Targeting neuronal nitric oxide synthase with gene transfer to modulate cardiac autonomic function
Microdomains of neuronal nitric oxide synthase (nNOS) are spatially localised within both autonomic neurons innervating the heart and post-junctional myocytes. This review examines the use of gene transfer to investigate the role of nNOS in cardiac autonomic control. Furthermore, it explores techniq...
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Veröffentlicht in: | Progress in Biophysics and Molecular Biology 2004-02, Vol.84 (2), p.321-344 |
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creator | Mohan, R.M Golding, S Heaton, D.A Danson, E.J Paterson, D.J |
description | Microdomains of neuronal nitric oxide synthase (nNOS) are spatially localised within both autonomic neurons innervating the heart and post-junctional myocytes. This review examines the use of gene transfer to investigate the role of nNOS in cardiac autonomic control. Furthermore, it explores techniques that may be used to improve upon gene delivery to the cardiac autonomic nervous system, potentially allowing more specific delivery of genes to the target neurons/myocytes. This may involve modification of the tropism of the adenoviral vector, or the use of alternative viral and non-viral gene delivery mechanisms to minimise potential immune responses in the host.
Here we show that adenoviral vectors provide an efficient method of gene delivery to cardiac–neural tissue. Functionally, adenovirus-nNOS can increase cardiac vagal responsiveness by facilitating cholinergic neurotransmission and decrease
β-adrenergic excitability. Whether gene transfer remains the preferred strategy for targeting cardiac autonomic impairment will depend on site-specific promoters eliciting sustained gene expression that results in restoration of physiological function. |
doi_str_mv | 10.1016/j.pbiomolbio.2003.11.013 |
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Here we show that adenoviral vectors provide an efficient method of gene delivery to cardiac–neural tissue. Functionally, adenovirus-nNOS can increase cardiac vagal responsiveness by facilitating cholinergic neurotransmission and decrease
β-adrenergic excitability. Whether gene transfer remains the preferred strategy for targeting cardiac autonomic impairment will depend on site-specific promoters eliciting sustained gene expression that results in restoration of physiological function.</description><identifier>ISSN: 0079-6107</identifier><identifier>EISSN: 1873-1732</identifier><identifier>DOI: 10.1016/j.pbiomolbio.2003.11.013</identifier><identifier>PMID: 14769442</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Adenoviridae - genetics ; Animals ; Autonomic nervous system ; Autonomic Nervous System - pathology ; Brain Stem - pathology ; Gene transfer ; Gene Transfer Techniques ; Heart ; Humans ; Models, Biological ; Myocardium - enzymology ; Myocardium - metabolism ; Myocardium - pathology ; Neurons - metabolism ; Nitric Oxide - metabolism ; Nitric oxide synthase ; Nitric Oxide Synthase - genetics ; Nitric Oxide Synthase - metabolism ; Nitric Oxide Synthase Type I</subject><ispartof>Progress in Biophysics and Molecular Biology, 2004-02, Vol.84 (2), p.321-344</ispartof><rights>2003</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c420t-4dc351951bc847d6df05ef46444b54cfd9636644631bdf19e2a60ce160fb8913</citedby><cites>FETCH-LOGICAL-c420t-4dc351951bc847d6df05ef46444b54cfd9636644631bdf19e2a60ce160fb8913</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.pbiomolbio.2003.11.013$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>313,314,780,784,792,3541,27913,27915,27916,45986</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/14769442$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mohan, R.M</creatorcontrib><creatorcontrib>Golding, S</creatorcontrib><creatorcontrib>Heaton, D.A</creatorcontrib><creatorcontrib>Danson, E.J</creatorcontrib><creatorcontrib>Paterson, D.J</creatorcontrib><title>Targeting neuronal nitric oxide synthase with gene transfer to modulate cardiac autonomic function</title><title>Progress in Biophysics and Molecular Biology</title><addtitle>Prog Biophys Mol Biol</addtitle><description>Microdomains of neuronal nitric oxide synthase (nNOS) are spatially localised within both autonomic neurons innervating the heart and post-junctional myocytes. This review examines the use of gene transfer to investigate the role of nNOS in cardiac autonomic control. Furthermore, it explores techniques that may be used to improve upon gene delivery to the cardiac autonomic nervous system, potentially allowing more specific delivery of genes to the target neurons/myocytes. This may involve modification of the tropism of the adenoviral vector, or the use of alternative viral and non-viral gene delivery mechanisms to minimise potential immune responses in the host.
Here we show that adenoviral vectors provide an efficient method of gene delivery to cardiac–neural tissue. Functionally, adenovirus-nNOS can increase cardiac vagal responsiveness by facilitating cholinergic neurotransmission and decrease
β-adrenergic excitability. Whether gene transfer remains the preferred strategy for targeting cardiac autonomic impairment will depend on site-specific promoters eliciting sustained gene expression that results in restoration of physiological function.</description><subject>Adenoviridae - genetics</subject><subject>Animals</subject><subject>Autonomic nervous system</subject><subject>Autonomic Nervous System - pathology</subject><subject>Brain Stem - pathology</subject><subject>Gene transfer</subject><subject>Gene Transfer Techniques</subject><subject>Heart</subject><subject>Humans</subject><subject>Models, Biological</subject><subject>Myocardium - enzymology</subject><subject>Myocardium - metabolism</subject><subject>Myocardium - pathology</subject><subject>Neurons - metabolism</subject><subject>Nitric Oxide - metabolism</subject><subject>Nitric oxide synthase</subject><subject>Nitric Oxide Synthase - genetics</subject><subject>Nitric Oxide Synthase - metabolism</subject><subject>Nitric Oxide Synthase Type I</subject><issn>0079-6107</issn><issn>1873-1732</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkE1v1DAQhi1URJfCX0A-cUuYSRwnOULFl1SJy94txx5vvUrsxXaA_nuy2pV67GVGIz3vjOZhjCPUCCg_HevT5OMS563WDUBbI9aA7Su2w6FvK-zb5obtAPqxkgj9LXub8xEAGuzlG3aLopejEM2OTXudDlR8OPBAa4pBzzz4krzh8Z-3xPNTKI86E__ryyM_UCBekg7ZUeIl8iXaddaFuNHJem24XksMcdnybg2m-BjesddOz5neX_sd23_7ur__UT38-v7z_vNDZUQDpRLWtB2OHU5mEL2V1kFHTkghxNQJ4-woW7lNssXJOhyp0RIMoQQ3DSO2d-zjZe0pxd8r5aIWnw3Nsw4U16wGwE4CnsHhApoUc07k1Cn5RacnhaDOetVRPetVZ70KUW16t-iH6411Wsg-B68-N-DLBaDt0T-eksrGUzBkfSJTlI3-5Sv_AeGBktI</recordid><startdate>20040201</startdate><enddate>20040201</enddate><creator>Mohan, R.M</creator><creator>Golding, S</creator><creator>Heaton, D.A</creator><creator>Danson, E.J</creator><creator>Paterson, D.J</creator><general>Elsevier Ltd</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20040201</creationdate><title>Targeting neuronal nitric oxide synthase with gene transfer to modulate cardiac autonomic function</title><author>Mohan, R.M ; Golding, S ; Heaton, D.A ; Danson, E.J ; Paterson, D.J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c420t-4dc351951bc847d6df05ef46444b54cfd9636644631bdf19e2a60ce160fb8913</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Adenoviridae - genetics</topic><topic>Animals</topic><topic>Autonomic nervous system</topic><topic>Autonomic Nervous System - pathology</topic><topic>Brain Stem - pathology</topic><topic>Gene transfer</topic><topic>Gene Transfer Techniques</topic><topic>Heart</topic><topic>Humans</topic><topic>Models, Biological</topic><topic>Myocardium - enzymology</topic><topic>Myocardium - metabolism</topic><topic>Myocardium - pathology</topic><topic>Neurons - metabolism</topic><topic>Nitric Oxide - metabolism</topic><topic>Nitric oxide synthase</topic><topic>Nitric Oxide Synthase - genetics</topic><topic>Nitric Oxide Synthase - metabolism</topic><topic>Nitric Oxide Synthase Type I</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mohan, R.M</creatorcontrib><creatorcontrib>Golding, S</creatorcontrib><creatorcontrib>Heaton, D.A</creatorcontrib><creatorcontrib>Danson, E.J</creatorcontrib><creatorcontrib>Paterson, D.J</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Progress in Biophysics and Molecular Biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mohan, R.M</au><au>Golding, S</au><au>Heaton, D.A</au><au>Danson, E.J</au><au>Paterson, D.J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Targeting neuronal nitric oxide synthase with gene transfer to modulate cardiac autonomic function</atitle><jtitle>Progress in Biophysics and Molecular Biology</jtitle><addtitle>Prog Biophys Mol Biol</addtitle><date>2004-02-01</date><risdate>2004</risdate><volume>84</volume><issue>2</issue><spage>321</spage><epage>344</epage><pages>321-344</pages><issn>0079-6107</issn><eissn>1873-1732</eissn><abstract>Microdomains of neuronal nitric oxide synthase (nNOS) are spatially localised within both autonomic neurons innervating the heart and post-junctional myocytes. This review examines the use of gene transfer to investigate the role of nNOS in cardiac autonomic control. Furthermore, it explores techniques that may be used to improve upon gene delivery to the cardiac autonomic nervous system, potentially allowing more specific delivery of genes to the target neurons/myocytes. This may involve modification of the tropism of the adenoviral vector, or the use of alternative viral and non-viral gene delivery mechanisms to minimise potential immune responses in the host.
Here we show that adenoviral vectors provide an efficient method of gene delivery to cardiac–neural tissue. Functionally, adenovirus-nNOS can increase cardiac vagal responsiveness by facilitating cholinergic neurotransmission and decrease
β-adrenergic excitability. Whether gene transfer remains the preferred strategy for targeting cardiac autonomic impairment will depend on site-specific promoters eliciting sustained gene expression that results in restoration of physiological function.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>14769442</pmid><doi>10.1016/j.pbiomolbio.2003.11.013</doi><tpages>24</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adenoviridae - genetics Animals Autonomic nervous system Autonomic Nervous System - pathology Brain Stem - pathology Gene transfer Gene Transfer Techniques Heart Humans Models, Biological Myocardium - enzymology Myocardium - metabolism Myocardium - pathology Neurons - metabolism Nitric Oxide - metabolism Nitric oxide synthase Nitric Oxide Synthase - genetics Nitric Oxide Synthase - metabolism Nitric Oxide Synthase Type I |
title | Targeting neuronal nitric oxide synthase with gene transfer to modulate cardiac autonomic function |
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