食品级二氧化钛 E171 的一代生殖毒性扩展研究,重点关注生殖和内分泌终点。

IF 3.3 4区 医学 Q2 REPRODUCTIVE BIOLOGY Reproductive toxicology Pub Date : 2024-08-20 DOI:10.1016/j.reprotox.2024.108687
Rodger V. Battersby , Janine Adam , Amy L. Williams , John M. DeSesso
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引用次数: 0

摘要

在一项延长一代生殖毒性(EOGRT)研究(经合组织测试 443)中,对 Sprague Dawley 大鼠进行了食品级二氧化钛 E171 的饲料添加试验。在交配前 10 周开始喂食剂量为 0、100、300 或 1000 毫克/千克体重/天的饲料,并在整个研究期间持续喂食。断奶后,幼崽被分配到群组 1A/1B(评估生殖毒性)、2A/2B(评估发育神经毒性)和 3(评估发育免疫毒性);此外,群组 1B 交配产生 F2 代,并对卫星 F0 动物进行结肠异常隐窝(ACF)评估。F0 动物没有全身毒性或生殖影响,没有与治疗相关的组织病理学变化,结肠中也没有 ACF。F0 和 F1 动物的血清雌二醇或睾酮浓度均无变化。F1 动物未发现与治疗相关的产前/产后发育变化,F1 组群 1B 动物的繁殖性能也未受到影响。F2 幼崽在出生前后(出生后第 4-8 天)的发育均未出现异常。在组群 2A/2B 中未观察到与治疗相关的发育神经毒性。虽然在组群 3 中未观察到与治疗相关的免疫毒性,但阳性对照没有引起预期的反应;将重复这部分研究。对血液和尿液的分析表明,饮食摄入 E171 后,胃肠道对其的系统吸收可以忽略不计。亲代全身毒性、生殖毒性、子代毒性和发育神经毒性的无观测不良效应水平(NOAEL)为 1000 毫克/千克体重/天。在发育免疫毒性方面,由于阳性对照的 T 细胞依赖性抗体反应不足,因此未确定无观测不良效应水平。我们的研究为 E171 的生殖毒性和肿瘤前病变潜力提供了可靠的数据。
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Extended one-generation reproductive toxicity study of food-grade titanium dioxide E171 with emphasis on reproductive and endocrine endpoints

Food-grade titanium dioxide E171 was administered in feed to Sprague Dawley rats in an extended one-generation reproductive toxicity (EOGRT) study (OECD Test 443). The dosed diet (0, 100, 300, or 1000 mg/kg body weight/day) started 10 weeks before mating and continued throughout the study. After weaning, pups were allocated to Cohorts 1 A/1B (to assess reproductive toxicity), 2 A/2B (to assess developmental neurotoxicity), and 3 (to assess developmental immunotoxicity); in addition, Cohort 1B was mated to produce an F2 generation and satellite F0 animals were evaluated for colonic aberrant crypt foci (ACF). In F0 animals, there were no systemic toxicity or reproductive effects, no treatment-related histopathological changes, and no ACF in the colon. Serum estradiol or testosterone concentrations were not changed in F0 or F1 animals. No pre-/postnatal developmental changes related to treatment were noted in F1 animals, and the reproductive performance of F1 Cohort 1B animals was unaffected. F2 pups showed no abnormalities in pre- or postnatal development (postnatal days 4–8). No treatment-related developmental neurotoxicity was observed in Cohorts 2 A/2B. Although no treatment-related immunotoxicity was observed in Cohort 3, the positive control did not induce the expected response; this segment of the study will be repeated. Analyses of blood and urine showed negligible systemic absorption of E171 from the gastrointestinal tract upon dietary ingestion. The no observed adverse effect level (NOAEL) for parental systemic toxicity, reproductive toxicity, offspring toxicity, and developmental neurotoxicity was considered 1000 mg/kg body weight/day. For developmental immunotoxicity, a NOAEL was not determined owing to insufficient T-cell-dependent antibody response in the positive control. Our study provides robust data on the reproductive toxicity and preneoplastic potential of E171.

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来源期刊
Reproductive toxicology
Reproductive toxicology 生物-毒理学
CiteScore
6.50
自引率
3.00%
发文量
131
审稿时长
45 days
期刊介绍: Drawing from a large number of disciplines, Reproductive Toxicology publishes timely, original research on the influence of chemical and physical agents on reproduction. Written by and for obstetricians, pediatricians, embryologists, teratologists, geneticists, toxicologists, andrologists, and others interested in detecting potential reproductive hazards, the journal is a forum for communication among researchers and practitioners. Articles focus on the application of in vitro, animal and clinical research to the practice of clinical medicine. All aspects of reproduction are within the scope of Reproductive Toxicology, including the formation and maturation of male and female gametes, sexual function, the events surrounding the fusion of gametes and the development of the fertilized ovum, nourishment and transport of the conceptus within the genital tract, implantation, embryogenesis, intrauterine growth, placentation and placental function, parturition, lactation and neonatal survival. Adverse reproductive effects in males will be considered as significant as adverse effects occurring in females. To provide a balanced presentation of approaches, equal emphasis will be given to clinical and animal or in vitro work. Typical end points that will be studied by contributors include infertility, sexual dysfunction, spontaneous abortion, malformations, abnormal histogenesis, stillbirth, intrauterine growth retardation, prematurity, behavioral abnormalities, and perinatal mortality.
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