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- Publisher Website: 10.1007/s11010-007-9691-3
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- PMID: 18165926
- WOS: WOS:000254204500005
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Article: Genistein potentiates protein kinase A activity in porcine coronary artery
Title | Genistein potentiates protein kinase A activity in porcine coronary artery |
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Authors | |
Keywords | cAMP Genistein Protein kinase A Relaxation Vascular smooth muscle |
Issue Date | 2008 |
Publisher | Springer New York LLC. The Journal's web site is located at http://springerlink.metapress.com/openurl.asp?genre=journal&issn=0300-8177 |
Citation | Molecular And Cellular Biochemistry, 2008, v. 311 n. 1-2, p. 37-44 How to Cite? |
Abstract | Soy consumption is associated with a lower risk of atherosclerotic disease in the oriental population. Genistein is a soy isoflavone bearing estrogenic properties. Previous experiments in our laboratory demonstrated the potentiation of endothelium-independent relaxation of coronary artery by both estrogen and genistein. The potentiating effects of both estrogen and genistein were mediated through the cAMP-signaling pathway. We hypothesize that genistein could enhance protein kinase A (PKA) activity in porcine coronary artery smooth muscle, thereby offering a mechanism for the potentiation of vascular relaxation by genistein. In our study, a high concentration of genistein (10 -4.5 M) significantly increased PKA activity in porcine coronary artery rings. While genistein at 10 -5.5 M and forskolin at 10 -7 M had no effect on PKA activity, the combination of the two compounds at the prescribed concentrations caused a significant increase in PKA activity. The increase in PKA activity by genistein was abolished by SQ 22536 (adenylate cyclase blocker), but not by NF 449 (Gs protein blocker) or ICI 182780 (estrogen receptor antagonist). Our results suggest that the action of genistein is mediated via adenylate cyclase, but does not appear to involve Gs protein or ICI 182780-sensitive estrogen receptor. © Springer Science+Business Media, LLC. 2007. |
Persistent Identifier | http://hdl.handle.net/10722/67306 |
ISSN | 2023 Impact Factor: 3.5 2023 SCImago Journal Rankings: 0.901 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Ng, William WH | en_HK |
dc.contributor.author | Keung, W | en_HK |
dc.contributor.author | Xu, YC | en_HK |
dc.contributor.author | Ng, KFJ | en_HK |
dc.contributor.author | Leung, GPH | en_HK |
dc.contributor.author | Vanhoutte, PM | en_HK |
dc.contributor.author | Choy, PC | en_HK |
dc.contributor.author | Man, RYK | en_HK |
dc.date.accessioned | 2010-09-06T05:53:49Z | - |
dc.date.available | 2010-09-06T05:53:49Z | - |
dc.date.issued | 2008 | en_HK |
dc.identifier.citation | Molecular And Cellular Biochemistry, 2008, v. 311 n. 1-2, p. 37-44 | en_HK |
dc.identifier.issn | 0300-8177 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/67306 | - |
dc.description.abstract | Soy consumption is associated with a lower risk of atherosclerotic disease in the oriental population. Genistein is a soy isoflavone bearing estrogenic properties. Previous experiments in our laboratory demonstrated the potentiation of endothelium-independent relaxation of coronary artery by both estrogen and genistein. The potentiating effects of both estrogen and genistein were mediated through the cAMP-signaling pathway. We hypothesize that genistein could enhance protein kinase A (PKA) activity in porcine coronary artery smooth muscle, thereby offering a mechanism for the potentiation of vascular relaxation by genistein. In our study, a high concentration of genistein (10 -4.5 M) significantly increased PKA activity in porcine coronary artery rings. While genistein at 10 -5.5 M and forskolin at 10 -7 M had no effect on PKA activity, the combination of the two compounds at the prescribed concentrations caused a significant increase in PKA activity. The increase in PKA activity by genistein was abolished by SQ 22536 (adenylate cyclase blocker), but not by NF 449 (Gs protein blocker) or ICI 182780 (estrogen receptor antagonist). Our results suggest that the action of genistein is mediated via adenylate cyclase, but does not appear to involve Gs protein or ICI 182780-sensitive estrogen receptor. © Springer Science+Business Media, LLC. 2007. | en_HK |
dc.language | eng | en_HK |
dc.publisher | Springer New York LLC. The Journal's web site is located at http://springerlink.metapress.com/openurl.asp?genre=journal&issn=0300-8177 | en_HK |
dc.relation.ispartof | Molecular and Cellular Biochemistry | en_HK |
dc.rights | The original publication is available at www.springerlink.com | - |
dc.subject | cAMP | en_HK |
dc.subject | Genistein | en_HK |
dc.subject | Protein kinase A | en_HK |
dc.subject | Relaxation | en_HK |
dc.subject | Vascular smooth muscle | en_HK |
dc.subject.mesh | Adenine - analogs and derivatives - metabolism - pharmacology | - |
dc.subject.mesh | Coronary Vessels - anatomy and histology - drug effects - metabolism | - |
dc.subject.mesh | Genistein - metabolism - pharmacology | - |
dc.subject.mesh | Muscle, Smooth, Vascular - drug effects - metabolism | - |
dc.subject.mesh | Protein Kinase Inhibitors - metabolism - pharmacology | - |
dc.title | Genistein potentiates protein kinase A activity in porcine coronary artery | en_HK |
dc.type | Article | en_HK |
dc.identifier.openurl | http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=0300-8177&volume=311&issue=1-2&spage=37&epage=44&date=2008&atitle=Genistein+potentiates+protein+kinase+A+activity+in+porcine+coronary+artery | en_HK |
dc.identifier.email | Ng, KFJ: jkfng@hkucc.hku.hk | en_HK |
dc.identifier.email | Leung, GPH: gphleung@hkucc.hku.hk | en_HK |
dc.identifier.email | Vanhoutte, PM: vanhoutt@hku.hk | en_HK |
dc.identifier.email | Man, RYK: rykman@hkucc.hku.hk | en_HK |
dc.identifier.authority | Ng, KFJ=rp00544 | en_HK |
dc.identifier.authority | Leung, GPH=rp00234 | en_HK |
dc.identifier.authority | Vanhoutte, PM=rp00238 | en_HK |
dc.identifier.authority | Man, RYK=rp00236 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1007/s11010-007-9691-3 | en_HK |
dc.identifier.pmid | 18165926 | - |
dc.identifier.scopus | eid_2-s2.0-41349091455 | en_HK |
dc.identifier.hkuros | 168516 | en_HK |
dc.identifier.hkuros | 143132 | - |
dc.identifier.hkuros | 214410 | - |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-41349091455&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 311 | en_HK |
dc.identifier.issue | 1-2 | en_HK |
dc.identifier.spage | 37 | en_HK |
dc.identifier.epage | 44 | en_HK |
dc.identifier.isi | WOS:000254204500005 | - |
dc.publisher.place | United States | en_HK |
dc.identifier.scopusauthorid | Ng, William WH=7401613562 | en_HK |
dc.identifier.scopusauthorid | Keung, W=19337708900 | en_HK |
dc.identifier.scopusauthorid | Xu, YC=35106482400 | en_HK |
dc.identifier.scopusauthorid | Ng, KFJ=13608809400 | en_HK |
dc.identifier.scopusauthorid | Leung, GPH=35963668200 | en_HK |
dc.identifier.scopusauthorid | Vanhoutte, PM=7202304247 | en_HK |
dc.identifier.scopusauthorid | Choy, PC=7006633002 | en_HK |
dc.identifier.scopusauthorid | Man, RYK=7004986435 | en_HK |
dc.identifier.issnl | 0300-8177 | - |