The insulin receptor is colocalized with the TRPV1 nociceptive ion channel and neuropeptides in pancreatic spinal and vagal primary sensory neurons

OBJECTIVES: Recent observations demonstrated the expression of the insulin receptor (InsR) and its functional interaction with the transient receptor potential vanilloid type 1 receptor (TRPV1) in sensory ganglion neurons. Because sensory nerves are implicated in pancreatic inflammatory processes,...

Teljes leírás

Elmentve itt :
Bibliográfiai részletek
Szerzők: Lázár Bence András
Jancsó Gábor
Oszlács Orsolya
Nagy Istvá
Sántha Péter
Dokumentumtípus: Cikk
Megjelent: 2018
Sorozat:PANCREAS 47 No. 1
doi:10.1097/MPA.0000000000000959

mtmt:3311693
Online Access:http://publicatio.bibl.u-szeged.hu/13365
Leíró adatok
Tartalmi kivonat:OBJECTIVES: Recent observations demonstrated the expression of the insulin receptor (InsR) and its functional interaction with the transient receptor potential vanilloid type 1 receptor (TRPV1) in sensory ganglion neurons. Because sensory nerves are implicated in pancreatic inflammatory processes, we studied the colocalization of the InsR with TRPV1 and proinflammatory neuropeptides in spinal and vagal pancreatic afferent neurons. METHODS: Immunohistochemistry and quantitative morphometry were used to analyze the expression of TRPV1, InsR, substance P (SP), and calcitonin gene-related peptide (CGRP) in retrogradely labeled pancreatic dorsal root ganglion (DRG) and nodose ganglion (NG) neurons. RESULTS: The proportions of retrogradely labeled pancreatic TRPV1-, InsR-, SP-, and CGRP-immunoreactive neurons amounted to 68%, 48%, 33%, and 54% in DRGs and 64%, 49%, 40%, and 25% in the NGs. Of the labeled DRG and NG neurons, 23% and 35% showed both TRPV1 and InsR immunoreactivity. Colocalization of the InsR with SP or CGRP was demonstrated in 14% and 28% of pancreatic DRG and 24% and 8% of pancreatic NG neurons. CONCLUSIONS: The present findings provide morphological basis for possible functional interactions among the nociceptive ion channel TRPV1, the InsR, and the proinflammatory neuropeptides SP and CGRP expressed by pancreatic DRG and NG neurons.
Terjedelem/Fizikai jellemzők:110-115
ISSN:0885-3177