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Inhibition of lipopolysaccharide-induced microglia activation by calcitonin gene related peptide and adrenomedullin

Calcitonin gene related peptide (CGRP) and adrenomedullin are potent biologically active peptides that have been proposed to play an important role in vascular and inflammatory diseases. Their function in the central nervous system is still unclear since they have been proposed as either pro-inflamm...

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Autores principales: Consonni, Alessandra, Morara, Stefano, Codazzi, Franca, Grohovaz, Fabio, Zacchetti, Daniele
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Academic Press 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3174421/
https://www.ncbi.nlm.nih.gov/pubmed/21803157
http://dx.doi.org/10.1016/j.mcn.2011.07.006
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author Consonni, Alessandra
Morara, Stefano
Codazzi, Franca
Grohovaz, Fabio
Zacchetti, Daniele
author_facet Consonni, Alessandra
Morara, Stefano
Codazzi, Franca
Grohovaz, Fabio
Zacchetti, Daniele
author_sort Consonni, Alessandra
collection PubMed
description Calcitonin gene related peptide (CGRP) and adrenomedullin are potent biologically active peptides that have been proposed to play an important role in vascular and inflammatory diseases. Their function in the central nervous system is still unclear since they have been proposed as either pro-inflammatory or neuroprotective factors. We investigated the effects of the two peptides on astrocytes and microglia, cells of the central nervous system that exert a strong modulatory activity in the neuroinflammatory processes. In particular, we studied the ability of CGRP and adrenomedullin to modulate microglia activation, i.e. its competence of producing and releasing pro-inflammatory cytokines/chemokines that are known to play a crucial role in neuroinflammation. In this work we show that the two neuropeptides exert a potent inhibitory effect on lipopolysaccharide-induced microglia activation in vitro, with strong inhibition of the release of pro-inflammatory mediators (such as NO, cytokines and chemokines). Both CGRP and adrenomedullin are known to promote cAMP elevation, this second messenger cannot fully account for the observed inhibitory effects, thereby suggesting that other signaling pathways are involved. Interestingly, the inhibitory effect of CGRP and adrenomedullin appears to be stimulus specific, since direct activation with pro-inflammatory cytokines was not affected. Our findings clarify aspects of microglia activation, and contribute to the comprehension of the switch from reparative to detrimental function that occurs when glia is exposed to different conditions. Moreover, they draw the attention to potential targets for novel pharmacological intervention in pathologies characterized by glia activation and neuroinflammation.
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spelling pubmed-31744212011-10-01 Inhibition of lipopolysaccharide-induced microglia activation by calcitonin gene related peptide and adrenomedullin Consonni, Alessandra Morara, Stefano Codazzi, Franca Grohovaz, Fabio Zacchetti, Daniele Mol Cell Neurosci Article Calcitonin gene related peptide (CGRP) and adrenomedullin are potent biologically active peptides that have been proposed to play an important role in vascular and inflammatory diseases. Their function in the central nervous system is still unclear since they have been proposed as either pro-inflammatory or neuroprotective factors. We investigated the effects of the two peptides on astrocytes and microglia, cells of the central nervous system that exert a strong modulatory activity in the neuroinflammatory processes. In particular, we studied the ability of CGRP and adrenomedullin to modulate microglia activation, i.e. its competence of producing and releasing pro-inflammatory cytokines/chemokines that are known to play a crucial role in neuroinflammation. In this work we show that the two neuropeptides exert a potent inhibitory effect on lipopolysaccharide-induced microglia activation in vitro, with strong inhibition of the release of pro-inflammatory mediators (such as NO, cytokines and chemokines). Both CGRP and adrenomedullin are known to promote cAMP elevation, this second messenger cannot fully account for the observed inhibitory effects, thereby suggesting that other signaling pathways are involved. Interestingly, the inhibitory effect of CGRP and adrenomedullin appears to be stimulus specific, since direct activation with pro-inflammatory cytokines was not affected. Our findings clarify aspects of microglia activation, and contribute to the comprehension of the switch from reparative to detrimental function that occurs when glia is exposed to different conditions. Moreover, they draw the attention to potential targets for novel pharmacological intervention in pathologies characterized by glia activation and neuroinflammation. Academic Press 2011-10 /pmc/articles/PMC3174421/ /pubmed/21803157 http://dx.doi.org/10.1016/j.mcn.2011.07.006 Text en © 2011 Elsevier Inc. https://creativecommons.org/licenses/by-nc-nd/3.0/ Open Access under CC BY-NC-ND 3.0 (https://creativecommons.org/licenses/by-nc-nd/3.0/) license
spellingShingle Article
Consonni, Alessandra
Morara, Stefano
Codazzi, Franca
Grohovaz, Fabio
Zacchetti, Daniele
Inhibition of lipopolysaccharide-induced microglia activation by calcitonin gene related peptide and adrenomedullin
title Inhibition of lipopolysaccharide-induced microglia activation by calcitonin gene related peptide and adrenomedullin
title_full Inhibition of lipopolysaccharide-induced microglia activation by calcitonin gene related peptide and adrenomedullin
title_fullStr Inhibition of lipopolysaccharide-induced microglia activation by calcitonin gene related peptide and adrenomedullin
title_full_unstemmed Inhibition of lipopolysaccharide-induced microglia activation by calcitonin gene related peptide and adrenomedullin
title_short Inhibition of lipopolysaccharide-induced microglia activation by calcitonin gene related peptide and adrenomedullin
title_sort inhibition of lipopolysaccharide-induced microglia activation by calcitonin gene related peptide and adrenomedullin
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3174421/
https://www.ncbi.nlm.nih.gov/pubmed/21803157
http://dx.doi.org/10.1016/j.mcn.2011.07.006
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