Back to Search
Start Over
Decrease of CD68 Synovial Macrophages in Celastrol Treated Arthritic Rats
- Source :
- PLoS ONE, PLoS ONE, Vol 10, Iss 12, p e0142448 (2015), Repositório Científico de Acesso Aberto de Portugal, Repositório Científico de Acesso Aberto de Portugal (RCAAP), instacron:RCAAP
- Publication Year :
- 2015
- Publisher :
- Public Library of Science, 2015.
-
Abstract
- Copyright: © 2015 Cascão et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited<br />Background: Rheumatoid arthritis (RA) is a chronic immune-mediated inflammatory disease characterized by cellular infiltration into the joints, hyperproliferation of synovial cells and bone damage. Available treatments for RA only induce remission in around 30% of the patients, have important adverse effects and its use is limited by their high cost. Therefore, compounds that can control arthritis, with an acceptable safety profile and low production costs are still an unmet need. We have shown, in vitro, that celastrol inhibits both IL-1β and TNF, which play an important role in RA, and, in vivo, that celastrol has significant anti-inflammatory properties. Our main goal in this work was to test the effect of celastrol in the number of sublining CD68 macrophages (a biomarker of therapeutic response for novel RA treatments) and on the overall synovial tissue cellularity and joint structure in the adjuvant-induced rat model of arthritis (AIA). Methods: Celastrol was administered to AIA rats both in the early (4 days after disease induction) and late (11 days after disease induction) phases of arthritis development. The inflammatory score, ankle perimeter and body weight were evaluated during treatment period. Rats were sacrificed after 22 days of disease progression and blood, internal organs and paw samples were collected for toxicological blood parameters and serum proinflammatory cytokine quantification, as well as histopathological and immunohistochemical evaluation, respectively. Results: Here we report that celastrol significantly decreases the number of sublining CD68 macrophages and the overall synovial inflammatory cellularity, and halted joint destruction without side effects. Conclusions: Our results validate celastrol as a promising compound for the treatment of arthritis.<br />RC was supported with a fellowship from Fundação para a Ciência e a Tecnologia (FCT, SFRH/BPD/92860/2013).
- Subjects :
- Pathology
Interleukin-1beta
Anti-Inflammatory Agents
Arthritis
lcsh:Medicine
Gene Expression
Cell Count
Inflammatory diseases
Arthritis, Rheumatoid
chemistry.chemical_compound
lcsh:Science
Multidisciplinary
Synovial Membrane
3. Good health
Cellular infiltration
Treatment Outcome
Celastrol
Rheumatoid arthritis
Cytokines
Tumor necrosis factor alpha
Female
medicine.symptom
Pentacyclic Triterpenes
Injections, Intraperitoneal
Research Article
medicine.medical_specialty
Antigens, Differentiation, Myelomonocytic
Inflammation
Proinflammatory cytokine
Adjuvants, Immunologic
Antigens, CD
medicine
Animals
Humans
Rats, Wistar
business.industry
Tumor Necrosis Factor-alpha
Macrophages
lcsh:R
Ankles
Hematoxylin staining
medicine.disease
Arthritis, Experimental
Triterpenes
Rats
Synovial Cell
chemistry
lcsh:Q
business
Subjects
Details
- Language :
- English
- ISSN :
- 19326203
- Volume :
- 10
- Issue :
- 12
- Database :
- OpenAIRE
- Journal :
- PLoS ONE
- Accession number :
- edsair.doi.dedup.....5be31a4f354a5dc848a33fe6195c2db0