Impaired Production and Diurnal Regulation of Vascular RvDn-3 DPA Increase Systemic Inflammation and Cardiovascular DiseaseNovelty and Significance [Clinical Track]

Publication Date:
2018-03-16
Publisher:
American Heart Association (AHA)
Print ISSN:
0009-7330
Electronic ISSN:
1524-4571
Topics:
Medicine
Keywords:
Biomarkers, Inflammation, Mechanisms, Pathophysiology, Physiology
Published by:
_version_ 1836398847759220736
autor Romain A. Colas, Patricia R. Souza, Mary E. Walker, Maudrian Burton, Zbigniew Zasłona, Annie M. Curtis, Raquel M. Marques, Jesmond Dalli
beschreibung Rationale:Diurnal mechanisms are central to regulating host responses. Recent studies uncovered a novel family of mediators termed as specialized proresolving mediators that terminate inflammation without interfering with the immune response.Objective:Herein, we investigated the diurnal regulation of specialized proresolving mediators in humans and their role in controlling peripheral blood leukocyte and platelet activation.Methods and Results:Using lipid mediator profiling and healthy volunteers, we found that plasma concentrations of n-3 docosapentaenoic acid-derived D-series resolvins (RvDn-3 DPA) were regulated in a diurnal manner. The production and regulation of these mediators was markedly altered in patients at risk of myocardial infarct. These changes were associated with decreased 5-lipoxygenase expression and activity, as well as increased systemic adenosine concentrations. We also found a significant negative correlation between plasma RvDn-3 DPA and markers of platelet, monocyte, and neutrophil activation, including CD63 and CD11b. Incubation of RvDn-3 DPA with peripheral blood from healthy volunteers and patients with cardiovascular disease significantly and dose-dependently decreased platelet and leukocyte activation. Furthermore, administration of RvD5n-3 DPA to ApoE−/− (apolipoprotein E deficient) mice significantly reduced platelet–leukocyte aggregates, vascular thromboxane B2 concentrations, and aortic lesions.Conclusions:These results demonstrate that peripheral blood RvDn-3 DPA are diurnally regulated in humans, and dysregulation in the production of these mediators may lead to cardiovascular disease.
citation_standardnr 6208007
datenlieferant ipn_articles
feed_id 321
feed_publisher American Heart Association (AHA)
feed_publisher_url http://www.americanheart.org/
insertion_date 2018-03-16
journaleissn 1524-4571
journalissn 0009-7330
publikationsjahr_anzeige 2018
publikationsjahr_facette 2018
publikationsjahr_intervall 7984:2015-2019
publikationsjahr_sort 2018
publisher American Heart Association (AHA)
quelle Circulation Research
relation http://circres.ahajournals.org/content/122/6/855.short?rss=1
schlagwort Biomarkers, Inflammation, Mechanisms, Pathophysiology, Physiology
search_space articles
shingle_author_1 Romain A. Colas, Patricia R. Souza, Mary E. Walker, Maudrian Burton, Zbigniew Zasłona, Annie M. Curtis, Raquel M. Marques, Jesmond Dalli
shingle_author_2 Romain A. Colas, Patricia R. Souza, Mary E. Walker, Maudrian Burton, Zbigniew Zasłona, Annie M. Curtis, Raquel M. Marques, Jesmond Dalli
shingle_author_3 Romain A. Colas, Patricia R. Souza, Mary E. Walker, Maudrian Burton, Zbigniew Zasłona, Annie M. Curtis, Raquel M. Marques, Jesmond Dalli
shingle_author_4 Romain A. Colas, Patricia R. Souza, Mary E. Walker, Maudrian Burton, Zbigniew Zasłona, Annie M. Curtis, Raquel M. Marques, Jesmond Dalli
shingle_catch_all_1 Impaired Production and Diurnal Regulation of Vascular RvDn-3 DPA Increase Systemic Inflammation and Cardiovascular DiseaseNovelty and Significance [Clinical Track]
Biomarkers, Inflammation, Mechanisms, Pathophysiology, Physiology
Rationale:Diurnal mechanisms are central to regulating host responses. Recent studies uncovered a novel family of mediators termed as specialized proresolving mediators that terminate inflammation without interfering with the immune response.Objective:Herein, we investigated the diurnal regulation of specialized proresolving mediators in humans and their role in controlling peripheral blood leukocyte and platelet activation.Methods and Results:Using lipid mediator profiling and healthy volunteers, we found that plasma concentrations of n-3 docosapentaenoic acid-derived D-series resolvins (RvDn-3 DPA) were regulated in a diurnal manner. The production and regulation of these mediators was markedly altered in patients at risk of myocardial infarct. These changes were associated with decreased 5-lipoxygenase expression and activity, as well as increased systemic adenosine concentrations. We also found a significant negative correlation between plasma RvDn-3 DPA and markers of platelet, monocyte, and neutrophil activation, including CD63 and CD11b. Incubation of RvDn-3 DPA with peripheral blood from healthy volunteers and patients with cardiovascular disease significantly and dose-dependently decreased platelet and leukocyte activation. Furthermore, administration of RvD5n-3 DPA to ApoE−/− (apolipoprotein E deficient) mice significantly reduced platelet–leukocyte aggregates, vascular thromboxane B2 concentrations, and aortic lesions.Conclusions:These results demonstrate that peripheral blood RvDn-3 DPA are diurnally regulated in humans, and dysregulation in the production of these mediators may lead to cardiovascular disease.
Romain A. Colas, Patricia R. Souza, Mary E. Walker, Maudrian Burton, Zbigniew Zasłona, Annie M. Curtis, Raquel M. Marques, Jesmond Dalli
American Heart Association (AHA)
0009-7330
00097330
1524-4571
15244571
shingle_catch_all_2 Impaired Production and Diurnal Regulation of Vascular RvDn-3 DPA Increase Systemic Inflammation and Cardiovascular DiseaseNovelty and Significance [Clinical Track]
Biomarkers, Inflammation, Mechanisms, Pathophysiology, Physiology
Rationale:Diurnal mechanisms are central to regulating host responses. Recent studies uncovered a novel family of mediators termed as specialized proresolving mediators that terminate inflammation without interfering with the immune response.Objective:Herein, we investigated the diurnal regulation of specialized proresolving mediators in humans and their role in controlling peripheral blood leukocyte and platelet activation.Methods and Results:Using lipid mediator profiling and healthy volunteers, we found that plasma concentrations of n-3 docosapentaenoic acid-derived D-series resolvins (RvDn-3 DPA) were regulated in a diurnal manner. The production and regulation of these mediators was markedly altered in patients at risk of myocardial infarct. These changes were associated with decreased 5-lipoxygenase expression and activity, as well as increased systemic adenosine concentrations. We also found a significant negative correlation between plasma RvDn-3 DPA and markers of platelet, monocyte, and neutrophil activation, including CD63 and CD11b. Incubation of RvDn-3 DPA with peripheral blood from healthy volunteers and patients with cardiovascular disease significantly and dose-dependently decreased platelet and leukocyte activation. Furthermore, administration of RvD5n-3 DPA to ApoE−/− (apolipoprotein E deficient) mice significantly reduced platelet–leukocyte aggregates, vascular thromboxane B2 concentrations, and aortic lesions.Conclusions:These results demonstrate that peripheral blood RvDn-3 DPA are diurnally regulated in humans, and dysregulation in the production of these mediators may lead to cardiovascular disease.
Romain A. Colas, Patricia R. Souza, Mary E. Walker, Maudrian Burton, Zbigniew Zasłona, Annie M. Curtis, Raquel M. Marques, Jesmond Dalli
American Heart Association (AHA)
0009-7330
00097330
1524-4571
15244571
shingle_catch_all_3 Impaired Production and Diurnal Regulation of Vascular RvDn-3 DPA Increase Systemic Inflammation and Cardiovascular DiseaseNovelty and Significance [Clinical Track]
Biomarkers, Inflammation, Mechanisms, Pathophysiology, Physiology
Rationale:Diurnal mechanisms are central to regulating host responses. Recent studies uncovered a novel family of mediators termed as specialized proresolving mediators that terminate inflammation without interfering with the immune response.Objective:Herein, we investigated the diurnal regulation of specialized proresolving mediators in humans and their role in controlling peripheral blood leukocyte and platelet activation.Methods and Results:Using lipid mediator profiling and healthy volunteers, we found that plasma concentrations of n-3 docosapentaenoic acid-derived D-series resolvins (RvDn-3 DPA) were regulated in a diurnal manner. The production and regulation of these mediators was markedly altered in patients at risk of myocardial infarct. These changes were associated with decreased 5-lipoxygenase expression and activity, as well as increased systemic adenosine concentrations. We also found a significant negative correlation between plasma RvDn-3 DPA and markers of platelet, monocyte, and neutrophil activation, including CD63 and CD11b. Incubation of RvDn-3 DPA with peripheral blood from healthy volunteers and patients with cardiovascular disease significantly and dose-dependently decreased platelet and leukocyte activation. Furthermore, administration of RvD5n-3 DPA to ApoE−/− (apolipoprotein E deficient) mice significantly reduced platelet–leukocyte aggregates, vascular thromboxane B2 concentrations, and aortic lesions.Conclusions:These results demonstrate that peripheral blood RvDn-3 DPA are diurnally regulated in humans, and dysregulation in the production of these mediators may lead to cardiovascular disease.
Romain A. Colas, Patricia R. Souza, Mary E. Walker, Maudrian Burton, Zbigniew Zasłona, Annie M. Curtis, Raquel M. Marques, Jesmond Dalli
American Heart Association (AHA)
0009-7330
00097330
1524-4571
15244571
shingle_catch_all_4 Impaired Production and Diurnal Regulation of Vascular RvDn-3 DPA Increase Systemic Inflammation and Cardiovascular DiseaseNovelty and Significance [Clinical Track]
Biomarkers, Inflammation, Mechanisms, Pathophysiology, Physiology
Rationale:Diurnal mechanisms are central to regulating host responses. Recent studies uncovered a novel family of mediators termed as specialized proresolving mediators that terminate inflammation without interfering with the immune response.Objective:Herein, we investigated the diurnal regulation of specialized proresolving mediators in humans and their role in controlling peripheral blood leukocyte and platelet activation.Methods and Results:Using lipid mediator profiling and healthy volunteers, we found that plasma concentrations of n-3 docosapentaenoic acid-derived D-series resolvins (RvDn-3 DPA) were regulated in a diurnal manner. The production and regulation of these mediators was markedly altered in patients at risk of myocardial infarct. These changes were associated with decreased 5-lipoxygenase expression and activity, as well as increased systemic adenosine concentrations. We also found a significant negative correlation between plasma RvDn-3 DPA and markers of platelet, monocyte, and neutrophil activation, including CD63 and CD11b. Incubation of RvDn-3 DPA with peripheral blood from healthy volunteers and patients with cardiovascular disease significantly and dose-dependently decreased platelet and leukocyte activation. Furthermore, administration of RvD5n-3 DPA to ApoE−/− (apolipoprotein E deficient) mice significantly reduced platelet–leukocyte aggregates, vascular thromboxane B2 concentrations, and aortic lesions.Conclusions:These results demonstrate that peripheral blood RvDn-3 DPA are diurnally regulated in humans, and dysregulation in the production of these mediators may lead to cardiovascular disease.
Romain A. Colas, Patricia R. Souza, Mary E. Walker, Maudrian Burton, Zbigniew Zasłona, Annie M. Curtis, Raquel M. Marques, Jesmond Dalli
American Heart Association (AHA)
0009-7330
00097330
1524-4571
15244571
shingle_title_1 Impaired Production and Diurnal Regulation of Vascular RvDn-3 DPA Increase Systemic Inflammation and Cardiovascular DiseaseNovelty and Significance [Clinical Track]
shingle_title_2 Impaired Production and Diurnal Regulation of Vascular RvDn-3 DPA Increase Systemic Inflammation and Cardiovascular DiseaseNovelty and Significance [Clinical Track]
shingle_title_3 Impaired Production and Diurnal Regulation of Vascular RvDn-3 DPA Increase Systemic Inflammation and Cardiovascular DiseaseNovelty and Significance [Clinical Track]
shingle_title_4 Impaired Production and Diurnal Regulation of Vascular RvDn-3 DPA Increase Systemic Inflammation and Cardiovascular DiseaseNovelty and Significance [Clinical Track]
timestamp 2025-06-30T23:33:35.037Z
titel Impaired Production and Diurnal Regulation of Vascular RvDn-3 DPA Increase Systemic Inflammation and Cardiovascular DiseaseNovelty and Significance [Clinical Track]
titel_suche Impaired Production and Diurnal Regulation of Vascular RvDn-3 DPA Increase Systemic Inflammation and Cardiovascular DiseaseNovelty and Significance [Clinical Track]
topic WW-YZ
uid ipn_articles_6208007