author_facet Plecevic, Sasa
Pechanova, Olga
Barta, Andrej
Vranic, Aleksandra
Jeremic, Jovana
Arsenijevic, Ljiljana
Jeremic, Nevena
Jakovljevic, Vladimir
Jevdjevic, Maja
Stanojevic, Dejan
Plecevic, Sasa
Pechanova, Olga
Barta, Andrej
Vranic, Aleksandra
Jeremic, Jovana
Arsenijevic, Ljiljana
Jeremic, Nevena
Jakovljevic, Vladimir
Jevdjevic, Maja
Stanojevic, Dejan
author Plecevic, Sasa
Pechanova, Olga
Barta, Andrej
Vranic, Aleksandra
Jeremic, Jovana
Arsenijevic, Ljiljana
Jeremic, Nevena
Jakovljevic, Vladimir
Jevdjevic, Maja
Stanojevic, Dejan
spellingShingle Plecevic, Sasa
Pechanova, Olga
Barta, Andrej
Vranic, Aleksandra
Jeremic, Jovana
Arsenijevic, Ljiljana
Jeremic, Nevena
Jakovljevic, Vladimir
Jevdjevic, Maja
Stanojevic, Dejan
Serbian Journal of Experimental and Clinical Research
Effects Of The Direct Renin Inhibitor Aliskiren On Oxidative Stress In Isolated Rat Heart
General Medicine
author_sort plecevic, sasa
spelling Plecevic, Sasa Pechanova, Olga Barta, Andrej Vranic, Aleksandra Jeremic, Jovana Arsenijevic, Ljiljana Jeremic, Nevena Jakovljevic, Vladimir Jevdjevic, Maja Stanojevic, Dejan 2335-075X Walter de Gruyter GmbH General Medicine http://dx.doi.org/10.1515/sjecr-2015-0025 <jats:title>Abstract</jats:title> <jats:p>Increased activity of the renin-angiotensin-aldosterone system (RAAS) plays a significant role in the development and progression of various cardio-metabolic diseases, such as hypertension, atherosclerosis and heart failure. Aliskiren is the newest antihypertensive drug and the first orally active direct renin inhibitor to become available for clinical use. This study investigated the acute and direct effects of Aliskiren on different parameters of oxidative stress on isolated rat heart. The hearts of male Wistar albino rats (n = 24, 8 per experimental group, age 8 weeks, body mass 180–200 g), were excised and retrogradely perfused according to the Langendorfftechnique at a gradually increasing perfusion pressure (40-120 cmH<jats:sub>2</jats:sub>O). Markers of oxidative stress (NO<jats:sub>2</jats:sub> <jats:sup>−</jats:sup>, TBARS, H<jats:sub>2</jats:sub>O<jats:sub>2</jats:sub> and O<jats:sub>2</jats:sub> <jats:sup>−</jats:sup>) were measured spectrophotometrically after perfusion with three different concentrations of Aliskiren (0.1 μM, 1 μM, and 10 μM). The results demonstrated possible dose-dependent cardioprotective properties of Aliskiren, particularly with higher CPP. Lipid peroxidation (TBARS) levels decreased with the highest dose of Aliskiren and higher CPP, and the same trend was observed in nitrite (NO<jats:sub>2</jats:sub> <jats:sup>−</jats:sup>) and hydrogen peroxide (H<jats:sub>2</jats:sub>O<jats:sub>2</jats:sub>) levels. These findings indicate that the acute effects of Aliskiren do not likely promote the production of reactive oxygen species upon higher pressure with the highest dose. Aliskiren may exert beneficial effects on oxidative stress biomarkers.</jats:p> Effects Of The Direct Renin Inhibitor Aliskiren On Oxidative Stress In Isolated Rat Heart Serbian Journal of Experimental and Clinical Research
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series Serbian Journal of Experimental and Clinical Research
source_id 49
title Effects Of The Direct Renin Inhibitor Aliskiren On Oxidative Stress In Isolated Rat Heart
title_unstemmed Effects Of The Direct Renin Inhibitor Aliskiren On Oxidative Stress In Isolated Rat Heart
title_full Effects Of The Direct Renin Inhibitor Aliskiren On Oxidative Stress In Isolated Rat Heart
title_fullStr Effects Of The Direct Renin Inhibitor Aliskiren On Oxidative Stress In Isolated Rat Heart
title_full_unstemmed Effects Of The Direct Renin Inhibitor Aliskiren On Oxidative Stress In Isolated Rat Heart
title_short Effects Of The Direct Renin Inhibitor Aliskiren On Oxidative Stress In Isolated Rat Heart
title_sort effects of the direct renin inhibitor aliskiren on oxidative stress in isolated rat heart
topic General Medicine
url http://dx.doi.org/10.1515/sjecr-2015-0025
publishDate 2015
physical 193-199
description <jats:title>Abstract</jats:title> <jats:p>Increased activity of the renin-angiotensin-aldosterone system (RAAS) plays a significant role in the development and progression of various cardio-metabolic diseases, such as hypertension, atherosclerosis and heart failure. Aliskiren is the newest antihypertensive drug and the first orally active direct renin inhibitor to become available for clinical use. This study investigated the acute and direct effects of Aliskiren on different parameters of oxidative stress on isolated rat heart. The hearts of male Wistar albino rats (n = 24, 8 per experimental group, age 8 weeks, body mass 180–200 g), were excised and retrogradely perfused according to the Langendorfftechnique at a gradually increasing perfusion pressure (40-120 cmH<jats:sub>2</jats:sub>O). Markers of oxidative stress (NO<jats:sub>2</jats:sub> <jats:sup>−</jats:sup>, TBARS, H<jats:sub>2</jats:sub>O<jats:sub>2</jats:sub> and O<jats:sub>2</jats:sub> <jats:sup>−</jats:sup>) were measured spectrophotometrically after perfusion with three different concentrations of Aliskiren (0.1 μM, 1 μM, and 10 μM). The results demonstrated possible dose-dependent cardioprotective properties of Aliskiren, particularly with higher CPP. Lipid peroxidation (TBARS) levels decreased with the highest dose of Aliskiren and higher CPP, and the same trend was observed in nitrite (NO<jats:sub>2</jats:sub> <jats:sup>−</jats:sup>) and hydrogen peroxide (H<jats:sub>2</jats:sub>O<jats:sub>2</jats:sub>) levels. These findings indicate that the acute effects of Aliskiren do not likely promote the production of reactive oxygen species upon higher pressure with the highest dose. Aliskiren may exert beneficial effects on oxidative stress biomarkers.</jats:p>
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author Plecevic, Sasa, Pechanova, Olga, Barta, Andrej, Vranic, Aleksandra, Jeremic, Jovana, Arsenijevic, Ljiljana, Jeremic, Nevena, Jakovljevic, Vladimir, Jevdjevic, Maja, Stanojevic, Dejan
author_facet Plecevic, Sasa, Pechanova, Olga, Barta, Andrej, Vranic, Aleksandra, Jeremic, Jovana, Arsenijevic, Ljiljana, Jeremic, Nevena, Jakovljevic, Vladimir, Jevdjevic, Maja, Stanojevic, Dejan, Plecevic, Sasa, Pechanova, Olga, Barta, Andrej, Vranic, Aleksandra, Jeremic, Jovana, Arsenijevic, Ljiljana, Jeremic, Nevena, Jakovljevic, Vladimir, Jevdjevic, Maja, Stanojevic, Dejan
author_sort plecevic, sasa
container_issue 3
container_start_page 193
container_title Serbian Journal of Experimental and Clinical Research
container_volume 16
description <jats:title>Abstract</jats:title> <jats:p>Increased activity of the renin-angiotensin-aldosterone system (RAAS) plays a significant role in the development and progression of various cardio-metabolic diseases, such as hypertension, atherosclerosis and heart failure. Aliskiren is the newest antihypertensive drug and the first orally active direct renin inhibitor to become available for clinical use. This study investigated the acute and direct effects of Aliskiren on different parameters of oxidative stress on isolated rat heart. The hearts of male Wistar albino rats (n = 24, 8 per experimental group, age 8 weeks, body mass 180–200 g), were excised and retrogradely perfused according to the Langendorfftechnique at a gradually increasing perfusion pressure (40-120 cmH<jats:sub>2</jats:sub>O). Markers of oxidative stress (NO<jats:sub>2</jats:sub> <jats:sup>−</jats:sup>, TBARS, H<jats:sub>2</jats:sub>O<jats:sub>2</jats:sub> and O<jats:sub>2</jats:sub> <jats:sup>−</jats:sup>) were measured spectrophotometrically after perfusion with three different concentrations of Aliskiren (0.1 μM, 1 μM, and 10 μM). The results demonstrated possible dose-dependent cardioprotective properties of Aliskiren, particularly with higher CPP. Lipid peroxidation (TBARS) levels decreased with the highest dose of Aliskiren and higher CPP, and the same trend was observed in nitrite (NO<jats:sub>2</jats:sub> <jats:sup>−</jats:sup>) and hydrogen peroxide (H<jats:sub>2</jats:sub>O<jats:sub>2</jats:sub>) levels. These findings indicate that the acute effects of Aliskiren do not likely promote the production of reactive oxygen species upon higher pressure with the highest dose. Aliskiren may exert beneficial effects on oxidative stress biomarkers.</jats:p>
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spelling Plecevic, Sasa Pechanova, Olga Barta, Andrej Vranic, Aleksandra Jeremic, Jovana Arsenijevic, Ljiljana Jeremic, Nevena Jakovljevic, Vladimir Jevdjevic, Maja Stanojevic, Dejan 2335-075X Walter de Gruyter GmbH General Medicine http://dx.doi.org/10.1515/sjecr-2015-0025 <jats:title>Abstract</jats:title> <jats:p>Increased activity of the renin-angiotensin-aldosterone system (RAAS) plays a significant role in the development and progression of various cardio-metabolic diseases, such as hypertension, atherosclerosis and heart failure. Aliskiren is the newest antihypertensive drug and the first orally active direct renin inhibitor to become available for clinical use. This study investigated the acute and direct effects of Aliskiren on different parameters of oxidative stress on isolated rat heart. The hearts of male Wistar albino rats (n = 24, 8 per experimental group, age 8 weeks, body mass 180–200 g), were excised and retrogradely perfused according to the Langendorfftechnique at a gradually increasing perfusion pressure (40-120 cmH<jats:sub>2</jats:sub>O). Markers of oxidative stress (NO<jats:sub>2</jats:sub> <jats:sup>−</jats:sup>, TBARS, H<jats:sub>2</jats:sub>O<jats:sub>2</jats:sub> and O<jats:sub>2</jats:sub> <jats:sup>−</jats:sup>) were measured spectrophotometrically after perfusion with three different concentrations of Aliskiren (0.1 μM, 1 μM, and 10 μM). The results demonstrated possible dose-dependent cardioprotective properties of Aliskiren, particularly with higher CPP. Lipid peroxidation (TBARS) levels decreased with the highest dose of Aliskiren and higher CPP, and the same trend was observed in nitrite (NO<jats:sub>2</jats:sub> <jats:sup>−</jats:sup>) and hydrogen peroxide (H<jats:sub>2</jats:sub>O<jats:sub>2</jats:sub>) levels. These findings indicate that the acute effects of Aliskiren do not likely promote the production of reactive oxygen species upon higher pressure with the highest dose. Aliskiren may exert beneficial effects on oxidative stress biomarkers.</jats:p> Effects Of The Direct Renin Inhibitor Aliskiren On Oxidative Stress In Isolated Rat Heart Serbian Journal of Experimental and Clinical Research
spellingShingle Plecevic, Sasa, Pechanova, Olga, Barta, Andrej, Vranic, Aleksandra, Jeremic, Jovana, Arsenijevic, Ljiljana, Jeremic, Nevena, Jakovljevic, Vladimir, Jevdjevic, Maja, Stanojevic, Dejan, Serbian Journal of Experimental and Clinical Research, Effects Of The Direct Renin Inhibitor Aliskiren On Oxidative Stress In Isolated Rat Heart, General Medicine
title Effects Of The Direct Renin Inhibitor Aliskiren On Oxidative Stress In Isolated Rat Heart
title_full Effects Of The Direct Renin Inhibitor Aliskiren On Oxidative Stress In Isolated Rat Heart
title_fullStr Effects Of The Direct Renin Inhibitor Aliskiren On Oxidative Stress In Isolated Rat Heart
title_full_unstemmed Effects Of The Direct Renin Inhibitor Aliskiren On Oxidative Stress In Isolated Rat Heart
title_short Effects Of The Direct Renin Inhibitor Aliskiren On Oxidative Stress In Isolated Rat Heart
title_sort effects of the direct renin inhibitor aliskiren on oxidative stress in isolated rat heart
title_unstemmed Effects Of The Direct Renin Inhibitor Aliskiren On Oxidative Stress In Isolated Rat Heart
topic General Medicine
url http://dx.doi.org/10.1515/sjecr-2015-0025