Department of Clinical Nutrition and Dietetics, Palestine Ahliya University, Bethlehem, Palestine.
Department of Pharmacology, University Medical Center, Johannes Gutenberg University, Mainz, Germany.
Handb Exp Pharmacol. 2024;285:639-664. doi: 10.1007/164_2024_717.
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.
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。