Targeting endothelial cells with adenovirus expressing nitric oxide synthase prevents elevation of blood pressure in stroke-prone spontaneously hypertensive rats.
Local adenoviral (Ad)-mediated gene transfer to the carotid artery of the stroke-prone spontaneously hypertensive rat (SHRSP) is successful in improving endothelial function. Here we explored the potential of systemic delivery of Ad encoding endothelial nitric oxide synthase (AdeNOS) to prevent elev...
Main Authors: | , , , , , , , , , |
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Format: | Journal article |
Language: | English |
Published: |
2005
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author | Miller, W Brosnan, M Graham, D Nicol, C Morecroft, I Channon, K Danilov, S Reynolds, P Baker, A Dominiczak, A |
author_facet | Miller, W Brosnan, M Graham, D Nicol, C Morecroft, I Channon, K Danilov, S Reynolds, P Baker, A Dominiczak, A |
author_sort | Miller, W |
collection | OXFORD |
description | Local adenoviral (Ad)-mediated gene transfer to the carotid artery of the stroke-prone spontaneously hypertensive rat (SHRSP) is successful in improving endothelial function. Here we explored the potential of systemic delivery of Ad encoding endothelial nitric oxide synthase (AdeNOS) to prevent elevation of blood pressure in the SHRSP using both nontargeted and vector targeting approaches. Systemic administration of nontargeted AdeNOS failed to modify the rise in blood pressure in SHRSP when administered during the 12th week of age (n = 5, P = 0.088, F = 3.0), an effect likely to result from sequestration of Ad by the liver. Rerouting Ad transduction using a bispecific antibody (anti-ACE/anti-Ad capsid, Fab9B9) that blocks Ad binding to the coxsackie and adenovirus receptor and simultaneously retargets AdeNOS to the angiotensin-converting enzyme resulted in efficient eNOS overexpression in the lung vasculature and a sustained hypotensive effect (n = 5, P = 0.007, F = 7.9). This study highlights the importance of vector targeting to achieve therapeutic gain and represents the first such study in cardiovascular gene therapy. |
first_indexed | 2024-03-06T21:42:00Z |
format | Journal article |
id | oxford-uuid:483e1ac7-c59c-4d3e-a94f-d01fdaa45b36 |
institution | University of Oxford |
language | English |
last_indexed | 2024-03-06T21:42:00Z |
publishDate | 2005 |
record_format | dspace |
spelling | oxford-uuid:483e1ac7-c59c-4d3e-a94f-d01fdaa45b362022-03-26T15:24:40ZTargeting endothelial cells with adenovirus expressing nitric oxide synthase prevents elevation of blood pressure in stroke-prone spontaneously hypertensive rats.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:483e1ac7-c59c-4d3e-a94f-d01fdaa45b36EnglishSymplectic Elements at Oxford2005Miller, WBrosnan, MGraham, DNicol, CMorecroft, IChannon, KDanilov, SReynolds, PBaker, ADominiczak, ALocal adenoviral (Ad)-mediated gene transfer to the carotid artery of the stroke-prone spontaneously hypertensive rat (SHRSP) is successful in improving endothelial function. Here we explored the potential of systemic delivery of Ad encoding endothelial nitric oxide synthase (AdeNOS) to prevent elevation of blood pressure in the SHRSP using both nontargeted and vector targeting approaches. Systemic administration of nontargeted AdeNOS failed to modify the rise in blood pressure in SHRSP when administered during the 12th week of age (n = 5, P = 0.088, F = 3.0), an effect likely to result from sequestration of Ad by the liver. Rerouting Ad transduction using a bispecific antibody (anti-ACE/anti-Ad capsid, Fab9B9) that blocks Ad binding to the coxsackie and adenovirus receptor and simultaneously retargets AdeNOS to the angiotensin-converting enzyme resulted in efficient eNOS overexpression in the lung vasculature and a sustained hypotensive effect (n = 5, P = 0.007, F = 7.9). This study highlights the importance of vector targeting to achieve therapeutic gain and represents the first such study in cardiovascular gene therapy. |
spellingShingle | Miller, W Brosnan, M Graham, D Nicol, C Morecroft, I Channon, K Danilov, S Reynolds, P Baker, A Dominiczak, A Targeting endothelial cells with adenovirus expressing nitric oxide synthase prevents elevation of blood pressure in stroke-prone spontaneously hypertensive rats. |
title | Targeting endothelial cells with adenovirus expressing nitric oxide synthase prevents elevation of blood pressure in stroke-prone spontaneously hypertensive rats. |
title_full | Targeting endothelial cells with adenovirus expressing nitric oxide synthase prevents elevation of blood pressure in stroke-prone spontaneously hypertensive rats. |
title_fullStr | Targeting endothelial cells with adenovirus expressing nitric oxide synthase prevents elevation of blood pressure in stroke-prone spontaneously hypertensive rats. |
title_full_unstemmed | Targeting endothelial cells with adenovirus expressing nitric oxide synthase prevents elevation of blood pressure in stroke-prone spontaneously hypertensive rats. |
title_short | Targeting endothelial cells with adenovirus expressing nitric oxide synthase prevents elevation of blood pressure in stroke-prone spontaneously hypertensive rats. |
title_sort | targeting endothelial cells with adenovirus expressing nitric oxide synthase prevents elevation of blood pressure in stroke prone spontaneously hypertensive rats |
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