Prévost Gaëtan, Picot Marie, Le Solliec Marie-Anne, Arabo Arnaud, Berrahmoune Hind, El Mehdi Mouna, Cherifi Saloua, Benani Alexandre, Nédélec Emmanuelle, Gobet Françoise, Brunel Valéry, Leprince Jérôme, Lefebvre Hervé, Anouar Youssef, Chartrel Nicolas
Normandie Univ, UNIROUEN, INSERM U1239, Laboratory of Neuronal and Neuroendocrine Differentiation and Communication (DC2N), Rouen, France.
Department of Endocrinology, Diabetes and Metabolic Diseases, Normandie Univ, UNIROUEN, Rouen University Hospital, Rouen, France.
Endocr Connect. 2019 Jul;8(7):941-951. doi: 10.1530/EC-19-0247.
Recent studies performed in mice revealed that the neuropeptide 26RFa regulates glucose homeostasis by acting as an incretin and by increasing insulin sensitivity. However, in humans, an association between 26RFa and the regulation of glucose homeostasis is poorly documented. In this study, we have thus investigated in detail the distribution of 26RFa and its receptor, GPR103, in the gut and the pancreas, and determined the response of this peptidergic system to an oral glucose challenge in obese patients.
Distribution of 26RFa and GPR103 was examined by immunohistochemistry using gut and pancreas tissue sections. Circulating 26RFa was determined using a specific radioimmunoassay in plasma samples collected during an oral glucose tolerance test.
26RFa and GPR103 are present all along the gut but are more abundant in the stomach and duodenum. In the stomach, the peptide and its receptor are highly expressed in the gastric glands, whereas in the duodenum, ileum and colon they are present in the enterocytes and the goblet cells. In the pancreatic islets, the 26RFa/GPR103 system is mostly present in the β cells. During an oral glucose tolerance test, plasma 26RFa profile is different between obese patients and healthy volunteers, and we found strong positive correlations between 26RFa blood levels and the BMI, and with various parameters of insulin secretion and insulin resistance.
The present data suggest an involvement of the 26RFa/GPR103 peptidergic system in the control of human glucose homeostasis.
最近在小鼠中进行的研究表明,神经肽26RFa通过作为肠促胰岛素和增加胰岛素敏感性来调节葡萄糖稳态。然而,在人类中,26RFa与葡萄糖稳态调节之间的关联鲜有文献记载。因此,在本研究中,我们详细研究了26RFa及其受体GPR103在肠道和胰腺中的分布,并确定了该肽能系统对肥胖患者口服葡萄糖挑战的反应。
使用肠道和胰腺组织切片,通过免疫组织化学检查26RFa和GPR103的分布。在口服葡萄糖耐量试验期间采集的血浆样本中,使用特异性放射免疫测定法测定循环中的26RFa。
26RFa和GPR103存在于整个肠道,但在胃和十二指肠中含量更高。在胃中,该肽及其受体在胃腺中高度表达,而在十二指肠、回肠和结肠中,它们存在于肠上皮细胞和杯状细胞中。在胰岛中,26RFa/GPR103系统主要存在于β细胞中。在口服葡萄糖耐量试验期间,肥胖患者和健康志愿者的血浆26RFa谱不同,并且我们发现26RFa血药浓度与BMI以及胰岛素分泌和胰岛素抵抗的各种参数之间存在强正相关。
目前的数据表明26RFa/GPR103肽能系统参与了人类葡萄糖稳态的控制。