Cycloartane-type triterpenoids from Combretum quadrangulare Kurz with PCSK9 secretion inhibitory activities

被引:0
|
作者
An, Chae-Yeong [1 ,2 ]
Pel, Pisey [1 ,2 ]
Bae, Mingoo [3 ,4 ]
Park, Chan-Woong [1 ,2 ]
Kwon, Haeun [5 ]
Lee, Hyun Suk [6 ]
Van Dung, Luong [6 ]
Kim, Changmu [7 ]
Lee, Dongho [5 ]
Choi, Young Hee [3 ,4 ]
Chin, Young-Won [1 ,2 ]
机构
[1] Seoul Natl Univ, Nat Prod Res Inst, Coll Pharm, Seoul 08826, South Korea
[2] Seoul Natl Univ, Res Inst Pharmaceut Sci, Coll Pharm, Seoul 08826, South Korea
[3] Dongguk Univ Seoul, Coll Pharm, 32 Dongguk Lo, Goyang Si 10326, Gyeonggi Do, South Korea
[4] Dongguk Univ Seoul, Integrated Res Inst Drug Dev, 32 Dongguk Lo, Goyang Si 10326, Gyeonggi Do, South Korea
[5] Korea Univ, Coll Life Sci & Biotechnol, Dept Plant Biotechnol, Seoul 02841, South Korea
[6] Dalat Univ, Ctr Biodivers & Climate Change Res, Phu Dong Thien Vuong 01, Dalat City, Lam Dong, Vietnam
[7] Natl Inst Biol Resources, Species Divers Res Div, Incheon 22689, South Korea
基金
新加坡国家研究基金会;
关键词
Combretum quadrangulare; Combretaceae; Cycloartane; Triterpenoid; VCD; PCSK9; LDL; Hypercholesterolemia; ABSOLUTE-CONFIGURATION; MOLECULES; THERAPY;
D O I
10.1016/j.phytochem.2024.114330
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
Nine previously undescribed (1-9) and seven known (10-16) cycloartane-type triterpenoids were isolated and characterized from Combretum quadrangulare Kurz using physicochemical and spectroscopic methods. The absolute configurations of these compounds were determined through modified Mosher's method and quantum chemical calculation of electronic circular dichroism (ECD) and vibrational circular dichroism (VCD) spectra. Their inhibitory activities against PCSK9 secretion were assessed, and a plausible structure-activity relationship was delineated. Compounds 2, 14, and 15 exhibited notable inhibitory effects on PCSK9 mRNA and protein levels, and significant PCSK9 mRNA inhibition was observed when co-treated with atorvastatin. Compound 15 showed the most potent activity, markedly enhancing LDL uptake compared to the negative control. In vivo pharmacokinetic studies confirmed that compound 15 exhibited higher distribution in the liver than plasma, where PCSK9 is predominantly synthesized. These findings emphasize the potential significance of the cycloartane-type triterpenoid scaffold in discovering PCSK9 inhibitors.
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页数:17
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