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蛇足石杉中的石松生物碱及其乙酰胆碱酯酶抑制活性。

Lycopodium alkaloids from Huperzia serrata and their cholinesterase inhibitory activities.

机构信息

State Key Laboratory of Phytochemistry and Plant Resources in West China, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming 650201, People's Republic of China; University of Chinese Academy of Sciences, Beijing 100049, People's Republic of China.

State Key Laboratory of Phytochemistry and Plant Resources in West China, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming 650201, People's Republic of China; University of Chinese Academy of Sciences, Beijing 100049, People's Republic of China.

出版信息

Phytochemistry. 2024 Jul;223:114114. doi: 10.1016/j.phytochem.2024.114114. Epub 2024 Apr 30.

Abstract

Huperzia serrata, belonging to the Lycopodiaceae family, has been traditionally utilized for the management of treating rheumatic numbness, arthritic pain, dysmenorrhea, and contusions. This plant is a rich source of lycopodium alkaloids, some of which have demonstrated notable cholinesterase inhibitory activity. The objective of this study was to identify lycopodium alkaloids with cholinesterase inhibitory properties from H. serrata. The structures of these alkaloids were elucidated by HRESIMS, NMR (including a H-N HMBC experiment), ECD methods and single-crystal X-ray diffraction. The inhibitory activities against acetylcholinesterase (AChE) and butyrylcholinesterase (BuChE) were assessed using a modified Ellman's method. Consequently, sixteen lycopodium alkaloids (1-16), including ten previously undescribed ones named huperradines A-G and huperradines I-K (1-7 and 9-11), along with one previously undescribed naturally occurring compound, huperradine H (8), were isolated from H. serrata. Among these, compounds 7 and 1 exhibited potent and moderate AChE inhibition, with IC values of 0.876 ± 0.039 μM and 13.125 ± 0.521 μM, respectively. Our results suggest that huperradine G (7) may be a promising lead compound for the development of new AChE inhibitors for Alzheimer's disease.

摘要

蛇足石杉,属于石松科,传统上用于治疗风湿麻木、关节炎疼痛、痛经和瘀伤。这种植物是石松生物碱的丰富来源,其中一些具有显著的胆碱酯酶抑制活性。本研究的目的是从蛇足石杉中鉴定具有胆碱酯酶抑制活性的石松生物碱。这些生物碱的结构通过高分辨质谱(HRESIMS)、核磁共振(包括 H-N HMBC 实验)、ECD 方法和单晶 X 射线衍射来阐明。使用改良的 Ellman 法评估它们对乙酰胆碱酯酶(AChE)和丁酰胆碱酯酶(BuChE)的抑制活性。因此,从蛇足石杉中分离得到十六种石松生物碱(1-16),包括十种以前未描述的命名为 huperradines A-G 和 huperradines I-K(1-7 和 9-11)以及一种以前未描述的天然存在的化合物 huperradine H(8)。其中,化合物 7 和 1 表现出较强和中等的 AChE 抑制活性,IC 值分别为 0.876 ± 0.039 μM 和 13.125 ± 0.521 μM。我们的结果表明,huperradine G(7)可能是开发治疗阿尔茨海默病的新型 AChE 抑制剂的有前途的先导化合物。

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