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- Publisher Website: 10.1016/j.niox.2009.11.005
- Scopus: eid_2-s2.0-73349099337
- PMID: 19931630
- WOS: WOS:000273642200005
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Article: The diversity of nNOS gene expression in avulsion-injured spinal motoneurons among laboratory rodents
Title | The diversity of nNOS gene expression in avulsion-injured spinal motoneurons among laboratory rodents | ||||||
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Authors | |||||||
Keywords | Avulsion Motoneuron Neuronal nitric oxide synthase Species-specific | ||||||
Issue Date | 2010 | ||||||
Publisher | Academic Press. The Journal's web site is located at http://www.elsevier.com/locate/yniox | ||||||
Citation | Nitric Oxide - Biology And Chemistry, 2010, v. 22 n. 1, p. 37-42 How to Cite? | ||||||
Abstract | Rats, mice, and hamsters are commonly used laboratory rodents in the experimental modeling strategies of avulsion-induced motoneuron degenerations. It is necessary to study the species-specific gene expression in spinal cord in response to avulsion. We carried out the brachial roots avulsion in all animals and compared the survival and nNOS gene expression in injured motoneurons and spinal segments among the three species. The results showed that avulsion-induced loss of motoneurons was greatest in mice than that in hamsters or rats. Avulsion induced decrease of nNOS mRNA level in injured spinal segments in all three species, but greater in amplitude in rats and mice than that in hamsters. However, the de novo nNOS protein expression in injured motoneurons was higher in rats than in hamsters, none in mice. This study strongly suggests that the species diversity of nNOS gene must be considered when estimating the role of nNOS in motoneuron degenerations. © 2009 Elsevier Inc. All rights reserved. | ||||||
Persistent Identifier | http://hdl.handle.net/10722/149725 | ||||||
ISSN | 2023 Impact Factor: 3.2 2023 SCImago Journal Rankings: 0.749 | ||||||
ISI Accession Number ID |
Funding Information: This work was supported by grants from the National Science Foundation Council of China (30672119) and grants from the Research Grants Council of Guangdong (2008B050100011). | ||||||
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Wang, J | en_US |
dc.contributor.author | Yan, L | en_US |
dc.contributor.author | Zhao, X | en_US |
dc.contributor.author | Wu, W | en_US |
dc.contributor.author | Zhou, LH | en_US |
dc.date.accessioned | 2012-06-26T05:57:40Z | - |
dc.date.available | 2012-06-26T05:57:40Z | - |
dc.date.issued | 2010 | en_US |
dc.identifier.citation | Nitric Oxide - Biology And Chemistry, 2010, v. 22 n. 1, p. 37-42 | en_US |
dc.identifier.issn | 1089-8603 | en_US |
dc.identifier.uri | http://hdl.handle.net/10722/149725 | - |
dc.description.abstract | Rats, mice, and hamsters are commonly used laboratory rodents in the experimental modeling strategies of avulsion-induced motoneuron degenerations. It is necessary to study the species-specific gene expression in spinal cord in response to avulsion. We carried out the brachial roots avulsion in all animals and compared the survival and nNOS gene expression in injured motoneurons and spinal segments among the three species. The results showed that avulsion-induced loss of motoneurons was greatest in mice than that in hamsters or rats. Avulsion induced decrease of nNOS mRNA level in injured spinal segments in all three species, but greater in amplitude in rats and mice than that in hamsters. However, the de novo nNOS protein expression in injured motoneurons was higher in rats than in hamsters, none in mice. This study strongly suggests that the species diversity of nNOS gene must be considered when estimating the role of nNOS in motoneuron degenerations. © 2009 Elsevier Inc. All rights reserved. | en_US |
dc.language | eng | en_US |
dc.publisher | Academic Press. The Journal's web site is located at http://www.elsevier.com/locate/yniox | en_US |
dc.relation.ispartof | Nitric Oxide - Biology and Chemistry | en_US |
dc.subject | Avulsion | - |
dc.subject | Motoneuron | - |
dc.subject | Neuronal nitric oxide synthase | - |
dc.subject | Species-specific | - |
dc.subject.mesh | Animals | en_US |
dc.subject.mesh | Cricetinae | en_US |
dc.subject.mesh | Gene Expression Regulation, Enzymologic - Genetics | en_US |
dc.subject.mesh | Immunohistochemistry | en_US |
dc.subject.mesh | Male | en_US |
dc.subject.mesh | Mice | en_US |
dc.subject.mesh | Mice, Inbred Balb C | en_US |
dc.subject.mesh | Motor Neurons - Enzymology - Pathology | en_US |
dc.subject.mesh | Nadph Dehydrogenase - Metabolism | en_US |
dc.subject.mesh | Nitric Oxide Synthase Type I - Genetics | en_US |
dc.subject.mesh | Rna, Messenger - Genetics | en_US |
dc.subject.mesh | Rats | en_US |
dc.subject.mesh | Rats, Sprague-Dawley | en_US |
dc.subject.mesh | Reverse Transcriptase Polymerase Chain Reaction | en_US |
dc.subject.mesh | Species Specificity | en_US |
dc.subject.mesh | Spinal Cord Injuries - Enzymology - Pathology | en_US |
dc.title | The diversity of nNOS gene expression in avulsion-injured spinal motoneurons among laboratory rodents | en_US |
dc.type | Article | en_US |
dc.identifier.email | Wu, W:wtwu@hkucc.hku.hk | en_US |
dc.identifier.authority | Wu, W=rp00419 | en_US |
dc.description.nature | link_to_subscribed_fulltext | en_US |
dc.identifier.doi | 10.1016/j.niox.2009.11.005 | en_US |
dc.identifier.pmid | 19931630 | - |
dc.identifier.scopus | eid_2-s2.0-73349099337 | en_US |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-73349099337&selection=ref&src=s&origin=recordpage | en_US |
dc.identifier.volume | 22 | en_US |
dc.identifier.issue | 1 | en_US |
dc.identifier.spage | 37 | en_US |
dc.identifier.epage | 42 | en_US |
dc.identifier.isi | WOS:000273642200005 | - |
dc.publisher.place | United States | en_US |
dc.identifier.scopusauthorid | Wang, J=36090272400 | en_US |
dc.identifier.scopusauthorid | Yan, L=7402671199 | en_US |
dc.identifier.scopusauthorid | Zhao, X=36665560200 | en_US |
dc.identifier.scopusauthorid | Wu, W=7407081122 | en_US |
dc.identifier.scopusauthorid | Zhou, LH=7404125592 | en_US |
dc.identifier.citeulike | 6189110 | - |
dc.identifier.issnl | 1089-8603 | - |