Cargando…

Update on the electrolytic IVC model for pre‐clinical studies of venous thrombosis

ESSENTIALS: Three key updates are provided on the electrolytic inferior vena cava model (EIM). The originally described stimulator equipment has been discontinued; we developed an alternative. The fibrinolytic system and the current and time dependency of the EIM was characterized. EIM allows the in...

Descripción completa

Detalles Bibliográficos
Autores principales: Palmer, Olivia R., Shaydakov, Maxim E., Rainey, Joshua P., Lawrence, Daniel A., Greve, Joan M., Diaz, José A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6055493/
https://www.ncbi.nlm.nih.gov/pubmed/30046728
http://dx.doi.org/10.1002/rth2.12074
_version_ 1783341183778422784
author Palmer, Olivia R.
Shaydakov, Maxim E.
Rainey, Joshua P.
Lawrence, Daniel A.
Greve, Joan M.
Diaz, José A.
author_facet Palmer, Olivia R.
Shaydakov, Maxim E.
Rainey, Joshua P.
Lawrence, Daniel A.
Greve, Joan M.
Diaz, José A.
author_sort Palmer, Olivia R.
collection PubMed
description ESSENTIALS: Three key updates are provided on the electrolytic inferior vena cava model (EIM). The originally described stimulator equipment has been discontinued; we developed an alternative. The fibrinolytic system and the current and time dependency of the EIM was characterized. EIM allows the investigation of the fibrinolytic system, critical for endovascular therapies. BACKGROUND: The electrolytic inferior vena cava model (EIM) is a murine venous thrombosis (VT) model that produces a non‐occlusive thrombus. The thrombus forms in the direction of blood flow, as observed in patients. The EIM is valuable for investigations of therapeutics due to the presence of continuous blood flow. However, the equipment used to induce thrombosis in the original model description was expensive and has since been discontinued. Further, the fibrinolytic system had not been previously studied in the EIM. OBJECTIVES: We aimed to provide an equipment alternative. Additionally, we further characterized the model through mapping the current and time dependency of thrombus resolution dynamics, and investigated the fibrinolytic system from acute to chronic VT. RESULTS: A voltage to current converter powered by a direct current power supply was constructed and validated, providing an added benefit of significantly reducing costs. The current and time dependency of thrombus volume dynamics was assessed by MRI, demonstrating the flexibility of the EIM to investigate both pro‐thrombotic and anti‐thrombotic conditions. Additionally, the fibrinolytic system was characterized in EIM. Centripetal distribution of plasminogen was observed over time, with peak staining at day 6 post thrombus induction. Both active circulating plasminogen activator inhibitor‐1 (PAI‐1) and vein wall gene expression of PAI‐1 peaked at day 2, coinciding with a relative decrease in tissue plasminogen activator and urokinase plasminogen activator. CONCLUSIONS: The EIM is a valuable model of VT that can now be performed at low cost and may be beneficial in investigations of the fibrinolytic system.
format Online
Article
Text
id pubmed-6055493
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-60554932018-07-25 Update on the electrolytic IVC model for pre‐clinical studies of venous thrombosis Palmer, Olivia R. Shaydakov, Maxim E. Rainey, Joshua P. Lawrence, Daniel A. Greve, Joan M. Diaz, José A. Res Pract Thromb Haemost Methodological Article ESSENTIALS: Three key updates are provided on the electrolytic inferior vena cava model (EIM). The originally described stimulator equipment has been discontinued; we developed an alternative. The fibrinolytic system and the current and time dependency of the EIM was characterized. EIM allows the investigation of the fibrinolytic system, critical for endovascular therapies. BACKGROUND: The electrolytic inferior vena cava model (EIM) is a murine venous thrombosis (VT) model that produces a non‐occlusive thrombus. The thrombus forms in the direction of blood flow, as observed in patients. The EIM is valuable for investigations of therapeutics due to the presence of continuous blood flow. However, the equipment used to induce thrombosis in the original model description was expensive and has since been discontinued. Further, the fibrinolytic system had not been previously studied in the EIM. OBJECTIVES: We aimed to provide an equipment alternative. Additionally, we further characterized the model through mapping the current and time dependency of thrombus resolution dynamics, and investigated the fibrinolytic system from acute to chronic VT. RESULTS: A voltage to current converter powered by a direct current power supply was constructed and validated, providing an added benefit of significantly reducing costs. The current and time dependency of thrombus volume dynamics was assessed by MRI, demonstrating the flexibility of the EIM to investigate both pro‐thrombotic and anti‐thrombotic conditions. Additionally, the fibrinolytic system was characterized in EIM. Centripetal distribution of plasminogen was observed over time, with peak staining at day 6 post thrombus induction. Both active circulating plasminogen activator inhibitor‐1 (PAI‐1) and vein wall gene expression of PAI‐1 peaked at day 2, coinciding with a relative decrease in tissue plasminogen activator and urokinase plasminogen activator. CONCLUSIONS: The EIM is a valuable model of VT that can now be performed at low cost and may be beneficial in investigations of the fibrinolytic system. John Wiley and Sons Inc. 2018-01-31 /pmc/articles/PMC6055493/ /pubmed/30046728 http://dx.doi.org/10.1002/rth2.12074 Text en © 2018 The Authors. Research and Practice in Thrombosis and Haemostasis published by Wiley Periodicals, Inc on behalf of International Society on Thrombosis and Haemostasis. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Methodological Article
Palmer, Olivia R.
Shaydakov, Maxim E.
Rainey, Joshua P.
Lawrence, Daniel A.
Greve, Joan M.
Diaz, José A.
Update on the electrolytic IVC model for pre‐clinical studies of venous thrombosis
title Update on the electrolytic IVC model for pre‐clinical studies of venous thrombosis
title_full Update on the electrolytic IVC model for pre‐clinical studies of venous thrombosis
title_fullStr Update on the electrolytic IVC model for pre‐clinical studies of venous thrombosis
title_full_unstemmed Update on the electrolytic IVC model for pre‐clinical studies of venous thrombosis
title_short Update on the electrolytic IVC model for pre‐clinical studies of venous thrombosis
title_sort update on the electrolytic ivc model for pre‐clinical studies of venous thrombosis
topic Methodological Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6055493/
https://www.ncbi.nlm.nih.gov/pubmed/30046728
http://dx.doi.org/10.1002/rth2.12074
work_keys_str_mv AT palmeroliviar updateontheelectrolyticivcmodelforpreclinicalstudiesofvenousthrombosis
AT shaydakovmaxime updateontheelectrolyticivcmodelforpreclinicalstudiesofvenousthrombosis
AT raineyjoshuap updateontheelectrolyticivcmodelforpreclinicalstudiesofvenousthrombosis
AT lawrencedaniela updateontheelectrolyticivcmodelforpreclinicalstudiesofvenousthrombosis
AT grevejoanm updateontheelectrolyticivcmodelforpreclinicalstudiesofvenousthrombosis
AT diazjosea updateontheelectrolyticivcmodelforpreclinicalstudiesofvenousthrombosis