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胡椒中的生物碱及其抗炎特性。

Alkaloids from Piper longum L and their Anti-inflammatory Properties.

作者信息

Phuong Tran Thi Thu, Nhiem Nguyen Xuan, Pham-The Hai, Phan Uyen Thi Tu, Huong Le Thanh, Nguyen Hai Dang

机构信息

University of Science and Technology of Hanoi (USTH), Vietnam Academy of Science and Technology (VAST), 18 Hoang Quoc Viet, Cau Giay, Hanoi, 100000, Viet Nam.

Institute of Marine Biochemistry, VAST, 18 Hoang Quoc Viet, Cau Giay, Hanoi, 100000, Viet Nam.

出版信息

Chem Biodivers. 2024 Dec;21(12):e202401224. doi: 10.1002/cbdv.202401224. Epub 2024 Oct 26.

DOI:10.1002/cbdv.202401224
PMID:39149874
Abstract

Piper longum L. (PL) is considered one of the most important species traditionally used for treating various ailments and has indicated the presence of alkaloids, flavonoids, and steroids. In this study, we isolated the chemical compounds of PL leaves, and measured NO, IL-6, iNOS, as well as COX-2 protein levels. In addition, molecular docking analysis was used to further understand the anti-inflammation effect of the compounds. We identified one new alkaloid named piperlongumine A (1) with ten known compounds (2-11). The new compound (1) and two other alkaloids 2E)-3-(4-hydroxy-3-methoxyphenyl)-1-(pyrrol-1-yl) propanone (7) and piperchabamide A (8) significantly reduced NO production in LPS-stimulated RAW 264.7 cells with the IC values of 0.97±0.05 μM, 0.91±0.07 μM, 1.63±0.14 μM, respectively. Moreover, at concentration of 2 μM, compound 1 inhibited approximately 98±0.64 % of IL-6 secretion, and decreased iNOS and COX-2 protein level by about 96 and 19 folds compared to LPS treatment alone, respectively. Furthermore, compounds 1, 7, and 8 were predicted to bind and inhibit IL-6, TNF-α, and iNOS, with compound 1 showing the highest binding energy of -7.09 kcal/mol. This study provides new insights for potential anti-inflammatory drug design and warrants further investigation.

摘要

荜茇被认为是传统上用于治疗各种疾病的最重要的物种之一,并且已表明其含有生物碱、黄酮类化合物和甾体类化合物。在本研究中,我们分离了荜茇叶的化学成分,并测量了一氧化氮(NO)、白细胞介素-6(IL-6)、诱导型一氧化氮合酶(iNOS)以及环氧化酶-2(COX-2)的蛋白水平。此外,还利用分子对接分析进一步了解这些化合物的抗炎作用。我们鉴定出一种名为荜茇明碱A(1)的新生物碱以及十种已知化合物(2 - 11)。新化合物(1)以及另外两种生物碱(E)-3-(4-羟基-3-甲氧基苯基)-1-(吡咯-1-基)丙酮(7)和胡椒酰胺A(8)显著降低了脂多糖(LPS)刺激的RAW 264.7细胞中NO的产生,其半数抑制浓度(IC)值分别为0.97±0.05 μM、0.91±0.07 μM、1.63±0.14 μM。此外,在浓度为2 μM时,化合物1抑制了约98±0.64%的IL-6分泌,与单独的LPS处理相比,iNOS和COX-2蛋白水平分别降低了约96倍和19倍。此外,预测化合物1、7和8可结合并抑制IL-6、肿瘤坏死因子-α(TNF-α)和iNOS,其中化合物1显示出最高的结合能为 -7.09 kcal/mol。本研究为潜在抗炎药物设计提供了新的见解,值得进一步研究。

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