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基于谱效关系的天麻抗神经炎症关键成分鉴定及其作用机制探究

Identification of key anti-neuroinflammatory components in Gastrodiae Rhizoma based on spectrum-effect relationships and its mechanism exploration.

作者信息

Ma Tianyu, Chen Panpan, Dong Hongjing, Wang Xiao

机构信息

Key Laboratory for Applied Technology of Sophisticated Analytic Instrument of Shandong Province, Shandong Analysis and Test Center, Qilu University of Technology (Shandong Academy of Sciences), Jinan 250014, China; School of Pharmaceutical Sciences, Shandong University of Traditional Chinese Medicine, Jinan 250355, China.

Key Laboratory for Natural Active Pharmaceutical Constituents Research in Universities of Shandong Province, School of Pharmaceutical Sciences, Qilu University of Technology (Shandong Academy of Sciences), Jinan 250014, China.

出版信息

J Pharm Biomed Anal. 2024 Sep 15;248:116266. doi: 10.1016/j.jpba.2024.116266. Epub 2024 May 29.

Abstract

Gastrodiae Rhizoma was proven to have anti-inflammatory activity based on its main component of 4-hydroxybenzyl alcohol (4-HBA) and gastrodin (GAS). However, the anti-inflammatory activity of other phenols has been less reported. In this study, the n-BuOH extract was selected as the active anti-inflammatory part of Gastrodiae Rhizoma based on the LPS-induced inflammatory BV-2 cells. The spectral-effect relationship analysis of the n-BuOH extract showed the main effective components were GAS, 4-HBA, parishin A (PA), parishin B (PB), and parishin C (PC). Among them, PB could reduce LPS-induced expression of nitric oxide (NO), intracellular ROS, TNF-α, IL-6, inducible nitric oxide synthase (iNOS), and cyclooxygenase-2 (COX-2). Molecular docking predicted that PB had a good binding capacity to AMPKα and SIRT1 proteins of -12.1 kJ/mol and -7.6 kJ/mol, respectively. The Western Blot results further demonstrated that PB could inhibit NF-κB pathway by activating AMPK/SIRT1 pathway, thus exerting anti-LPS-induced neuroinflammatory effects. This study provides a referable idea for solving the problem of unclear action of TCM with complex compositions and is of great significance for the development of innovative medicines of traditional Chinese medicine.

摘要

天麻已被证明基于其主要成分4-羟基苄醇(4-HBA)和天麻素(GAS)具有抗炎活性。然而,其他酚类的抗炎活性报道较少。在本研究中,基于脂多糖(LPS)诱导的炎症性BV-2细胞,选择正丁醇提取物作为天麻的活性抗炎部位。正丁醇提取物的谱效关系分析表明,主要有效成分是天麻素、4-羟基苄醇、巴利森苷A(PA)、巴利森苷B(PB)和巴利森苷C(PC)。其中,PB可降低LPS诱导的一氧化氮(NO)、细胞内活性氧(ROS)、肿瘤坏死因子-α(TNF-α)、白细胞介素-6(IL-6)、诱导型一氧化氮合酶(iNOS)和环氧化酶-2(COX-2)的表达。分子对接预测PB分别与AMPKα和SIRT1蛋白具有良好的结合能力,结合能分别为-12.1 kJ/mol和-7.6 kJ/mol。蛋白质免疫印迹结果进一步证明,PB可通过激活AMPK/SIRT1途径抑制NF-κB途径,从而发挥抗LPS诱导的神经炎症作用。本研究为解决成分复杂的中药作用机制不明确的问题提供了可参考的思路,对中药创新药物的开发具有重要意义。

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