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Dual effects of noradrenaline on astroglial production of chemokines and pro-inflammatory mediators. [artículo]

Por: Caso, Javier Rubén [Instituto de Investigación i+12] | García Bueno, Borja [Instituto de Investigación i+12] | Hinojosa, Ara E [Instituto de Investigación i+12] | Leza, Juan Carlos [Instituto de Investigación i+12] | Madrigal, José LM [Instituto de Investigación i+12].
Colaborador(es): Instituto de Investigación imas12.
Editor: Journal of neuroinflammation, 2013Descripción: 10:81.Recursos en línea: Acceso libre Resumen: Noradrenaline (NA) is known to limit neuroinflammation. However, the previously described induction by NA of a chemokine involved in the progression of immune/inflammatory processes, such as chemokine (C-C motif) ligand 2 (CCL2)/monocyte chemotactic protein-1 (MCP-1), apparently contradicts NA anti-inflammatory actions. In the current study we analyzed NA regulation of astroglial chemokine (C-X3-C motif) ligand 1 (CX3CL1), also known as fractalkine, another chemokine to which both neuroprotective and neurodegenerative actions have been attributed. In addition, NA effects on other chemokines and pro-inflammatory mediators were also analyzed.
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Formato Vancouver:
Hinojosa AE, Caso JR, García-Bueno B, Leza JC, Madrigal JL. Dual effects of noradrenaline on astroglial production of chemokines and pro-inflammatory mediators. J Neuroinflammation. 2013 Jul 9;10:81.

PMID: 23837880

Contiene 65 referencias

Noradrenaline (NA) is known to limit neuroinflammation. However, the previously described induction by NA of a chemokine involved in the progression of immune/inflammatory processes, such as chemokine (C-C motif) ligand 2 (CCL2)/monocyte chemotactic protein-1 (MCP-1), apparently contradicts NA anti-inflammatory actions. In the current study we analyzed NA regulation of astroglial chemokine (C-X3-C motif) ligand 1 (CX3CL1), also known as fractalkine, another chemokine to which both neuroprotective and neurodegenerative actions have been attributed. In addition, NA effects on other chemokines and pro-inflammatory mediators were also analyzed.

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