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基于细胞学评价的鱼油抗炎活性研究OACHSSCD

Study on the anti-inflammatory activity of fish oil based on cellular evaluation

中文摘要英文摘要

目的:针对市售鱼油产品抗炎活性参差不齐,且缺乏统一评价方法的现状,本研究旨在建立一套基于 HepG2 与 Caco-2 细胞炎症模型的体外鱼油抗炎活性评价体系,为产品效能的客观比较和质量控制提供依据.方法:通过筛选异丙醇、鱼油、脂多糖(lipopolysaccharide,LPS)的最佳工作浓度,构建 LPS 诱导的HepG2 与 Caco-2 细胞炎症模型.采用实时荧光定量 PCR(RT-qPCR)与酶联免疫吸附测定(enzyme-linked immunosorbent assay,ELISA)两种检测技术,验证该模型评价鱼油抗炎活性的适用性,并据此对 10 款市售鱼油产品进行抗炎活性评价.结果:确定体积分数小于或等于 2.5%的异丙醇和质量浓度小于或等于900μg/mL的鱼油对细胞存活率无抑制作用,并筛选出用于构建炎症模型的最佳 LPS 质量浓度(HepG2 细胞:1 μg/mL;Caco-2 细胞:3μg/mL.相较于反映动态转录水平的 RT-qPCR,ELISA 法在表征鱼油剂量-抑制效应关系时呈现更优的线性与稳定性,其线性相关系数R2>0.98,批内和批间精密度以及稳定性的变异系数均小于 15%,符合方法学要求.应用该模型评价 10 种市售鱼油产品,显示不同产品的抗炎活性存在显著异质性,其中特定产品(YY-4、YY-6)在两种细胞模型上均表现出较强的抗炎抑制效果.结论:本研究所建立的以ELISA 为核心检测手段的标准化体外评价体系,适用于鱼油产品的抗炎活性评价,可为产品的功能评价与品质分级提供可靠的技术支撑.

Aims:In view of the inconsistent anti-inflammatory activities of commercial fish oil products and the lack of a unified evaluation method,this study aims to establish an in vitro evaluation system for the anti-inflammatory activity of fish oil based on HepG2 and Caco-2 cell inflammation models,so as to provide a basis for the objective comparison of product efficacy and quality control.Methods:Optimal concentrations of isopropanol,fish oil,and lipopolysaccharide(LPS)were selected to establish LPS-induced inflammatory models in HepG2 and Caco-2 cells.The applicability of the established models for evaluating the anti-inflammatory activity of fish oil was verified using realtime quantitative polymerase chain reaction(RTqPCR)and enzymelinked immunosorbent assay(ELISA);and the antiinflammatory activities of 10 commercial fish oil products were subsequently evaluated.Results:Isopropanol(≤2.5%)and fish oil(≤900μg/mL)exhibited no inhibitory effects on cell viability.Lipopolysaccharide(LPS)at 1 μg/mL and 3 μg/mL was selected for establishing inflammatory models in HepG2 and Caco-2 cells,respectively.Compared with RTqPCR,which reflected dynamic transcriptional levels,the ELISA method showed superior linearity and stability in characterizing the doseinhibitory effect relationship of fish oil.The linear correlation coefficient R2 was greater than 0.98.The intra and interassay precision coefficients of variation were less than 15%;and the stability CV was less than 15%,all of which met the methodological requirements.The established model was applied to evaluate 10 commercially available fish oil products.The results demonstrated significant heterogeneity in antiinflammatory activities among different products,among which specific products(YY-4,YY-6)exhibited strong antiinflammatory inhibitory effects in both cell models.Conclusions:The established standardized in vitro evaluation system with ELISA as the core detection method is suitable for evaluating the anti-inflammatory activity of fish oil products.It can provide reliable technical support for the functional evaluation and quality grading of fish oil products.

彭张美子;赵微;叶子弘;汤近天;张雅芬

中国计量大学 生命科学学院 国家市场监督管理总局重点实验室(微生物计量检测与生物制品质量安全),浙江 杭州 310018中国计量大学 生命科学学院 国家市场监督管理总局重点实验室(微生物计量检测与生物制品质量安全),浙江 杭州 310018中国计量大学 生命科学学院 国家市场监督管理总局重点实验室(微生物计量检测与生物制品质量安全),浙江 杭州 310018中国计量大学 生命科学学院 国家市场监督管理总局重点实验室(微生物计量检测与生物制品质量安全),浙江 杭州 310018中国计量大学 生命科学学院 国家市场监督管理总局重点实验室(微生物计量检测与生物制品质量安全),浙江 杭州 310018

轻工纺织

鱼油炎症模型抗炎活性评价

fish oilinflammation modelanti-inflammatory activity evaluation

《中国计量大学学报》 2026 (1)

115-127,13

浙江省重点研发计划项目(No.2023C02037)

10.3969/j.issn.2096-2835.2026.01.013

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