Taxifolin Glycoside Blocks Human ether-a-go-go Related Gene K+ Channels

被引:6
作者
Yun, Jihyun [1 ]
Bae, Hyemi [1 ]
Choi, Sun Eun [5 ]
Kim, Jung-Ha [4 ]
Choi, Young Wook [6 ]
Lim, Inja [1 ]
Lee, Chung Soo [2 ]
Lee, Min Won [6 ]
Ko, Jae-Hong [1 ]
Seo, Seong Jun [3 ]
Bang, Hyoweon [1 ]
机构
[1] Chung Ang Univ, Coll Med, Dept Physiol, Seoul 156756, South Korea
[2] Chung Ang Univ, Coll Med, Dept Pharmacol, Seoul 156756, South Korea
[3] Chung Ang Univ, Coll Med, Dept Dermatol, Seoul 156756, South Korea
[4] Chung Ang Univ, Coll Med, Dept Family Med, Seoul 156756, South Korea
[5] Nambu Univ, Dept Cosmetol Sci, Kwangju 506706, South Korea
[6] Chung Ang Univ, Coll Pharm, Seoul 156756, South Korea
关键词
hERG K+ channel; Long QT syndrome; Patch clamp; Taxifolin glycoside; TORSADE-DE-POINTES; ATOPIC-DERMATITIS; DRUG DEVELOPMENT; NC/NGA MICE; PROLONGATION;
D O I
10.4196/kjpp.2013.17.1.37
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Taxifolin glycoside is a new drug candidate for the treatment of atopic dermatitis (AD). Many drugs cause side effects such as long QT syndrome by blocking the human ether-a-go-go related gene (hERG) K.+ channels. To determine whether taxifolin glycoside would block hERG K+ channels, we recorded hERG K+ currents using a whole-cell patch clamp technique. We found that taxifolin glycoside directly blocked hERG K+ current in a concentration-dependent manner (EC50=9.6 +/- 0.7 mu M). The activation curve of hERG K+ channels was negatively shifted by taxifolin glycoside. In addition, taxifolin glycoside accelerated the activation time constant and reduced the onset of the inactivation time constant. These results suggest that taxifolin glycoside blocks hERG K+ channels that function by facilitating activation and inactivation process.
引用
收藏
页码:37 / 42
页数:6
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