Matsubara M - Search Results

1

Olopatadine ameliorates rat experimental cutaneous inflammation by improving skin barrier function.

Tamura T, Matsubara M, Amano T, Chida M. Tamura T, et al. Among authors: matsubara m. Pharmacology. 2008;81(2):118-26. doi: 10.1159/000110112. Epub 2007 Oct 26. Pharmacology. 2008. PMID: 17962722

2

Histamine H1 receptor antagonist blocks histamine-induced proinflammatory cytokine production through inhibition of Ca2+-dependent protein kinase C, Raf/MEK/ERK and IKK/I kappa B/NF-kappa B signal cascades.

Matsubara M, Tamura T, Ohmori K, Hasegawa K. Matsubara M, et al. Biochem Pharmacol. 2005 Feb 1;69(3):433-49. doi: 10.1016/j.bcp.2004.10.006. Epub 2004 Dec 9. Biochem Pharmacol. 2005. PMID: 15652235

3

Effects of olopatadine hydrochloride, an antihistamine drug, on skin inflammation induced by repeated topical application of oxazolone in mice.

Tamura T, Matsubara M, Takada C, Hasegawa K, Suzuki K, Ohmori K, Karasawa A. Tamura T, et al. Among authors: matsubara m. Br J Dermatol. 2004 Dec;151(6):1133-42. doi: 10.1111/j.1365-2133.2004.06172.x. Br J Dermatol. 2004. PMID: 15606507

4

Properties of olopatadine hydrochloride, a new antiallergic/antihistaminic drug.

Ohmori K, Hasegawa K, Tamura T, Miyake K, Matsubara M, Masaki S, Karasawa A, Urayama N, Horikoshi K, Kajita J, Hasegawa M, Taniguchi K, Komada T, Kawamoto Y. Ohmori K, et al. Among authors: matsubara m. Arzneimittelforschung. 2004;54(12):809-29. doi: 10.1055/s-0031-1297036. Arzneimittelforschung. 2004. PMID: 15646365 Review.

5

Olopatadine hydrochloride suppresses the rebound phenomenon after discontinuation of treatment with a topical steroid in mice with chronic contact hypersensitivity.

Tamura T, Matsubara M, Hasegawa K, Ohmori K, Karasawa A. Tamura T, et al. Among authors: matsubara m. Clin Exp Allergy. 2005 Jan;35(1):97-103. doi: 10.1111/j.1365-2222.2005.02147.x. Clin Exp Allergy. 2005. PMID: 15649273

6

Differential regulation of IL-4 expression and degranulation by anti-allergic olopatadine in rat basophilic leukemia (RBL-2H3) cells.

Matsubara M, Masaki S, Ohmori K, Karasawa A, Hasegawa K. Matsubara M, et al. Biochem Pharmacol. 2004 Apr 1;67(7):1315-26. doi: 10.1016/j.bcp.2003.12.008. Biochem Pharmacol. 2004. PMID: 15013847

7

Comparison of the antiatherosclerotic effects of dihydropyridine calcium channel blocker and HMG-CoA reductase inhibitor on hypercholesterolemic rabbits.

Takayama M, Matsubara M, Arakawa E, Takada C, Ina Y, Hasegawa K, Yao K. Takayama M, et al. Among authors: matsubara m. Vascul Pharmacol. 2007 Apr;46(4):302-8. doi: 10.1016/j.vph.2006.11.004. Epub 2006 Nov 23. Vascul Pharmacol. 2007. PMID: 17197250

8

Benidipine, an anti-hypertensive drug, inhibits reactive oxygen species production in polymorphonuclear leukocytes and oxidative stress in salt-loaded stroke-prone spontaneously hypertensive rats.

Matsubara M, Akizuki O, Ikeda J, Saeki K, Yao K, Sasaki K. Matsubara M, et al. Eur J Pharmacol. 2008 Feb 2;580(1-2):201-13. doi: 10.1016/j.ejphar.2007.10.072. Epub 2007 Nov 1. Eur J Pharmacol. 2008. PMID: 18048030

9

Effects of benidipine, a dihydropyridine-Ca2+ channel blocker, on expression of cytokine-induced adhesion molecules and chemoattractants in human aortic endothelial cells.

Matsubara M, Hasegawa K. Matsubara M, et al. Eur J Pharmacol. 2004 Sep 13;498(1-3):303-14. doi: 10.1016/j.ejphar.2004.07.086. Eur J Pharmacol. 2004. PMID: 15364009

10

Blockade of T-type voltage-dependent Ca2+ channels by benidipine, a dihydropyridine calcium channel blocker, inhibits aldosterone production in human adrenocortical cell line NCI-H295R.

Akizuki O, Inayoshi A, Kitayama T, Yao K, Shirakura S, Sasaki K, Kusaka H, Matsubara M. Akizuki O, et al. Among authors: matsubara m. Eur J Pharmacol. 2008 Apr 28;584(2-3):424-34. doi: 10.1016/j.ejphar.2008.02.001. Epub 2008 Feb 12. Eur J Pharmacol. 2008. PMID: 18331727

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