4.7 Article

Eugenol interacts with cardiac sodium channel and reduces heart excitability and arrhythmias

期刊

LIFE SCIENCES
卷 282, 期 -, 页码 -

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.lfs.2021.119761

关键词

Eugenol; Sodium channel; Na(v)1.5; Arrhythmia; Heart

资金

  1. Sao Paulo Research Foundation (FAPESP) [2019/21304-4, 2018/22830-9, 2018/20777-3]
  2. Brazilian Coordination for the Improvement of Higher Education Personnel (CAPES)
  3. National Council for Scientific and Technological Development (CNPq)
  4. Internal Program of Initiation in sciences (PICIN) of Universidade do Estado da Bahia
  5. CNPq [304257/2020-6]

向作者/读者索取更多资源

Eugenol, a natural compound found in aromatic plants, has been shown to have antiarrhythmic activity by reducing sodium current, shifting inactivation curve, delaying recovery from inactivation, and blocking the channel in the inactivated state. These findings suggest that eugenol interacts with Na(v)1.5 to exert its antiarrhythmic effects.
Aims: Eugenol is a natural compound found in the essential oils of many aromatic plants. The compound is used as a local anesthetic because of its inhibitory effect on the voltage-gated Na+ channels (Na-v), which are expressed in the nociceptive neurons. Eugenol has shown wide range of activities in the cardiovascular system; most of these activities are attributed to the modulation of voltage-sensitive Ca2+ channels. However, its action on Na(v)1.5, the main subtype of Na-v expressed in the mammalian myocardium, is unknown. The interaction of eugenol with Na(v)1.5 could also contribute to its antiarrhythmic properties in vitro and ex vivo. We investigated the compound's effect on sodium current (I-Na) and its possible cardiac antiarrhythmic activity. Methods: The effect of eugenol on cardiac contractility was investigated using isolated atrium from guinea pig (for isometric force measurements). The compound's effect on I-Na was evaluated using human embryonic cell transiently expressing human Na(v)1.5 and patch-clamp technique. Key findings: Eugenol caused negative inotropic and chronotropic effects in the atria. In the ex vivo arrhythmia model, eugenol decreased atrial pacing disturbance induced by ouabain. Eugenol reduced the I-Na in a concentration-dependent manner. Furthermore, the compound left-shifted the stationary inactivation curve, delayed recovery from inactivation of the I-Na, and preferentially blocked the channel in the inactivated state. Importantly, eugenol was able to attenuate the late sodium current. All these aspects are considered to be antiarrhythmic. Significance: Overall, our findings demonstrate that eugenol has antiarrhythmic activity due, at least in part, to its interaction with Na(v)1.5.

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