Journal
PHARMACEUTICS
Volume 15, Issue 6, Pages -Publisher
MDPI
DOI: 10.3390/pharmaceutics15061683
Keywords
dapagliflozin; lipopolysaccharide; hypotension; inflammation; diabetes; iNOS
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In this study, it was found that the SGLT2 inhibitor dapagliflozin attenuated lipopolysaccharide-induced hypotension by inhibiting vasodilation and reducing cytokine levels. This protective effect was independent of glycemic control and applicable to patients with different glucose levels.
Sodium-glucose cotransporter-2 (SGLT2) inhibitors have been suggested to have anti-inflammatory properties in diabetes. The goal of this study was to evaluate the role of the SGLT2 inhibitor dapagliflozin (DAPA) in the attenuation of lipopolysaccharide (LPS)-induced hypotension. Male Wistar albino rats were divided into normal and diabetic groups and received DAPA (1 mg/kg/day) for two weeks followed by a single dose of 10 mg/kg LPS. Blood pressure was recorded throughout the study and the circulatory levels of cytokines were assessed using a multiplex array, while the aortas were harvested for analysis. DAPA attenuated the vasodilation and hypotension caused by LPS. Mean arterial pressure (MAP) was preserved in the normal and diabetic DAPA-treated septic groups (MAP = 83.17 & PLUSMN; 5.27, 98.43 & PLUSMN; 5.57 mmHg) compared to the vehicle-treated septic groups (MAP = 65.60 & PLUSMN; 3.31, 68.21 & PLUSMN; 5.88 mmHg). Most of the cytokines induced by LPS were decreased in the DAPA-treated septic groups. In the aorta, the inducible nitric oxide synthase-derived nitric oxide had lower expression in the DAPA-treated rats. In contrast, the expression of & alpha;-smooth muscle actin, a marker of the vessel's contractile state, was higher in the DAPA-treated rats in comparison with non-treated septic rats. These findings revealed that the protective role of DAPA against LPS-induced hypotension is likely to be glucose-lowering independent, as was observed in the non-diabetic septic group. Taken together, the results show that DAPA has a potential effect in the prevention of the hemodynamic disturbances of sepsis regardless of glycemia levels.
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