Table 1.
Effects of empagliflozin on vascular function in ALDH2*2 mice using wire myograph.
WT | Vehicle | EtOH | Empa | |
---|---|---|---|---|
Maximal Contractile Force (mN/mg) | 0.44 ± 0.03 | 0.35 ± 0.01# | 0.29 ± 0.02$ | 0.45 ± 0.04%* |
Maximal Relaxation (%) | 91.8 ± 1.4% | 81.1 ± 4.0%# | 47.0 ± 13.2%$ | 91.2 ± 1.7%* |
Data correspond to results presented in Fig. 7 (E and F). The maximal contractile force was recorded in response to 1 μM endothelin-1 (ET-1), and the relaxation maximal relaxation (%) was recorded in response to 1 mM acetylcholine in mouse aortas isolated from WT, vehicle, EtOH, and Empa groups. WT group, wild-type Aldh2 mice; vehicle group, solvent (PEG/DMSO) control– treated ALDH2*1/*2 mice; EtOH group, alcohol-treated ALDH2*1/*2 mice; Empa group, ethanol- and Empa-treated ALDH2*1/*2 mice. Data represent six mice for each group. Data are expressed as means ± SEM.
Vehicle versus WT group: #P < 0.05
EtOH versus vehicle group: $P < 0.05
EtOH versus Empa group: *P < 0.05, calculated by a one-way ANOVA with Bonferroni correction.