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Rat salivary gland ligation causes reversible secretory hypofunction

AIM: To determine the influence of inflammation on salivary secretion. Secretion by salivary glands involves interactions between nerves, blood vessels and salivary cells. The present study investigated the effects of inflammation on rat submandibular gland function following acute ductal obstructio...

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Detalles Bibliográficos
Autores principales: Carpenter, G H, Osailan, S M, Correia, P, Paterson, K P, Proctor, G B
Formato: Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1859985/
https://www.ncbi.nlm.nih.gov/pubmed/17305704
http://dx.doi.org/10.1111/j.1365-201X.2006.01662.x
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author Carpenter, G H
Osailan, S M
Correia, P
Paterson, K P
Proctor, G B
author_facet Carpenter, G H
Osailan, S M
Correia, P
Paterson, K P
Proctor, G B
author_sort Carpenter, G H
collection PubMed
description AIM: To determine the influence of inflammation on salivary secretion. Secretion by salivary glands involves interactions between nerves, blood vessels and salivary cells. The present study investigated the effects of inflammation on rat submandibular gland function following acute ductal obstruction. METHODS: Under recovery anaesthesia a metal clip was placed on the main duct of the submandibular gland. After 24 h salivary secretion was evoked by nerve and methacholine stimulation. For recovery experiments the clip was removed after 24 h and the animal left to recover for 3 days when salivary function was again assessed. RESULTS: By 24 h of obstruction an inflammatory infiltrate had developed within the obstructed gland and stimulated salivary flows were just 20% of the normal secretion, whilst protein secretion and ion reabsorption were also severely impaired. If ductal obstruction was removed after 24 h the salivary function returned to normal after 3 days of recovery. In vitro analysis of cells from 24-h ligated glands revealed normal changes in intracellular calcium (the main secondary messenger involved in fluid secretion) in response to methacholine stimulation. Protein secretion from isolated cells indicated some changes in particular to methacholine-induced protein secretion although a significant protein secretion was still seen in response to isoprenaline – the main stimulus for protein secretion. CONCLUSION: This report demonstrates reversible salivary inhibition associated with an inflammatory infiltrate within the salivary gland.
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spelling pubmed-18599852007-05-03 Rat salivary gland ligation causes reversible secretory hypofunction Carpenter, G H Osailan, S M Correia, P Paterson, K P Proctor, G B Acta Physiol (Oxf) Gastro-Intestinal AIM: To determine the influence of inflammation on salivary secretion. Secretion by salivary glands involves interactions between nerves, blood vessels and salivary cells. The present study investigated the effects of inflammation on rat submandibular gland function following acute ductal obstruction. METHODS: Under recovery anaesthesia a metal clip was placed on the main duct of the submandibular gland. After 24 h salivary secretion was evoked by nerve and methacholine stimulation. For recovery experiments the clip was removed after 24 h and the animal left to recover for 3 days when salivary function was again assessed. RESULTS: By 24 h of obstruction an inflammatory infiltrate had developed within the obstructed gland and stimulated salivary flows were just 20% of the normal secretion, whilst protein secretion and ion reabsorption were also severely impaired. If ductal obstruction was removed after 24 h the salivary function returned to normal after 3 days of recovery. In vitro analysis of cells from 24-h ligated glands revealed normal changes in intracellular calcium (the main secondary messenger involved in fluid secretion) in response to methacholine stimulation. Protein secretion from isolated cells indicated some changes in particular to methacholine-induced protein secretion although a significant protein secretion was still seen in response to isoprenaline – the main stimulus for protein secretion. CONCLUSION: This report demonstrates reversible salivary inhibition associated with an inflammatory infiltrate within the salivary gland. Blackwell Publishing Ltd 2007-03-01 /pmc/articles/PMC1859985/ /pubmed/17305704 http://dx.doi.org/10.1111/j.1365-201X.2006.01662.x Text en © 2007 The Authors Journal compilation © 2007 Scandinavian Physiological Society https://creativecommons.org/licenses/by/2.5/ Reuse of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation
spellingShingle Gastro-Intestinal
Carpenter, G H
Osailan, S M
Correia, P
Paterson, K P
Proctor, G B
Rat salivary gland ligation causes reversible secretory hypofunction
title Rat salivary gland ligation causes reversible secretory hypofunction
title_full Rat salivary gland ligation causes reversible secretory hypofunction
title_fullStr Rat salivary gland ligation causes reversible secretory hypofunction
title_full_unstemmed Rat salivary gland ligation causes reversible secretory hypofunction
title_short Rat salivary gland ligation causes reversible secretory hypofunction
title_sort rat salivary gland ligation causes reversible secretory hypofunction
topic Gastro-Intestinal
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1859985/
https://www.ncbi.nlm.nih.gov/pubmed/17305704
http://dx.doi.org/10.1111/j.1365-201X.2006.01662.x
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