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使用光开关磺脲类药物对胰岛素释放进行光学控制。

Optical control of insulin release using a photoswitchable sulfonylurea.

作者信息

Broichhagen Johannes, Schönberger Matthias, Cork Simon C, Frank James A, Marchetti Piero, Bugliani Marco, Shapiro A M James, Trapp Stefan, Rutter Guy A, Hodson David J, Trauner Dirk

机构信息

Department of Chemistry, Ludwig-Maximilians-Universität München, and Munich Center for Integrated Protein Science, Butenandtstrasse 5-13, 81377 München, Germany.

Division of Biosciences, Department of Neuroscience, Physiology and Pharmacology, University College London, London WC1E 6BT, UK.

出版信息

Nat Commun. 2014 Oct 14;5:5116. doi: 10.1038/ncomms6116.

Abstract

Sulfonylureas are widely prescribed for the treatment of type 2 diabetes mellitus (T2DM). Through their actions on ATP-sensitive potassium (KATP) channels, sulfonylureas boost insulin release from the pancreatic beta cell mass to restore glucose homeostasis. A limitation of these compounds is the elevated risk of developing hypoglycemia and cardiovascular disease, both potentially fatal complications. Here, we describe the design and development of a photoswitchable sulfonylurea, JB253, which reversibly and repeatedly blocks KATP channel activity following exposure to violet-blue light. Using in situ imaging and hormone assays, we further show that JB253 bestows light sensitivity upon rodent and human pancreatic beta cell function. Thus, JB253 enables the optical control of insulin release and may offer a valuable research tool for the interrogation of KATP channel function in health and T2DM.

摘要

磺脲类药物被广泛用于治疗2型糖尿病(T2DM)。通过作用于ATP敏感性钾(KATP)通道,磺脲类药物促进胰岛素从胰腺β细胞群释放,以恢复葡萄糖稳态。这些化合物的一个局限性是发生低血糖和心血管疾病的风险增加,这两种都是潜在的致命并发症。在此,我们描述了一种可光开关的磺脲类药物JB253的设计与开发,其在暴露于蓝紫光后可逆且反复地阻断KATP通道活性。通过原位成像和激素测定,我们进一步表明JB253赋予啮齿动物和人类胰腺β细胞功能光敏感性。因此,JB253能够实现对胰岛素释放的光学控制,并可能为研究健康状态和T2DM中KATP通道功能提供有价值的研究工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e996/4214423/b144bbcff946/ncomms6116-f1.jpg

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