期刊论文详细信息
The Japanese Journal of Pharmacology
Facilitation of Acetylcholine Release by SK-951, a Benzofuran Derivative, via the 5-Hydroxytryptamine4 Receptor in Guinea Pig Stomach
Yasuko Sakurai-Yamashita2  Motohiro Takeda1  Katsura Tsukamoto1  Tsunemasa Suzuki1  Kohtaro Taniyama2 
[1]Pharmaceutical Laboratory,Sanwa Kagaku Kenkyusho Co.,Ltd.,Shiosaki 363,Hokusei-cho,Inabe-gun,Mie 511-0406,Japan
[2]Department of Pharmacology,Nagasaki University School of Medicine,Sakamoto 1-12-4,Nagasaki 852-8523,Japan
关键词: SK-951;    [125I]SB207710 binding;    Acetylcholine release;    5-Hydroxytryptamine4 receptor;    Guinea pig stomach;   
DOI  :  10.1254/jjp.82.138
学科分类:药理学
来源: Nihon Yakuri Gakkai Henshuubu / Japanese Pharmacological Society
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【 摘 要 】
References(22)Cited-By(1)Facilitation of acetylcholine(ACh) release by SK-951((−)4-amino-N-[2-(1-azabicyclo[3.3.0]octan-5-yl)ethyl]-5-chloro-2, 3-dihydro-2-methylbenzo[b]furan-7-carboxamine hemifumarate), a benzofuran derivative, via the 5-hydroxytryptamine(5-HT)4 receptor in guinea pig stomach was examined by in vitro receptor autoradiography and functional studies.[125I]SB207710 binding was detected in the myenteric plexus of the gastric corpus.High densities of binding sites were observed in the myenteric plexus and a moderate density in the muscle layer.SK-951 inhibited the binding of [125I]SB207710, a specific 5-HT4-receptor ligand, as in the case of SB204070, a specific 5-HT4-receptor antagonist, thus indicating the presence of 5-HT4 receptors in guinea pig stomach.SK-951 as well as 5-HT enhanced the electrically stimulated twitch contractions of gastric corpus strips, which were sensitive to tetrodotoxin and atropine, and enhanced electrically stimulated release of ACh from corporal strips, which was tetrodotoxin-sensitive and Ca2+-dependent.The enhancements of twitch contractions and ACh release by SK-951 were antagonized by GR113808, a selective 5-HT4-receptor antagonist.Thus, SK-951 binds to 5-HT4 receptors of the guinea pig gastric corpus and may accelerate gastric motility due to facilitation of ACh release.
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