Benzylisoquinoline Alkaloids from the Stems of Limacia scandens and Their Potential as Autophagy Inhibitors.

Hee-Ju Lee, Eun-Jin Park, Byeol Ryu, Hyo-Moon Cho, Duc-Trong Nghiem, Ha-Thanh-Tung Pham, Cheol-Ho Pan, Won-Keun Oh
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引用次数: 1

Abstract

Limacia scandens is traditionally used to treat depression and affective disorders in Malaysia. The chemical compositions have been reported to include bisbenzylisoquinoline and aporphine-type alkaloids in the genus Limacia Lour., but studies on the components of L. scandens have rarely been reported. Therefore, this study was conducted to determine new benzylisoquinoline alkaloid derivatives with autophagy regulation activity from this plant. Bioactivity-guided isolation was applied to various column chromatography methods using RP-18, Sephadex LH-20 open column chromatography, and preparative HPLC. The chemical structures of the isolated compounds were elucidated through spectroscopic data analysis, including NMR, HR-ESI-MS, and ECD data. In addition, isolated compounds were tested for autophagy-regulating activity in HEK293 cells expressing GFP-L3. Three new dimeric benzylisoquinoline alkaloids (1-3), one new 4-hydroxybenzoic acid-conjugated benzylisoquinoline alkaloid (4), and six known compounds (5-10) were isolated from the stems of L. scandens. All compounds (1-10) were screened for autophagy regulation in HEK293 cells stably expressing the GFP-LC3 plasmid. Among the isolated compounds, 1, 2, and 4 showed autophagic regulation activity that blocked the process of combining autophagosomes and lysosomes. They also inhibit the protein degradation process from the autolysosome as inhibitors of autophagy. Novel benzylisoquinoline alkaloids from L. scandens showed potent potency for the inhibition of autophagic flux. This study provides potential candidates for developing natural autophagy inhibitors for disease prevention and treatment.

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椴树茎中的苯基异喹啉类生物碱及其作为自噬抑制剂的潜力。
马来亚树在马来西亚传统上用于治疗抑郁症和情感障碍。据报道,其化学成分包括双苄基异喹啉和阿波啡型生物碱。但对其成分的研究鲜有报道。因此,本研究旨在从该植物中寻找具有自噬调节活性的新型苯基异喹啉生物碱衍生物。生物活性引导分离应用于RP-18、Sephadex LH-20开放式柱层析和制备型高效液相色谱等多种柱层析方法。通过NMR、HR-ESI-MS和ECD等波谱数据对化合物的化学结构进行了鉴定。此外,分离的化合物在表达GFP-L3的HEK293细胞中检测自噬调节活性。从香草茎中分离得到3个新的二聚苯基异喹啉生物碱(1-3)、1个新的4-羟基苯甲酸共轭苯基异喹啉生物碱(4)和6个已知化合物(5-10)。所有化合物(1-10)在稳定表达GFP-LC3质粒的HEK293细胞中进行自噬调节筛选。在分离的化合物中,1、2和4显示自噬调节活性,阻断自噬体和溶酶体结合的过程。它们也作为自噬的抑制剂抑制自噬体的蛋白质降解过程。新型苯基异喹啉生物碱对自噬通量有较强的抑制作用。该研究为开发用于疾病预防和治疗的天然自噬抑制剂提供了潜在的候选物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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