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茚三酮对葡萄糖诱导的胰岛素释放的抑制作用。

Ninhydrin inhibition of glucose-induced insulin release.

作者信息

McDaniel M L, Roth C E, Fink C J, Swanson J A, Lacy P E

出版信息

Diabetologia. 1977 Dec;13(6):603-6. doi: 10.1007/BF01236314.

Abstract

Ninhydrin, a compound which shares chemical properties strikingly similar to alloxan was found to mimic basically the inhibitory effect of alloxan on glucose-induced insulin release. Exposure of pancreatic islets for five minutes to 85 mumol/l ninhydrin produced approximately ninety percent inhibition of subsequent glucose-induced insulin release without altering basal secretion. Both D-glucose and D-mannose provided substantial protection against the inhibitory effect of ninhydrin, and the alpha anomer of D-glucose was more effective than the beta anomer in preventing ninhydrin inhibition of insulin release. Evidence for a common site of inhibition by ninhydrin and alloxan in the insulin release process is discussed.

摘要

茚三酮是一种化学性质与四氧嘧啶极为相似的化合物,它被发现基本上能模拟四氧嘧啶对葡萄糖诱导的胰岛素释放的抑制作用。将胰岛暴露于85微摩尔/升的茚三酮中五分钟,会对随后的葡萄糖诱导的胰岛素释放产生约90%的抑制作用,而不会改变基础分泌。D-葡萄糖和D-甘露糖都能对茚三酮的抑制作用提供显著的保护,并且D-葡萄糖的α异头物在防止茚三酮抑制胰岛素释放方面比β异头物更有效。文中讨论了茚三酮和四氧嘧啶在胰岛素释放过程中共同抑制位点的证据。

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