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Epoxyeicosatrienoic acid analog attenuates angiotensin II hypertension and kidney injury

Epoxyeicosatrienoic acids (EETs) contribute to blood pressure regulation leading to the concept that EETs can be therapeutically targeted for hypertension and the associated end organ damage. In the present study, we investigated anti-hypertensive and kidney protective actions of an EET analog, EET-...

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Autores principales: Hye Khan, Md. Abdul, Falck, John R., Manthati, Vijaya L., Campbell, William B., Imig, John D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4172029/
https://www.ncbi.nlm.nih.gov/pubmed/25295006
http://dx.doi.org/10.3389/fphar.2014.00216
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author Hye Khan, Md. Abdul
Falck, John R.
Manthati, Vijaya L.
Campbell, William B.
Imig, John D.
author_facet Hye Khan, Md. Abdul
Falck, John R.
Manthati, Vijaya L.
Campbell, William B.
Imig, John D.
author_sort Hye Khan, Md. Abdul
collection PubMed
description Epoxyeicosatrienoic acids (EETs) contribute to blood pressure regulation leading to the concept that EETs can be therapeutically targeted for hypertension and the associated end organ damage. In the present study, we investigated anti-hypertensive and kidney protective actions of an EET analog, EET-B in angiotensin II (ANG II)-induced hypertension. EET-B was administered in drinking water for 14 days (10 mg/kg/d) and resulted in a decreased blood pressure elevation in ANG II hypertension. At the end of the two-week period, blood pressure was 30 mmHg lower in EET analog-treated ANG II hypertensive rats. The vasodilation of mesenteric resistance arteries to acetylcholine was impaired in ANG II hypertension; however, it was improved with EET-B treatment. Further, EET-B protected the kidney in ANG II hypertension as evidenced by a marked 90% decrease in albuminuria and 54% decrease in nephrinuria. Kidney histology demonstrated a decrease in renal tubular cast formation in EET analog-treated hypertensive rats. In ANG II hypertension, EET-B treatment markedly lowered renal inflammation. Urinary monocyte chemoattractant protein-1 excretion was decreased by 55% and kidney macrophage infiltration was reduced by 52% with EET-B treatment. Overall, our results demonstrate that EET-B has anti-hypertensive properties, improves vascular function, and decreases renal inflammation and injury in ANG II hypertension.
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spelling pubmed-41720292014-10-07 Epoxyeicosatrienoic acid analog attenuates angiotensin II hypertension and kidney injury Hye Khan, Md. Abdul Falck, John R. Manthati, Vijaya L. Campbell, William B. Imig, John D. Front Pharmacol Pharmacology Epoxyeicosatrienoic acids (EETs) contribute to blood pressure regulation leading to the concept that EETs can be therapeutically targeted for hypertension and the associated end organ damage. In the present study, we investigated anti-hypertensive and kidney protective actions of an EET analog, EET-B in angiotensin II (ANG II)-induced hypertension. EET-B was administered in drinking water for 14 days (10 mg/kg/d) and resulted in a decreased blood pressure elevation in ANG II hypertension. At the end of the two-week period, blood pressure was 30 mmHg lower in EET analog-treated ANG II hypertensive rats. The vasodilation of mesenteric resistance arteries to acetylcholine was impaired in ANG II hypertension; however, it was improved with EET-B treatment. Further, EET-B protected the kidney in ANG II hypertension as evidenced by a marked 90% decrease in albuminuria and 54% decrease in nephrinuria. Kidney histology demonstrated a decrease in renal tubular cast formation in EET analog-treated hypertensive rats. In ANG II hypertension, EET-B treatment markedly lowered renal inflammation. Urinary monocyte chemoattractant protein-1 excretion was decreased by 55% and kidney macrophage infiltration was reduced by 52% with EET-B treatment. Overall, our results demonstrate that EET-B has anti-hypertensive properties, improves vascular function, and decreases renal inflammation and injury in ANG II hypertension. Frontiers Media S.A. 2014-09-23 /pmc/articles/PMC4172029/ /pubmed/25295006 http://dx.doi.org/10.3389/fphar.2014.00216 Text en Copyright © 2014 Hye Khan, Falck, Manthati, Campbell and Imig. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Hye Khan, Md. Abdul
Falck, John R.
Manthati, Vijaya L.
Campbell, William B.
Imig, John D.
Epoxyeicosatrienoic acid analog attenuates angiotensin II hypertension and kidney injury
title Epoxyeicosatrienoic acid analog attenuates angiotensin II hypertension and kidney injury
title_full Epoxyeicosatrienoic acid analog attenuates angiotensin II hypertension and kidney injury
title_fullStr Epoxyeicosatrienoic acid analog attenuates angiotensin II hypertension and kidney injury
title_full_unstemmed Epoxyeicosatrienoic acid analog attenuates angiotensin II hypertension and kidney injury
title_short Epoxyeicosatrienoic acid analog attenuates angiotensin II hypertension and kidney injury
title_sort epoxyeicosatrienoic acid analog attenuates angiotensin ii hypertension and kidney injury
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4172029/
https://www.ncbi.nlm.nih.gov/pubmed/25295006
http://dx.doi.org/10.3389/fphar.2014.00216
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