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1.
Biol. Res ; 47: 1-8, 2014. graf
Artículo en Inglés | LILACS | ID: biblio-950737

RESUMEN

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.


Asunto(s)
Humanos , Artritis Reumatoide/metabolismo , Bolsa Sinovial/citología , Mediadores de Inflamación/metabolismo , Angelica sinensis/química , Proliferación Celular/efectos de los fármacos , Fibroblastos/efectos de los fármacos , Artritis Reumatoide/patología , Proteínas Recombinantes/farmacología , Ensayo de Inmunoadsorción Enzimática , Extractos Vegetales/farmacología , Dinoprostona/metabolismo , Immunoblotting , FN-kappa B/efectos de los fármacos , Raíces de Plantas/química , Metaloproteinasas de la Matriz/efectos de los fármacos , Metaloproteinasas de la Matriz/metabolismo , Medicina de Hierbas , Ciclooxigenasa 2/efectos de los fármacos , Ciclooxigenasa 2/metabolismo , Interleucina-1beta/farmacología , Cultivo Primario de Células , Reacción en Cadena en Tiempo Real de la Polimerasa , Fibroblastos/citología , Fibroblastos/metabolismo , Citometría de Flujo , Articulación de la Rodilla/citología , Acetatos
2.
Biol. Res ; 43(2): 225-231, 2010. ilus
Artículo en Inglés | LILACS | ID: lil-567537

RESUMEN

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.


Asunto(s)
Humanos , Acetatos/farmacología , Artritis Reumatoide/patología , Fibroblastos/efectos de los fármacos , Interleucina-1beta/antagonistas & inhibidores , Moraceae/química , Proliferación Celular/efectos de los fármacos , /biosíntesis , Dinoprostona/biosíntesis , Ensayo de Inmunoadsorción Enzimática , Fibroblastos/patología , Interleucina-1beta/farmacología , Metaloproteinasas de la Matriz/biosíntesis , Reacción en Cadena de la Polimerasa
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