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抗胃泌素(SC - 15396)对小鼠胰腺腺泡淀粉酶释放及2 - 脱氧葡萄糖摄取的影响。

Effect of antigastrin (SC-15396) on amylase release and 2-deoxyglucose uptake in mouse pancreatic acini.

作者信息

Iwamoto Y, Nakamura R, Akanuma Y, Kuzuya T

出版信息

Digestion. 1985;31(1):31-6. doi: 10.1159/000199174.

Abstract

The effects of antigastrin (SC-15396) on amylase release and 2-deoxyglucose uptake were studied in dispersed acini from mouse pancreas. Antigastrin at concentrations between 0.5 and 2 mM inhibited cholecystokinin (CCK)-stimulated amylase release and 2-deoxyglucose uptake in a dose-dependent fashion. Antigastrin at concentrations between 0.5 and 2 mM inhibited carbachol-stimulated amylase release and 2-deoxyglucose uptake as well. In addition, the drug (2 mM) inhibited bombesin-stimulated amylase release and 2-deoxyglucose uptake. In contrast, the stimulation of amylase release by Ca2+ ionophore A23187 was not inhibited by antigastrin. The results, therefore, suggest that antigastrin nonselectively inhibits the actions of these secretagogues probably at their receptor sites.

摘要

研究了抗胃泌素(SC - 15396)对小鼠胰腺分散腺泡淀粉酶释放和2 - 脱氧葡萄糖摄取的影响。浓度在0.5至2 mM之间的抗胃泌素以剂量依赖方式抑制胆囊收缩素(CCK)刺激的淀粉酶释放和2 - 脱氧葡萄糖摄取。浓度在0.5至2 mM之间的抗胃泌素也抑制卡巴胆碱刺激的淀粉酶释放和2 - 脱氧葡萄糖摄取。此外,该药物(2 mM)抑制蛙皮素刺激的淀粉酶释放和2 - 脱氧葡萄糖摄取。相反,抗胃泌素不抑制Ca2 +离子载体A23187刺激的淀粉酶释放。因此,结果表明抗胃泌素可能在其受体部位非选择性地抑制这些促分泌素的作用。

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