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肾上腺素能受体在胰腺内分泌中的表达和功能。

Adrenoceptor Expression and Function in the Endocrine Pancreas.

机构信息

Department of Clinical Nutrition and Dietetics, Palestine Ahliya University, Bethlehem, Palestine.

Department of Pharmacology, University Medical Center, Johannes Gutenberg University, Mainz, Germany.

出版信息

Handb Exp Pharmacol. 2024;285:639-664. doi: 10.1007/164_2024_717.

Abstract

The sympathetic nervous system plays an important role in the regulation of endocrine pancreatic function, most importantly insulin release. Among the nine adrenoceptor (AR) subtypes, the α-AR appears to be the subtype most abundantly expressed in the human pancreas. While α- and β-AR have opposing effects, the net response to sympathetic stimulation is inhibition of insulin secretion mediated by α-AR located in the plasma membrane of pancreatic β cells. This inhibition may be present physiologically as evidenced by increased insulin secretion in healthy and diabetic humans and animals in response to α-AR antagonists, a finding that was confirmed in all studies. Based on such data and on an association of an α-AR polymorphism, that increases receptor expression levels, with an elevated risk for diabetes, increased α-AR signaling in the pancreatic β cells has been proposed as a risk factor for the development of type 2 diabetes. Thus, the α-AR was proposed as a drug target for the treatment of some forms of type 2 diabetes. Drug research and development programs leveraging this mechanism have reached the clinical stage, but none have resulted in an approved medicine due to a limited efficacy. While β-AR agonists can increase circulating insulin levels in vivo, it remains controversial whether this includes a direct effect on β cells or occurs secondary to general metabolic effects. Therefore, the regulation of endocrine pancreatic function is physiologically interesting but may be of limited therapeutic relevance.

摘要

交感神经系统在调节内分泌胰腺功能方面起着重要作用,尤其是胰岛素的释放。在九种肾上腺素能受体 (AR) 亚型中,α-AR 似乎是在人胰腺中表达最丰富的亚型。虽然 α-和 β-AR 具有相反的作用,但交感神经刺激的净反应是通过位于胰腺 β 细胞质膜上的 α-AR 介导的胰岛素分泌抑制。这种抑制在生理上可能存在,这可以从健康和糖尿病患者和动物对 α-AR 拮抗剂的反应中观察到胰岛素分泌增加得到证实,所有研究都证实了这一点。基于这些数据以及与增加受体表达水平的 α-AR 多态性的关联,与糖尿病风险增加相关,胰腺 β 细胞中增加的 α-AR 信号传导被提出是 2 型糖尿病发展的危险因素。因此,α-AR 被提议作为治疗某些 2 型糖尿病的药物靶点。利用这一机制的药物研发计划已经进入临床阶段,但由于疗效有限,没有一种药物获得批准。虽然β-AR 激动剂可以在体内增加循环胰岛素水平,但这是否包括对β细胞的直接作用,或者是否继发于一般代谢作用,仍存在争议。因此,内分泌胰腺功能的调节在生理学上很有趣,但可能在治疗相关性方面有限。

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