Characterization of bronchiolar metaplasia of the alveolar epithelium in female Sprague-Dawley rats exposed to 3,3′,4,4′,5-pentachlorobiphenyl (PCB126)

被引:15
|
作者
Brix, AE
Jokinen, MP
Walker, NJ
Sells, DM
Nyska, A
机构
[1] Expt Pathol Labs Inc, Res Triangle Pk, NC 27709 USA
[2] Charles River Co, Pathol Associates Inc, Durham, NC 27713 USA
[3] NIEHS, Environm Toxicol Program, Res Triangle Pk, NC 27709 USA
[4] Battelle Columbus, Columbus, OH 43201 USA
关键词
PCB126; bronchiolar metaplasia; alveolar epithelium; Toxic Equivalency Factor;
D O I
10.1080/01926230490431817
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
To test the dioxin toxic equivalency factor methodology, the National Toxicology Program conducted a series of 2-year rat bioassays of dioxin-like compounds. Following gavage exposure of female Harlan Sprague - Dawley rats to 2,3', 4,4', 5-pentachlorobiphenyl (PCB126), pulmonary alveolar epithelium at the junction of terminal bronchioles and along alveolar ducts was replaced by cuboidal to columnar ciliated cells. Scattered among these were cells exhibiting characteristics consistent with those of Clara cells; they lacked cilia and had a smooth apical surface that protruded into the alveolar space. This lesion was not typical of alveolar epithelial hyperplasia seen in rodent lungs; therefore, studies were done to characterize the lesion. Results of periodic acid-Schiff (PAS) staining, alcian blue (AB) staining, and GSTPi immunohistochemical staining of the lesions seen in treated rats were more similar to normal bronchiolar epithelium than normal alveolar epithelium or alveolar epithelial hyperplasia. These findings, along with the morphology of the cells, provide evidence that this lesion is closer in character to bronchiolar epithelium than alveolar type I or alveolar type II epithelium, and as a result, was called bronchiolar metaplasia.
引用
收藏
页码:333 / 337
页数:5
相关论文
共 50 条
  • [21] Excretion of 3,3′,4,4′,5-Pentachlorobiphenyl (PCB126) from Rat Liver Following Oral Administration of Lactobacillus reuteri and Lactobacillus acidophilus
    Suzuki, Takehito
    Yamazaki, Kaora
    Shinoda, Tadashi
    Shirai, Mitsuyuki
    Yoshikawa, Hiroshi
    Noguchi, Yurika
    Ito, Tetsuro
    Ishii, Yasuo
    Takizawa, Tatsuya
    Morita, Hidetoshi
    FOOD SCIENCE AND TECHNOLOGY RESEARCH, 2014, 20 (04) : 821 - 828
  • [22] Behavioral assessments of learning and attention in rats exposed perinatally to 3,3′,4,4′,5-pentachlorobiphenyl (PCB 126) (vol 21, pg 381, 1999)
    Bushnell, PJ
    Rice, DC
    NEUROTOXICOLOGY AND TERATOLOGY, 1999, 21 (06) : 733 - 733
  • [23] Dataset of transcriptomic changes that occur in human preadipocytes over a 3-day course of exposure to 3,3 ' ,4,4 ' ,5-Pentachlorobiphenyl (PCB126)
    Gourronc, Francoise A.
    Helm, Brynn K.
    Robertson, Larry W.
    Chimenti, Michael S.
    Lehmler, Hans-Joachim
    Ankrum, James A.
    Klingelhutz, Aloysius J.
    DATA IN BRIEF, 2022, 45
  • [24] Developmental toxicity of PCB 126 (3,3',4,4',5-pentachlorobiphenyl) in nestling American kestrels (Falco sparverius)
    Hoffman, DJ
    Melancon, MJ
    Klein, PN
    Rice, CP
    Eisemann, JD
    Hines, RK
    Spann, JW
    Pendleton, GW
    FUNDAMENTAL AND APPLIED TOXICOLOGY, 1996, 34 (02): : 188 - 200
  • [25] Low-frequency hearing loss following perinatal exposure to 3,3′,4,4′,5-pentachlorobiphenyl (PCB 126) in rats
    Crofton, KM
    Rice, DC
    NEUROTOXICOLOGY AND TERATOLOGY, 1999, 21 (03) : 299 - 301
  • [26] Increase in cardiovascular pathology in female sprague-dawley rats following chronic treatment with 2,3,7,8-tetrachlorodibenzo-p-dioxin and 3,3′,4,4′,5-pentachlorobiphenyl
    Micheal P. Jokinen
    Nigel J. Walker
    Amy E. Brix
    Donald M. Sells
    Joseph K. Haseman
    Abraham Nyska
    Cardiovascular Toxicology, 2003, 3 (4)
  • [27] Early Life Exposure to Low Levels of AHR Agonist PCB126 (3,3′,4,4′,5-Pentachlorobiphenyl) Reprograms Gene Expression in Adult Brain
    Aluru, Neelakanteswar
    Karchner, Sibel I.
    Glazer, Lilah
    TOXICOLOGICAL SCIENCES, 2017, 160 (02) : 386 - 397
  • [28] Transcriptome sequencing of 3,3′,4,4′,5-Pentachlorobiphenyl (PCB126)-treated human preadipocytes demonstrates progressive changes in pathways associated with inflammation and diabetes
    Gourronc, Francoise A.
    Helm, Brynn K.
    Robertson, Larry W.
    Chimenti, Michael S.
    Joachim-Lehmler, Hans
    Ankrum, James A.
    Klingelhutz, Aloysius J.
    TOXICOLOGY IN VITRO, 2022, 83
  • [29] The effects of 3,3′,4,4′,5-pentachlorobiphenyl (PCB 126) on mink (Mustela vison) reproduction and kit survivability and growth
    Beckett, K. J.
    Yamini, B.
    Bursian, S. J.
    ARCHIVES OF ENVIRONMENTAL CONTAMINATION AND TOXICOLOGY, 2008, 54 (01) : 123 - 129
  • [30] Metabolism of H-3-retinol by lake trout (Salvelinus namaycush) pre-exposed to 3,3',4,4',5-pentachlorobiphenyl (PCB 126)
    Palace, VP
    Klaverkamp, JF
    Baron, CL
    Brown, SB
    AQUATIC TOXICOLOGY, 1997, 39 (3-4) : 321 - 332