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Rat Model of Parkes Weber Syndrome
The Parkes Weber syndrome is a congenital vascular malformation, characterized by varicose veins, arterio-venous fistulas and overgrown limbs. No broadly accepted animal model of Parkes Weber syndrome has been described. We created side-to-side arterio-venous fistula between common femoral vessels w...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4517880/ https://www.ncbi.nlm.nih.gov/pubmed/26217941 http://dx.doi.org/10.1371/journal.pone.0133752 |
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author | Bojakowski, Krzysztof Janusz, Gabriela Grabowska, Iwona Zegrocka-Stendel, Oliwia Surowiecka-Pastewka, Agnieszka Kowalewska, Magdalena Maciejko, Dorota Koziak, Katarzyna |
author_facet | Bojakowski, Krzysztof Janusz, Gabriela Grabowska, Iwona Zegrocka-Stendel, Oliwia Surowiecka-Pastewka, Agnieszka Kowalewska, Magdalena Maciejko, Dorota Koziak, Katarzyna |
author_sort | Bojakowski, Krzysztof |
collection | PubMed |
description | The Parkes Weber syndrome is a congenital vascular malformation, characterized by varicose veins, arterio-venous fistulas and overgrown limbs. No broadly accepted animal model of Parkes Weber syndrome has been described. We created side-to-side arterio-venous fistula between common femoral vessels with proximal non-absorbable ligature on common femoral vein limiting the enlargement of the vein diameter in Wistar rats. Contralateral limb was sham operated. Invasive blood pressure measurements in both iliac and inferior cava veins were performed in rats 30 days after fistula creation. Tight circumference and femoral bone length were measured. Histopathology and morphology of soleus muscle, extensor digitorum longus muscle, and the common femoral vessel were analyzed. 30 days following arterio-venous fistula creation, a statistically significant elevation of blood pressure in common iliac vein and limb overgrowth was observed. Limb enlargement was caused by muscle overgrowth, varicose veins formation and bone elongation. Arterio-venous fistula with proximal outflow limitation led to significant increase of femoral vein circumference and venous wall thickness. Our study indicates that the described rat model mimics major clinical features characteristic for the human Parkes Weber syndrome: presence of arterio-venous fistula, venous hypertension and dilatation, varicose veins formation, and the limb hypertrophy. We reveal that limb overgrowth is caused by bone elongation, muscle hypertrophy, and venous dilatation. The newly established model will permit detailed studies on the mechanisms underlying the disease and on the efficacy of novel therapeutic strategies for the Parkes Weber syndrome treatment. |
format | Online Article Text |
id | pubmed-4517880 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-45178802015-07-31 Rat Model of Parkes Weber Syndrome Bojakowski, Krzysztof Janusz, Gabriela Grabowska, Iwona Zegrocka-Stendel, Oliwia Surowiecka-Pastewka, Agnieszka Kowalewska, Magdalena Maciejko, Dorota Koziak, Katarzyna PLoS One Research Article The Parkes Weber syndrome is a congenital vascular malformation, characterized by varicose veins, arterio-venous fistulas and overgrown limbs. No broadly accepted animal model of Parkes Weber syndrome has been described. We created side-to-side arterio-venous fistula between common femoral vessels with proximal non-absorbable ligature on common femoral vein limiting the enlargement of the vein diameter in Wistar rats. Contralateral limb was sham operated. Invasive blood pressure measurements in both iliac and inferior cava veins were performed in rats 30 days after fistula creation. Tight circumference and femoral bone length were measured. Histopathology and morphology of soleus muscle, extensor digitorum longus muscle, and the common femoral vessel were analyzed. 30 days following arterio-venous fistula creation, a statistically significant elevation of blood pressure in common iliac vein and limb overgrowth was observed. Limb enlargement was caused by muscle overgrowth, varicose veins formation and bone elongation. Arterio-venous fistula with proximal outflow limitation led to significant increase of femoral vein circumference and venous wall thickness. Our study indicates that the described rat model mimics major clinical features characteristic for the human Parkes Weber syndrome: presence of arterio-venous fistula, venous hypertension and dilatation, varicose veins formation, and the limb hypertrophy. We reveal that limb overgrowth is caused by bone elongation, muscle hypertrophy, and venous dilatation. The newly established model will permit detailed studies on the mechanisms underlying the disease and on the efficacy of novel therapeutic strategies for the Parkes Weber syndrome treatment. Public Library of Science 2015-07-28 /pmc/articles/PMC4517880/ /pubmed/26217941 http://dx.doi.org/10.1371/journal.pone.0133752 Text en © 2015 Bojakowski et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Bojakowski, Krzysztof Janusz, Gabriela Grabowska, Iwona Zegrocka-Stendel, Oliwia Surowiecka-Pastewka, Agnieszka Kowalewska, Magdalena Maciejko, Dorota Koziak, Katarzyna Rat Model of Parkes Weber Syndrome |
title | Rat Model of Parkes Weber Syndrome |
title_full | Rat Model of Parkes Weber Syndrome |
title_fullStr | Rat Model of Parkes Weber Syndrome |
title_full_unstemmed | Rat Model of Parkes Weber Syndrome |
title_short | Rat Model of Parkes Weber Syndrome |
title_sort | rat model of parkes weber syndrome |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4517880/ https://www.ncbi.nlm.nih.gov/pubmed/26217941 http://dx.doi.org/10.1371/journal.pone.0133752 |
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