Alkaloids from Corydalis decumbens suppress neuronal excitability in primary cultures of mouse neocortical neurons

被引:24
作者
Huang, Qilong [1 ]
Chen, Juan [1 ]
Zhang, Wanjin [1 ]
Zhou, Baoping [1 ]
Zhang, Chunlei [1 ]
Gerwick, William H. [2 ,3 ]
Cao, Zhengyu [1 ]
机构
[1] China Pharmaceut Univ, Sch Tridit Chinese Pharm, Jiangsu Prov Key Lab TCM Evaluat & Translat Dev, Nanjing 211198, Jiangsu, Peoples R China
[2] Univ Calif San Diego, Scripps Inst Oceanog, Ctr Marine Biotechnol & Biomed, La Jolla, CA 92093 USA
[3] Univ Calif San Diego, Skaggs Sch Pharm & Pharmaceut Sci, La Jolla, CA 92093 USA
基金
中国国家自然科学基金;
关键词
Corydalis decumbens; Chemical correlation; Alkaloids; Neuron excitability; ANTIINFLAMMATORY ACTIVITIES; ISOQUINOLINE ALKALOIDS; CA2+ OSCILLATIONS; MEDICINAL-PLANTS; PROTOPINE; TETRAHYDROPALMATINE; INHIBITION; CHANNELS;
D O I
10.1016/j.phytochem.2018.03.006
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Eight previously undescribed alkaloids, named corydemine, dihydrocorydemine, corydedine, 8,13-dioxo-14-hydroxytetrahydropalmatine, egenine-alpha-N-oxide, egenine-beta-N-oxide, 7'-O-ethylegenine-alpha-N-oxide, and 7'-O-ethylegenine-beta-N-oxide, together with three known ones, muramine, L-tetrahydropalmatine, and (+)-egenine, were isolated from the bulbs of Corydalis decumbens. Their structures were elucidated by comprehensive spectroscopic analysis and chemical correlation. The isolated compounds were tested for their ability to modulate neuronal excitability in primary cultured neocortical neurons. Four of the compounds, corydemine, dihydrocorydemine, muramine, and L-tetrahydropalmatine, inhibited neuronal excitability with IC50 values of 3.6, 16.7, 13.5 and 14.0 mu M, respectively. (C) 2018 Elsevier Ltd. All rights reserved.
引用
收藏
页码:85 / 92
页数:8
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