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Vasoactive intestinal peptide attenuates liver ischemia/reperfusion injury in mice via the cyclic adenosine monophosphate-protein kinase a pathway.
- Source :
-
Liver transplantation : official publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society [Liver Transpl] 2013 Sep; Vol. 19 (9), pp. 945-56. Date of Electronic Publication: 2013 Jul 26. - Publication Year :
- 2013
-
Abstract
- Hepatic ischemia/reperfusion injury (IRI), an exogenous, antigen-independent, local inflammation response, occurs in multiple clinical settings, including liver transplantation, hepatic resection, trauma, and shock. The nervous system maintains extensive crosstalk with the immune system through neuropeptide and peptide hormone networks. This study examined the function and therapeutic potential of the vasoactive intestinal peptide (VIP) neuropeptide in a murine model of liver warm ischemia (90 minutes) followed by reperfusion. Liver ischemia/reperfusion (IR) triggered an induction of gene expression of intrinsic VIP; this peaked at 24 hours of reperfusion and coincided with a hepatic self-healing phase. Treatment with the VIP neuropeptide protected livers from IRI; this was evidenced by diminished serum alanine aminotransferase levels and well-preserved tissue architecture and was associated with elevated intracellular cyclic adenosine monophosphate (cAMP)-protein kinase A (PKA) signaling. The hepatocellular protection rendered by VIP was accompanied by diminished neutrophil/macrophage infiltration and activation, reduced hepatocyte necrosis/apoptosis, and increased hepatic interleukin-10 (IL-10) expression. Strikingly, PKA inhibition restored liver damage in otherwise IR-resistant VIP-treated mice. In vitro, VIP not only diminished macrophage tumor necrosis factor α/IL-6/IL-12 expression in a PKA-dependent manner but also prevented necrosis/apoptosis in primary mouse hepatocyte cultures. In conclusion, our findings document the importance of VIP neuropeptide-mediated cAMP-PKA signaling in hepatic homeostasis and cytoprotection in vivo. Because the enhancement of neural modulation differentially regulates local inflammation and prevents hepatocyte death, these results provide the rationale for novel approaches to managing liver IRI in transplant patients.<br /> (© 2013 American Association for the Study of Liver Diseases.)
- Subjects :
- Animals
Apoptosis
Caspase 3 metabolism
Flow Cytometry methods
Hepatocytes cytology
Hepatocytes metabolism
Homeostasis
Immune System
Inflammation
Interleukin-10 metabolism
L-Lactate Dehydrogenase metabolism
Liver metabolism
Macrophages cytology
Macrophages metabolism
Male
Mice
Mice, Inbred C57BL
Necrosis
Neutrophils cytology
Peroxidase metabolism
Time Factors
Cyclic AMP metabolism
Cyclic AMP-Dependent Protein Kinases metabolism
Liver pathology
Reperfusion Injury pathology
Vasoactive Intestinal Peptide chemistry
Subjects
Details
- Language :
- English
- ISSN :
- 1527-6473
- Volume :
- 19
- Issue :
- 9
- Database :
- MEDLINE
- Journal :
- Liver transplantation : official publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society
- Publication Type :
- Academic Journal
- Accession number :
- 23744729
- Full Text :
- https://doi.org/10.1002/lt.23681