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养殖三斑海马提取物中生物活性化合物的鉴定以及TNF-α和COX-2的抑制作用

Identification of bioactive compounds and inhibitory effects of TNF-α and COX-2 in the extract from cultured three-spot seahorse ().

作者信息

Chen Yung-Husan, Chang Yu-Wei, Ma Chu-Wen, Luo Lian-Zhong, Lu Ting-Jang, Yao Jeng-Yuan

机构信息

Xiamen Key Laboratory of Marine Medicinal Natural Products Resources Xiamen Medical College Xiamen China.

Fujian Provincial University Marine Biomedical Resources Engineering Research center Xiamen Medical College Xiamen China.

出版信息

Food Sci Nutr. 2023 Nov 27;12(2):1095-1104. doi: 10.1002/fsn3.3824. eCollection 2024 Feb.

Abstract

Three-spot seahorse () has been consumed as traditional Chinese medicine in Asian society. This study was designed to analyze the bioactive compounds of the solvent extracts from cultured three-spot seahorse by high pressure liquid chromatography coupled with electrospray ionization tandem mass spectrometry (HPLC-ESI/MS/MS). Subsequently, their biological activities were evaluated and confirmed by cell modes and Western blot analysis. Experimental results indicated that taurine and arginine were the primary bioactive compounds identified and quantified without pre- or post-column derivatization within 20 min retention time. The analytical method was established and validated with intraday/interday RSD from 0.25% to 3.34% and with recovery from 87.8% to 91.2%. As compared to other extracts, water layer extract (WLE) contained the most taurine and arginine contents of 6.807 and 0.437 mg/g (dry basis), respectively. In the meanwhile, WLE also showed anti-inflammatory activity on LPS-induced NO production and inhibited the protein expression of TNF-α and COX-2 by Western blot analysis with better cell viability.

摘要

三斑海马()在亚洲社会一直被用作传统中药。本研究旨在通过高压液相色谱-电喷雾电离串联质谱法(HPLC-ESI/MS/MS)分析养殖三斑海马溶剂提取物中的生物活性化合物。随后,通过细胞模型和蛋白质印迹分析对其生物活性进行了评估和确认。实验结果表明,牛磺酸和精氨酸是在20分钟保留时间内无需柱前或柱后衍生化即可鉴定和定量的主要生物活性化合物。所建立的分析方法经日内/日间相对标准偏差(RSD)为0.25%至3.34%、回收率为87.8%至91.2%验证。与其他提取物相比,水层提取物(WLE)中牛磺酸和精氨酸含量最高,分别为6.807和0.437毫克/克(干基)。同时, WLE对脂多糖诱导的一氧化氮产生也显示出抗炎活性,并通过蛋白质印迹分析抑制肿瘤坏死因子-α(TNF-α)和环氧合酶-2(COX-2)的蛋白质表达,且细胞活力更好。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a16d/10867490/7c5ab959b0eb/FSN3-12-1095-g001.jpg

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