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. Author manuscript; available in PMC: 2023 Jun 27.
Published in final edited form as: Sci Transl Med. 2023 Jan 25;15(680):eabp9952. doi: 10.1126/scitranslmed.abp9952

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.