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Volumn 67, Issue 22, 2000, Pages 2759-2766

Interaction of lidocaine with the cardiac sodium channel. Effects of low extracellular pH are consistent with an external blocking site

Author keywords

Cardiac sodium channel; Class I antiarrythmic; Ischaemia; Lidocaine

Indexed keywords

ANTIARRHYTHMIC AGENT; LIDOCAINE; SODIUM CHANNEL;

EID: 0034692901     PISSN: 00243205     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0024-3205(00)00855-9     Document Type: Article
Times cited : (10)

References (20)
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    • Wyse, K.R.1    Ye, V.2    Campbell, T.J.3
  • 6
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    • Importance of physico-chemical properties in determining the kinetics of the effects of Class I antiarrhythmic drugs on maximum rate of depolarization in guinea-pig ventricle
    • Sep
    • (1983) Br J Pharmacol , vol.80 , Issue.1 , pp. 33-40
    • Campbell, T.J.1
  • 9
    • 0027140475 scopus 로고
    • Dissecting lidocaine action: Diethylamide and phenol mimic modes of lidocaine block of sodium channels from heart and skeletal muscle
    • Dec
    • (1993) Biophys J , vol.65 , Issue.6 , pp. 2335-2347
    • Zamponi, G.W.1    French, R.J.2
  • 14
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    • Local anesthetics: Hydrophilic and hydrophobic pathways for the drug-receptor reaction
    • Apr
    • (1977) J Gen Physiol , vol.69 , Issue.4 , pp. 497-515
    • Hille, B.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.