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1.
In Vitro Cell Dev Biol Anim ; 48(1): 43-53, 2012 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-22179678

RESUMO

Interleukin-1ß (IL-1ß) induces the expression of matrix metalloproteinases (MMPs) implicated in cartilage and joint degradation in osteoarthritis (OA) and rheumatoid arthritis (RA). Polyoxypregnane glycoside (PPG), active compound was identified from Dregea volubilis extract by chemical analysis, shown to exert chondroprotective effects in cartilage explant models. However, no studies have been undertaken for the molecular investigation of whether PPG constituents protect the human articular chondrocyte (HAC). In the present studies, HAC was co-treated with IL-1ß and PPG. The expression of MMPs, type II collagen, phosphorylation of mitogen-activated protein kinases (MAPKs) and NF-κB signaling pathway were determined by Western immunoblotting. PPG (6.25-25 µM) decreased the IL-1ß-induced HA release from chondrocyte to culture medium. The mode of action of PPG was likely mediated through inhibiting expression of MMP-1, -3 and -13 in the medium, which was associated with the inhibition of mRNA expression. PPG had no effect on IL-1ß-induced phosphorylation of MAPK pathway. Conversely, PPG decreased phosphorylation of IκB kinase and IκBα degradation. Taken together, these results indicate that PPG may inhibit cartilage degradation in OA and may also be used as nutritional supplement for maintaining joint integrity and function.


Assuntos
Condrócitos/metabolismo , Interleucina-1beta/antagonistas & inibidores , Metaloproteinases da Matriz/metabolismo , NF-kappa B/metabolismo , Extratos Vegetais/farmacologia , Animais , Apocynaceae/química , Células Cultivadas , Condrócitos/citologia , Colágeno Tipo II/genética , Colágeno Tipo II/metabolismo , Regulação da Expressão Gênica/efeitos dos fármacos , Glicosídeos/farmacologia , Humanos , Interleucina-1beta/administração & dosagem , Metaloproteinases da Matriz/genética , Quinases de Proteína Quinase Ativadas por Mitógeno/metabolismo , NF-kappa B/genética , Fosforilação/efeitos dos fármacos , Extratos Vegetais/química , Saponinas/farmacologia , Transdução de Sinais/efeitos dos fármacos , Suínos
2.
J Vet Sci ; 9(3): 317-25, 2008 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-18716453

RESUMO

Hip dysplasia (HD) is one of the most important bone and joint diseases in dogs. Making the radiographic diagnosis is sometime possible when the disease has markedly progressed. Chondroitin sulfate (CS) and hyaluronan (HA) are the most important cartilage biomolecules that are elevated in the serum taken from dogs with osteoarthritis. The serum CS and HA can be detected by an ELISA technique, with using monoclonal antibodies against CS epitope 3B3 and WF6 and the HA chain as the primary antibodies. The aim of this study was to compare the levels of serum CS (both epitopes) and HA in non-HD and HD dogs. All 123 dogs were categorized into 2 groups. The non-HD group was composed of 98 healthy dogs, while the HD group was comprised of 25 HD dogs. Blood samples were collected for analyzing the serum CS and HA levels with using the ELISA technique. The results showed that the average serum level of the CS epitope WF6 in the HD group (2,594 +/- 3,036.10 ng/ml) was significantly higher than that in the non-HD group (465 +/- 208.97 ng/ml) (p < 0.01) while the epitope 3B3 in the HD group (105 +/- 100.05 ng/ml) was significantly lower than that in the non-HD group (136 +/- 142.03 ng/ml) (p < 0.05). The amount of serum HA in the HD group (134.74 +/- 59.71 ng/ml) was lower than that in the non HD group (245.45 +/- 97.84 ng/ml) (p < 0.05). The results indicate that the serum CS and HA levels might be used as biomarkers for osteoarthritis in HD dogs.


Assuntos
Biomarcadores/sangue , Sulfatos de Condroitina/sangue , Doenças do Cão/sangue , Displasia Pélvica Canina/sangue , Ácido Hialurônico/sangue , Osteoartrite/veterinária , Animais , Peso Corporal , Cães , Ensaio de Imunoadsorção Enzimática , Feminino , Displasia Pélvica Canina/epidemiologia , Masculino , Osteoartrite/sangue , Prevalência , Caracteres Sexuais
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