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1.
Braz. oral res. (Online) ; 31: e16, 2017. tab, graf
Artículo en Inglés | LILACS | ID: biblio-839530

RESUMEN

Abstract Recent studies investigating protease-activated receptor type 2 (PAR-2) suggest an association between the receptor and periodontal inflammation. It is known that gingipain, a bacterial protease secreted by the important periodontopathogen Porphyromonas gingivalis can activate PAR-2. Previous studies by our group found that PAR-2 is overexpressed in the gingival crevicular fluid (GCF) of patients with moderate chronic periodontitis (MP). The present study aimed at evaluating whether PAR-2 expression is associated with chronic periodontitis severity. GCF samples and clinical parameters, including plaque and bleeding on probing indices, probing pocket depth and clinical attachment level, were collected from the control group (n = 19) at baseline, and from MP patients (n = 19) and severe chronic periodontitis (SP) (n = 19) patients before and 6 weeks after periodontal non-surgical treatment. PAR-2 and gingipain messenger RNA (mRNA) in the GCF of 4 periodontal sites per patient were evaluated by Reverse Transcription Polymerase Chain Reaction (RT-qPCR). PAR-2 and gingipain expressions were greater in periodontitis patients than in control group patients. In addition, the SP group presented increased PAR-2 and gingipain mRNA levels, compared with the MP group. Furthermore, periodontal treatment significantly reduced (p <0.05) PAR-2 expression in patients with periodontitis. In conclusion, PAR-2 is associated with chronic periodontitis severity and with gingipain levels in the periodontal pocket, thus suggesting that PAR-2 expression in the GCF reflects the severity of destruction during periodontal infection.


Asunto(s)
Humanos , Masculino , Femenino , Adulto , Persona de Mediana Edad , Líquido del Surco Gingival/química , Receptor PAR-2/análisis , Periodontitis Crónica/patología , Valores de Referencia , Índice de Severidad de la Enfermedad , Cisteína Endopeptidasas/análisis , Biomarcadores/análisis , Estudios de Casos y Controles , Expresión Génica , Índice Periodontal , Índice de Placa Dental , Pérdida de la Inserción Periodontal , Porphyromonas gingivalis , Estadísticas no Paramétricas , Adhesinas Bacterianas/análisis
2.
Clinics ; 66(7): 1199-1202, 2011. ilus
Artículo en Inglés | LILACS | ID: lil-596908

RESUMEN

INTRODUCTION: Asthma affects approximately 10 percent of the world's population. Sensitization to allergens is an important risk factor, and exposure to allergens is associated with disease severity. METHODS: We performed skin tests to evaluate allergen sensitization to mites, cockroaches, cats, dogs, and molds in 73 asthmatic patients. Enzyme Linked Immunosorbent Assay was used to assay the mite and cockroach allergens found in dust from the bedding, hammocks, bedroom floors, living rooms, and kitchens of 29 patients and 14 controls. RESULTS: Fifty patients (68.5 percent) had positive skin test responses. There were positive responses to D. pteronyssinus (52.0 percent), B. tropicalis (53.4 percent), T. putrescentiae (15.0 percent), E. maynei (12.3 percent), L. destructor (8.2 percent), B. germanica (20.5 percent), P. americana (21.9 percent), Felis catus (10.9 percent), C. herbarium (2.7 percent), A. alternata (4.1 percent), and P. notatun (1.3 percent). The exposure to mite and cockroach allergens was similar in the patients and the controls. The Dermatophagoides pteronyssinus Group 1 levels were highest in the beds and hammocks. The Blattella germanica Group 1 levels were highest in the kitchens, living rooms and hammocks. DISCUSSION: The positive skin tests to mites, cockroaches and cats were consistent with previous studies. D pteronyssinus was the most prevalent home dust mite, and hammocks were a source of allergens. To improve asthma prophylaxis, it is important to determine its association with mite allergen exposure in hammocks.


Asunto(s)
Adolescente , Adulto , Animales , Femenino , Humanos , Masculino , Persona de Mediana Edad , Adulto Joven , Alérgenos/inmunología , Asma/inmunología , Polvo/inmunología , Antígenos Dermatofagoides/análisis , Proteínas de Artrópodos/análisis , Estudios de Casos y Controles , Cucarachas , Cisteína Endopeptidasas/análisis , Polvo/análisis , Ensayo de Inmunoadsorción Enzimática , Ácaros , Factores de Riesgo , Pruebas Cutáneas , Estadísticas no Paramétricas
3.
The Korean Journal of Parasitology ; : 89-92, 2002.
Artículo en Inglés | WPRIM | ID: wpr-95663

RESUMEN

The cysteine proteases of Paragonimus westermani metacercariae are involved in metacercarial excystment, host immune modulation, and possibly in tissue penetration. In order to clarify the origin of the enzymes, 28 and 27 kDa cysteine proteases in metacercarial excretory-secretory products were purified through the FPLC system using Mono Q column chromatography. The polyclonal antibodies to the enzymes were produced in BALB/c mice. Immunolocalization studies revealed that both cysteine proteases were distributed at the linings of excretory bladder and excretory concretions of the metacercariae. It was suggested that the excretory epithelium of P. westermani undertake the secretory function of metacercarial cysteine proteases, in addition to its role as a route for eliminating waste products.


Asunto(s)
Animales , Ratones , Cromatografía Liquida , Biología Computacional , Cisteína Endopeptidasas/análisis , Inmunohistoquímica , Ratones Endogámicos BALB C , Paragonimus/anatomía & histología
4.
Braz. j. microbiol ; 32(1): 6-9, Jan.-Mar. 2001. tab, graf
Artículo en Inglés | LILACS | ID: lil-297657

RESUMEN

The influence of the addition of Amaranthus cruenthus seed meal to the medium, as nutrient and growth factor, on protease production by Bacillus subtilis 3411 was studied. Tests were carried out in a rotary shaker and in mechanically stirred fermenters. The influence of aeration was also evaluated. The addition of amaranth in a concentration of 20 g/L resulted in 400 per cente increase in protease production. Aeration up to 750 r.p.m. and 1 L/L.min had a favorable effect.


Asunto(s)
Amaranthus , Bacillus subtilis , Cisteína Endopeptidasas/análisis , Aireación , Fermentación
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