食品科学 ›› 2026, Vol. 47 ›› Issue (8): 240-249.doi: 10.7506/spkx1002-6630-20251003-003

• 营养卫生 • 上一篇    下一篇

不同低分子质量κ-卡拉胶对高脂饮食小鼠降脂活性

蔡海珠,陈菁,张国芸,郑珊珊,覃海丽,何融,宋兵兵,钟赛意   

  1. (1.广东海洋大学食品科技学院,广东省水产品加工与安全重点实验室,广东省海洋生物制品工程实验室,广东省海洋食品工程技术研究中心,广东 湛江 524088;2.广东海洋大学深圳研究院,广东 深圳 518108)
  • 出版日期:2026-04-25 发布日期:2026-05-15
  • 基金资助:
    深圳市国际合作项目(GJHZ20240218114715029);深圳市科技重大专项(可持续发展专项)(KCXFZ20240903094014019); 广东省高校重点领域专项(2023ZDZX2025);广东省高校科技创新团队项目(2021KCXTD021)

Hypolipidemic Activity of κ-Carrageenans of Different Molecular Masses in Mice Fed High-Fat Diet

CAI Haizhu, CHEN Jing, ZHANG Guoyun, ZHENG Shanshan, QIN Haili, HE Rong, SONG Bingbing, ZHONG Saiyi   

  1. (1. Guangdong Provincial Key Laboratory of Aquatic Product Processing and Safety, Guangdong Province Engineering Laboratory for Marine Biological Products, Guangdong Provincial Engineering Technology Research Center of Seafood, College of Food Science and Technology, Guangdong Ocean University, Zhanjiang 524088, China; 2. Shenzhen Institute of Guangdong Ocean University, Shenzhen 518108, China)
  • Online:2026-04-25 Published:2026-05-15

摘要: 本研究采用光催化降解法制备不同低分子质量κ-卡拉胶样品(5.2、15.5、36.2 kDa),通过高脂饮食诱导的肥胖小鼠模型系统评价其降脂功效。通过检测小鼠体质量、附睾脂肪质量、口服葡萄糖耐量、血清血脂4 项(甘油三酯(triglyceride,TG)、总胆固醇(total cholesterol,TC)、低密度脂蛋白胆固醇(low-density lipoprotein cholesterol,LDL-C)、高密度脂蛋白胆固醇(high-density lipoprotein cholesterol,HDL-C))、炎症因子(白细胞介素-6(interleukin-6,IL-6)和肿瘤坏死因子-α(tumor necrosis factor-α,TNF-α))、肝脏脂质含量以及肝脏、结肠和脂肪组织的病理形态学变化,综合评估不同分子质量κ-卡拉胶样品的活性差异。结果表明,所有降解κ-卡拉胶均表现出降脂活性,且效果呈现分子质量依赖性。其中,15.5 kDa的κ-卡拉胶表现出最优的综合降脂效果,能显著抑制高脂饮食小鼠的体质量和附睾脂肪质量增长(P<0.05),改善糖耐量异常;有效调节血脂水平,使血清TC、TG和LDL-C水平分别降低12.40%、8.74%和5.02%,并显著提升HDL-C水平(提升11.34%);同时,它能显著降低血清中炎症因子IL-6水平,并有效减轻肝脏脂肪变性。本研究揭示了κ-卡拉胶的降脂活性与其分子质量密切相关,且发现降脂效果并非随分子质量降低而简单增强。本研究为深入理解κ-卡拉胶的生物活性提供了新的实验证据,可为开发具有特定分子质量特征的κ-卡拉胶降脂功能性食品提供新的数据支持和理论参考。

关键词: κ-卡拉胶;低分子质量;降脂;高脂肥胖

Abstract: In this study, the lipid-lowering effects of κ-carrageenans with different molecular masses (5.2, 15.5 and 36.2 kDa), prepared using a photocatalytic degradation method, were compared in a mouse model of obesity induced by a high-fat diet. Body mass, epididymal fat mass, oral glucose tolerance, four serum lipid parameters (triglycerides (TG), total cholesterol (TC), low-density lipoprotein cholesterol (LDL-C), and high-density lipoprotein cholesterol (HDL-C)), inflammatory factors (interleukin-6 (IL-6) and tumor necrosis factor-α (TNF-α)), hepatic lipid content, and pathomorphological changes in the liver, colon, and adipose tissue of mice were measured. The results indicated that all degraded κ-carrageenans exhibited lipid-lowering activity in a molecular mass-dependent manner. Among these, the 15.5 kDa κ-carrageenan demonstrated the most pronounced lipid-lowering effect. It significantly inhibited body mass gain and epididymal fat accumulation in high-fat diet-fed mice (P < 0.05) and alleviated impaired glucose tolerance, effectively regulating blood lipid levels, reducing serum TC, TG and LDL-C by 12.40%, 8.74%, and 5.02% respectively, whilst significantly increasing HDL-C levels by 11.34%. Additionally, it significantly reduced serum levels of the inflammatory cytokine IL-6 and effectively alleviated hepatic steatosis. This study revealed that the lipid-lowering activity of κ-carrageenan is closely related to its molecular mass, but does not simply increase as its molecular mass decreases. This study provides new experimental evidence for an in-depth understanding of the biological activity of κ-carrageenan, and offers new data support and theoretical references for the development of κ-carrageenan-based functional foods with specific molecular mass characteristics.

Key words: κ-carrageenan; low molecular mass; lipid-lowering; high fat-induced obesity

中图分类号: