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1.
J Invest Surg ; 20(3): 157-66, 2007.
Artigo em Inglês | MEDLINE | ID: mdl-17613690

RESUMO

Bioabsorbable fixation is commonly used in soft tissue procedures performed in the shoulder. ArthroRivettrade mark tacks (referred to as rivets here), made from a copolymer of 82% poly-L-lactic acid and 18% polyglycolic acid, were developed for the Bankart procedure. Although a previous in vivo study demonstrated favorable comparison of the fixation strength and absorption characteristics of this device with that of polyglyconate bioabsorbable tacks, there have been no published biomechanical studies of this rivet in the shoulder. Fourteen shoulders were harvested from fresh-frozen cadavers of average age 74 years (46-89). Biomechanical testing was performed by measuring the energy, or work, required to anteriorly displace the humeral head 6 mm from the glenoid. Each shoulder was tested intact, vented, and before and after repair of a simulated Bankart lesion at 0, 45, and 90 degrees of abduction with and without maximal external rotation. Overall, the average work required ranged from 54.7 N-mm to 178.27 N-mm. Although the biomechanical performance of the rivet, based on resistance to anterior displacement of the humeral head, was indistinguishable from that of the suture repair, the statistical power of the test was low due to the large variance in the cadaver specimens. The results, in general, correlated well with those of previously published studies, suggesting the suitability of the bioabsorbable rivet for use in Bankart repair.


Assuntos
Implantes Absorvíveis , Teste de Materiais , Procedimentos Ortopédicos/instrumentação , Articulação do Ombro/patologia , Articulação do Ombro/cirurgia , Idoso , Idoso de 80 Anos ou mais , Fenômenos Biomecânicos , Humanos , Técnicas In Vitro , Ácido Láctico , Pessoa de Meia-Idade , Procedimentos Ortopédicos/métodos , Poliésteres , Ácido Poliglicólico , Polímeros , Articulação do Ombro/fisiologia
2.
Carcinogenesis ; 23(11): 1953-60, 2002 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-12419846

RESUMO

Prebiotics such as fructans, and probiotics such as Lactobacilli or Bifidobacteria, or a combination of prebiotics and probiotics (synbiotics) are thought to be protective against colon cancer. Therefore, we studied whether the prebiotic inulin enriched with oligofructose (Raftilose-Synergy1, briefly, Synergy1, 10% of the diet), probiotics [Bifidobacterium lactis (Bb12) and Lactobacillus rhamnosus (LGG), each at 5x10(8) c.f.u./g diet] or synbiotics (a combination of the two) protect rats against azoxymethane (AOM)-induced colon cancer. Male F344 rats were divided into: Controls; PRE, which were fed a diet containing Synergy1; PRO, fed a diet containing LGG and Bb12; PREPRO, fed a diet containing Synergy1, LGG and BB12. Ten days after beginning the diets, rats were treated with AOM (15 mg/kg s.c. two times); dietary treatments were continued for the entire experiment. Thirty-one weeks after AOM, rats treated with Synergy1 (PRE and PREPRO groups) had a significantly lower (P < 0.001) number of tumours (adenomas and cancers) than rats without Synergy1 (colorectal tumours/rat were 1.9 +/- 1.7, 1.1 +/- 1.1, 2.2 +/- 1.4 and 0.9 +/- 1.2 in Controls, PRE, PRO and PREPRO groups, respectively, means +/- SD). A slight, not significant effect of probiotics in reducing malignant tumours was also observed (P = 0.079). Caecal short-chain fatty acids (SCFA) were higher (P < 0.001) in the groups treated with Synergy1. Apoptosis was increased in the normal mucosa of the PRO group, while no variation was observed in the tumours. Colonic proliferation was lower in the PRE group as compared with Controls. Glutathione S-transferase placental enzyme pi type expression, and to a lesser extent, inducible NO synthase were depressed in the tumours from rats in the PRE and PREPRO groups. Cycloxygenase-2 expression was increased in the tumours of control rats but not in those from PRE, PRO or PREPRO rats. In conclusion, prebiotic administration in the diet decreases AOM-induced carcinogenesis in rats.


Assuntos
Adenocarcinoma/prevenção & controle , Adenoma/prevenção & controle , Antineoplásicos Fitogênicos/uso terapêutico , Protocolos de Quimioterapia Combinada Antineoplásica/uso terapêutico , Bifidobacterium/fisiologia , Neoplasias do Colo/prevenção & controle , Inulina/uso terapêutico , Lactobacillus/fisiologia , Oligossacarídeos/uso terapêutico , Probióticos/uso terapêutico , Adenocarcinoma/induzido quimicamente , Adenocarcinoma/enzimologia , Adenoma/induzido quimicamente , Adenoma/enzimologia , Animais , Antineoplásicos Fitogênicos/administração & dosagem , Antineoplásicos Fitogênicos/farmacologia , Apoptose/efeitos dos fármacos , Azoximetano/toxicidade , Carcinógenos/toxicidade , Ceco , Divisão Celular/efeitos dos fármacos , Neoplasias do Colo/induzido quimicamente , Neoplasias do Colo/enzimologia , Ciclo-Oxigenase 2 , Dieta , Ensaios de Seleção de Medicamentos Antitumorais , Sinergismo Farmacológico , Indução Enzimática/efeitos dos fármacos , Ácidos Graxos Voláteis/metabolismo , Conteúdo Gastrointestinal , Glutationa S-Transferase pi , Glutationa Transferase/metabolismo , Mucosa Intestinal/efeitos dos fármacos , Mucosa Intestinal/enzimologia , Inulina/administração & dosagem , Inulina/farmacologia , Isoenzimas/metabolismo , Masculino , Proteínas de Neoplasias/metabolismo , Oligossacarídeos/administração & dosagem , Oligossacarídeos/farmacologia , Prostaglandina-Endoperóxido Sintases/metabolismo , Ratos , Ratos Endogâmicos F344
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