Cargando…

Implication of Free Fatty Acids in Thrombin Generation and Fibrinolysis in Vascular Inflammation in Zucker Rats and Evolution with Aging

Background: The metabolic syndrome (MetS) and aging are associated with modifications in blood coagulation factors, vascular inflammation, and increased risk of thrombosis. Objectives: Our aim was to determine concomitant changes in thrombin generation in the blood compartment and at the surface of...

Descripción completa

Detalles Bibliográficos
Autores principales: Lagrange, Jérémy, Didelot, Mélusine, Mohamadi, Amel, Walton, Lucy A., Bloemen, Saartje, de Laat, Bas, Louis, Huguette, Thornton, Simon N., Derby, Brian, Sherratt, Michael J., Fève, Bruno, Challande, Pascal, Akhtar, Riaz, Cruickshank, J. Kennedy, Lacolley, Patrick, Regnault, Véronique
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5702631/
https://www.ncbi.nlm.nih.gov/pubmed/29213245
http://dx.doi.org/10.3389/fphys.2017.00949
_version_ 1783281562239893504
author Lagrange, Jérémy
Didelot, Mélusine
Mohamadi, Amel
Walton, Lucy A.
Bloemen, Saartje
de Laat, Bas
Louis, Huguette
Thornton, Simon N.
Derby, Brian
Sherratt, Michael J.
Fève, Bruno
Challande, Pascal
Akhtar, Riaz
Cruickshank, J. Kennedy
Lacolley, Patrick
Regnault, Véronique
author_facet Lagrange, Jérémy
Didelot, Mélusine
Mohamadi, Amel
Walton, Lucy A.
Bloemen, Saartje
de Laat, Bas
Louis, Huguette
Thornton, Simon N.
Derby, Brian
Sherratt, Michael J.
Fève, Bruno
Challande, Pascal
Akhtar, Riaz
Cruickshank, J. Kennedy
Lacolley, Patrick
Regnault, Véronique
author_sort Lagrange, Jérémy
collection PubMed
description Background: The metabolic syndrome (MetS) and aging are associated with modifications in blood coagulation factors, vascular inflammation, and increased risk of thrombosis. Objectives: Our aim was to determine concomitant changes in thrombin generation in the blood compartment and at the surface of vascular smooth muscle cells (VSMCs) and its interplay with adipokines, free fatty acids (FFA), and metalloproteinases (MMPs) in obese Zucker rats that share features of the human MetS. Methods: Obese and age-matched lean Zucker rats were compared at 25 and 80 weeks of age. Thrombin generation was assessed by calibrated automated thrombography (CAT). Results: Endogenous thrombin potential (ETP) was increased in obese rats independent of platelets and age. Clot half-lysis time was delayed with obesity and age. Interleukin (IL)-1β and IL-13 were increased with obesity and age respectively. Addition of exogenous fibrinogen, leptin, linoleic, or palmitic acid increased thrombin generation in plasma whereas adiponectin had an opposite effect. ETP was increased at the surface of VSMCs from obese rats and addition of exogenous palmitic acid further enhanced ETP values. Gelatinase activity was increased in aorta at both ages in obese rats and MMP-2 activity was increased in VSMCs from obese rats. Conclusions: Our study demonstrated in MetS an early prothrombotic phenotype of the blood compartment reinforced by procoagulant properties of dedifferentiated and inflammatory VSMCs. Mechanisms involved (1) increased fibrinogen and impaired fibrinolysis and (2) increased saturated fatty acids responsible for additive procoagulant effects. Whether specifically targeting this hypercoagulability using direct thrombin inhibitors would improve outcome in MetS is worth investigating.
format Online
Article
Text
id pubmed-5702631
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-57026312017-12-06 Implication of Free Fatty Acids in Thrombin Generation and Fibrinolysis in Vascular Inflammation in Zucker Rats and Evolution with Aging Lagrange, Jérémy Didelot, Mélusine Mohamadi, Amel Walton, Lucy A. Bloemen, Saartje de Laat, Bas Louis, Huguette Thornton, Simon N. Derby, Brian Sherratt, Michael J. Fève, Bruno Challande, Pascal Akhtar, Riaz Cruickshank, J. Kennedy Lacolley, Patrick Regnault, Véronique Front Physiol Physiology Background: The metabolic syndrome (MetS) and aging are associated with modifications in blood coagulation factors, vascular inflammation, and increased risk of thrombosis. Objectives: Our aim was to determine concomitant changes in thrombin generation in the blood compartment and at the surface of vascular smooth muscle cells (VSMCs) and its interplay with adipokines, free fatty acids (FFA), and metalloproteinases (MMPs) in obese Zucker rats that share features of the human MetS. Methods: Obese and age-matched lean Zucker rats were compared at 25 and 80 weeks of age. Thrombin generation was assessed by calibrated automated thrombography (CAT). Results: Endogenous thrombin potential (ETP) was increased in obese rats independent of platelets and age. Clot half-lysis time was delayed with obesity and age. Interleukin (IL)-1β and IL-13 were increased with obesity and age respectively. Addition of exogenous fibrinogen, leptin, linoleic, or palmitic acid increased thrombin generation in plasma whereas adiponectin had an opposite effect. ETP was increased at the surface of VSMCs from obese rats and addition of exogenous palmitic acid further enhanced ETP values. Gelatinase activity was increased in aorta at both ages in obese rats and MMP-2 activity was increased in VSMCs from obese rats. Conclusions: Our study demonstrated in MetS an early prothrombotic phenotype of the blood compartment reinforced by procoagulant properties of dedifferentiated and inflammatory VSMCs. Mechanisms involved (1) increased fibrinogen and impaired fibrinolysis and (2) increased saturated fatty acids responsible for additive procoagulant effects. Whether specifically targeting this hypercoagulability using direct thrombin inhibitors would improve outcome in MetS is worth investigating. Frontiers Media S.A. 2017-11-22 /pmc/articles/PMC5702631/ /pubmed/29213245 http://dx.doi.org/10.3389/fphys.2017.00949 Text en Copyright © 2017 Lagrange, Didelot, Mohamadi, Walton, Bloemen, de Laat, Louis, Thornton, Derby, Sherratt, Fève, Challande, Akhtar, Cruickshank, Lacolley and Regnault. 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 Physiology
Lagrange, Jérémy
Didelot, Mélusine
Mohamadi, Amel
Walton, Lucy A.
Bloemen, Saartje
de Laat, Bas
Louis, Huguette
Thornton, Simon N.
Derby, Brian
Sherratt, Michael J.
Fève, Bruno
Challande, Pascal
Akhtar, Riaz
Cruickshank, J. Kennedy
Lacolley, Patrick
Regnault, Véronique
Implication of Free Fatty Acids in Thrombin Generation and Fibrinolysis in Vascular Inflammation in Zucker Rats and Evolution with Aging
title Implication of Free Fatty Acids in Thrombin Generation and Fibrinolysis in Vascular Inflammation in Zucker Rats and Evolution with Aging
title_full Implication of Free Fatty Acids in Thrombin Generation and Fibrinolysis in Vascular Inflammation in Zucker Rats and Evolution with Aging
title_fullStr Implication of Free Fatty Acids in Thrombin Generation and Fibrinolysis in Vascular Inflammation in Zucker Rats and Evolution with Aging
title_full_unstemmed Implication of Free Fatty Acids in Thrombin Generation and Fibrinolysis in Vascular Inflammation in Zucker Rats and Evolution with Aging
title_short Implication of Free Fatty Acids in Thrombin Generation and Fibrinolysis in Vascular Inflammation in Zucker Rats and Evolution with Aging
title_sort implication of free fatty acids in thrombin generation and fibrinolysis in vascular inflammation in zucker rats and evolution with aging
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5702631/
https://www.ncbi.nlm.nih.gov/pubmed/29213245
http://dx.doi.org/10.3389/fphys.2017.00949
work_keys_str_mv AT lagrangejeremy implicationoffreefattyacidsinthrombingenerationandfibrinolysisinvascularinflammationinzuckerratsandevolutionwithaging
AT didelotmelusine implicationoffreefattyacidsinthrombingenerationandfibrinolysisinvascularinflammationinzuckerratsandevolutionwithaging
AT mohamadiamel implicationoffreefattyacidsinthrombingenerationandfibrinolysisinvascularinflammationinzuckerratsandevolutionwithaging
AT waltonlucya implicationoffreefattyacidsinthrombingenerationandfibrinolysisinvascularinflammationinzuckerratsandevolutionwithaging
AT bloemensaartje implicationoffreefattyacidsinthrombingenerationandfibrinolysisinvascularinflammationinzuckerratsandevolutionwithaging
AT delaatbas implicationoffreefattyacidsinthrombingenerationandfibrinolysisinvascularinflammationinzuckerratsandevolutionwithaging
AT louishuguette implicationoffreefattyacidsinthrombingenerationandfibrinolysisinvascularinflammationinzuckerratsandevolutionwithaging
AT thorntonsimonn implicationoffreefattyacidsinthrombingenerationandfibrinolysisinvascularinflammationinzuckerratsandevolutionwithaging
AT derbybrian implicationoffreefattyacidsinthrombingenerationandfibrinolysisinvascularinflammationinzuckerratsandevolutionwithaging
AT sherrattmichaelj implicationoffreefattyacidsinthrombingenerationandfibrinolysisinvascularinflammationinzuckerratsandevolutionwithaging
AT fevebruno implicationoffreefattyacidsinthrombingenerationandfibrinolysisinvascularinflammationinzuckerratsandevolutionwithaging
AT challandepascal implicationoffreefattyacidsinthrombingenerationandfibrinolysisinvascularinflammationinzuckerratsandevolutionwithaging
AT akhtarriaz implicationoffreefattyacidsinthrombingenerationandfibrinolysisinvascularinflammationinzuckerratsandevolutionwithaging
AT cruickshankjkennedy implicationoffreefattyacidsinthrombingenerationandfibrinolysisinvascularinflammationinzuckerratsandevolutionwithaging
AT lacolleypatrick implicationoffreefattyacidsinthrombingenerationandfibrinolysisinvascularinflammationinzuckerratsandevolutionwithaging
AT regnaultveronique implicationoffreefattyacidsinthrombingenerationandfibrinolysisinvascularinflammationinzuckerratsandevolutionwithaging