Results were normalized by protein concentration and NO synthase activity was expressed as pmol/mg min. NE, ACh and SNP were acquired from Sigma Chemical Co. (St. Louis, MO). Except when described, all other drugs and reagents were purchased from Merck, Sharp & Döhme (Whitehouse Station, NJ). Comparisons were made by ANOVA followed by Tukey–Kramer test. Anti-infection Compound Library research buy Values were reported as mean ± standard error of mean (SEM). Statistical significance was set as P < 0.05. After 30 min of stabilization, basal perfusion pressure in mesenteric vascular bed from B2−/− (48 ± 1.8 mmHg; n = 8;

P < 0.05) was significantly higher when compared to WT (40 ± 1.4 mmHg; n = 11) and B1−/− (41 ± 1.0 mmHg; n = 8) preparations. Injection of vasoconstrictor NE on isolated vascular preparations elicited rapid and dose-related constriction that increased to a single peak and then declined to basal perfusion pressure, usually within 2 min ( Fig. 1A). NE injection promoted similar responses in all vascular preparations from WT, B1−/− and B2−/−, as demonstrated in Fig. 1B.

The endothelial function of mesenteric arterioles was assessed through the effect of ACh (an endothelium-dependent relaxating agent) and SNP (an endothelium-independent relaxating agent) in pre-contracted vessels (NE 10 μmol/L). In all experiments, ACh produced a significant dose-dependent reduction in perfusion pressure (at the doses of 0.1, 1 and 10 nmols). As shown in Fig. 2, vascular response to ACh was markedly reduced in B1−/− and B2−/− preparations when compared to WT responses, for all tested BIBW2992 nmr doses. In all groups,

SNP injection elicited a consistent decrease in perfusion pressure (about 60% of contraction induced by NE perfusion at the dose of 10 nmols). No significant differences were detected among strains for all tested doses of SNP (Fig. 3). Since the NO metabolites reflect the overall NO production in the organism, we determined the plasma nitrite/nitrate concentration in blood samples obtained from WT, B1−/− and B2−/− mice. A significant decrease in circulating NO levels was detected in both B1−/− and B2−/− when compared to WT samples. Data are shown Leukocyte receptor tyrosine kinase in Fig. 4. Vascular NO production was assessed in mesenteric arterioles sections incubated with DAF-2 DA, a sensitive fluorescent indicator for detection of NO. Images are shown in Fig. 5A. The fluorescence intensity of DAF-2 DA was significantly diminished in vessels from B1−/− and B2−/− when compared to WT samples, indicating that basal NO production was decreased in mesenteric arterioles from both strains (Fig. 5B). The NOS activity was assessed in homogenates of mesenteric vessels by biochemical conversion of l-[3H] arginine to l-[3H] citrulline in presence of substrate and co-factors.