Inhibition of human ether-à-go-go-related gene K+ currents expressed in HEK293 cells by three gingerol components from ginger

Author:

Liu Miaomaio1,Yang Yakun1,Zhang Muqing1,Xue Yucong1,Zheng Bin1,Zhang Yuanyuan1,Liu Yu1,Chu Xi2,Sun Zhenqing3,Han Xue45

Affiliation:

1. School of Pharmacy, Hebei University of Chinese Medicine , Shijiazhuang, Hebei , China

2. The Fourth Hospital of Hebei Medical University , Shijiazhuang, Hebei , China

3. Qingdao Hospital of Traditional Chinese Medicine (Qingdao Hiser hospital) , Qingdao, Shandong , China

4. Affiliated Hospital, Hebei University of Chinese Medicine , Shijiazhuang, Hebei , China

5. Hebei Key Laboratory of Integrative Medicine on Liver-Kidney Patterns, Hebei University of Chinese Medicine , Shijiazhuang, Hebei , China

Abstract

Abstract Objectives Gingerols are bioactive compounds derived from ginger, our experiment investigates the effects of 6-, 8- and 10-Gin on the human ether-à-go-go-related gene (hERG) K+ channels by using patch clamp technology. Key findings hERG K+ currents were suppressed by 6-, 8- and 10-Gin in a concentration-dependent manner. The IC50 values of 6-, 8- and 10-Gin were 41.5, 16.1 and 86.5 μM for the hERG K+ currents, respectively. The maximum inhibitory effects caused by 6-, 8- and 10-Gin were 44.3% ± 2.0%, 88.6% ± 1.3% and 63.1% ± 1.1%, respectively, and the effects were almost completely reversible. Conclusion These findings suggest that 8-Gin is the most potent hERG K+ channel inhibitor among gingerol components and may offer a new approach for understanding and treating cancer.

Funder

Nature Fund of Hebei Province

Project of Science and Technology Research Project of Hebei Province

Publisher

Oxford University Press (OUP)

Subject

Pharmaceutical Science,Pharmacology

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