Literature DB >> 17706639

Antiarrhythmic effect of newly synthesized compound 44Bu on model of aconitine-induced arrhythmia -- compared to lidocaine.

Ladislava Bartosova1, Filip Novak, Marketa Bebarova, Marek Frydrych, Vit Brunclik, Radka Opatrilova, Jana Kolevska, Petr Mokry, Peter Kollar, Vera Strnadova, Pavel Suchy.   

Abstract

The antiarrhythmic action of the newly developed compound 44Bu (an original compound that was synthesized at our Faculty of Pharmacy) was tested on a model of aconitine-induced arrhythmia and compared with the effect of lidocaine. Both tested substances were administered either as therapeutic or prophylactic agents. 44Bu was highly effective in reducing the occurrence of ventricular fibrillation from 94% to 8% by therapeutic administration, and to 0% by prophylactic administration. The overall mortality rate was significantly reduced by 44Bu from 100% to 25% in the case of therapeutic administration, and to 0% in the case of prophylactic administration. In contrast, there was not any significant difference between therapeutic and prophylactic administration of lidocaine. The occurrence of ventricular fibrillation dropped from 94% to 50% with therapeutic administration, and to 67% with prophylactic administration of lidocaine. The overall mortality rate was significantly reduced from 100% to 63% and to 67%, respectively. We conclude that the 44Bu compound is a highly effective agent in suppressing aconitine-induced arrhythmias. The antiarrhythmic effect of 44Bu was significantly more evident in comparison with lidocaine, particularly in the case of its prophylactic administration.

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Year:  2007        PMID: 17706639     DOI: 10.1016/j.ejphar.2007.07.044

Source DB:  PubMed          Journal:  Eur J Pharmacol        ISSN: 0014-2999            Impact factor:   4.432


  6 in total

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Authors:  Kai Yang; Jie Liang; Qinfan Li; Xiangya Kong; Rui Chen; Yimin Jin
Journal:  World J Microbiol Biotechnol       Date:  2012-12-27       Impact factor: 3.312

2.  Gallic Acid Inhibits Mesaconitine-Activated TRPV1-Channel-Induced Cardiotoxicity.

Authors:  Shu Han; Liyuan Bao; Weifei Li; Kaiyang Liu; Ya'nan Tang; Xitao Han; Ziqin Liu; Hongyue Wang; Fengting Zhang; Shuo Mi; Hong Du
Journal:  Evid Based Complement Alternat Med       Date:  2022-04-13       Impact factor: 2.650

3.  L-Type Calcium Channel Inhibition Contributes to the Proarrhythmic Effects of Aconitine in Human Cardiomyocytes.

Authors:  Jianjun Wu; Xiangchong Wang; Ying Ying Chung; Cai Hong Koh; Zhenfeng Liu; Huicai Guo; Qiang Yuan; Chuan Wang; Suwen Su; Heming Wei
Journal:  PLoS One       Date:  2017-01-05       Impact factor: 3.240

4.  Design, synthesis, and biological evaluation of arylmethylpiperidines as Kv1.5 potassium channel inhibitors.

Authors:  Lingyue Zhao; Qian Yang; Yiqun Tang; Qidong You; Xiaoke Guo
Journal:  J Enzyme Inhib Med Chem       Date:  2022-12       Impact factor: 5.051

5.  Attenuated Structural Transformation of Indaconitine during Sand Frying Process and Anti-Arrhythmic Effects of Its Transformed Products.

Authors:  Yan Wang; Pei Tao; Yu-Jie Wang
Journal:  Evid Based Complement Alternat Med       Date:  2022-02-17       Impact factor: 2.629

6.  Inhibition of the INa/K and the activation of peak INa contribute to the arrhythmogenic effects of aconitine and mesaconitine in guinea pigs.

Authors:  Xiang-Chong Wang; Qing-Zhong Jia; Yu-Lou Yu; Han-Dong Wang; Hui-Cai Guo; Xin-di Ma; Chun-Tong Liu; Xue-Yan Chen; Qing-Feng Miao; Bing-Cai Guan; Su-Wen Su; He-Ming Wei; Chuan Wang
Journal:  Acta Pharmacol Sin       Date:  2020-08-03       Impact factor: 6.150

  6 in total

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