Autor: |
Pilaiwanwadee Hutamekalin, Kohei Takeda, Mitsuhiro Tani, Yuko Tsuga, Naoki Ogawa, Nobuaki Mizutani, Shin Yoshino |
Jazyk: |
angličtina |
Rok vydání: |
2010 |
Předmět: |
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Zdroj: |
Journal of Pharmacological Sciences, Vol 112, Iss 1, Pp 56-63 (2010) |
Druh dokumentu: |
article |
ISSN: |
1347-8613 |
DOI: |
10.1254/jphs.09180FP |
Popis: |
It was investigated whether the C3a-receptor antagonist (C3aRA) SB 290157 was involved in the suppression of anti-OVA pAb–induced arthritis because it is well known that anaphylatoxin C3a plays a crucial role in the development of an effective inflammatory response during complement activation. Anti-OVA pAb–induced arthritis was induced in DBA/1J mice by administration of anti-OVA pAb 0.5 h prior to intra-articular (i.a.) injection of OVA (0 h). Two peaks of joint swelling were observed at 0.5 and 3 h. The role of C3aRA in arthritis was investigated by injection of SB 290157 at concentrations of 10 and 30 mg/kg at 0 and 2 h. The antagonist was able to reduce joint swelling only at 3 h, and about 50% inhibition of joint swelling was observed with the concentration of 30 mg/kg. The C3 level was significantly decreased at 3 h compared with naïve mice showing complement consumption. Furthermore, the C3 activation was observed and increased corresponding to the graded concentration of anti-OVA pAb. The results also revealed that the C3aRA was able to reduce the expression of IL-1β in synovial tissue. Taken together, the results suggested that C3aRA may be effective in the inhibition of arthritis. Keywords:: rheumatoid arthritis, OVA, anti-OVA antibody–induced arthritis, C3a-receptor antagonist, inflammation |
Databáze: |
Directory of Open Access Journals |
Externí odkaz: |
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