Shimizu I - Search Results

1

Na+ influx-induced decrease of (Na+ + K+)-ATPase activity in rat brain slices: role of Ca2+.

Matsuda T, Shimizu I, Baba A. Matsuda T, et al. Among authors: shimizu i. Eur J Pharmacol. 1991 Nov 12;204(3):257-63. doi: 10.1016/0014-2999(91)90850-p. Eur J Pharmacol. 1991. PMID: 1663455

2

Postnatal change in a Ca(2+)-mediated decrease in (Na+ + K+)-ATPase activity in rat brain slices.

Matsuda T, Shimizu I, Baba A. Matsuda T, et al. Among authors: shimizu i. Brain Res. 1992 Feb 14;572(1-2):349-51. doi: 10.1016/0006-8993(92)90499-y. Brain Res. 1992. PMID: 1319275

3

Glucose and oxygen deprivation induces a Ca(2+)-mediated decrease in (Na(+)+K+)-ATPase activity in rat brain slices.

Matsuda T, Shimizu I, Murata Y, Baba A. Matsuda T, et al. Among authors: shimizu i. Brain Res. 1992 Apr 3;576(2):263-70. doi: 10.1016/0006-8993(92)90689-7. Brain Res. 1992. PMID: 1387578

4

Pharmacological actions of AH-9700 on micturition reflex in anesthetized rats.

Shimizu I, Kawashima K, Ishii D, Oku S, Kohayakawa H, Oka M. Shimizu I, et al. Eur J Pharmacol. 2001 Jan 26;412(2):171-9. doi: 10.1016/s0014-2999(00)00937-7. Eur J Pharmacol. 2001. PMID: 11165228

5

DSR-98776, a novel selective mGlu5 receptor negative allosteric modulator with potent antidepressant and antimanic activity.

Kato T, Takata M, Kitaichi M, Kassai M, Inoue M, Ishikawa C, Hirose W, Yoshida K, Shimizu I. Kato T, et al. Among authors: shimizu i. Eur J Pharmacol. 2015 Jun 15;757:11-20. doi: 10.1016/j.ejphar.2015.03.024. Epub 2015 Mar 28. Eur J Pharmacol. 2015. PMID: 25823809

6

The in vitro pharmacology and non-clinical cardiovascular safety studies of a novel 5-HT₄ receptor agonist, DSP-6952.

Tsubouchi T, Kunimatsu T, Tsujimoto S, Kiyoshi A, Katsura Y, Oku S, Chihara K, Mine Y, Yamada T, Shimizu I, Bando K. Tsubouchi T, et al. Among authors: shimizu i. Eur J Pharmacol. 2018 May 5;826:96-105. doi: 10.1016/j.ejphar.2018.02.037. Epub 2018 Mar 1. Eur J Pharmacol. 2018. PMID: 29501863 Free article.

7

DSP-6952, a novel 5-HT₄ receptor partial agonist, inhibits visceral hypersensitivity and ameliorates gastrointestinal dysfunction in experimental animals.

Mine Y, Itakura T, Oku S, Asada R, Shimizu I. Mine Y, et al. Among authors: shimizu i. Eur J Pharmacol. 2018 May 5;826:123-132. doi: 10.1016/j.ejphar.2018.02.005. Epub 2018 Feb 9. Eur J Pharmacol. 2018. PMID: 29428470 Free article.

8

Lack of dopamine supersensitivity in rats after chronic administration of blonanserin: Comparison with haloperidol.

Hashimoto T, Baba S, Ikeda H, Oda Y, Hashimoto K, Shimizu I. Hashimoto T, et al. Among authors: shimizu i. Eur J Pharmacol. 2018 Jul 5;830:26-32. doi: 10.1016/j.ejphar.2018.04.014. Epub 2018 Apr 22. Eur J Pharmacol. 2018. PMID: 29684390 Free article.

9

Effects of (+)-pentazocine and 1,3-di-o-tolylguanidine (DTG), sigma (sigma) ligands, on micturition in anaesthetized rats.

Shimizu I, Kawashima K, Ishii D, Oka M. Shimizu I, et al. Br J Pharmacol. 2000 Oct;131(3):610-6. doi: 10.1038/sj.bjp.0703593. Br J Pharmacol. 2000. PMID: 11015314 Free PMC article.

10

RU486, a progestin antagonist, binds to progesterone receptors in a human endometrial cancer cell line and reverses the growth inhibition by progestins.

Terakawa N, Shimizu I, Tanizawa O, Matsumoto K. Terakawa N, et al. Among authors: shimizu i. J Steroid Biochem. 1988 Aug;31(2):161-6. doi: 10.1016/0022-4731(88)90049-0. J Steroid Biochem. 1988. PMID: 2457133

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