Zobrazeno 1 - 10
of 155
pro vyhledávání: '"Hironaka AIHARA"'
Autor:
Masaaki Kimura, Hiroaki Araki, Hironaka Aihara, Yasuko Karasawa, Kazuaki Kawashima, Shigeru Okuyama, Susumu Otomo, Hiroko Shimamura-Harada
Publikováno v:
General Pharmacology: The Vascular System. 22:143-150
1. 1. We examined the effects of minaprine on cerebral infarction produced by occluding of unilateral middle cerebral artery (MCA) above the rhinal fissure in stroke-prone spontaneously hypertensive rats (SHRSP). 2. 2. Oral administration of minaprin
Publikováno v:
European Journal of Pharmacology. 178:343-350
The H2-receptor antagonistic activities and properties of IT-066 were investigated in rabbit isolated gastric mucosal cell and were compared with those of famotidine and cimetidine. IT-066 inhibited dose dependently the histamine-stimulated [14C]amin
Autor:
Katsuharu Tsuchida, Makoto Muramatsu, Katsuyoshi Kaneko, Ryuzaburo Yamazaki, Takashi Yamada, Naoyoshi Ogawa, Hironaka Aihara
Publikováno v:
Cardiovascular Drug Reviews. 8:45-55
Publikováno v:
Neurochemistry International. 16:301-307
5-Hydroxytryptamine (serotonin, 5-HT) and 5-HT(2) receptor agonist 4-bromo-2,5-dimethoxyphenylisopropylamine (DOB) inhibited K(+)-induced [(3)H]acetylcholine ([(3)H]ACh) release from slices and crude synaptosomes of rat cerebral cortex. Minaprine [3(
Publikováno v:
Japanese journal of pharmacology. 57(1)
3-Amino-4-[4-[4-(1-piperidinomethyl)-2-pyridyloxy]-cis-2-butenylamino]-3-cyclobutene-1, 2-dione hydrochloride (IT-066) showed a highly potent and long lasting H2-receptor blocking action in guinea pig atria. The inhibitory effect of IT-066 on the his
Effect of salvianolic acid A, a depside from roots of Salvia miltiorrhiza, on gastric H+,K(+)-ATPase
Autor:
Haruko Kijima, Susumu Otomo, Shigeru Murakami, Makoto Muramatsu, L N Li, Yoshihiko Isobe, Hironaka Aihara, C B Ai
Publikováno v:
Planta medica. 56(4)
Salvianolic acid A, a depside from the roots of Salvia miltiorrhiza, inhibited pig gastric H+,K(+)-ATPase and pNPPase with 50% inhibition values (IC50) of 5.2 x 10(-7) M and 1.7 x 10(-6) M, respectively. Kinetic studies revealed that the inhibition p
Autor:
Masahiro Harada, Susumu Otomo, Hideo Okumura, T. Takamura, T. Kobayashi, Hironaka Aihara, Nobuo Ikekawa, Takao Yamamuro, Shohei Higuchi
Publikováno v:
Bone and mineral. 9(2)
The effect of 26,27-hexafluoro-1,25-dihydroxyvitamin D3 (F6-1,25(OH)2D3) on experimental osteoporosis in the rat induced by a combination of immobilization and ovariectomy was evaluated. F6-1,25(OH)2D3 increased the femur score and the photo-density.
Publikováno v:
Neuropharmacology. 29(1)
2-Deoxy-D-glucose (2-DG) administered intraperitoneally, dose-dependently increased the secretion of gastric acid, and the changes were comparable with those on the activity of choline acetyltransferase (CAT) and acetylcholinesterase (AChE) in the st
The antiseoretory properties of a new histamine H2-receptor antagonist, IT-066, in vitro and in vivo
Publikováno v:
European Journal of Pharmacology. 183:302-303
Publikováno v:
Journal of Cardiovascular Pharmacology. 18:769
We examined the calcium antagonistic action of CD-349, a dihydropyridine derivative, on goat cardiac Purkinje fibers using the two-microelectrode voltage-clamp method. CD-349 at a concentration of 10(-5) M shortened the action potential duration with