Structure-activity relationship of Baifuzi-cerebrosides on BKCa channel activation

被引:7
|
作者
Zhou, Li [1 ]
Zhang, Yu-Jiao [1 ]
Gao, Li-Juan [2 ]
Ye, Ying [2 ]
Qi, Jian-Hua [2 ]
Qi, Zhi [1 ]
机构
[1] Xiamen Univ, Dept Basic Med Sci, Coll Med, Xiamen 361102, Peoples R China
[2] Zhejiang Univ, Coll Pharmaceut Sci, Hangzhou 310058, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
Baifuzi-cerebroside; Ischemic stroke; BKCa channel; RECEPTOR POTENTIAL CHANNELS; CA2+-ACTIVATED K+ CHANNELS; FATTY-ACIDS; POTASSIUM CHANNELS; ISCHEMIC STROKE; ION CHANNELS; CONDUCTANCE; MODULATION; BETA; REPOLARIZATION;
D O I
10.1016/j.ejmech.2014.01.007
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Our previous study reported that a mixture of cerebrosides from traditional Chinese medicine Baifuzi could activate BKCa channel. It is curious to know the effect of each single cerebroside on the channel. Here we isolated 5 pure cerebrosides from the mixture and determined their chemical structures. The most potent one increased the single channel open probability 6 folds with EC50 value of 1.0 mu M. The structure activity relationship revealed that acyl chain length of cerebrosides has potent effect, while configuration of double bond at C8-C9 on their long chain base has weak effect on the channel activity. Thus, this research provides a guide for design and synthesis of a lead cerebroside with more potent effect on the BKCa channel. (C) 2014 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:301 / 307
页数:7
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