癌变·畸变·突变 ›› 2026, Vol. 38 ›› Issue (1): 64-70.doi: 10.3969/j.issn.1004-616x.2026.01.011

• 检测硏究 • 上一篇    

乳糖-N-四糖的安全性毒理学评价

张悦1, 刘梦思2, 乔文英2, 陈博文2, 李翔1, 刘汉霞1   

  1. 1. 中国质量检验检测科学研究院, 北京 100176;
    2. 中国检验检疫科学研究院综合检测中心, 北京 100123
  • 收稿日期:2025-08-13 修回日期:2025-11-16 发布日期:2026-01-30
  • 通讯作者: 李翔, 刘汉霞
  • 基金资助:
    中国质量检验检测科学研究院基本科研业务费项目(2024JK0026)

Toxicological safety study of lactose-N-tetraosaccharide

ZHANG Yue1, LIU Mengsi2, QIAO Wenying2, CHEN Bowen2, LI Xiang1, LIU Hanxia1   

  1. 1. Chinese Academy of Quality and Inspection & Testing, Beijing 100176;
    2. Comprehensive Testing Center of Chinese Academy of Inspection and Quarantine, Beijing 100123, China
  • Received:2025-08-13 Revised:2025-11-16 Published:2026-01-30

摘要: 目的: 依据食品安全国家标准对乳糖-N-四糖(LNT)的安全性进行毒理学评价。方法: 急性经口毒性试验采用限量法,对20只ICR小鼠一次性灌胃20 g/kg的LNT,连续2周观察小鼠的毒性反应。细菌回复突变试验选用组氨酸缺陷型鼠伤寒沙门氏菌TA97a、TA98、TA100、TA102、TA1535共5个菌株,在加与不加S9的条件下进行两次试验。哺乳动物红细胞微核试验采用30 h两次以5.0 g/kg为最高剂量,中、低剂量分别为2.5、1.25 g/kg给予ICR小鼠灌胃,同时设置溶媒对照组和阳性对照组。体外染色体畸变试验选用中国仓鼠肺(CHL)细胞株,在加和不加S9条件下设0.8、2.0、5.0 mg/mL共3个浓度,同时设置DMEM阴性对照及阳性对照。90天经口毒性试验设置2.5、5.0、10.0 g/kg共3个剂量组,同时设置溶媒对照组,观察SD大鼠亚慢性毒性反应。结果: 急性经口毒性试验显示LNT对小鼠LD50大于20 g/kg;3个致突变试验结果均为阴性;90天经口毒性试验中,雌性大鼠未见明显异常,其未观察到有害作用剂量(NOAEL)为10.0 g/kg,雄性大鼠体质量增长以及摄食量下降,其NOAEL为5.0 g/kg。结论: LNT连续灌胃90天对雌性大鼠无不良影响,可致雄性大鼠体质量增长以及摄食量下降,因此LNT在食品领域应用的安全性需考虑性别差异。

关键词: 乳糖-N-四糖, 急性经口毒性试验, 遗传毒性试验, 90天经口毒性试验

Abstract: OBJECTIVE: To evaluate safety of lactose-N-tetrasaccharide (LNT) according to national food safety standards. METHODS: Acute oral toxicity test was performed using the limit method. Twenty ICR mice were administered 20 g/kg of LNT via gavage once,and the toxic effects were observed for two consecutive weeks. Bacterial reverse mutation test: Five histidine-deficient Salmonella Typhimurium strains (TA97a,TA98, TA100, TA102, and TA1535) were used, and two tests were conducted with and without S9. For the mammalian erythrocyte micronucleus test, ICR mice were administered LNT twice via gavage at a maximum dose of 5.0 g/kg,with medium and low doses of 2.5 and 1.25 g/kg,respectively,over 30 hours. A solvent control group and a positive control group were also included. For the in vitro chromosomal aberration test, Chinese hamster lung (CHL) cell line was used,and three concentrations (0.8,2.0,and 5.0 mg/mL) were set up with and without S9. A DMEM negative control and a positive control group were also included. A 90-day oral toxicity test was conducted with three dosage groups (2.5,5.0,and 10.0 g/kg) and a solvent control group to observe sub-chronic toxicity in SD rats. RESULTS: The acute oral toxicity test showed that the LD50 of LNT in mice was greater than 20 g/kg; all three mutagenicity tests were negative. In the 90-day oral toxicity test, no significant abnormalities were observed in female rats, with a no-adverse-effect level (NOAEL) of 10.0 g/kg. Male rats showed weight gain and decreased food intake, with a NOAEL of 5.0 g/kg. CONCLUSION: Continuous gavage administration of LNT for 90 days had no adverse effects on female rats, but it caused weight gain and decreased food intake in male rats. Therefore, the safety of LNT in food applications needs to consider gender differences.

Key words: lactose-N-tetrasaccharide, acute oral toxicity test, genotoxicity test, 90-day oral toxicity test

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