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A 32% decrease in the expression of inducible nitric oxide synthase (iNOS) (but not endothelial nitric oxide synthase; eNOS) in eosinophils from l-NAME-treated rats was observed.
Amniotic fluid MBP levels increased with increasing DBP doses, and high variability in maternal urinary levels of MBP between rats was observed.
Increased fecal excretion of 14C-labeled PFOA and PFOS in rats was observed after multi-day administration cholestyramine per os, accompanied by a concurrent reduction in concentrations of the substances in the liver and plasma.
As shown in Figure 5, the highest SUV in rats was observed over the heart region for which the SUV value at 60 min amounted to 75% of the 2-min value.
A significant decrease of plasma uric acid levels (P < 0.05) and hepatic impairment in male rats was observed after oral administration of a SLS (mean size: 120 μm) suspensions of the optimum formulation, compared to suspensions of pure AP.
Additionally, a significant increase in B1 receptor protein expression in renal cortex of Ang II-infused rats was observed compared to control suggesting that bradykinin receptor activation could account for the effect of enalapril to enhance the actions of tempol.
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Rats were observed for 24 hours.
The rats were observed for defecation.
Pain-related behaviors in rats were observed at specific time points.
Rats were observed for abnormal behavior and physical condition after carrageenan injection.
Rats were observed for survival and assessed for liver injury by serum alanine transaminase (ALT) measurement and histological analysis.
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