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SCH 28080的胃抗分泌及细胞保护活性

Gastric antisecretory and cytoprotective activities of SCH 28080.

作者信息

Long J F, Chiu P J, Derelanko M J, Steinberg M

出版信息

J Pharmacol Exp Ther. 1983 Jul;226(1):114-20.

PMID:6864535
Abstract

SCH 28080 (2-methyl-8-(phenylmethoxy)imidazo[1,2-a]pyridine-3-acetonitrile) is a novel antiulcer agent which has both antisecretory and cytoprotective activities. The antisecretory ED50 values in the pylorus-ligated rat were 3.7 mg/kg p.o. and 2.8 mg/kg i.p., being 7 and 10 times more potent than cimetidine, respectively. In dogs, SCH 28080 was effective in inhibiting acid secretion stimulated by histamine (ED50 of 0.09 mg/kg i.v. and 4.4 mg/kg p.o.), dimaprit, pentagastrin, insulin and feeding. The cytoprotective activity of SCH 28080 was demonstrated by inhibition of ethanol-induced gastric lesions in a dose-dependent manner in rats (ED50:3.0 mg/kg p.o.). SCH 28080 was active in similar dose ranges (1-10 mg/kg) by both p.o. and i.v. routes of administration. This gastric cytoprotective activity was not affected by indomethacin pretreatment. Furthermore, the gastric potential difference was effectively sustained by SCH 28080 (3, 10 and 30 mg/kg p.o.) after intragastric ethanol. SCH 28080 (1-30 mg/kg p.o.) also inhibited gastric ulcers provoked by aspirin, aspirin + acid, indomethacin and stress (cold-restraint) in rats. The data support the concept that it is possible to have combined antisecretory and cytoprotectant actions in a single molecule which is not a prostaglandin.

摘要

SCH 28080(2-甲基-8-(苄氧基)咪唑并[1,2-a]吡啶-3-乙腈)是一种新型抗溃疡药物,具有抗分泌和细胞保护活性。在幽门结扎大鼠中,抗分泌ED50值经口服为3.7毫克/千克,经腹腔注射为2.8毫克/千克,分别比西咪替丁强7倍和10倍。在犬类中,SCH 28080能有效抑制组胺(静脉注射ED50为0.09毫克/千克,口服为4.4毫克/千克)、二甲双胍、五肽胃泌素、胰岛素和进食刺激引起的胃酸分泌。SCH 28080的细胞保护活性通过在大鼠中以剂量依赖性方式抑制乙醇诱导的胃损伤得以证明(ED50:口服3.0毫克/千克)。SCH 28080经口服和静脉注射途径在相似剂量范围(1 - 10毫克/千克)均有活性。这种胃细胞保护活性不受吲哚美辛预处理的影响。此外,在胃内给予乙醇后,SCH 28080(口服3、10和30毫克/千克)能有效维持胃电位差。SCH 28080(口服1 - 30毫克/千克)还能抑制大鼠中由阿司匹林、阿司匹林 + 酸、吲哚美辛和应激(冷束缚)诱发的胃溃疡。这些数据支持了在一个非前列腺素的单一分子中可能同时具有抗分泌和细胞保护作用的概念。

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