The vagus nerve and nicotinic receptors modulate experimental pancreatitis severity in mice

The nervous system, through the vagus nerve, controls inflammation by decreasing the release of tumor necrosis factor-alpha from endotoxin stimulated macrophages. This anti-inflammatory effect is mediated by an interaction of acetylcholine, the principal neurotransmitter of the vagus nerve, with mac...

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Vydané v:Gastroenterology (New York, N.Y. 1943) Ročník 130; číslo 6; s. 1822
Hlavní autori: van Westerloo, David J, Giebelen, Ilona A, Florquin, Sandrine, Bruno, Marco J, Larosa, Gregory J, Ulloa, Luis, Tracey, Kevin J, van der Poll, T
Médium: Journal Article
Jazyk:English
Vydavateľské údaje: United States 01.05.2006
Predmet:
Animals
Biopsy, Needle
Ceruletide
Disease Models, Animal
Female
Immunohistochemistry
Mice
Mice, Inbred C57BL
Nicotinic Antagonists - pharmacology
Pancreatitis - drug therapy
Pancreatitis - pathology
Pancreatitis - physiopathology
Probability
Receptors, Nicotinic - metabolism
Risk Factors
Sensitivity and Specificity
Severity of Illness Index
Vagotomy
Vagus Nerve - physiology
ISSN:0016-5085
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Popis
Shrnutí:The nervous system, through the vagus nerve, controls inflammation by decreasing the release of tumor necrosis factor-alpha from endotoxin stimulated macrophages. This anti-inflammatory effect is mediated by an interaction of acetylcholine, the principal neurotransmitter of the vagus nerve, with macrophage cholinergic nicotinic receptors expressing the alpha7 subunit. To determine the role of this "nicotinic anti-inflammatory pathway" in experimental pancreatitis, we induced pancreatitis in mice by 12 hourly intraperitoneal injections of cerulein. Pancreatitis was preceded by unilateral left cervical vagotomy or pretreatment with the nicotinic receptor antagonist mecamylamine or by pretreatment with the selective alpha7 nicotinic receptor agonist 3-(2,4-dimethoxybenzylidene) anabaseine (GTS-21). Vagotomy or pretreatment with mecamylamine resulted in an enhanced severity of pancreatitis, as reflected by histology, edema, plasma hydrolases, and interleukin-6 levels. Furthermore, the number of neutrophils migrated to the pancreas was increased in these mice, as shown by myeloperoxidase content and intrapancreatic staining of neutrophils. Conversely, GTS-21 pretreatment strongly decreased the severity of pancreatitis. Pancreatitis-associated pulmonary inflammation was independent of the integrity of the vagus nerve and nicotinic receptors. This study provides the first evidence for a therapeutic potential of the vagus nerve and the "nicotinic anti-inflammatory pathway" in attenuating inflammation and injury during experimental pancreatitis.
Bibliografia:ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-Feature-1
content type line 23
ISSN:0016-5085
DOI:10.1053/j.gastro.2006.02.022