食品科学 ›› 2024, Vol. 45 ›› Issue (8): 145-152.doi: 10.7506/spkx1002-6630-20230708-074

• 营养卫生 • 上一篇    下一篇

荔枝落果中A型低聚原花青素抑制类甜蛋白促炎机制

罗杨合,曾诗蔼,李洛欣,谢翀,闫景坤,李玉婷,罗英捷,赵雷   

  1. (1.广西康养食品科学与技术重点实验室(贺州学院),广西 贺州 542899;2.华南农业大学食品学院,广东 广州 510642;3.东莞理工学院生命健康技术学院,广东 东莞 523808;4.营家健康科技(广东)有限公司,广东 东莞 523000)
  • 出版日期:2024-04-25 发布日期:2024-05-01
  • 基金资助:
    广西康养食品科学与技术重点实验室开放课题(GXKYSYS202204);东莞市重点领域研发项目(20221200300082); 广东省自然科学基金项目(2023A1515012599);广州市科技计划项目(2023B01J2004); “十四五”广东省农业科技创新十大主攻方向“揭榜挂帅”项目(2023SDZG04)

Inhibitory Mechanism of A-type Oligomeric Proanthocyanidins from Abscising Litchi Fruits on Proinflammation Induced by Litchi Thaumatin-like Protein

LUO Yanghe, ZENG Shi’ai, LI Luoxin, XIE Chong, YAN Jingkun, LI Yuting, LUO Yingjie, ZHAO Lei   

  1. (1. Guangxi Key Laboratory of Health Care Food Science and Technology (Hezhou University), Hezhou 542899, China; 2. College of Food Science, South China Agricultural University, Guangzhou 510642, China; 3. School of Life and Health Technology, Dongguan University of Technology, Dongguan 523808, China; 4. Inkea Health Technology Co. Ltd., Dongguan 523000, China)
  • Online:2024-04-25 Published:2024-05-01

摘要: 以荔枝落果中的A型低聚原花青素为研究对象,探讨其对荔枝类甜蛋白(litchi thaumatin-like protein,LcTLP)促炎的抑制机理。采用乙醇提取、大孔吸附树脂纯化以及制备液相色谱仪等从荔枝落果中分离得到A型低聚原花青素(A-type oligomeric proanthocyanidins,A-OPC)纯化物,并对A-OPC结构鉴定,主要成分为原花青素A2、2 个A型原花青素三聚体和1 个A型四聚体,纯度达88.69%。利用LcTLP诱导构建RAW264.7细胞炎症模型,A-OPC的添加可抑制LcTLP诱导RAW264.7细胞的一氧化氮、细胞炎症因子白细胞介素-6和肿瘤坏死因子-α的分泌,在120 μg/mL质量浓度下,抑制率分别可达58.38%、39.80%和86.31%(P<0.01)。蛋白免疫印迹分析发现,在120 μg/mL质量浓度下A-OPC可降低诱导型一氧化氮合酶和环氧合酶2的表达量,并显著降低p65、核因子κB抑制蛋白、c-Jun氨基末端激酶、细胞外信号调节蛋白激酶和p38的磷酸化水平,说明A-OPC通过下调核转录因子-κB和丝裂原活化蛋白激酶通路中下游蛋白的磷酸化水平抑制LcTLP诱导的炎症反应。

关键词: 荔枝落果;A型低聚原花青素;荔枝类甜蛋白;抗炎机制

Abstract: This study investigated the mechanism by which A-type oligomeric proanthocyanidins (A-OPC) from abscising litchi fruits inhibit proinflammation induced by litchi thaumatin-like protein (LcTLP). A-OPC were prepared by sequential ethanol extraction and purification by macroporous adsorption resin and preparative liquid chromatography. Structural analysis showed that A-OPC were mainly composed of proanthocyanidin A2, two A-type proanthocyanidin trimers and one A-type tetramer, with a purity of 88.69%. At 120 μg/mL concentration, A-OPC inhibited the secretion of nitric oxide (NO), interleukin (IL)-6 and tumor necrosis factor-α (TNF-α) by 58.38%, 39.80% and 86.31% in RAW264.7 cells treated with LcTLP, respectively (P < 0.01). Western blot showed that 120 μg/mL A-OPC reduced the expression of inducible nitric oxide synthase (iNOS) and cyclooxygenase-2 (COX-2), and significantly decreased the phosphorylation levels of p65, inhibitor of NF-κB (IκBα), c-Jun N-terminal kinase (JNK), extracellular signal-regulated kinase (ERK) and p38. Therefore, A-OPC down-regulated the phosphorylation levels of downstream proteins in the nuclear transcription factor-κB (NF-κB) and mitogen-activated protein kinase (MAPK) signaling pathways, thereby suppressing LcTLP-induced inflammatory response.

Key words: litchi fruit; A-type oligomeric proanthocyanidins; litchi thaumatin-like protein; anti-inflammatory mechanism

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