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The neuropeptide 26RFa in the human gut and pancreas: potential involvement in glucose homeostasis

Authors :
Gaëtan Prévost
Marie Picot
Marie-Anne Le Solliec
Arnaud Arabo
Hind Berrahmoune
Mouna El Mehdi
Saloua Cherifi
Alexandre Benani
Emmanuelle Nédélec
Françoise Gobet
Valéry Brunel
Jérôme Leprince
Hervé Lefebvre
Youssef Anouar
Nicolas Chartrel
Source :
Endocrine Connections, Vol 8, Iss 7, Pp 941-951 (2019)
Publication Year :
2019
Publisher :
Bioscientifica, 2019.

Abstract

Objective: 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. Design and methods: 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. Results: 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 level s and the BMI, and with various parameters of insulin secretion and insulin resistance.

Details

Language :
English
ISSN :
20493614
Volume :
8
Issue :
7
Database :
Directory of Open Access Journals
Journal :
Endocrine Connections
Publication Type :
Academic Journal
Accession number :
edsdoj.58db3563f3444deaba9118db380d275d
Document Type :
article
Full Text :
https://doi.org/10.1530/EC-19-0247