Key result
Combined ACE and soluble epoxide hydrolase inhibition cuts absolute survival by ~31% in heart failure rats.
Why the study?
Does combined treatment with an ACE inhibitor and a soluble epoxide hydrolase inhibitor improve survival and renal function in Ren-2 transgenic hypertensive rats with aorto-caval fistula-induced congestive heart failure?
Does combined treatment with an ACE inhibitor and a soluble epoxide hydrolase inhibitor improve survival and renal function in Ren-2 transgenic hypertensive rats with aorto-caval fistula-induced congestive heart failure?
Absolute Event Rate: 53% vs 84%
p-value: p=<0.05
Addition of a soluble epoxide hydrolase inhibitor to ACE inhibitor treatment unexpectedly worsens survival in a rat model of volume-overload heart failure, suggesting this combination is not a viable therapeutic strategy.
Combined ACEi-sEHi therapy worsened survival in this rat HF model; hypothesis-generating and should not inform clinical practice.
We showed recently that increasing kidney epoxyeicosatrienoic acids (EETs) by blocking soluble epoxide hydrolase (sEH), an enzyme responsible for EETs degradation, retarded the development of renal dysfunction and progression of aorto-caval fistula(ACF)-induced congestive heart failure (CHF) in Ren-2 transgenic hypertensive rats (TGR). In that study the final survival rate of untreated ACF TGR was only 14 % but increased to 41 % after sEH blockade. Here we examined if sEH inhibition added to renin-angiotensin system (RAS) blockade would further enhance protection against ACF-induced CHF in TGR. The treatment regimens were started one week after ACF creation and the follow-up period was 50 weeks. RAS was blocked using angiotensin-converting enzyme inhibitor (ACEi, trandolapril, 6 mg/l) and sEH with an sEH inhibitor (sEHi, c-AUCB, 3 mg/l). Renal hemodynamics and excretory function were determined two weeks post-ACF, just before the onset of decompensated phase of CHF. 29 weeks post-ACF no untreated animal survived. ACEi treatment greatly improved the survival rate, to 84 % at the end of study. Surprisingly, combined treatment with ACEi and sEHi worsened the rate (53 %). Untreated ACF TGR exhibited marked impairment of renal function and the treatment with ACEi alone or combined with sEH inhibition did not prevent it. In conclusion, addition of sEHi to ACEi treatment does not provide better protection against CHF progression and does not increase the survival rate in ACF TGR: indeed, the rate decreases significantly. Thus, combined treatment with sEHi and ACEi is not a promising approach to further attenuate renal dysfunction and retard progression of CHF.
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Kala et al. (2017) studied Congestive heart failure and renal dysfunction (n=169). Angiotensin-converting enzyme inhibitor (trandolapril) combined with soluble epoxide hydrolase inhibitor (c-AUCB) vs. Angiotensin-converting enzyme inhibitor (trandolapril) alone was evaluated on Survival rate at 50 weeks (p=<0.05). Combined treatment with an ACE inhibitor and a soluble epoxide hydrolase inhibitor significantly worsened the 50-week survival rate to 53% compared to 84% with ACE inhibitor alone in rats with heart failure.
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