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1.
Actual. osteol ; 13(1): 58-66, Ene - Abr. 2017. ilus
Artigo em Inglês | LILACS | ID: biblio-1118913

RESUMO

Connexins (Cxs) are a family of transmembrane proteins that form gap junctions and hemi-channels, which mediate cell-cell communication between neighboring cells and the respective extracellular milieu in different tissues. Most tissues and cell types throughout the body express one or more Cx proteins, highlighting its importance in regulating cell growth, differentiation, adhesion, migration, cell death and others. Moreover, Cx can propagate intracellular signals through its C-terminus domain, and thus function beyond a mere channel. Cx43 is the most highly expressed and most well studied Cx in bone and musculoskeletal tissues, although Cx40, Cx45, Cx46 and more recently, the Cx37 have been described in bone tissue, along with Cx26, Cx32 and Cx39 in other musculoskeletal tissues. Here, we discuss the basic structure of gap junctions and the role of the Cxs in musculoskeletal tissue, with special focus on Cx37. (AU)


Las conexinas (Cxs) son una familia de proteínas transmembrana que forman uniones en hendidura y hemicanales encargados de mediar la comunicación entre células vecinas y el respectivo medio extracelular en diferentes tejidos. La mayoría de los tejidos y células expresan una o más proteínas conexina, jugando un papel importante en la regulación de la proliferación celular, diferenciación, adhesión, migración y muerte celular, entre otras funciones. Además de actuar como un canal, las conexinas pueden propagar señales intracelulares a través del dominio C-terminal. La Cx43 es la conexina mas expresada y mejor estudiada en el tejido óseo y el músculo, aunque las Cx40, Cx45, Cx46, y mas recientemente Cx37, son también detectadas en el hueso. A su vez la expresión de la Cx26, Cx32 y Cx39 ha sido observada en otros tejidos músculoesqueléticos. En este manuscrito describimos la estructura básica de las uniones tipo gap y el papel que las Cxs, y en especial la Cx37, tienen en tejidos músculo-esqueléticos. (AU)


Assuntos
Humanos , Osso e Ossos/metabolismo , Reabsorção Óssea/prevenção & controle , Conexinas/fisiologia , Osteoblastos/metabolismo , Osteócitos/metabolismo , Tendões/metabolismo , Transdução de Sinais/fisiologia , Cartilagem/metabolismo , Comunicação Celular/fisiologia , Fenômenos Fisiológicos Celulares , Junções Comunicantes/efeitos dos fármacos , Junções Comunicantes/fisiologia , Conexina 43/fisiologia , Músculo Esquelético/metabolismo , Conservadores da Densidade Óssea/uso terapêutico , Ligamentos/metabolismo , Antiarrítmicos/efeitos adversos
2.
Journal of Korean Medical Science ; : 983-988, 2016.
Artigo em Inglês | WPRIM | ID: wpr-224846

RESUMO

Numerous musculoskeletal disorders are caused by thickened ligament, tendon stiffness, or fibrosis of joint capsule. Relaxin, a peptide hormone, can exert collagenolytic effect on ligamentous and fibrotic tissues. We hypothesized that local injection of relaxin could be used to treat entrapment neuropathy and adhesive capsulitis. Because hormonal effect depends on the receptor of the hormone on the target cell, it is important to confirm the presence of such hormonal receptor at the target tissue before the hormone therapy is initiated. The aim of this study was to determine whether there were relaxin receptors in the ligament, tendon, and joint capsular tissues of rats and to identify the distribution of relaxin receptors in these tissues. Transverse carpal ligaments (TCLs), inguinal ligaments, anterior cruciate ligaments (ACLs), Achilles tendons, and shoulder joint capsules were obtained from male Wistar rats. Western blot analysis was used to identify relaxin receptor isoforms RXFP1 and RXFP2. The distribution of relaxin receptors was determined by immunohistochemical staining. The RXFP1 isoform was found in all tissues examined. The RXFP2 isoform was present in all tissues but the TCLs. Its expression in ACLs tissues was relatively weak compared to that in other tissues. Our results revealed that RXFP1 and RXFP2 were distributed in distinctly different patterns according to the type of tissue (vascular endothelial cells, fibroblast-like cells) they were identified.


Assuntos
Animais , Masculino , Ratos , Western Blotting , Regulação da Expressão Gênica , Imuno-Histoquímica , Ligamentos/metabolismo , Ratos Wistar , Receptores Acoplados a Proteínas G/genética , Receptores de Peptídeos/genética , Articulação do Ombro/metabolismo , Tendões/metabolismo
3.
Artigo em Inglês | IMSEAR | ID: sea-18187

RESUMO

BACKGROUND & OBJECTIVE: Accumulation of collagen and changes in its physiochemical properties contribute to the development of secondary complications of diabetes. We undertook this study to see the effects of taurine on the content and characteristics of collagen from tail tendon of rats fed with high fructose diet. METHODS: The rats were divided into four groups of six each: control group (CON), taurine-supplemented control group (CON+TAU), taurine supplemented (FRU+TAU) and not supplemented fructose-fed group (FRU). The physico-chemical properties of collagen isolated from the tail tendon were studied. RESULTS: Fructose administration caused accumulation of collagen in tail tendon. Enhanced glycation and advanced glycation end products (AGE)-linked fluorescence together with alterations in aldehyde content, solubility pattern, susceptibility to denaturing agents and shrinkage temperature were observed in fructose-fed rats. Elevated b component of type I collagen was evidenced from the SDS gel pattern of collagen from the fructose-fed rats. Simultaneous administration of taurine alleviated these changes. INTERPRETATION & CONCLUSION: Taurine administration to fructose-rats had a positive influence on both quantitative and qualitative properties of collagen. The results of the present study suggested a role for the action of taurine in delaying diabetic complications and the possible use of taurine as an adjuvant therapeutic measure in the management of diabetes and its complications.


Assuntos
Aminoácidos/química , Fenômenos Fisiológicos da Nutrição Animal , Animais , Antioxidantes/farmacologia , Colágeno/química , Colágeno Tipo I/metabolismo , Frutose/metabolismo , /metabolismo , Peroxidação de Lipídeos , Masculino , Modelos Animais , Pepsina A/química , Ratos , Ratos Wistar , Sais/farmacologia , Dodecilsulfato de Sódio/química , Solubilidade , Cauda , Taurina/química , Temperatura , Tendões/metabolismo
4.
Yonsei Medical Journal ; : 26-29, 1999.
Artigo em Inglês | WPRIM | ID: wpr-63769

RESUMO

Growth factors have the ability to stimulate matrix synthesis and cell proliferation in rabbit flexor tendon. Maximal stimulation effects of growth factors have a wide variation. It depends upon the different anatomic sites of the tendon segment, the kinds of growth factor, the concentration of growth factors, and the time sequence. Since proliferation was an early component of intrinsic tendon healing, we investigated the short-term dose response to four different growth factors on in vitro rabbit's tendon culture. We evaluated the effects according to the various concentrations of recombinant human insulin-like growth factor 1 (IGF), recombinant human epidermal growth factor (EGF), fibroblast growth factor (FGF), and recombinant human platelet-derived growth factor-BB (PDGF). Fetal calf serum was the most potent stimulator of cell proliferation and protein synthesis in in vitro rabbit's tendon culture. Matrix synthesis and cell proliferation were stimulated dose-dependently by IGF between the doses of 50 and 150 ng/ml. The maximum mitogenic effect of EGF was observed at the concentration of 100 ng/ml (1.3 times more than the media-only control culture). The rabbit's tendon responded significantly dose-dependently to PDGF, whereas there was no significant response to FGF.


Assuntos
Coelhos , Animais , Divisão Celular/efeitos dos fármacos , Relação Dose-Resposta a Droga , Substâncias de Crescimento/farmacologia , Técnicas de Cultura de Órgãos , Proteínas/biossíntese , Tendões/metabolismo , Tendões/efeitos dos fármacos , Tendões/citologia
5.
Rev. venez. cir. ortop. traumatol ; 26(2): 85-90, oct. 1994. ilus
Artigo em Espanhol | LILACS | ID: lil-252079

RESUMO

Diferentes tipos de injertos ligamentarios autólogos han sido utilizados como reemplazo en las lesiones o rupturas del ligamento cruzado anterior. En el presente trabajo realizamos la evaluación de las propiedades biomecánicas del tendón patelar y de Aquiles, sometiéndolos a fuerzas máximas de tensión con velocidad constante, para determinar su resistencia y capacidad de elongación, comparándolos con las propiedades mecánicas del ligamento cruzado anterior, publicados en estudios previos por otros autores. El tendón de Aquiles resultó ser muy rígido, con desgarro temprano de sus fibras proximales, por su disposición anatómica y menor espesor que la extremidad distal en su inserción calcánea


Assuntos
Humanos , Masculino , Feminino , Tendões/cirurgia , Tendões/metabolismo , Transplantes , Ligamentos Articulares/cirurgia , Fenômenos Biomecânicos , Tendão do Calcâneo
6.
Rev. bras. biol ; 50(3): 689-93, ago. 1990. ilus
Artigo em Inglês | LILACS | ID: lil-93653

RESUMO

Particularidades topoquímicas da reaçäo de diferentes tipos de estruturas contendo colágeno, com Cancanavalina A (Con A) näo tem sido considerados até agora. A presença de disponibilidade de resíduos de glicose em moléculas de colágeno de intestino, fígado, cartilagem e tendäo säo verificados usando Con A e peroxidase de rábano silvestre (HRP). Em cortes de intestino, cartilagem e tendäo, o método usando Con A-HRP só foi significativamente positivo quando os cortes eram submetidos a um tratamento prévio com papaína sugerindo a presença de glicoproteínas e proteoglicanas da matriz extracelular (ECM), interagindo com resíduos laterais de carboidratos das moléculas de colágeno ou causando algum bloqueio estérico como ocorre em regiöes com alto estado de compactaçäo


Assuntos
Ratos , Animais , Colágeno/metabolismo , Concanavalina A/metabolismo , Matriz Extracelular/metabolismo , Glucose/metabolismo , Cartilagem/metabolismo , Peroxidase do Rábano Silvestre , Intestino Grosso/metabolismo , Fígado/metabolismo , Tendões/metabolismo
7.
Indian J Exp Biol ; 1981 Jan; 19(1): 37-9
Artigo em Inglês | IMSEAR | ID: sea-60349
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