Neural and Behavioral Sciences Penn State College of Medicine, Department of Neural and Behavioral Sciences, 500 University Drive-MC H109 Hershey, PA 17033-0850, USA.
Neural and Behavioral Sciences Penn State College of Medicine, Department of Neural and Behavioral Sciences, 500 University Drive-MC H109 Hershey, PA 17033-0850, USA.
Biochem Pharmacol. 2014 Feb 15;87(4):535-42. doi: 10.1016/j.bcp.2013.12.001. Epub 2013 Dec 16.
The pancreas consists of two major divisions, the exocrine and the endocrine pancreas. Recent data from our laboratory have shown that the functions of the two divisions are under modulatory regulation by separate neurocircuits that originate in the dorsal motor nucleus of the vagus (DMV). Metabotropic glutamate receptors (mGluRs) are expressed throughout the central nervous system and have been implicated in the modulation of synaptic transmission. mGluRs consist of three groups of receptors, which can be distinguished based on their pharmacological properties and second messenger systems. Group I mGluRs predominantly increase, whereas group II and III mGluRs decrease synaptic transmission. Group II and group III mGluRs are present on excitatory and inhibitory synaptic terminals impinging on pancreas-projecting DMV neurons. We have shown that group II mGluRs regulate both exocrine pancreatic secretions and insulin release, whereas group III mGluRs only regulate insulin release. Several mGluR agonists and antagonists have been shown to have clinical uses for disorders accompanied by abnormal synaptic transmission, including anxiety and Parkinson's disease. Moreover, a negative allosteric modulator of Group I mGluRs is effective in alleviating symptoms of gastro-esophageal reflux disease (GERD). Since the role of the three mGluR groups in mediating different gastrointestinal (GI) functions appears to be highly specific, the use of agonists or antagonists directed at a single receptor group could potentially provide highly selective targets for the treatment of GI disorders including GERD, functional dyspepsia and acute pancreatitis.
胰腺由两个主要部分组成,外分泌腺和内分泌腺。我们实验室的最新数据表明,这两个部分的功能受到来自迷走神经背核(DMV)的独立神经回路的调节。代谢型谷氨酸受体(mGluRs)在中枢神经系统中广泛表达,并被认为参与了突触传递的调节。mGluRs 由三组受体组成,它们可以根据其药理学特性和第二信使系统来区分。I 组 mGluRs 主要增强,而 II 组和 III 组 mGluRs 则降低突触传递。II 组和 III 组 mGluRs 存在于投射到胰腺的 DMV 神经元的兴奋性和抑制性突触末梢上。我们已经表明,II 组 mGluRs 调节外分泌胰腺分泌和胰岛素释放,而 III 组 mGluRs 仅调节胰岛素释放。已经证明几种 mGluR 激动剂和拮抗剂对伴有异常突触传递的疾病(包括焦虑症和帕金森病)具有临床用途。此外,I 组 mGluRs 的负变构调节剂在缓解胃食管反流病(GERD)的症状方面有效。由于三组 mGluRs 在介导不同胃肠道(GI)功能方面的作用似乎高度特异,针对单个受体组的激动剂或拮抗剂的使用可能为治疗 GI 疾病(包括 GERD、功能性消化不良和急性胰腺炎)提供高度选择性的靶标。