OBJETIVO: Analisar as características de tendões de Aquiles de ratos após indução de processo inflamatório localizado na pata. MÉTODOS: Foram utilizados três grupos experimentais: grupo inflamado com carragenina na pata de rato (G1); grupo salina (G2) e grupo controle (G3). Após 4 horas os animais foram eutanaziados e o tendão de Aquiles foi removido. RESULTADOS:Não foram observadas diferenças significativas nas análises de proteínas não colagênicas, glicosaminoglicanos e hidroxiprolina, mas uma tendência a diminuição foi verificada em G1. Em organização de moléculas de colágeno não foram observadas diferenças entre os grupos. Com respeito à atividade de MMPs, foi observada uma presença maior da isoforma ativa da MMP-2 em G1, sugerindo que a remodelação do tecido está ocorrendo. CONCLUSÃO: Desta forma, nós concluímos que o processo inflamatório desencadeado em pata de rato pode afetar o remodelamento de tendões situados próximo ao local inflamado. Nível de Evidência I, Estudos Prognósticos - Investigação do Efeito de Característica de um Paciente Sobre o Desfecho da Doença.

OBJECTIVE: To analyze the characteristics of the Achilles tendon of rats after induction of localized inflammation in the rat paw. METHODS: In our study three groups were used: inflamed group with carrageenan in rat paw (G1); saline group (G2) and control group (G3). After 4 hours the animals were euthanized and the Achilles tendon removed. RESULTS: No significant differences were observed in the analysis of non-collagenous proteins, glycosaminoglycans and hydroxyproline in the groups but a tendency of reduction was verified in G1. About the organization of collagen molecules, no differences were observed between groups. With respect to MMPs activity, a stronger presence of the active isoform of MMP-2 in G1 was observed, suggesting that the remodeling was occurring. CONCLUSION: Thus, we conclude that the inflammatory process in rat paw may affect the remodeling of tendons located near the inflamed site. Level of Evidence I, Prognostic Studies - Investigating the Effect of a Patient Characteristic on the Outcome of Disease.

The composition and organization of the extracellular matrix of ostrich articular cartilage was investigated, using samples from the proximal and distal surfaces of the tarsometatarsus. For morphological analysis, sections were stained with toluidine blue and analyzed by polarized light microscopy. For biochemical analysis, extracellular matrix components were extracted with 4 M guanidinium chloride, fractionated on DEAE-Sephacel and analyzed by SDS-PAGE. Glycosaminoglycans were analyzed by electrophoresis in agarose gels. Structural analysis showed that the fibrils were arranged in different directions, especially on the distal surface. The protein and glycosaminoglycan contents of this region were higher than in the other regions. SDS-PAGE showed the presence of proteins with molecular masses ranging from 17 to 121 kDa and polydisperse components of 67, 80-100, and 250-300 kDa in all regions. The analysis of glycosaminoglycans in agarosepropylene diamine gels revealed the presence of only chondroitin-sulfate. The electrophoretic band corresponding to putative decorin was a small proteoglycan containing chondroitin-sufate and not dermatan-sulfate, unlike other cartilages. The higher amounts of proteins and glycosaminoglycans and the multidirectional arrangement of fibrils seen in the distal region may be correlated with the higher compression normally exerted on this region.

In order to evaluate the effect of chaotropic agents on proteoglycan and non-collagenous proteins, chicken xiphoid cartilage was treated with guanidine-HCI and MgCl2 in different concentrations (1M to 5M), and different periods of time (12, 24, 48 and 72hr). The maximum yield of uronic acid was obtained with 3M MgCl2 (73.3 per cent). Concentrations of 4M and 5M of MgCl2 showed that much less uronic acid was removed, 55.3 per cent and 38.1 respectively. Extraction with 3M MgCl2 and 3M guanidine-HCl resulted better efficiency when performed for 48 hr. Analysis by SDS-PAGE of the extracts obtained with guanidine-HCl and MgCl, in different concentrations pointed out that most components are equally removed with the two solvents, showing that the extraction with MgCl2 is an alternative assay to remove non-collagenous proteins from extracellular matrix.