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Capsaicin-sensitive sensory fibers in the islets of Langerhans contribute to defective insulin secretion in Zucker diabetic rat, an animal model for some aspects of human type 2 diabetes

Gram, Dorte X. ; Ahrén, Bo LU ; Nagy, Istvan ; Olsen, Uffe B. ; Brand, Christian L. ; Sundler, Frank ; Tabanera, Rene ; Svendsen, Ove ; Carr, Richard D. and Santha, Peter , et al. (2007) In European Journal of Neuroscience 25(1). p.213-223
Abstract
The system that regulates insulin secretion from beta-cells in the islet of Langerhans has a capsaicin-sensitive inhibitory component. As calcitonin gene-related peptide (CGRP)-expressing primary sensory fibers innervate the islets, and a major proportion of the CGRP-containing primary sensory neurons is sensitive to capsaicin, the islet-innervating sensory fibers may represent the capsaicin-sensitive inhibitory component. Here, we examined the expression of the capsaicin receptor, vanilloid type 1 transient receptor potential receptor (TRPV1) in CGRP-expressing fibers in the pancreatic islets, and the effect of selective elimination of capsaicin-sensitive primary afferents on the decline of glucose homeostasis and insulin secretion in... (More)
The system that regulates insulin secretion from beta-cells in the islet of Langerhans has a capsaicin-sensitive inhibitory component. As calcitonin gene-related peptide (CGRP)-expressing primary sensory fibers innervate the islets, and a major proportion of the CGRP-containing primary sensory neurons is sensitive to capsaicin, the islet-innervating sensory fibers may represent the capsaicin-sensitive inhibitory component. Here, we examined the expression of the capsaicin receptor, vanilloid type 1 transient receptor potential receptor (TRPV1) in CGRP-expressing fibers in the pancreatic islets, and the effect of selective elimination of capsaicin-sensitive primary afferents on the decline of glucose homeostasis and insulin secretion in Zucker diabetic fatty (ZDF) rats, which are used to study various aspects of human type 2 diabetes mellitus. We found that CGRP-expressing fibers in the pancreatic islets also express TRPV1. Furthermore, we also found that systemic capsaicin application before the development of hyperglycemia prevents the increase of fasting, non-fasting, and mean 24-h plasma glucose levels, and the deterioration of glucose tolerance assessed on the fifth week following the injection. These effects were accompanied by enhanced insulin secretion and a virtually complete loss of CGRP- and TRPV1-coexpressing islet-innervating fibers. These data indicate that CGRP-containing fibers in the islets are capsaicin sensitive, and that elimination of these fibers contributes to the prevention of the deterioration of glucose homeostasis through increased insulin secretion in ZDF rats. Based on these data we propose that the activity of islet-innervating capsaicin-sensitive fibers may have a role in the development of reduced insulin secretion in human type 2 diabetes mellitus. (Less)
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organization
publishing date
type
Contribution to journal
publication status
published
subject
keywords
primary sensory neuron, CGRP, low-grade inflammation, TRPV1
in
European Journal of Neuroscience
volume
25
issue
1
pages
213 - 223
publisher
Wiley-Blackwell
external identifiers
  • wos:000243682100021
  • scopus:33846194056
ISSN
1460-9568
DOI
10.1111/j.1460-9568.2006.05261.x
language
English
LU publication?
yes
id
e22e52c8-22ad-4f93-aaa4-157625e7865d (old id 676666)
date added to LUP
2016-04-01 12:32:40
date last changed
2024-02-24 12:05:20
@article{e22e52c8-22ad-4f93-aaa4-157625e7865d,
  abstract     = {{The system that regulates insulin secretion from beta-cells in the islet of Langerhans has a capsaicin-sensitive inhibitory component. As calcitonin gene-related peptide (CGRP)-expressing primary sensory fibers innervate the islets, and a major proportion of the CGRP-containing primary sensory neurons is sensitive to capsaicin, the islet-innervating sensory fibers may represent the capsaicin-sensitive inhibitory component. Here, we examined the expression of the capsaicin receptor, vanilloid type 1 transient receptor potential receptor (TRPV1) in CGRP-expressing fibers in the pancreatic islets, and the effect of selective elimination of capsaicin-sensitive primary afferents on the decline of glucose homeostasis and insulin secretion in Zucker diabetic fatty (ZDF) rats, which are used to study various aspects of human type 2 diabetes mellitus. We found that CGRP-expressing fibers in the pancreatic islets also express TRPV1. Furthermore, we also found that systemic capsaicin application before the development of hyperglycemia prevents the increase of fasting, non-fasting, and mean 24-h plasma glucose levels, and the deterioration of glucose tolerance assessed on the fifth week following the injection. These effects were accompanied by enhanced insulin secretion and a virtually complete loss of CGRP- and TRPV1-coexpressing islet-innervating fibers. These data indicate that CGRP-containing fibers in the islets are capsaicin sensitive, and that elimination of these fibers contributes to the prevention of the deterioration of glucose homeostasis through increased insulin secretion in ZDF rats. Based on these data we propose that the activity of islet-innervating capsaicin-sensitive fibers may have a role in the development of reduced insulin secretion in human type 2 diabetes mellitus.}},
  author       = {{Gram, Dorte X. and Ahrén, Bo and Nagy, Istvan and Olsen, Uffe B. and Brand, Christian L. and Sundler, Frank and Tabanera, Rene and Svendsen, Ove and Carr, Richard D. and Santha, Peter and Wierup, Nils and Hansen, Anker J.}},
  issn         = {{1460-9568}},
  keywords     = {{primary sensory neuron; CGRP; low-grade inflammation; TRPV1}},
  language     = {{eng}},
  number       = {{1}},
  pages        = {{213--223}},
  publisher    = {{Wiley-Blackwell}},
  series       = {{European Journal of Neuroscience}},
  title        = {{Capsaicin-sensitive sensory fibers in the islets of Langerhans contribute to defective insulin secretion in Zucker diabetic rat, an animal model for some aspects of human type 2 diabetes}},
  url          = {{http://dx.doi.org/10.1111/j.1460-9568.2006.05261.x}},
  doi          = {{10.1111/j.1460-9568.2006.05261.x}},
  volume       = {{25}},
  year         = {{2007}},
}