Inhibition of soluble epoxide hydrolase improves the impaired pressure-natriuresis relationship and attenuates the development of hypertension and hypertension-associated end-organ damage in Cyp1a1-Ren-2 transgenic rats
Language English Country Netherlands Media print
Document type Comparative Study, Journal Article, Research Support, Non-U.S. Gov't
Grant support
F32 NS009699
NINDS NIH HHS - United States
F32 NS010499
NINDS NIH HHS - United States
P01 DK038226
NIDDK NIH HHS - United States
R01 HL059699
NHLBI NIH HHS - United States
PubMed
21720266
PubMed Central
PMC3777565
DOI
10.1097/hjh.0b013e328349062f
Knihovny.cz E-resources
- MeSH
- Angiotensin II Type 1 Receptor Blockers pharmacology MeSH
- Cytochrome P-450 CYP1A1 genetics MeSH
- Epoxide Hydrolases antagonists & inhibitors MeSH
- Glomerular Filtration Rate drug effects physiology MeSH
- Hypertension, Malignant chemically induced physiopathology prevention & control MeSH
- Indoles adverse effects MeSH
- Enzyme Inhibitors pharmacology MeSH
- Blood Pressure drug effects physiology MeSH
- Rats MeSH
- Kidney blood supply pathology physiopathology MeSH
- Losartan pharmacology MeSH
- Disease Models, Animal MeSH
- Natriuresis drug effects physiology MeSH
- Kidney Diseases physiopathology prevention & control MeSH
- Rats, Transgenic MeSH
- Regional Blood Flow drug effects physiology MeSH
- Renin genetics MeSH
- Animals MeSH
- Check Tag
- Rats MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Comparative Study MeSH
- Names of Substances
- Angiotensin II Type 1 Receptor Blockers MeSH
- Cytochrome P-450 CYP1A1 MeSH
- Epoxide Hydrolases MeSH
- indole-3-carbinol MeSH Browser
- Indoles MeSH
- Enzyme Inhibitors MeSH
- Losartan MeSH
- Ren2 protein, rat MeSH Browser
- Renin MeSH
OBJECTIVE: In the present study, we compared the effects of treatment with the novel soluble epoxide hydrolase (sEH) inhibitor (c-AUCB) with those of the AT1 receptor antagonist losartan on blood pressure (BP), autoregulation of renal blood flow (RBF) and on glomerular filtration rate (GFR) and the pressure-natriuresis relationship in response to stepwise reduction in renal arterial pressure (RAP) in Cyp1a1-Ren-2 transgenic rats. METHODS: Hypertension was induced in Cyp1a1-Ren-2 rats through dietary administration for 11 days of the natural xenobiotic indole-3-carbinol (I3C) which activates the renin gene. Treatment with c-AUCB and losartan was started 48 h before initiating administration of the diet containing I3C. Rats were prepared for renal functional studies to evaluate in-vivo renal autoregulatory efficiency when RAP was gradually decreased by an aortic clamp. RESULTS: I3C administration resulted in the development of severe hypertension which was associated with markedly lower basal RBF and GFR and substantially impaired autoregulatory efficiency as well as a suppression of the pressure-natriuresis relationship when compared with noninduced rats. Treatment with c-AUCB significantly decreased BP, improved autoregulatory efficiency of RBF and GFR and the slope of pressure-natriuresis relationship. Treatment with losartan completely prevented the impaired autoregulation and pressure-natriuresis relationship as well as the development of hypertension in I3C-induced rats. CONCLUSION: Our present findings indicate that chronic treatment with the sEH inhibitor c-AUCB substantially attenuates the development of malignant hypertension in I3C-induced rats likely via improvement of the renal autoregulatory efficiency and the pressure-natriuresis relationship.
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Epoxyeicosanoids in hypertension