INVESTIGADORES
CARRANZA Maria Andrea
congresos y reuniones científicas
Título:
Nitric oxide (NO), prostanoids (PR) and oxidative stress (OS) during experimental endotoxemia in fructose (F).overloaded rats
Autor/es:
PEREDO, HORACIO A; CARRANZA, ANDREA; AZICH, ANABELLA; MAYER, MARCOS A; INGARAMO, PI; RONCO, MT; PUYÓ, ANA MARÍA; GALLEANO, MÓNICA
Lugar:
Santiago de Chile
Reunión:
Congreso; VI Meeting of SFRBM South American Group; 2009
Institución organizadora:
Society of Free Radicals
Resumen:
Nitric oxide (NO), prostanoids (PR) and oxidative stress (OS) during experimental endotoxemia in fructose (F).overloaded rats H.A. Peredeo, M.A. Carranza, A. Azich, M. Mayer, P.I. Ingaramo, M.T. Ronco, M.A. Puyo, M. Galleano Facultad de Farmacia y Bioquimica, Universidad de Buenos Aires, IFISE, Universidad Nacional de Rosario and CONICET, Argentina The aim of this work was to study NO and PR production and OS markers during experimental endotoxemia in control and F-overloaded rats, considered a modelo f metabolic syndrome. Male Sprague-Dawley rats were grouped in controls (C, tap water, n=16) or F (F solution, 10% w/v, n=16) and treated for 15 weeks. Six hours previous to sacrifice, 8 animals from each group received LPS (4mg/kg, ip) (C-LPS and F-LPS groups) and the remaining received physiologic solution (C and F). The following parameters were measured: blood NO/hemoglobin (by ESR), plasma nitrites and nitrates (NOx), liver iNOS expression, TBARS, plasma 8-isoprostanes (8-iso, ELISA), and vascular PR production in aorta and mesenteric bed (HPLC). NoHb (UA) NOx (µ M) iNOS (UA) TBARS (µ M) 8-iso (pg/ml) C <0.5 9±0.7 2.5±1.3 1.7±0.2 184±45 F <0.5 13.1±0.6 0.6±0.3 1.53±0.06 192±26 C-LPS 19±2 264±11 68±3a 2.9±0.09 3557±400a F-LPS 11±1b 212±18a,b 55±6a,b 2.6±0.2a 2960±620a a p<0.05vs.C and F< b p<0.05vs.C-LPS (ANOVA) PLS increased the release of PR in both vascular preparations (p<0.05) in C but not in F group. Results showed that NO and PR production were lower in F-LPS rats as compared woth C-LPS group, suggesting an impaired response to LPS-challenge in F rats. Supported by UBA, CONICET and ANPCyT.