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Dimethyl lithospermate B, an extract of Danshen, suppresses arrhythmogenesis associated with the Brugada syndrome

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dc.contributor.authorFish, Jeffrey M.-
dc.contributor.authorWelchons, Daniel R.-
dc.contributor.authorKim, Young-Sup-
dc.contributor.authorLee, Suk-Ho-
dc.contributor.authorHo, Won-Kyung-
dc.contributor.authorAntzelevitch, Charles-
dc.date.accessioned2010-01-07T05:11:09Z-
dc.date.available2010-01-07T05:11:09Z-
dc.date.issued2005-03-15-
dc.identifier.citationCirculation. 2006 Mar 21;113(11):1393-400. Epub 2006 Mar 13.en
dc.identifier.issn1524-4539 (Electronic)-
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Citation&list_uids=16534004-
dc.identifier.urihttps://hdl.handle.net/10371/28226-
dc.description.abstractBACKGROUND: Dimethyl lithospermate B (dmLSB) is an extract of Danshen, a traditional Chinese herbal remedy, which slows inactivation of INa, leading to increased inward current during the early phases of the action potential (AP). We hypothesized that this action would be antiarrhythmic in the setting of Brugada syndrome. METHODS AND RESULTS: The Brugada syndrome phenotype was created in canine arterially perfused right ventricular wedge preparations with the use of either terfenadine or verapamil to inhibit INa and ICa or pinacidil to activate IK-ATP. AP recordings were simultaneously recorded from epicardial and endocardial sites together with an ECG. Terfenadine, verapamil, and pinacidil each induced all-or-none repolarization at some epicardial sites but not others, leading to ST-segment elevation as well as an increase in both epicardial and transmural dispersions of repolarization (EDR and TDR, respectively) from 12.9+/-9.6 to 107.0+/-54.8 ms and from 22.4+/-8.1 to 82.2+/-37.4 ms, respectively (P<0.05; n=9). Under these conditions, phase 2 reentry developed as the epicardial AP dome propagated from sites where it was maintained to sites at which it was lost, generating closely coupled extrasystoles and ventricular tachycardia and fibrillation. Addition of dmLSB (10 micromol/L) to the coronary perfusate restored the epicardial AP dome, reduced EDR and TDR to 12.4+/-18.1 and 24.4+/-26.7 ms, respectively (P<0.05; n=9), and abolished phase 2 reentry-induced extrasystoles and ventricular tachycardia and fibrillation in 9 of 9 preparations. CONCLUSIONS: Our data suggest that dmLSB is effective in eliminating the arrhythmogenic substrate responsible for the Brugada syndrome and that it deserves further study as a pharmacological adjunct to implanted cardioverter/defibrillator usage.en
dc.language.isoenen
dc.publisherAmerican Heart Associationen
dc.subjectAnimalsen
dc.subjectArrhythmias, Cardiac/etiology/*prevention & controlen
dc.subjectBiological Transport/drug effectsen
dc.subjectCalcium Channel Blockers/toxicityen
dc.subjectDogsen
dc.subjectDrug Evaluation, Preclinicalen
dc.subjectDrugs, Chinese Herbal/isolation & purification/*therapeutic useen
dc.subjectElectrocardiography/drug effectsen
dc.subjectFemaleen
dc.subjectMaleen
dc.subjectPinacidil/toxicityen
dc.subjectPlant Extracts/isolation & purification/*therapeutic useen
dc.subjectPlant Roots/chemistryen
dc.subjectPotassium Channels/agonistsen
dc.subjectSalvia miltiorrhiza/*chemistryen
dc.subjectSodium/metabolismen
dc.subjectSodium Channel Blockers/toxicityen
dc.subjectSodium Channels/*agonists/physiologyen
dc.subjectStimulation, Chemicalen
dc.subjectTerfenadine/toxicityen
dc.subjectVerapamil/toxicityen
dc.titleDimethyl lithospermate B, an extract of Danshen, suppresses arrhythmogenesis associated with the Brugada syndromeen
dc.typeArticleen
dc.contributor.AlternativeAuthor김영섭-
dc.contributor.AlternativeAuthor이석호-
dc.contributor.AlternativeAuthor호원경-
dc.identifier.doi10.1161/CIRCULATIONAHA.105.601690-
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