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
Jazyk angličtina Země Nizozemsko Médium print
Typ dokumentu srovnávací studie, časopisecké články, práce podpořená grantem
Grantová podpora
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-zdroje
- MeSH
- blokátory receptoru 1 pro angiotenzin II farmakologie MeSH
- cytochrom P-450 CYP1A1 genetika MeSH
- epoxid hydrolasy antagonisté a inhibitory MeSH
- hodnoty glomerulární filtrace účinky léků fyziologie MeSH
- hypertenze maligní chemicky indukované patofyziologie prevence a kontrola MeSH
- indoly škodlivé účinky MeSH
- inhibitory enzymů farmakologie MeSH
- krevní tlak účinky léků fyziologie MeSH
- krysa rodu Rattus MeSH
- ledviny krevní zásobení patologie patofyziologie MeSH
- losartan farmakologie MeSH
- modely nemocí na zvířatech MeSH
- natriuréza účinky léků fyziologie MeSH
- nemoci ledvin patofyziologie prevence a kontrola MeSH
- potkani transgenní MeSH
- regionální krevní průtok účinky léků fyziologie MeSH
- renin genetika MeSH
- zvířata MeSH
- Check Tag
- krysa rodu Rattus MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- srovnávací studie MeSH
- Názvy látek
- blokátory receptoru 1 pro angiotenzin II MeSH
- cytochrom P-450 CYP1A1 MeSH
- epoxid hydrolasy MeSH
- indole-3-carbinol MeSH Prohlížeč
- indoly MeSH
- inhibitory enzymů MeSH
- losartan MeSH
- Ren2 protein, rat MeSH Prohlížeč
- 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