P4.18 ANTIHYPERTENSIVE ACTIVITY OF LONG CHAIN FATTY ACID DERIVATIVES OF FLAVONOIDS VIA INHIBITION OF RENIN-ANGIOTENSIN-ALDOSTERONE SYSTEM (RAAS)

Hypertension is a contributing factor to pathophysiology of vascular damage and accelerated arterial stiffening. Renin-angiotensin-aldosterone system (RAAS) inhibitors are widely used for treatment of persistent hypertension. Along with conventional antihypertensive therapy, nutritional intervention...

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Main Authors: Bhullar Khushwant Singh, Zia ullah, Rupasinghe Vasantha
Format: Article
Language:English
Published: Atlantis Press 2013-11-01
Series:Artery Research
Online Access:https://www.atlantis-press.com/article/125939030/view
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spelling doaj-bf943f1f576d41fb8491f1f5759ca14f2020-11-25T03:20:19ZengAtlantis PressArtery Research 1876-44012013-11-0171010.1016/j.artres.2013.10.136P4.18 ANTIHYPERTENSIVE ACTIVITY OF LONG CHAIN FATTY ACID DERIVATIVES OF FLAVONOIDS VIA INHIBITION OF RENIN-ANGIOTENSIN-ALDOSTERONE SYSTEM (RAAS)Bhullar Khushwant SinghZia ullahRupasinghe VasanthaHypertension is a contributing factor to pathophysiology of vascular damage and accelerated arterial stiffening. Renin-angiotensin-aldosterone system (RAAS) inhibitors are widely used for treatment of persistent hypertension. Along with conventional antihypertensive therapy, nutritional intervention has also gained attention as arterial and vascular complications are closely associated with dietary and lifestyle risk factors. Flavonoids and omega-3 polyunsaturated fatty acids (PUFA) are the key antihypertensive biomolecules emerging to prevent and manage hypertension. In the current study, twelve long chain fatty acid derivatives of isoquercitrin (Q3G) and phloridzin (PZ) were investigated for inhibition of angiotensin-converting enzyme (ACE), renin and aldosterone synthase in comparison to their parent compounds in vitro. The linoleic and α-linolenic esters of PZ were the strongest (IC50 69.9–70.8 μM) while Q3G and PZ (IC50 >200 μM) were the weakest renin inhibitors in vitro (p<0.05). Similar to renin inhibition, PZ derivatives exhibited stronger ACE inhibition compared to Q3G. The eicosapentaenoic acid (EPA) ester of PZ (IC50 16.03 μM) was the strongest, while PZ (IC50 123.96 μM) was the weakest ACE inhibitor (p<0.05) among all tested compounds. However, all investigated compounds had no effect on aldosterone synthase inhibition (p<0.05). Overall, the results showed that phloridzin derivatives were stronger antihypertensive agents than isoquercitrin. It is indicated from our study that these novel compounds as dual RAAS inhibitors may be used as potent bioactive ingredients to develop functional foods and nutraceuticals for prevention and treatment of high blood pressure.https://www.atlantis-press.com/article/125939030/view
collection DOAJ
language English
format Article
sources DOAJ
author Bhullar Khushwant Singh
Zia ullah
Rupasinghe Vasantha
spellingShingle Bhullar Khushwant Singh
Zia ullah
Rupasinghe Vasantha
P4.18 ANTIHYPERTENSIVE ACTIVITY OF LONG CHAIN FATTY ACID DERIVATIVES OF FLAVONOIDS VIA INHIBITION OF RENIN-ANGIOTENSIN-ALDOSTERONE SYSTEM (RAAS)
Artery Research
author_facet Bhullar Khushwant Singh
Zia ullah
Rupasinghe Vasantha
author_sort Bhullar Khushwant Singh
title P4.18 ANTIHYPERTENSIVE ACTIVITY OF LONG CHAIN FATTY ACID DERIVATIVES OF FLAVONOIDS VIA INHIBITION OF RENIN-ANGIOTENSIN-ALDOSTERONE SYSTEM (RAAS)
title_short P4.18 ANTIHYPERTENSIVE ACTIVITY OF LONG CHAIN FATTY ACID DERIVATIVES OF FLAVONOIDS VIA INHIBITION OF RENIN-ANGIOTENSIN-ALDOSTERONE SYSTEM (RAAS)
title_full P4.18 ANTIHYPERTENSIVE ACTIVITY OF LONG CHAIN FATTY ACID DERIVATIVES OF FLAVONOIDS VIA INHIBITION OF RENIN-ANGIOTENSIN-ALDOSTERONE SYSTEM (RAAS)
title_fullStr P4.18 ANTIHYPERTENSIVE ACTIVITY OF LONG CHAIN FATTY ACID DERIVATIVES OF FLAVONOIDS VIA INHIBITION OF RENIN-ANGIOTENSIN-ALDOSTERONE SYSTEM (RAAS)
title_full_unstemmed P4.18 ANTIHYPERTENSIVE ACTIVITY OF LONG CHAIN FATTY ACID DERIVATIVES OF FLAVONOIDS VIA INHIBITION OF RENIN-ANGIOTENSIN-ALDOSTERONE SYSTEM (RAAS)
title_sort p4.18 antihypertensive activity of long chain fatty acid derivatives of flavonoids via inhibition of renin-angiotensin-aldosterone system (raas)
publisher Atlantis Press
series Artery Research
issn 1876-4401
publishDate 2013-11-01
description Hypertension is a contributing factor to pathophysiology of vascular damage and accelerated arterial stiffening. Renin-angiotensin-aldosterone system (RAAS) inhibitors are widely used for treatment of persistent hypertension. Along with conventional antihypertensive therapy, nutritional intervention has also gained attention as arterial and vascular complications are closely associated with dietary and lifestyle risk factors. Flavonoids and omega-3 polyunsaturated fatty acids (PUFA) are the key antihypertensive biomolecules emerging to prevent and manage hypertension. In the current study, twelve long chain fatty acid derivatives of isoquercitrin (Q3G) and phloridzin (PZ) were investigated for inhibition of angiotensin-converting enzyme (ACE), renin and aldosterone synthase in comparison to their parent compounds in vitro. The linoleic and α-linolenic esters of PZ were the strongest (IC50 69.9–70.8 μM) while Q3G and PZ (IC50 >200 μM) were the weakest renin inhibitors in vitro (p<0.05). Similar to renin inhibition, PZ derivatives exhibited stronger ACE inhibition compared to Q3G. The eicosapentaenoic acid (EPA) ester of PZ (IC50 16.03 μM) was the strongest, while PZ (IC50 123.96 μM) was the weakest ACE inhibitor (p<0.05) among all tested compounds. However, all investigated compounds had no effect on aldosterone synthase inhibition (p<0.05). Overall, the results showed that phloridzin derivatives were stronger antihypertensive agents than isoquercitrin. It is indicated from our study that these novel compounds as dual RAAS inhibitors may be used as potent bioactive ingredients to develop functional foods and nutraceuticals for prevention and treatment of high blood pressure.
url https://www.atlantis-press.com/article/125939030/view
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