全氟正烷酸(PFDA)灌胃28天对雌性Harlan Sprague-Dawley大鼠和B6C3F1/N小鼠的免疫毒性和肝毒性作用。

IF 2.4 4区 医学 Q3 TOXICOLOGY Journal of Immunotoxicology Pub Date : 2018-12-01 DOI:10.1080/1547691X.2018.1445145
Rachel P Frawley, Matthew Smith, Mark F Cesta, Schantel Hayes-Bouknight, Chad Blystone, Grace E Kissling, Shawn Harris, Dori Germolec
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引用次数: 30

摘要

聚氟烷基和全氟烷基物质(PFAS)是化学和热稳定、疏水、疏脂的化合物,用于防染剂和水、油表面活性剂中,并与免疫抑制和过氧化物酶体增殖活性有关。全氟-正癸酸(PFDA, (CF3(CF2)8COOH)是一种氟化直链脂肪酸化合物,据报道可在啮齿动物模型中诱导胸腺萎缩和可逆性骨髓细胞减少。本研究的目的是评估PFDA的潜在免疫毒性,因为它的结构与其他免疫抑制剂PFASs相似。雌性Harlan Sprague-Dawley大鼠每日灌胃0 ~ 2.0 mg PFDA/kg,连续28 d。雌性B6C3F1/N小鼠以0 ~ 5.0 mg /kg PFDA灌胃1次/周,连续灌胃4周。评估了动物对脾和骨髓免疫细胞群的影响,以及先天、体液和细胞介导的免疫。还评估了小鼠对流感病毒的抵抗力。0.5 mg /kg/d PFDA处理大鼠出现治疗相关性肝细胞坏死和肝肿大。PFDA浓度≥0.625 mg /kg/周时,小鼠肝脏肿大(26-89%),而5.0 mg /kg/周时,小鼠脾脏萎缩(20%)。5.0 mg PFDA/kg/周可使小鼠脾细胞总数、Ig +和NK +细胞减少(17.6 ~ 27%)。≥1.25 mg PFDA/kg/周时,脾脏CD3+、CD4+、CD8+和Mac3+细胞数量减少(10.5-39%)。pfda暴露大鼠的白细胞亚群未见变化。≥0.25 mg PFDA/kg/d时,大鼠肝脏固定组织巨噬细胞的吞噬能力下降(比活性为24-39%)。pfda对体液和细胞介导的免疫、宿主抵抗和骨髓祖细胞的影响是有限的。这些数据表明,暴露于PFDA可能以与PFAS类别一致的方式在大鼠肝脏中诱导不良反应,并可能改变小鼠淋巴组织中免疫细胞群的平衡。
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Immunotoxic and hepatotoxic effects of perfluoro-n-decanoic acid (PFDA) on female Harlan Sprague-Dawley rats and B6C3F1/N mice when administered by oral gavage for 28 days.

Poly- and perfluoroalkyl substances (PFAS) are chemically and thermally stable, hydrophobic, lipophobic compounds used in stain repellants and water and oil surfactants, and associated with immunosuppression and peroxisome proliferator activity. Perfluoro-n-decanoic acid (PFDA, (CF3(CF2)8COOH), a fluorinated straight chain fatty acid compound, is reported to induce thymic atrophy and reversible bone marrow hypocellularity in rodent models. The objective of this study was to assess potential immunotoxicity of PFDA, due to its structural similarity to other immunosuppressive PFASs. Female Harlan Sprague-Dawley rats were exposed to 0-2.0 mg PFDA/kg by oral gavage daily for 28 d. Female B6C3F1/N mice were exposed once/week to 0-5.0 mg PFDA/kg by gavage for 4 weeks. Animals were evaluated for effects on immune cell populations in spleen and bone marrow, and innate, humoral-, and cell-mediated immunity. Mice were also evaluated for resistance to Influenza virus. Treatment-related hepatocyte necrosis and hepatomegaly were observed in rats treated with 0.5 mg PFDA/kg/d. In mice, hepatomegaly (26-89%) was observed following exposure to ≥0.625 mg PFDA/kg/week, while splenic atrophy (20%) was observed at 5.0 mg PFDA/kg/week. At 5.0 mg PFDA/kg/week, total spleen cells, and Ig + and NK + cells were decreased (17.6-27%). At ≥ 1.25 mg PFDA/kg/week the numbers of splenic CD3+, CD4+, CD8+, and Mac3+ cells were decreased (10.5-39%). No changes were observed in leukocyte subpopulations in PFDA-exposed rats. Phagocytosis by fixed-tissue macrophages was decreased in liver (specific activity, 24-39%) at ≥0.25 mg PFDA/kg/d in rats. PFDA-induced effects on humoral- and cell-mediated immunity, host resistance, and bone marrow progenitor cells were limited. These data suggest that exposure to PFDA may induce adverse effects in rat liver in a manner consistent with the PFAS class, and may also alter the balance of immune cell populations in lymphoid tissues in mice.

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来源期刊
Journal of Immunotoxicology
Journal of Immunotoxicology 医学-毒理学
CiteScore
6.70
自引率
3.00%
发文量
26
审稿时长
1 months
期刊介绍: The Journal of Immunotoxicology is an open access, peer-reviewed journal that provides a needed singular forum for the international community of immunotoxicologists, immunologists, and toxicologists working in academia, government, consulting, and industry to both publish their original research and be made aware of the research findings of their colleagues in a timely manner. Research from many subdisciplines are presented in the journal, including the areas of molecular, developmental, pulmonary, regulatory, nutritional, mechanistic, wildlife, and environmental immunotoxicology, immunology, and toxicology. Original research articles as well as timely comprehensive reviews are published.
期刊最新文献
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