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Article: Cardiac effects of the extract and active components of radix stephaniae tetrandrae: II. Myocardial infarct, arrhythmias, coronary arterial flow and heart rate in the isolated perfused rat heart

TitleCardiac effects of the extract and active components of radix stephaniae tetrandrae: II. Myocardial infarct, arrhythmias, coronary arterial flow and heart rate in the isolated perfused rat heart
Authors
KeywordsArrhythmia
Fangchinoline
Infarct size
Langendorff perfused rat heart
Radix stephaniae tetrandrae
Tetrandrine
Verapamil
Issue Date2001
PublisherElsevier Inc. The Journal's web site is located at http://www.elsevier.com/locate/lifescie
Citation
Life Sciences, 2001, v. 68 n. 25, p. 2863-2872 How to Cite?
AbstractThe primary purpose of the present study was to compare the cardioprotective effects of the extract from radix stephaniae tetrandrae (RST) and its individual compounds, tetrandrine (Tet) and fanchinoline (Fan). Secondly, we also compared the cardiac effects of the individual compounds and the RST extract with those of verapamil, a classical Ca2+ channel blocker. The Langendorff isolated perfused rat heart preparation was used. Regional ischaemia and reperfusion was employed to induce myocardial infarct and arrhythmia. Infarct, arrhythmia, heart rate and coronary artery flow were determined in hearts treated with vehicle, RST extract, Tet, Fan, or verapamil. It was found that RST extract, of which only 9% was Tet, and Tet alone produced equally potent ameliorating effects on arrhythmia and infarct induced by ischaemia and reperfusion without further inhibiting ischaemia-reduced heart rate and coronary artery flow. Fan had no effects on arrhythmia and infarct induced by ischaemia and reperfusion; but it induced S-T segment elevation and further reduced heart rate and coronary artery flow during ischaemia. Verapamil also ameliorated the effects of ischaemia and reperfusion on arrhythmia and infarct. It should be noted that 1 μM verapamil, that produced comparable effects on infarct and arrhythmia to the RST extract and Tet, further inhibited heart rate during ischaemia. The results indicate that the RST extract produces equally potent cardioprotective and anti-arrhythmic effects as Tet alone. Both RST extract and Tet may be better choices for the treatment of arrhythmia and infarct induced by myocardial ischaemia and reperfusion than the classical Ca2+ channel blocker, verapamil as they do not further reduce heart rate during ischaemia.
Persistent Identifierhttp://hdl.handle.net/10722/224117
ISSN
2021 Impact Factor: 6.780
2020 SCImago Journal Rankings: 1.131
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorYu, XC-
dc.contributor.authorWu, S-
dc.contributor.authorWang, GY-
dc.contributor.authorShan, J-
dc.contributor.authorWong, TM-
dc.contributor.authorChen, CF-
dc.contributor.authorPang, KT-
dc.date.accessioned2016-03-24T03:09:18Z-
dc.date.available2016-03-24T03:09:18Z-
dc.date.issued2001-
dc.identifier.citationLife Sciences, 2001, v. 68 n. 25, p. 2863-2872-
dc.identifier.issn0024-3205-
dc.identifier.urihttp://hdl.handle.net/10722/224117-
dc.description.abstractThe primary purpose of the present study was to compare the cardioprotective effects of the extract from radix stephaniae tetrandrae (RST) and its individual compounds, tetrandrine (Tet) and fanchinoline (Fan). Secondly, we also compared the cardiac effects of the individual compounds and the RST extract with those of verapamil, a classical Ca2+ channel blocker. The Langendorff isolated perfused rat heart preparation was used. Regional ischaemia and reperfusion was employed to induce myocardial infarct and arrhythmia. Infarct, arrhythmia, heart rate and coronary artery flow were determined in hearts treated with vehicle, RST extract, Tet, Fan, or verapamil. It was found that RST extract, of which only 9% was Tet, and Tet alone produced equally potent ameliorating effects on arrhythmia and infarct induced by ischaemia and reperfusion without further inhibiting ischaemia-reduced heart rate and coronary artery flow. Fan had no effects on arrhythmia and infarct induced by ischaemia and reperfusion; but it induced S-T segment elevation and further reduced heart rate and coronary artery flow during ischaemia. Verapamil also ameliorated the effects of ischaemia and reperfusion on arrhythmia and infarct. It should be noted that 1 μM verapamil, that produced comparable effects on infarct and arrhythmia to the RST extract and Tet, further inhibited heart rate during ischaemia. The results indicate that the RST extract produces equally potent cardioprotective and anti-arrhythmic effects as Tet alone. Both RST extract and Tet may be better choices for the treatment of arrhythmia and infarct induced by myocardial ischaemia and reperfusion than the classical Ca2+ channel blocker, verapamil as they do not further reduce heart rate during ischaemia.-
dc.languageeng-
dc.publisherElsevier Inc. The Journal's web site is located at http://www.elsevier.com/locate/lifescie-
dc.relation.ispartofLife Sciences-
dc.subjectArrhythmia-
dc.subjectFangchinoline-
dc.subjectInfarct size-
dc.subjectLangendorff perfused rat heart-
dc.subjectRadix stephaniae tetrandrae-
dc.subjectTetrandrine-
dc.subjectVerapamil-
dc.subject.meshAlkaloids - therapeutic use-
dc.subject.meshBenzylisoquinolines-
dc.subject.meshCalcium Channel Blockers - therapeutic use-
dc.subject.meshDrugs, Chinese Herbal - therapeutic use-
dc.subject.meshMyocardial Infarction - physiopathology - prevention & control-
dc.titleCardiac effects of the extract and active components of radix stephaniae tetrandrae: II. Myocardial infarct, arrhythmias, coronary arterial flow and heart rate in the isolated perfused rat heart-
dc.typeArticle-
dc.identifier.emailWu, S: swua@hkucc.hku.hk-
dc.identifier.emailWong, TM: wongtakm@hkucc.hku.hk-
dc.identifier.doi10.1016/S0024-3205(01)01067-0-
dc.identifier.pmid11432452-
dc.identifier.scopuseid_2-s2.0-0035844011-
dc.identifier.hkuros60027-
dc.identifier.volume68-
dc.identifier.issue25-
dc.identifier.spage2863-
dc.identifier.epage2872-
dc.identifier.isiWOS:000168753700010-
dc.publisher.placeUnited States-
dc.identifier.issnl0024-3205-

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