The neuropeptide calcitonin gene-related peptide (CGRP) prevents inflammatory liver injury in mice

被引:49
|
作者
Kroeger, Irena [1 ,2 ]
Erhardt, Annette [1 ]
Abt, Dominik [2 ]
Fischer, Michael [3 ]
Biburger, Markus [4 ]
Rau, Thomas [5 ]
Neuhuber, Winfried L. [6 ]
Tiegs, Gisa [1 ]
机构
[1] Univ Med Ctr Hamburg Eppendorf, Ctr Internal Med, Div Expt Immunol & Hepatol, D-20246 Hamburg, Germany
[2] Univ Erlangen Nurnberg, Inst Expt & Clin Pharmacol & Toxicol, Erlangen, Germany
[3] Univ Erlangen Nurnberg, Inst Physiol & Expt Pathophysiol, Erlangen, Germany
[4] Univ Hosp Erlangen Nuremberg, Dept Med 3, Nikolaus Fiebiger Ctr Mol Med, Lab Expt Immunol & Immunotherapy, Erlangen, Germany
[5] Univ Med Ctr Hamburg Eppendorf, Inst Expt & Clin Pharmacol & Toxicol, D-20246 Hamburg, Germany
[6] Univ Erlangen Nurnberg, Inst Anat 1, Erlangen, Germany
关键词
Calcitonin gene-related peptide; Inducible cAMP early repressor; Interleukin-10; Liver inflammation; TNF alpha; TUMOR-NECROSIS-FACTOR; NITRIC-OXIDE; TNF-ALPHA; SIGNAL-TRANSDUCTION; LETHAL ENDOTOXEMIA; ADENYLATE-CYCLASE; KUPFFER CELLS; PROTECT MICE; SUBSTANCE-P; RAT MODEL;
D O I
10.1016/j.jhep.2009.03.022
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background/Aims: Calcitonin gene-related peptide (CGRP) is a potent vasodilator and supposed to be responsible for neurogenic inflammation involved in migraine. Its role in inflammatory diseases of other organs is controversial and poorly investigated regarding liver inflammation, although the organ is innervated by CGRP containing primary sensory nerve fibers. Methods:Male Balb/c and IL-10(-/-) mice were pretreated with either alpha CGRP or the CGRP receptor antagonists CGRP(8-37) or BIBN4096BS. Immune-mediated liver injury was induced by administration of lipopolysaccharide (LPS) or tumor necrosis factor-alpha (TNF alpha) to galactosamine (GalN)-sensitized mice and evaluated by serum transaminase activities and cytokine levels. Furthermore, intrahepatic CGRP receptor expression and hepatic CGRP concentrations were examined. Results: CGRP receptor I was expressed by immune cells and hepatocytes in human and murine liver. During liver injury CGRP receptor expression was increased whereas hepatic CGRP concentrations concomitantly decreased. While CGRP receptor antagonists failed to affect liver damage, pretreatment with alpha CGRP protected mice from GalN/LPS-induced liver injury by suppression of the pro-inflammatory cytokine response independently from IL-10 but related to the induction of the transcriptional repressor inducible cAMP early repressor (ICER). In contrast, aCGRP failed to protect against GalN/TNF alpha-induced liver failure. Conclusion: In the liver, CGRP exerts anti-inflammatory properties, which are characterized by a reduced production of pro-inflammatory cytokines. (C) 2009 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:342 / 353
页数:12
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