmacol. 2006. PMID: 16736156

10

Effect of YM598, a selective endothelin ETA receptor antagonist, on endothelin-1-induced bone formation.

Someya A, Yuyama H, Fujimori A, Ukai M, Fukushima S, Sasamata M. Someya A, et al. Among authors: ukai m. Eur J Pharmacol. 2006 Aug 14;543(1-3):14-20. doi: 10.1016/j.ejphar.2006.06.035. Epub 2006 Jun 27. Eur J Pharmacol. 2006. PMID: 16843458

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