Ito H - Search Results

1

Pharmacological properties of a novel gastrointestinal prokinetic benzamide selective for human 5-HT4 receptor versus human 5-HT3 receptor.

Nagakura Y, Akuzawa S, Miyata K, Kamato T, Suzuki T, Ito H, Yamaguchi T. Nagakura Y, et al. Among authors: ito h. Pharmacol Res. 1999 May;39(5):375-82. doi: 10.1006/phrs.1998.0454. Pharmacol Res. 1999. PMID: 10328995

2

L-365,260, a potent CCK-B/gastrin receptor antagonist, suppresses gastric acid secretion induced by histamine and bethanechol as well as pentagastrin in rats.

Nishida A, Yuki H, Tsutsumi R, Miyata K, Kamato T, Ito H, Yamano M, Honda K. Nishida A, et al. Among authors: ito h. Jpn J Pharmacol. 1992 Feb;58(2):137-45. doi: 10.1254/jjp.58.137. Jpn J Pharmacol. 1992. PMID: 1354760 Free article.

3

Characterization of YM060, a potent and selective 5-hydroxytryptamine3 receptor antagonist, in rabbit nodose ganglion and N1E-115 neuroblastoma cells.

Ito H, Hidaka K, Miyata K, Kamato T, Nishida A, Honda K. Ito H, et al. J Pharmacol Exp Ther. 1992 Dec;263(3):1127-32. J Pharmacol Exp Ther. 1992. PMID: 1469624

4

Role of the serotonin3 receptor in stress-induced defecation.

Miyata K, Kamato T, Nishida A, Ito H, Yuki H, Yamano M, Tsutsumi R, Katsuyama Y, Honda K. Miyata K, et al. Among authors: ito h. J Pharmacol Exp Ther. 1992 Apr;261(1):297-303. J Pharmacol Exp Ther. 1992. PMID: 1560375

5

Pharmacologic profile of (R)-5-[(1-methyl-3-indolyl)carbonyl]-4,5,6,7-tetrahydro-1H- benzimidazole hydrochloride (YM060), a potent and selective 5-hydroxytryptamine3 receptor antagonist, and its enantiomer in the isolated tissue.

Miyata K, Kamato T, Nishida A, Ito H, Katsuyama Y, Iwai A, Yuki H, Yamano M, Tsutsumi R, Ohta M, et al. Miyata K, et al. Among authors: ito h. J Pharmacol Exp Ther. 1991 Oct;259(1):15-21. J Pharmacol Exp Ther. 1991. PMID: 1656016

6

Antiemetic effects of YM060, a potent and selective serotonin (5HT)3-receptor antagonist, in ferrets and dogs.

Kamato T, Miyata K, Ito H, Yuki H, Yamano M, Honda K. Kamato T, et al. Among authors: ito h. Jpn J Pharmacol. 1991 Nov;57(3):387-95. doi: 10.1254/jjp.57.387. Jpn J Pharmacol. 1991. PMID: 1813664 Free article.

7

Serotonin (5-HT)3 receptor blocking activities of YM060, a novel 4,5,6,7-tetrahydrobenzimidazole derivative, and its enantiomer in anesthetized rats.

Miyata K, Kamato T, Yamano M, Nishida A, Ito H, Katsuyama Y, Yuki H, Tsutsumi R, Ohta M, Takeda M, et al. Miyata K, et al. Among authors: ito h. J Pharmacol Exp Ther. 1991 Nov;259(2):815-9. J Pharmacol Exp Ther. 1991. PMID: 1941629

8

Gastrin receptor antagonist YM022 prevents hypersecretion after long-term acid suppression.

Nishida A, Kobayashi-Uchida A, Akuzawa S, Takinami Y, Shishido T, Kamato T, Ito H, Yamano M, Yuki H, Nagakura Y, et al. Nishida A, et al. Among authors: ito h. Am J Physiol. 1995 Nov;269(5 Pt 1):G699-705. doi: 10.1152/ajpgi.1995.269.5.G699. Am J Physiol. 1995. PMID: 7491961

9

Inhibitory effect of YM060 on 5-HT3 receptor-mediated depolarization in colonic myenteric neurons of the guinea pig.

Ito H, Tamura K. Ito H, et al. Eur J Pharmacol. 1995 Sep 5;283(1-3):107-12. doi: 10.1016/0014-2999(95)00296-w. Eur J Pharmacol. 1995. PMID: 7498299

10

Comparative study of the affinities of the 5-HT3 receptor antagonists, YM060, YM114 (KAE-393), granisetron and ondansetron in rat vagus nerve and cerebral cortex.

Ito H, Akuzawa S, Tsutsumi R, Kiso T, Kamato T, Nishida A, Yamano M, Miyata K. Ito H, et al. Neuropharmacology. 1995 Jun;34(6):631-7. doi: 10.1016/0028-3908(95)00033-3. Neuropharmacology. 1995. PMID: 7566499

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