Why the study?
Because adding a soluble epoxide hydrolase inhibitor to ACE inhibitor surprisingly increased heart failure mortality in Ren-2 transgenic hypertensive rats, and these rats exhibit sex-related mortality differences, researchers examined whether sex-related differentiation exists in response to these treatments.
Does combined treatment with ACEi and sEHi improve survival compared to ACEi alone in male and female hypertensive rats with ACF-induced heart failure?
Does combined treatment with ACEi and sEHi improve survival compared to ACEi alone in male and female hypertensive rats with ACF-induced heart failure?
In a hypertensive rat model of heart failure, the addition of an sEH inhibitor to ACE inhibitor therapy worsened survival in males but improved survival in females, highlighting critical sex-linked differences in pharmacological response.
Sex-specific survival effects with combined ACEi-sEHi require cautious interpretation; leaves open relevance to human heart failure.
We found recently that in Ren-2 transgenic hypertensive rats (TGR) addition of soluble epoxide hydrolase inhibitor (sEHi) to treatment with angiotensin-converting enzyme inhibitor (ACEi), surprisingly, increased the mortality due to heart failure (HF) induced by creation of the aorto-caval fistula (ACF). Since TGR exhibit sex-related differences in mortality, we examined here if such differentiation exists also in the response to the treatment with ACEi (trandolapril), alone or combined with sEHi [cis-4-[4-(3-adamantan-1-yl-ureido)cyclohexyloxy]benzoic acid, (c-AUCB)]. ACEi improved survival in males to 74 % (vs. 0 %) and in females to 65 % (vs. 32 %). ACEi and sEHi combined also improved the survival in male ACF TGR, however, it was significantly less (38 %) than after ACEi alone. In contrast, in females the combined treatment significantly improved the final survival rate (84 %). There were no significant sex-linked differences in survival rate in untreated or treated normotensive Hannover Sprague-Dawley rats. In conclusion, in HF patients with co-existing hypertension and RAS hyperactivity, the sex may co-determine the rate of HF progression, and can influence the effectiveness of the therapeutic measures applied. Therefore, in the relevant pre-clinical studies the sex-linked differences should be seriously considered. Our data indicate that TGR might be an optimal model for such studies.
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Kala et al. (2019) studied this question.
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