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- Publisher Website: 10.1016/j.bcp.2012.05.002
- Scopus: eid_2-s2.0-84864138148
- PMID: 22583923
- WOS: WOS:000307135600011
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Article: Effects of the natural flavone trimethylapigenin on cardiac potassium currents
Title | Effects of the natural flavone trimethylapigenin on cardiac potassium currents |
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Authors | |
Keywords | Acetylcholine-Activated K + Current Hkv1.5 Open Channel Blocker Trimethylapigenin |
Issue Date | 2012 |
Publisher | Elsevier Inc. The Journal's web site is located at http://www.elsevier.com/locate/biochempharm |
Citation | Biochemical Pharmacology, 2012, v. 84 n. 4, p. 498-506 How to Cite? |
Abstract | The natural flavones and polymethylflavone have been reported to have cardiovascular protective effects. In the present study, we determined whether quecertin, apigenin and their methylated compounds (3,7,3′,4′-tetramethylquecertin, 3,5,7,3′,4′-pentamethylquecertin, 7,4′-dimethylapigenin, and 5,7,4′-trimethylapigenin) would block the atrial specific potassium channel hKv1.5 using a whole-cell patch voltage-clamp technique. We found that only trimethylapigenin showed a strong inhibitory effect on hKv1.5 channel current. This compound suppressed hKv1.5 current in HEK 293 cell line (IC 50 = 6.4 μM), and the ultra-rapid delayed rectify K + current I Kur in human atrial myocytes (IC 50 = 8.0 μM) by binding to the open channels and showed a use- and frequency-dependent manner. In addition, trimethylapigenin decreased transient outward potassium current (I to) in human atrial myocytes, inhibited acetylcholine-activated K + current (IC 50 = 6.8 μM) in rat atrial myocytes. Interestingly, trimethylapigenin had a weak inhibition of hERG channel current. Our results indicate that trimethyapigenin significantly inhibits the atrial potassium currents hKv1.5/I Kur and I KACh, which suggests that trimethylapigenin may be a potential candidate for anti-atrial fibrillation. © 2012 Elsevier Inc. All rights reserved. |
Persistent Identifier | http://hdl.handle.net/10722/163493 |
ISSN | 2023 Impact Factor: 5.3 2023 SCImago Journal Rankings: 1.365 |
ISI Accession Number ID |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Liu, Y | en_US |
dc.contributor.author | Xu, XH | en_US |
dc.contributor.author | Liu, Z | en_US |
dc.contributor.author | Du, XL | en_US |
dc.contributor.author | Chen, KH | en_US |
dc.contributor.author | Xin, X | en_US |
dc.contributor.author | Jin, ZD | en_US |
dc.contributor.author | Shen, JZ | en_US |
dc.contributor.author | Hu, Y | en_US |
dc.contributor.author | Li, GR | en_US |
dc.contributor.author | Jin, MW | en_US |
dc.date.accessioned | 2012-09-05T05:32:16Z | - |
dc.date.available | 2012-09-05T05:32:16Z | - |
dc.date.issued | 2012 | en_US |
dc.identifier.citation | Biochemical Pharmacology, 2012, v. 84 n. 4, p. 498-506 | en_US |
dc.identifier.issn | 0006-2952 | en_US |
dc.identifier.uri | http://hdl.handle.net/10722/163493 | - |
dc.description.abstract | The natural flavones and polymethylflavone have been reported to have cardiovascular protective effects. In the present study, we determined whether quecertin, apigenin and their methylated compounds (3,7,3′,4′-tetramethylquecertin, 3,5,7,3′,4′-pentamethylquecertin, 7,4′-dimethylapigenin, and 5,7,4′-trimethylapigenin) would block the atrial specific potassium channel hKv1.5 using a whole-cell patch voltage-clamp technique. We found that only trimethylapigenin showed a strong inhibitory effect on hKv1.5 channel current. This compound suppressed hKv1.5 current in HEK 293 cell line (IC 50 = 6.4 μM), and the ultra-rapid delayed rectify K + current I Kur in human atrial myocytes (IC 50 = 8.0 μM) by binding to the open channels and showed a use- and frequency-dependent manner. In addition, trimethylapigenin decreased transient outward potassium current (I to) in human atrial myocytes, inhibited acetylcholine-activated K + current (IC 50 = 6.8 μM) in rat atrial myocytes. Interestingly, trimethylapigenin had a weak inhibition of hERG channel current. Our results indicate that trimethyapigenin significantly inhibits the atrial potassium currents hKv1.5/I Kur and I KACh, which suggests that trimethylapigenin may be a potential candidate for anti-atrial fibrillation. © 2012 Elsevier Inc. All rights reserved. | en_US |
dc.language | eng | en_US |
dc.publisher | Elsevier Inc. The Journal's web site is located at http://www.elsevier.com/locate/biochempharm | en_US |
dc.relation.ispartof | Biochemical Pharmacology | en_US |
dc.subject | Acetylcholine-Activated K + Current | en_US |
dc.subject | Hkv1.5 | en_US |
dc.subject | Open Channel Blocker | en_US |
dc.subject | Trimethylapigenin | en_US |
dc.title | Effects of the natural flavone trimethylapigenin on cardiac potassium currents | en_US |
dc.type | Article | en_US |
dc.identifier.email | Li, GR:grli@hkucc.hku.hk | en_US |
dc.identifier.authority | Li, GR=rp00476 | en_US |
dc.description.nature | link_to_subscribed_fulltext | en_US |
dc.identifier.doi | 10.1016/j.bcp.2012.05.002 | en_US |
dc.identifier.pmid | 22583923 | - |
dc.identifier.scopus | eid_2-s2.0-84864138148 | en_US |
dc.identifier.hkuros | 202912 | - |
dc.identifier.isi | WOS:000307135600011 | - |
dc.publisher.place | United States | en_US |
dc.identifier.scopusauthorid | Liu, Y=55071922600 | en_US |
dc.identifier.scopusauthorid | Xu, XH=37082609600 | en_US |
dc.identifier.scopusauthorid | Liu, Z=55228841900 | en_US |
dc.identifier.scopusauthorid | Du, XL=53263675600 | en_US |
dc.identifier.scopusauthorid | Chen, KH=55228781400 | en_US |
dc.identifier.scopusauthorid | Xin, X=37462585400 | en_US |
dc.identifier.scopusauthorid | Jin, ZD=37461509500 | en_US |
dc.identifier.scopusauthorid | Shen, JZ=55073430400 | en_US |
dc.identifier.scopusauthorid | Hu, Y=50261872200 | en_US |
dc.identifier.scopusauthorid | Li, GR=7408462932 | en_US |
dc.identifier.scopusauthorid | Jin, MW=35932258500 | en_US |
dc.identifier.citeulike | 11092493 | - |
dc.identifier.issnl | 0006-2952 | - |