Secondary Metabolites of the Lichen Lethariella cladonioides and Their Neuroprotective Potential.

IF 3.6 2区 生物学 Q2 CHEMISTRY, MEDICINAL Journal of Natural Products Pub Date : 2025-02-28 Epub Date: 2025-02-18 DOI:10.1021/acs.jnatprod.4c01359
Lei Zhang, Wen-Hua Chao, Cui-Cui Tan, Zhi-Ying Dou, Feng Qiu, Yu-Ming Liu, Jing-Jing Wang, Li-Ning Wang
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Abstract

In the pathogenesis of neurodegenerative diseases, particularly Alzheimer's disease, cholinergic neuron dysfunction and neuroinflammation are integral components. Against this backdrop, within the vast array of potential sources under exploration, Lethariella cladonioides, a remarkable lichen with profound ethnopharmacological significance among various Chinese ethnic minorities, has recently emerged as a promising candidate. Through our comprehensive phytochemical investigation, five undescribed diphenylmethanes (1-5), three unreported depsides (6-8), and one novel diphenylether (9), along with 16 known compounds, were successfully isolated and identified. Their structures were elucidated by spectroscopic analysis and X-ray crystallography. Specifically, compounds 3-7 and 9 exhibited acetylcholinesterase inhibitory activity, while compounds 1, 2, and 4 significantly inhibited NO production by LPS in RAW264.7 cells. Collectively, these findings suggest that L. cladonioides has potential value in preventing and treating neurodegenerative diseases. This potential lies in its ability to potentially retard disease progression or alleviate symptoms by enhancing cholinergic transmission and mitigating neuroinflammation.

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苔藓次生代谢物及其神经保护作用。
在神经退行性疾病,特别是阿尔茨海默病的发病机制中,胆碱能神经元功能障碍和神经炎症是不可缺少的组成部分。在这样的背景下,在大量的潜在来源中,在中国各少数民族中具有深远民族药理学意义的地衣Lethariella cladonioides最近成为一个有希望的候选物种。通过我们全面的植物化学调查,成功分离和鉴定了5种未描述的二苯基甲烷(1-5),3种未报道的深度(6-8)和1种新的二苯基醚(9),以及16种已知化合物。通过光谱分析和x射线晶体学对其结构进行了表征。具体而言,化合物3-7和9表现出乙酰胆碱酯酶抑制活性,而化合物1、2和4显著抑制LPS在RAW264.7细胞中产生NO。综上所述,这些发现提示枝状乳杆菌在预防和治疗神经退行性疾病方面具有潜在的价值。这种潜力在于它能够通过增强胆碱能传递和减轻神经炎症来潜在地延缓疾病进展或减轻症状。
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来源期刊
CiteScore
9.10
自引率
5.90%
发文量
294
审稿时长
2.3 months
期刊介绍: The Journal of Natural Products invites and publishes papers that make substantial and scholarly contributions to the area of natural products research. Contributions may relate to the chemistry and/or biochemistry of naturally occurring compounds or the biology of living systems from which they are obtained. Specifically, there may be articles that describe secondary metabolites of microorganisms, including antibiotics and mycotoxins; physiologically active compounds from terrestrial and marine plants and animals; biochemical studies, including biosynthesis and microbiological transformations; fermentation and plant tissue culture; the isolation, structure elucidation, and chemical synthesis of novel compounds from nature; and the pharmacology of compounds of natural origin. When new compounds are reported, manuscripts describing their biological activity are much preferred. Specifically, there may be articles that describe secondary metabolites of microorganisms, including antibiotics and mycotoxins; physiologically active compounds from terrestrial and marine plants and animals; biochemical studies, including biosynthesis and microbiological transformations; fermentation and plant tissue culture; the isolation, structure elucidation, and chemical synthesis of novel compounds from nature; and the pharmacology of compounds of natural origin.
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