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. 2018 Apr 30;2018:8309698. doi: 10.1155/2018/8309698

Figure 5.

Figure 5

Nrf2 KO mice are protected against impairment of myocardial diastolic function following AMI. (a) I/R injury resulted in an impairment of diastolic function (evaluated with prolonged deceleration time (DT)), (b) E/A relation, and (c) relaxation time (IVRT) in WT mice (white box plots), whereas preexisting diastolic dysfunction was not aggravated in Nrf2 KO mice (blue box plots). In eNOS KO mice (A, red box plots), diastolic dysfunction evidenced by increased DT as compared to WT mice (Supplementary Table 1) was not further exacerbated after AMI. WT mice: n = 9, Nrf2 KO mice: n = 8; Browne-Forsythe test p > 0.05, means ± quartiles, one-way ANOVA p < 0.05, ∗∗ p < 0.01 except for eNOS KO mice n = 4‐5, unpaired t-test.