您的账号已在其他设备登录,您当前账号已强迫下线,
如非您本人操作,建议您在会员中心进行密码修改

确定
收藏 | 浏览24 | 下载0

Objective To deter mice the role of glucose in the control of insulin secretion and the possible mechanisms with which glucose fails to exert its effects on adenosine triphosphate-sensitive K+ channels. Methods NMRI mice islets were used to investigate the amount of insulin secretion and the changes of energy state in islets when the activity of adenosine triphosphate-sensitive K+channels was eliminated by diazoxide. Isolated islets were cutured in PRMI1640 medium for 18 hours, and were divided into 6 batches randomly, with 10 islets per batch (n=20). These were placed in 1.0 ml Krebs medium containing 250 μ mol/L diazoxide, 30 mmol/LK+and variou glucose concentrations, respectively, and incubated in 37℃ water for 60 minutes. A portion of the supernatant was withdrawn at the end of the incubation for insulin assay, the islets were treated with trichloracetic acid and diethyl ether for the measurements of ATP, ADP, GTP, and UTP. Results Under our experimental conditions, insulin secretion increased f

作者:肖常青;施焕中

来源:中华内科杂志 1998 年 37卷 zk期

知识库介绍

临床诊疗知识库该平台旨在解决临床医护人员在学习、工作中对医学信息的需求,方便快速、便捷的获取实用的医学信息,辅助临床决策参考。该库包含疾病、药品、检查、指南规范、病例文献及循证文献等多种丰富权威的临床资源。

详细介绍
热门关注
免责声明:本知识库提供的有关内容等信息仅供学习参考,不代替医生的诊断和医嘱。

收藏
| 浏览:24 | 下载:0
作者:
肖常青;施焕中
来源:
中华内科杂志 1998 年 37卷 zk期
标签:
Insulin Potassium channels Energy metabolism
Objective To deter mice the role of glucose in the control of insulin secretion and the possible mechanisms with which glucose fails to exert its effects on adenosine triphosphate-sensitive K+ channels. Methods NMRI mice islets were used to investigate the amount of insulin secretion and the changes of energy state in islets when the activity of adenosine triphosphate-sensitive K+channels was eliminated by diazoxide. Isolated islets were cutured in PRMI1640 medium for 18 hours, and were divided into 6 batches randomly, with 10 islets per batch (n=20). These were placed in 1.0 ml Krebs medium containing 250 μ mol/L diazoxide, 30 mmol/LK+and variou glucose concentrations, respectively, and incubated in 37℃ water for 60 minutes. A portion of the supernatant was withdrawn at the end of the incubation for insulin assay, the islets were treated with trichloracetic acid and diethyl ether for the measurements of ATP, ADP, GTP, and UTP. Results Under our experimental conditions, insulin secretion increased f