Human-derived nanoparticles and vascular response to injury in rabbit carotid arteries: Proof of principle
Maria A K Schwartz1, John C Lieske2, Vivek Kumar2, Gerard Farell-Baril2, Virginia M Miller1,31Departments of Physiology and Biomedical Engineering, Internal Medicine; 2Division of Nephrology, and 3Surgery, Mayo Clinic College of Medicine, Rochester, MN, USAAbstract: Self-calcifying, self-replicating...
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Dove Medical Press
2008
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oai:doaj.org-article:299671bc75bf4553aefcadac5a705b2c2021-12-02T02:31:37ZHuman-derived nanoparticles and vascular response to injury in rabbit carotid arteries: Proof of principle1176-91141178-2013https://doaj.org/article/299671bc75bf4553aefcadac5a705b2c2008-06-01T00:00:00Zhttp://www.dovepress.com/human-derived-nanoparticles-and-vascular-response-to-injury-in-rabbit--a1842https://doaj.org/toc/1176-9114https://doaj.org/toc/1178-2013Maria A K Schwartz1, John C Lieske2, Vivek Kumar2, Gerard Farell-Baril2, Virginia M Miller1,31Departments of Physiology and Biomedical Engineering, Internal Medicine; 2Division of Nephrology, and 3Surgery, Mayo Clinic College of Medicine, Rochester, MN, USAAbstract: Self-calcifying, self-replicating nanoparticles have been isolated from calcified human tissues. However, it is unclear if these nanoparticles participate in disease processes. Therefore, this study was designed to preliminarily test the hypothesis that human-derived nanoparticles are causal to arterial disease processes. One carotid artery of 3 kg male rabbits was denuded of endothelium; the contralateral artery remained unoperated as a control. Each rabbit was injected intravenously with either saline, calcified, or decalcified nanoparticles cultured from calcified human arteries or kidney stones. After 35 days, both injured and control arteries were removed for histological examination. Injured arteries from rabbits injected with saline showed minimal, eccentric intimal hyperplasia. Injured arteries from rabbits injected with calcified kidney stone- and arterial-derived nanoparticles occluded, sometimes with canalization. The calcified kidney stone-derived nanoparticles caused calcifications within the occlusion. Responses to injury in rabbits injected with decalcified kidney stone-derived nanoparticles were similar to those observed in saline-injected animals. However, decalcified arterial-derived nanoparticles produced intimal hyperplasia that varied from moderate to occlusion with canalization and calcifi cation. This study offers the first evidence that there may be a causal relationship between human-derived nanoparticles and response to injury including calcification in arteries with damaged endothelium.Keywords: arterial calcification, endothelial injury, intimal hyperplasia Maria A K SchwartzJohn C LieskeVivek KumarGerard Farell-BarilVirginia M MillerDove Medical PressarticleMedicine (General)R5-920ENInternational Journal of Nanomedicine, Vol 2008, Iss Issue 2, Pp 243-248 (2008) |
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Medicine (General) R5-920 Maria A K Schwartz John C Lieske Vivek Kumar Gerard Farell-Baril Virginia M Miller Human-derived nanoparticles and vascular response to injury in rabbit carotid arteries: Proof of principle |
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Maria A K Schwartz1, John C Lieske2, Vivek Kumar2, Gerard Farell-Baril2, Virginia M Miller1,31Departments of Physiology and Biomedical Engineering, Internal Medicine; 2Division of Nephrology, and 3Surgery, Mayo Clinic College of Medicine, Rochester, MN, USAAbstract: Self-calcifying, self-replicating nanoparticles have been isolated from calcified human tissues. However, it is unclear if these nanoparticles participate in disease processes. Therefore, this study was designed to preliminarily test the hypothesis that human-derived nanoparticles are causal to arterial disease processes. One carotid artery of 3 kg male rabbits was denuded of endothelium; the contralateral artery remained unoperated as a control. Each rabbit was injected intravenously with either saline, calcified, or decalcified nanoparticles cultured from calcified human arteries or kidney stones. After 35 days, both injured and control arteries were removed for histological examination. Injured arteries from rabbits injected with saline showed minimal, eccentric intimal hyperplasia. Injured arteries from rabbits injected with calcified kidney stone- and arterial-derived nanoparticles occluded, sometimes with canalization. The calcified kidney stone-derived nanoparticles caused calcifications within the occlusion. Responses to injury in rabbits injected with decalcified kidney stone-derived nanoparticles were similar to those observed in saline-injected animals. However, decalcified arterial-derived nanoparticles produced intimal hyperplasia that varied from moderate to occlusion with canalization and calcifi cation. This study offers the first evidence that there may be a causal relationship between human-derived nanoparticles and response to injury including calcification in arteries with damaged endothelium.Keywords: arterial calcification, endothelial injury, intimal hyperplasia |
format |
article |
author |
Maria A K Schwartz John C Lieske Vivek Kumar Gerard Farell-Baril Virginia M Miller |
author_facet |
Maria A K Schwartz John C Lieske Vivek Kumar Gerard Farell-Baril Virginia M Miller |
author_sort |
Maria A K Schwartz |
title |
Human-derived nanoparticles and vascular response to injury in rabbit carotid arteries: Proof of principle |
title_short |
Human-derived nanoparticles and vascular response to injury in rabbit carotid arteries: Proof of principle |
title_full |
Human-derived nanoparticles and vascular response to injury in rabbit carotid arteries: Proof of principle |
title_fullStr |
Human-derived nanoparticles and vascular response to injury in rabbit carotid arteries: Proof of principle |
title_full_unstemmed |
Human-derived nanoparticles and vascular response to injury in rabbit carotid arteries: Proof of principle |
title_sort |
human-derived nanoparticles and vascular response to injury in rabbit carotid arteries: proof of principle |
publisher |
Dove Medical Press |
publishDate |
2008 |
url |
https://doaj.org/article/299671bc75bf4553aefcadac5a705b2c |
work_keys_str_mv |
AT mariaakschwartz humanderivednanoparticlesandvascularresponsetoinjuryinrabbitcarotidarteriesproofofprinciple AT johnclieske humanderivednanoparticlesandvascularresponsetoinjuryinrabbitcarotidarteriesproofofprinciple AT vivekkumar humanderivednanoparticlesandvascularresponsetoinjuryinrabbitcarotidarteriesproofofprinciple AT gerardfarellbaril humanderivednanoparticlesandvascularresponsetoinjuryinrabbitcarotidarteriesproofofprinciple AT virginiammiller humanderivednanoparticlesandvascularresponsetoinjuryinrabbitcarotidarteriesproofofprinciple |
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1718402398594007040 |