The effect of dehydroepiandrosterone on inflammatory response of astroglial cells
- Authors: Buyanova S.M.1,2, Chistyakov D.V.2, Astakhova A.A.2, Sergeeva M.G.2
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Affiliations:
- Faculty of Bioengineering and Bioinformatics
- Belozersky Institute of Physico-Chemical Biology
- Issue: Vol 11, No 4 (2017)
- Pages: 304-310
- Section: Articles
- URL: https://journals.rcsi.science/1990-7478/article/view/213274
- DOI: https://doi.org/10.1134/S199074781704002X
- ID: 213274
Cite item
Abstract
An increased interest in neuroinflammation is conditioned by its involvement in various pathological processes in the brain. Astrocytes play an important role in neuroinflammation, participating in its regulation, throwing out a large number of signaling molecules. Steroid compounds, actively produced by astrocytes, are of interest with regards to the regulation of inflammatory processes in the central nervous system. In the present work the effect of dehydroepiandrosterone (DHEA) on astroglial cells (cultured primary rat astrocytes) in a model of inflammation was studied. The inflammatory response was stimulated with lipopolysaccharide (LPS). Expression levels of pro-inflammatory factor TNFα, antinflammatory interleukin IL-10, and both pro- and antiinflammatory protein COX-2 were measured. The expression of IL-10, COX-2, and TNFα mRNA was determined by real-time PCR, COX-2 protein level by immunoblotting method, TNFα and IL-10 release by enzyme immunoassay. The effect of short-term (30 min) and long-term (24 h) exposure to DHEA was evaluated. It was shown that DHEA potentiates LPS-stimulated (1) increase in the IL-10 mRNA level; (2) IL-10 release; (3) does not affect TNFα level, and (4) exerts a weak pulsating bidirectional effect on COX-2. Using trilostane, an inhibitor of 3β-hydroxysteroid dehydrogenase, a key enzyme of DHEA metabolism, it was shown that DHEA metabolites make the main contribution to its effect. Thus, DHEA is of interest as a stimulant of anti-inflammatory processes in the brain.
About the authors
S. M. Buyanova
Faculty of Bioengineering and Bioinformatics; Belozersky Institute of Physico-Chemical Biology
Author for correspondence.
Email: sofia.buyanova@gmail.com
Russian Federation, Moscow, 119234; Moscow, 119992
D. V. Chistyakov
Belozersky Institute of Physico-Chemical Biology
Email: sofia.buyanova@gmail.com
Russian Federation, Moscow, 119992
A. A. Astakhova
Belozersky Institute of Physico-Chemical Biology
Email: sofia.buyanova@gmail.com
Russian Federation, Moscow, 119992
M. G. Sergeeva
Belozersky Institute of Physico-Chemical Biology
Email: sofia.buyanova@gmail.com
Russian Federation, Moscow, 119992