Dual effects of noradrenaline on astroglial production of chemokines and pro-inflammatory mediators

• Published in: Journal of neuroinflammation Vol. 10; no. 1; p. 81
• Main Authors: Hinojosa, Ara E, Caso, Javier R, García-Bueno, Borja, Leza, Juan C, Madrigal, José L M
• Format: Journal Article
• Language: English
• Published: England BioMed Central Ltd 09.07.2013; BioMed Central
• Subjects: Animals; Astrocytes; Astrocytes - drug effects; Astrocytes - metabolism; Brain research; Chemokines; Chemokines - biosynthesis; Hypotheses; Inflammation; Inflammation Mediators - metabolism; Inflammation Mediators - physiology; Ligands; Neurodegeneration; Nitric oxide; Noradrenaline; Norepinephrine - pharmacology; Norepinephrine - physiology; Physiological aspects; Polymerase chain reaction; Primary Cell Culture; Proteins; Random Allocation; Rats; Rats, Wistar; Rodents; Studies; Spain
• ISSN: 1742-2094; 1742-2094
• DOI: 10.1186/1742-2094-10-81

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. Primary astrocyte-enriched cultures were obtained from neonatal Wistar rats. These cells were incubated for different time durations with combinations of NA and lipopolysaccharide (LPS). The expression and synthesis of different proteins was measured by RT-PCR and enzyme-linked immunosorbent assay (ELISA) or enzyme immunoassays. Data were analyzed by one-way analysis of variance (ANOVA), followed by Newman-Keuls multiple comparison tests. The data presented here show that in control conditions, NA induces the production of CX3CL1 in rat cultured astrocytes, but in the presence of an inflammatory stimulus, such as LPS, NA has the opposite effect inhibiting CX3CL1 production. This inversion of NA effect was also observed for MCP-1. Based on the observation of this dual action, NA regulation of different chemokines and pro-inflammatory cytokines was also analyzed, observing that in most cases NA exerts an inhibitory effect in the presence of LPS. One characteristic exception was the induction of cyclooxygenase-2 (COX-2), where a summative effect was detected for both LPS and NA. These data suggest that NA effects on astrocytes can adapt to the presence of an inflammatory agent reducing the production of certain cytokines, while in basal conditions NA may have the opposite effect and help to maintain moderate levels of these cytokines.