Cardiac effects and toxicity of chloroquine: a short update

被引:54
作者
Mubagwa, Kanigula [1 ,2 ,3 ]
机构
[1] Katholieke Univ Leuven, Dept Cardiovasc Sci, Leuven, Belgium
[2] Univ Catholique Bukavu, Dept Basic Sci, Fac Med, Bukavu, DEM REP CONGO
[3] Univ Leuven, Dept Cardiovasc Sci, Campus Gasthuisberg,Herestr 49, B-3000 Leuven, Belgium
关键词
Chloroquine; Hydroxychloroquine; Cardiac; Ion channel; Muscarinic receptor; Autophagy; SYSTEMIC-LUPUS-ERYTHEMATOSUS; TRANSIENT OUTWARD CURRENT; EPICARDIAL BORDER ZONE; RAT SOLEUS MUSCLE; ANTIMALARIAL-DRUGS; MUSCARINIC ANTAGONIST; MOLECULAR-MECHANISMS; HEART-FAILURE; AUTOPHAGY; INHIBITION;
D O I
10.1016/j.ijantimicag.2020.106057
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
There is currently increased interest in the use of the antimalarial drugs chloroquine and hydroxychloroquine for the treatment of other diseases, including cancer and viral infections such as coronavirus disease 2019 (COVID-19). However, the risk of cardiotoxic effects tends to limit their use. In this review, the effects of these drugs on the electrical and mechanical activities of the heart as well as on remodelling of cardiac tissue are presented and the underlying molecular and cellular mechanisms are discussed. The drugs can have proarrhythmic as well as antiarrhythmic actions resulting from their inhibition of ion channels, including voltage-dependent Na+ and Ca2+ channels, background and voltage-dependent K+ channels, and pacemaker channels. The drugs also exert a vagolytic effect due at least in part to a muscarinic receptor antagonist action. They also interfere with normal autophagy flux, an effect that could aggravate ischaemia/reperfusion injury or post-infarct remodelling. Most of the toxic effects occur at high concentrations, following prolonged drug administration or in the context of drug associations. (C) 2020 The Author(s). Published by Elsevier B.V.
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页数:10
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