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内分泌胰腺生长抑素受体的功能与表达

Function and expression of somatostatin receptors of the endocrine pancreas.

作者信息

Strowski Mathias Z, Blake Allan D

机构信息

Medizinische Klinik mit Schwerpunkt Hepatologie und Gastroenterologie, Charité-Universitätsmedizin Berlin, Berlin, Germany.

出版信息

Mol Cell Endocrinol. 2008 May 14;286(1-2):169-79. doi: 10.1016/j.mce.2008.02.007. Epub 2008 Feb 17.

Abstract

Somatostatin (SST) regulates multiple biological processes via five genetically distinct, G-protein coupled receptors. Clinical interest in therapy for neuroendocrine and metabolic disorders has resulted in the development of new tools for exploring the function of somatostatin receptors (SSTRs). The development of highly SSTR-selective agonists and antagonists, animal models with the deletion of individual SSTRs, as well as SSTR-specific antibodies have all been utilized in delineating SSTR functions. In the pancreas, SST is a potent regulator of insulin and glucagon secretion. Indeed, the inappropriate regulation of pancreatic A- and B-cell function in metabolic diseases provides an impetus to evaluate the SSTRs as therapeutic targets. By combining the results obtained from molecular biology, pharmacology and immunochemical studies the current review provides a summary of important recent developments which have extended our knowledge of SST actions in the endocrine pancreas.

摘要

生长抑素(SST)通过五种基因不同的G蛋白偶联受体调节多种生物学过程。对神经内分泌和代谢紊乱治疗的临床兴趣推动了探索生长抑素受体(SSTRs)功能的新工具的开发。高SSTR选择性激动剂和拮抗剂的开发、单个SSTR基因缺失的动物模型以及SSTR特异性抗体都已被用于阐明SSTR的功能。在胰腺中,SST是胰岛素和胰高血糖素分泌的有效调节剂。事实上,代谢疾病中胰腺A细胞和B细胞功能的不当调节促使人们将SSTRs作为治疗靶点进行评估。通过结合分子生物学、药理学和免疫化学研究获得的结果,本综述总结了近期的重要进展,这些进展扩展了我们对SST在内分泌胰腺中作用的认识。

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