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1.
Rev. Soc. Bras. Med. Trop ; 40(2): 156-162, mar.-abr. 2007. tab, graf
Artículo en Inglés | LILACS | ID: lil-452615

RESUMEN

We analyzed the kinetics of cytokine production by mononuclear cells from 17 patients who had been treated for paracoccidioidomycosis, using the stimulus of gp43 peptide groups (43kDa glycoprotein of Paracoccidioides brasiliensis) at 0.1 and 1µM, gp43 (1µg/ml) and crude Paracoccidioides brasiliensis antigen (PbAg; 75µg/ml). IFN-gamma production was a maximum at 144 hours in relation to the G2 and G8 peptide groups at 1µM and was greatest at 144 hours when stimulated by gp43 and by PbAg. The maximum TNF-alpha production was at 144 hours for the G2 group (0.1µM) and for gp43. IL-10 production was highest after 48 and 72 hours for G7 and G6 at 1µM, respectively. We also suggest the best time for analysis of IL4 production. These results may contribute towards future studies with gp43 peptides and encourage further investigations with the aim of understanding the influence of these peptides on the production of inflammatory and regulatory cytokines.


Analisamos a cinética da produção de citocinas de células mononucleares de 17 pacientes com paracoccidioidomicose tratada, usando como estímulo: grupos de peptídeos da gp43 (glicoproteina de 43kDa de Paracoccidioides brasiliensis) a 0,1 e 1µM, gp43 (1µg/mL) e antígeno bruto de Paracoccidioides brasiliensis - AgPb (75µg/mL). A produção de IFN-gama foi máxima em 144 horas frente aos grupos de peptídeos G2 e G8 a 1µM e maior em 144 horas quando estimuladas por gp43 e por AgPb. A produção de TNF-alfa foi máxima em 144 horas para G2 (0,1µM) e para gp43. A produção de IL-10 foi maior após 48 e 72 horas para G7 e G6 a 1µM, respectivamente. Sugerimos também o melhor período para a análise da produção de IL4. Tais resultados podem contribuir para estudos com peptídeos da gp43, estimulando investigações posteriores visando entender a influência de tais peptídeos na produção de citocinas inflamatórias e regulatórias.


Asunto(s)
Humanos , Citocinas/biosíntesis , Proteínas Fúngicas/farmacología , Leucocitos Mononucleares/inmunología , Paracoccidioides/química , Paracoccidioidomicosis/inmunología , Proteínas Fúngicas/aislamiento & purificación , Interferón gamma/biosíntesis , /biosíntesis , /biosíntesis , Leucocitos Mononucleares/efectos de los fármacos , Paracoccidioides/inmunología , Factores de Tiempo , Factor de Necrosis Tumoral alfa/biosíntesis
2.
Arch. med. res ; 30(1): 69-73, ene.-feb. 1999. tab, graf
Artículo en Inglés | LILACS | ID: lil-256624

RESUMEN

Background. Cu,Zn-superoxide-dismutase, Cu,Zn-SOD, can be obtained from different sources with different anti-inflammatory activities. In this study we compared the antiinflammatory capacity of the marine yeast Debaryomyces hanseii Cu,Zn-SOD (Dh-SOD) with that of bovine erythrocytes (Be-SOD) in preventive an a therapeutic fashion. Methods. Edema was induced by carrageenan injection into the rat hind paw and was evaluated using a mercury plethysmograph. Development of the inflammatory process was followed by volume displacement at time 0 (carrageenan injection), 1, 2, 3, 4, 5, 6, 9, 12, and 24 h thereafter. Three different SOD doses were used in preliminary experiments to prevent edema: 10, 100, and U/kg. Results. The results indicate that, at the lowest dose (10 U/kg), both SOD samples are effective in reducing inflammation in both the prostaglandin and amplification phases (-24.8 percent and -17.5 percent in the case of Be-SOD, and 11.8 percent and -18.7 percent in the case of Dh-SOD, respectively) (p<0.05). At 100 U/kg, Be-SOD also shows good anti-inflammatory activity in all edema phases (-27.1 percent in the serotonin phase; -19.4 percent in the prostaglandin phase; and -20 percent in the amplification phase) (p<0.05), but Dh-SOD was less effective (-10.9 percent, -9.1 percent, and -5.7 percent). At the highest dose tested (1000 U/kg), Dh-SOD was, again more effective than Be-SOD in all three edema phases (-33.1 percent and -1.5 percent; -17.9 percent and -2.6 percent; and -13.8 percent and 6.7 percent, respectively) (p >0.05). When evaluated as a therapeutic alternative, single doses of DH-SOD at 1,000 U/kg, and Be-SOD at 100 U/kg, both showed good anti-inflammatory activities (-31.7 percent and -23.5 percent, respectively) (p < 0.05). Conclusion. For therapy purposes alone, DH-SOD appears to be a better anti-inflammatory agent than Be-SOD in carrageenan-induced edema


Asunto(s)
Humanos , Animales , Ratas , Antiinflamatorios no Esteroideos/uso terapéutico , Edema/tratamiento farmacológico , Proteínas Fúngicas/uso terapéutico , Superóxido Dismutasa/uso terapéutico , Carragenina/toxicidad , Bovinos , Edema/inducido químicamente , Eritrocitos/enzimología , Proteínas Fúngicas/farmacología , Ratas Wistar , Superóxido Dismutasa/farmacología , Levaduras/enzimología
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