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阿尔及利亚酚类化合物的研究(采用液相色谱-电喷雾串联质谱分析、抗氧化活性和酶抑制法)及其在食品和营养保健品应用中的潜在意义

Investigation of Algerian Phenolic Compounds (Using LC-ESI-MS/MS Analysis, Antioxidant Activity, and Enzyme Inhibition) and Their Potential Implications for Food and Nutraceutical Applications.

作者信息

Goudjil Sabrina, Boussekine Samira, Goudjil Sarra, Goudjil Hanane, Yilmaz Mustafa Abdullah, Ola Mohammad Shamsul, Ali Ahmad, Cakir Oguz

机构信息

Laboratory of Bioactive Molecules and Applications, Department of Applied Biology, Faculty of Exact Sciences and Natural and Life Sciences, Echahid Cheikh Larbi Tebessi University, Tebessa 12000, Algeria.

Laboratory of Didactics of Physical and Chemical Sciences and Applications, Assia Djebar Higher Normal School of Constantine, Constantine 25000, Algeria.

出版信息

Antioxidants (Basel). 2024 Nov 4;13(11):1350. doi: 10.3390/antiox13111350.

DOI:10.3390/antiox13111350
PMID:39594492
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11590885/
Abstract

Investigations into the phenolic constituents of the butanolic fraction of were optimized using LC-ESI-MS/MS analysis, identifying and quantifying at least 23 fingerprint phytochemical compounds. The major phenolic compounds were epicatechin (99.916 ± 2.208 mg/g), isoquercetrin (53.31 ± 1.172 mg/g), chlorogenic acid (47.457 ± 1.010 mg/g), quinic acid (37.819 ± 1.406 mg/g), rutin (29.98 ± 0.740 mg/g), hesperidin (5.296 ± 0.177 mg/g, detected for the first time in the species), astragalin (1.774 ± 0.020 mg/g), and nicotiflorin (1.482 ± 0.016 mg/g). The antioxidant properties of the lyophilized butanolic fraction were evaluated using DPPH, GOR, ABTS, CUPRAC, and reducing power assays, all of which demonstrated that there was strong activity. Additionally, the neuroprotective effect was evaluated in vitro, showing a potent inhibitory effect on acetylcholinesterase (AChE) with an IC50 of 43.65 ± 2.10 µg/mL. The antidiabetic effect was investigated through -amylase inhibition (IC50 = 91.19 ± 0.10 µg/mL), showing high inhibitory activity. In addition, the butanolic extract exhibited significant urease inhibition with an IC50 of 26.36 ± 0.05 µg/mL. These results suggest that Algerian has potential as a therapeutic agent for managing diabetes complications and as a natural source of AChE inhibitors, making it a promising subject for the treatment of urease-related conditions. Its high concentrations of natural antioxidants, such as epicatechin, isoquercetrin, chlorogenic acid, quinic acid, rutin, hesperidin, and astragalin, make it suitable for integration into medicine, pharmaceuticals, cosmetics, and the food sector.

摘要

采用液相色谱 - 电喷雾串联质谱(LC - ESI - MS/MS)分析方法,对某植物丁醇部位的酚类成分进行了研究优化,鉴定并定量了至少23种指纹图谱植物化学化合物。主要酚类化合物有表儿茶素(99.916±2.208毫克/克)、异槲皮苷(53.31±1.172毫克/克)、绿原酸(47.457±1.010毫克/克)、奎尼酸(37.819±1.406毫克/克)、芦丁(29.98±0.740毫克/克)、橙皮苷(5.296±0.177毫克/克,首次在该物种中检测到)、紫云英苷(1.774±0.020毫克/克)和烟花苷(1.482±0.016毫克/克)。使用1,1 - 二苯基 - 2 - 三硝基苯肼(DPPH)、总抗氧化能力(GOR)、2,2'-联氮 - 双 - 3 - 乙基苯并噻唑啉 - 6 - 磺酸(ABTS)、铜离子还原抗氧化能力(CUPRAC)和还原能力测定法对冻干丁醇部位的抗氧化性能进行了评估,所有这些方法均表明其具有较强的活性。此外,还进行了体外神经保护作用评估,结果显示对乙酰胆碱酯酶(AChE)具有强效抑制作用,半数抑制浓度(IC50)为43.65±2.10微克/毫升。通过α - 淀粉酶抑制作用(IC50 = 91.19±0.10微克/毫升)研究了其抗糖尿病作用,显示出高抑制活性。此外,丁醇提取物对脲酶表现出显著抑制作用,IC50为26.36±0.05微克/毫升。这些结果表明,阿尔及利亚的该植物有潜力作为治疗糖尿病并发症的治疗剂以及乙酰胆碱酯酶抑制剂的天然来源,使其成为治疗与脲酶相关病症的有前景的研究对象。其高浓度的天然抗氧化剂,如表儿茶素、异槲皮苷、绿原酸、奎尼酸、芦丁、橙皮苷和紫云英苷,使其适合应用于医药、制药、化妆品和食品领域。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0561/11590885/9cd78dc26559/antioxidants-13-01350-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0561/11590885/4f0f689bbde4/antioxidants-13-01350-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0561/11590885/c7c61ac00fa0/antioxidants-13-01350-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0561/11590885/3d6fbf3225c8/antioxidants-13-01350-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0561/11590885/80df920b299c/antioxidants-13-01350-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0561/11590885/9cd78dc26559/antioxidants-13-01350-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0561/11590885/4f0f689bbde4/antioxidants-13-01350-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0561/11590885/c7c61ac00fa0/antioxidants-13-01350-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0561/11590885/3d6fbf3225c8/antioxidants-13-01350-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0561/11590885/80df920b299c/antioxidants-13-01350-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0561/11590885/9cd78dc26559/antioxidants-13-01350-g005.jpg

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