Yang Zihan, Gao Yuan, Wu Weijie, Mu Honglei, Liu Ruiling, Fang Xiangjun, Gao Haiyan, Chen Hangjun
Food Science Institute, Zhejiang Academy of Agricultural Sciences, Hangzhou, China.
Key Laboratory of Postharvest Handling of Fruits, Ministry of Agriculture and Rural Affairs, Hangzhou, China.
Front Nutr. 2023 Jan 11;9:1111283. doi: 10.3389/fnut.2022.1111283. eCollection 2022.
Lotus root () is a common medicinal-food dual-use vegetable. In this study, the effects of lotus root extract on acute alcoholism were investigated.
The Walle-Hoch method was used to determine the ADH activity of lotus root extracts . Lotus root methanol extract were identified by UPLC-QTOF-MS/MS based metabolomics analysis. Then 109 active ingredients with achievable oral doses and drug-like properties were explored using the TCMSP platform. SwissTargetPrediction Database to predict lotus root treatment targets for acute alcoholismSTRING database (https://www.string-db.org/) was used to construct protein-protein interaction network graphs. Gene ontology (GO) functional, Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment analysis of genes common to lotus root and alcoholism by Metascap database. Molecular docking simulations were performed using AutoDock 1.5.6 software. Animal experiments verified the relieving effect of lotus root extract on acute alcoholism after intervention.
Results indicated the methanol extract of lotus root showed the highest activation rate of ethanol dehydrogenase (18.87%). The 433 compounds of lotus root methanol extract were identified by UPLC-QTOF-MS/MS based metabolomics analysis. Bioinformatics analysis indicate that there were 224 intersectioning targets between lotus root extract and acute alcoholism. KEGG enrichment analysised shows that lotus root extract may play a role in treating acute alcoholism by intervening with the neuroactive ligand-receptor interaction pathway. The protein-protein interaction network (PPI) analysis found that HSP90AA1, MAPK1 and STAT3 played a key role in lotus root extract-modulated PPI networks. Molecular docking showed that (7R, 8S)-dihydrodihydrodipine cypressol had the best binding ability with MAPK1. Experiments in mice indicate that lotus root extract improved the activity of liver alcohol dehydrogenase (ADH), acetaldehyde dehydrogenase (ALDH), catalase (CAT), superoxide dismutase (SOD) and glutathione peroxidase (GSH-PX), increase glutathione (GSH) and reduce malondialdehyde (MDA) levels, decrease glutamate transaminase (AST), alanine transaminase (ALT) and alkaline phosphatase (AKP) in the serum of mice with acute alcoholism, and accelerate the metabolic rate of alcohol after drinking. This study reveals the mechanism of lotus root to alleviate acute alcoholism, which provides a basis for further research on functional foods using lotus root and offers new possibilities for the treatment of acute alcoholism.
The results of the current study showed that the methanolic extract of lotus root had the highest activation rate of ethanol dehydrogenase. Network pharmacology results suggest that lotus root extract may play a role in the treatment of alcoholism by regulating signaling pathways, such as neuroactive ligand-receptor interactions, as well as biological processes, such as regulation of secretion, regulation of ion transport, response to lipopolysaccharides, and response to alcohol. Animal experiments confirmed the therapeutic effect of lotus root on acute alcoholism mechanistically through activation of alcohol catabolic enzyme, reduction of oxidative stress and protection of liver function.
莲藕是一种常见的药食两用蔬菜。本研究探讨了莲藕提取物对急性酒精中毒的影响。
采用瓦勒-霍赫法测定莲藕提取物的乙醇脱氢酶(ADH)活性。通过基于超高效液相色谱-四极杆飞行时间串联质谱(UPLC-QTOF-MS/MS)的代谢组学分析鉴定莲藕甲醇提取物。然后利用中药系统药理学数据库与分析平台(TCMSP)探索109种具有可实现口服剂量和类药性质的活性成分。使用瑞士靶点预测数据库预测莲藕治疗急性酒精中毒的靶点。利用STRING数据库(https://www.string-db.org/)构建蛋白质-蛋白质相互作用网络图。通过Metascap数据库对莲藕和酒精中毒共同基因进行基因本体(GO)功能、京都基因与基因组百科全书(KEGG)通路富集分析。使用AutoDock 1.5.6软件进行分子对接模拟。动物实验验证了莲藕提取物干预后对急性酒精中毒的缓解作用。
结果表明莲藕甲醇提取物的乙醇脱氢酶激活率最高(18.87%)。通过基于UPLC-QTOF-MS/MS的代谢组学分析鉴定出莲藕甲醇提取物中的433种化合物。生物信息学分析表明莲藕提取物与急性酒精中毒之间存在224个交集靶点。KEGG富集分析表明莲藕提取物可能通过干预神经活性配体-受体相互作用途径在治疗急性酒精中毒中发挥作用。蛋白质-蛋白质相互作用网络(PPI)分析发现热休克蛋白90α家族成员1(HSP90AA1)、丝裂原活化蛋白激酶1(MAPK1)和信号转导和转录激活因子3(STAT3)在莲藕提取物调节的PPI网络中起关键作用。分子对接表明(7R,8S)-二氢二氢松脂醇与MAPK1具有最佳结合能力。小鼠实验表明莲藕提取物提高了急性酒精中毒小鼠肝脏乙醇脱氢酶(ADH)、乙醛脱氢酶(ALDH)、过氧化氢酶(CAT)、超氧化物歧化酶(SOD)和谷胱甘肽过氧化物酶(GSH-PX)的活性,增加了谷胱甘肽(GSH)含量,降低了丙二醛(MDA)水平,降低了急性酒精中毒小鼠血清中的谷氨酸转氨酶(AST)、丙氨酸转氨酶(ALT)和碱性磷酸酶(AKP),并加速了饮酒后酒精的代谢速率。本研究揭示了莲藕缓解急性酒精中毒的机制,为进一步研究以莲藕为原料的功能性食品提供了依据,并为急性酒精中毒的治疗提供了新的可能性。
本研究结果表明莲藕甲醇提取物的乙醇脱氢酶激活率最高。网络药理学结果表明莲藕提取物可能通过调节神经活性配体-受体相互作用等信号通路以及分泌调节、离子转运调节、对脂多糖的反应和对酒精的反应等生物学过程在酒精中毒治疗中发挥作用。动物实验通过激活酒精分解代谢酶、减轻氧化应激和保护肝功能从机制上证实了莲藕对急性酒精中毒的治疗作用。