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1.
Biol. Res ; 47: 1-8, 2014. graf
Artigo em Inglês | LILACS | ID: biblio-950737

RESUMO

BACKGROUND: The root of Angelica sinensis (AS), also known as "Dang-gui," was a popular herbal medicine widely used in the treatment of gynecological diseases in China, Korea, and Japan for a long time. This study aimed to determine the effects of ethyl acetate fraction from Angelica sinensis (EAAS) on the interleukin-1ß (IL-1ß)-induced proliferation of rheumatoid arthritis synovial fibroblasts (RASFs), and production of matrix metalloproteinases (MMPs), cyclooxygenase (COX) 2, and prostaglandin E2 (PGE2), involved in articular bone and cartilage destruction, by RASFs. RESULTS: RASF proliferation was evaluated with cholecystokinin octapeptide (CCK-8) reagent in the presence of IL-1ß with/without EAAS. Expression of MMPs, tissue inhibitor of metalloproteinases-1 (TIMP-1), COXs, PGE2, and intracellular mitogen-activated protein kinase (MAPK) signaling molecules, including p-ERK, p-p38, p-JNK, and NF-κB, were examined using immunoblotting or semi-quantitative reverse transcription-polymerase chain reaction and enzyme-linked immunosorbent assay. EAAS inhibited IL-1ß-induced RASF proliferation; MMP-1, MMP-3, and COX-2 mRNA and protein expressions; and PGE2 production. EAAS also inhibits the phosphorylation of ERK-1/2, p38, and JNK, and activation of NF-κB by IL-1ß. CONCLUSION: EAAS might be a new therapeutic modality for rheumatoid arthritis management.


Assuntos
Humanos , Artrite Reumatoide/metabolismo , Bolsa Sinovial/citologia , Mediadores da Inflamação/metabolismo , Angelica sinensis/química , Proliferação de Células/efeitos dos fármacos , Fibroblastos/efeitos dos fármacos , Artrite Reumatoide/patologia , Proteínas Recombinantes/farmacologia , Ensaio de Imunoadsorção Enzimática , Extratos Vegetais/farmacologia , Dinoprostona/metabolismo , Immunoblotting , NF-kappa B/efeitos dos fármacos , Raízes de Plantas/química , Metaloproteinases da Matriz/efeitos dos fármacos , Metaloproteinases da Matriz/metabolismo , Medicina Herbária , Ciclo-Oxigenase 2/efeitos dos fármacos , Ciclo-Oxigenase 2/metabolismo , Interleucina-1beta/farmacologia , Cultura Primária de Células , Reação em Cadeia da Polimerase em Tempo Real , Fibroblastos/citologia , Fibroblastos/metabolismo , Citometria de Fluxo , Articulação do Joelho/citologia , Acetatos
2.
Biol. Res ; 43(2): 225-231, 2010. ilus
Artigo em Inglês | LILACS | ID: lil-567537

RESUMO

Objectives: The objective of this study is to determine the effects of Ethyl acetate fraction from Cudrania tricuspidata (EACT) on the interleukin-1b (IL-1b)-induced proliferation of rheumatoid synovial fbroblasts (RASFs) and production of matrix metalloproteinases (MMPs), cyclooxygenase (COX) and prostaglandin E2 (PGE2) by RASFs. Materials and Methods: The proliferation of RASFs was evaluated with CCK-8 reagent in the presence of IL-1b with/without EACT. The expression of MMPs, TIMP-1, COXs, PGE2 and intracellular MAPK signalings, including p-ERK, p-p38, p-JNK and NF-kB were examined by immunoblotting or semi-quantitative reverse transcription-polymerase chain reaction (RT-PCR) and ELISA in conditions as described above. Results: EACT inhibits IL-1β-induced proliferation of RASFs and MMP-1, 3, COX-2 mRNA and protein expression, PGE2 production induced with IL-1b. EACT also inhibits the phosphorylation of ERK-1/2, p38, JNK and activation of NF-kB by IL-1b. Conclusions: These results suggest that EACT might be involved in synovial fbroblast proliferation and MMPs, COX-2, and PGE2 production, which are involved in joint destruction in rheumatoid arthritis (RA), indicating that this might be a new therapeutic modality for management of rheumatoid arthritis.


Assuntos
Humanos , Acetatos/farmacologia , Artrite Reumatoide/patologia , Fibroblastos/efeitos dos fármacos , Interleucina-1beta/antagonistas & inibidores , Moraceae/química , Proliferação de Células/efeitos dos fármacos , /biossíntese , Dinoprostona/biossíntese , Ensaio de Imunoadsorção Enzimática , Fibroblastos/patologia , Interleucina-1beta/farmacologia , Metaloproteinases da Matriz/biossíntese , Reação em Cadeia da Polimerase
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