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Effects of Recombinant Human Type I Pancreatic Elastase on Human Atherosclerotic Arteries

RATIONALE: At physiologic pressures, elastic fibers constrain artery diameter. Local treatment of atherosclerotic arteries with PRT-201, a recombinant type I elastase, could result in fragmentation and removal of elastin fibers and increased vessel diameter. OBJECTIVE: To investigate the use of PRT-...

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Autores principales: Burke, Steven K., Macdonald, Karen, Moss, Emma, Bunton, David, Starcher, Barry, Wong, Marco D., Bland, Kimberly S., Franano, F. Nicholas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Journal of Cardiovascular Pharmacology 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4272232/
https://www.ncbi.nlm.nih.gov/pubmed/25490419
http://dx.doi.org/10.1097/FJC.0000000000000149
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author Burke, Steven K.
Macdonald, Karen
Moss, Emma
Bunton, David
Starcher, Barry
Wong, Marco D.
Bland, Kimberly S.
Franano, F. Nicholas
author_facet Burke, Steven K.
Macdonald, Karen
Moss, Emma
Bunton, David
Starcher, Barry
Wong, Marco D.
Bland, Kimberly S.
Franano, F. Nicholas
author_sort Burke, Steven K.
collection PubMed
description RATIONALE: At physiologic pressures, elastic fibers constrain artery diameter. Local treatment of atherosclerotic arteries with PRT-201, a recombinant type I elastase, could result in fragmentation and removal of elastin fibers and increased vessel diameter. OBJECTIVE: To investigate the use of PRT-201 as a treatment for human atherosclerotic arteries. METHODS AND RESULTS: Arteries were harvested from donor legs amputated due to severe peripheral artery disease or from recently deceased persons who donated their bodies to science. Three- to four-centimeter artery segments were studied on a perfusion myograph to obtain baseline diameter data. After treatment with PRT-201 3.6 mg/mL or saline for 30 minutes myography was repeated. PRT-201 treatment resulted in an increase in vessel diameter across a range of transmural pressures. Average anterior tibial artery diameter increased by 0.78 ± 0.21 mm (27% ± 12%), whereas average posterior tibial artery diameter increased by 0.58 ± 0.30 mm (21% ± 11%), both P < 0.001. Elastin content as measured by desmosine radioimmunoassay was reduced by approximately 50%, P < 0.001. CONCLUSIONS: The results suggest that PRT-201 treatment of atherosclerotic peripheral arteries in patients could increase artery diameter, and thus luminal area, possibly alleviating some of the symptoms of peripheral artery disease.
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spelling pubmed-42722322014-12-23 Effects of Recombinant Human Type I Pancreatic Elastase on Human Atherosclerotic Arteries Burke, Steven K. Macdonald, Karen Moss, Emma Bunton, David Starcher, Barry Wong, Marco D. Bland, Kimberly S. Franano, F. Nicholas J Cardiovasc Pharmacol Original Article RATIONALE: At physiologic pressures, elastic fibers constrain artery diameter. Local treatment of atherosclerotic arteries with PRT-201, a recombinant type I elastase, could result in fragmentation and removal of elastin fibers and increased vessel diameter. OBJECTIVE: To investigate the use of PRT-201 as a treatment for human atherosclerotic arteries. METHODS AND RESULTS: Arteries were harvested from donor legs amputated due to severe peripheral artery disease or from recently deceased persons who donated their bodies to science. Three- to four-centimeter artery segments were studied on a perfusion myograph to obtain baseline diameter data. After treatment with PRT-201 3.6 mg/mL or saline for 30 minutes myography was repeated. PRT-201 treatment resulted in an increase in vessel diameter across a range of transmural pressures. Average anterior tibial artery diameter increased by 0.78 ± 0.21 mm (27% ± 12%), whereas average posterior tibial artery diameter increased by 0.58 ± 0.30 mm (21% ± 11%), both P < 0.001. Elastin content as measured by desmosine radioimmunoassay was reduced by approximately 50%, P < 0.001. CONCLUSIONS: The results suggest that PRT-201 treatment of atherosclerotic peripheral arteries in patients could increase artery diameter, and thus luminal area, possibly alleviating some of the symptoms of peripheral artery disease. Journal of Cardiovascular Pharmacology 2014-12 2014-12-09 /pmc/articles/PMC4272232/ /pubmed/25490419 http://dx.doi.org/10.1097/FJC.0000000000000149 Text en Copyright © 2014 by Lippincott Williams & Wilkins This is an open access article distributed under the terms of the Creative Commons Attribution-Noncommercial-No Derivatives 3.0 License, where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially.
spellingShingle Original Article
Burke, Steven K.
Macdonald, Karen
Moss, Emma
Bunton, David
Starcher, Barry
Wong, Marco D.
Bland, Kimberly S.
Franano, F. Nicholas
Effects of Recombinant Human Type I Pancreatic Elastase on Human Atherosclerotic Arteries
title Effects of Recombinant Human Type I Pancreatic Elastase on Human Atherosclerotic Arteries
title_full Effects of Recombinant Human Type I Pancreatic Elastase on Human Atherosclerotic Arteries
title_fullStr Effects of Recombinant Human Type I Pancreatic Elastase on Human Atherosclerotic Arteries
title_full_unstemmed Effects of Recombinant Human Type I Pancreatic Elastase on Human Atherosclerotic Arteries
title_short Effects of Recombinant Human Type I Pancreatic Elastase on Human Atherosclerotic Arteries
title_sort effects of recombinant human type i pancreatic elastase on human atherosclerotic arteries
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4272232/
https://www.ncbi.nlm.nih.gov/pubmed/25490419
http://dx.doi.org/10.1097/FJC.0000000000000149
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