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- Publisher Website: 10.1016/j.bbrc.2007.05.113
- Scopus: eid_2-s2.0-34250172430
- PMID: 17544367
- WOS: WOS:000247582500014
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Article: Nitric oxide modulation of voltage-gated calcium current by S-nitrosylation and cGMP pathway in cultured rat hippocampal neurons
Title | Nitric oxide modulation of voltage-gated calcium current by S-nitrosylation and cGMP pathway in cultured rat hippocampal neurons |
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Authors | |
Keywords | cGMP pathway Hippocampus Nitric oxide S-Nitrosylation Voltage-gated calcium currents |
Issue Date | 2007 |
Publisher | Academic Press. The Journal's web site is located at http://www.elsevier.com/wps/find/journaldescription.cws_home/622790/description |
Citation | Biochemical And Biophysical Research Communications, 2007, v. 359 n. 3, p. 481-485 How to Cite? |
Abstract | Nitric oxide (NO) plays an important role in many physiological and pathophysiological processes in the brain. In this study, we examined the mechanistic effects of an NO donor, diethylenetriamine/nitric oxide adduct (DETA/NO) on the voltage-gated calcium currents in cultured rat hippocampal neurons. DETA/NO stimulated the calcium currents and slightly increased the channel sensitivity to depolarizing voltages. The effect of DETA/NO on the calcium current was blocked by either depleting the NO in DETA/NO or by pretreating the neurons with NEM, a thiol-specific alkylating agent, suggesting an involvement of S-nitrosylation in the current response to NO. In addition, activation of the cGMP pathway by 8-Br-cGMP inhibited the calcium current in the neurons. Also, inhibition of guanylyl cyclase by 1H-[1,2,4] oxadiazolo [4,3-a] quinoxalin-1-one (ODQ) increased the current response to DETA/NO. Taken together, our results demonstrate that both S-nitrosylation and cGMP pathway are involved in the NO modulation of the hippocampal calcium current. © 2007 Elsevier Inc. All rights reserved. |
Persistent Identifier | http://hdl.handle.net/10722/171757 |
ISSN | 2023 Impact Factor: 2.5 2023 SCImago Journal Rankings: 0.770 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Jian, K | en_US |
dc.contributor.author | Chen, M | en_US |
dc.contributor.author | Cao, X | en_US |
dc.contributor.author | Zhu, XH | en_US |
dc.contributor.author | Fung, ML | en_US |
dc.contributor.author | Gao, TM | en_US |
dc.date.accessioned | 2012-10-30T06:16:49Z | - |
dc.date.available | 2012-10-30T06:16:49Z | - |
dc.date.issued | 2007 | en_US |
dc.identifier.citation | Biochemical And Biophysical Research Communications, 2007, v. 359 n. 3, p. 481-485 | en_US |
dc.identifier.issn | 0006-291X | en_US |
dc.identifier.uri | http://hdl.handle.net/10722/171757 | - |
dc.description.abstract | Nitric oxide (NO) plays an important role in many physiological and pathophysiological processes in the brain. In this study, we examined the mechanistic effects of an NO donor, diethylenetriamine/nitric oxide adduct (DETA/NO) on the voltage-gated calcium currents in cultured rat hippocampal neurons. DETA/NO stimulated the calcium currents and slightly increased the channel sensitivity to depolarizing voltages. The effect of DETA/NO on the calcium current was blocked by either depleting the NO in DETA/NO or by pretreating the neurons with NEM, a thiol-specific alkylating agent, suggesting an involvement of S-nitrosylation in the current response to NO. In addition, activation of the cGMP pathway by 8-Br-cGMP inhibited the calcium current in the neurons. Also, inhibition of guanylyl cyclase by 1H-[1,2,4] oxadiazolo [4,3-a] quinoxalin-1-one (ODQ) increased the current response to DETA/NO. Taken together, our results demonstrate that both S-nitrosylation and cGMP pathway are involved in the NO modulation of the hippocampal calcium current. © 2007 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/wps/find/journaldescription.cws_home/622790/description | en_US |
dc.relation.ispartof | Biochemical and Biophysical Research Communications | en_US |
dc.subject | cGMP pathway | - |
dc.subject | Hippocampus | - |
dc.subject | Nitric oxide | - |
dc.subject | S-Nitrosylation | - |
dc.subject | Voltage-gated calcium currents | - |
dc.subject.mesh | Animals | en_US |
dc.subject.mesh | Calcium Channels - Metabolism | en_US |
dc.subject.mesh | Cyclic Gmp - Metabolism | en_US |
dc.subject.mesh | Hippocampus - Drug Effects - Metabolism | en_US |
dc.subject.mesh | Ion Channel Gating | en_US |
dc.subject.mesh | Neurons - Drug Effects - Metabolism | en_US |
dc.subject.mesh | Nitric Oxide - Metabolism | en_US |
dc.subject.mesh | Nitrogen - Metabolism | en_US |
dc.subject.mesh | Polyamines - Pharmacology | en_US |
dc.subject.mesh | Rats | en_US |
dc.subject.mesh | Rats, Sprague-Dawley | en_US |
dc.subject.mesh | Signal Transduction | en_US |
dc.subject.mesh | Tissue Culture Techniques | en_US |
dc.title | Nitric oxide modulation of voltage-gated calcium current by S-nitrosylation and cGMP pathway in cultured rat hippocampal neurons | en_US |
dc.type | Article | en_US |
dc.identifier.email | Fung, ML:fungml@hkucc.hku.hk | en_US |
dc.identifier.authority | Fung, ML=rp00433 | en_US |
dc.description.nature | link_to_subscribed_fulltext | en_US |
dc.identifier.doi | 10.1016/j.bbrc.2007.05.113 | en_US |
dc.identifier.pmid | 17544367 | - |
dc.identifier.scopus | eid_2-s2.0-34250172430 | en_US |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-34250172430&selection=ref&src=s&origin=recordpage | en_US |
dc.identifier.volume | 359 | en_US |
dc.identifier.issue | 3 | en_US |
dc.identifier.spage | 481 | en_US |
dc.identifier.epage | 485 | en_US |
dc.identifier.isi | WOS:000247582500014 | - |
dc.publisher.place | United States | en_US |
dc.identifier.scopusauthorid | Jian, K=36929518800 | en_US |
dc.identifier.scopusauthorid | Chen, M=35285618500 | en_US |
dc.identifier.scopusauthorid | Cao, X=36985373700 | en_US |
dc.identifier.scopusauthorid | Zhu, XH=7406186945 | en_US |
dc.identifier.scopusauthorid | Fung, ML=7101955092 | en_US |
dc.identifier.scopusauthorid | Gao, TM=7101845480 | en_US |
dc.identifier.issnl | 0006-291X | - |