Literature DB >> 20067830

In utero and lactational exposure to 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) induces disruption of glands of the prostate and fibrosis in rhesus monkeys.

Akihiro Arima1, Hirohito Kato, Ryota Ise, Yojiro Ooshima, Ayumi Inoue, Atsunobu Muneoka, Shunichi Kamimura, Toshio Fukusato, Shunichiro Kubota, Hiroshi Sumida, Mineo Yasuda.   

Abstract

We investigated the effects that 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) exposure has on the prostate in rhesus monkey offspring. Dams received 0, 30 or 300 ng/kg TCDD subcutaneously on Day 20 of gestation, and then 5% of the initial dose was injected every 30 days until Day 90 after delivery. The offspring were maintained until reaching sexual maturity, and examined histopathologically. Dose-dependent decreases in glands of the prostate and widespread fibrosis were observed in offspring. It is noteworthy that 7 years from the final lactational TCDD exposure, inflammatory cell infiltration and disruption of glands of the prostate were still observed. Differential mRNA expression associated with fibrosis, inflammatory response and disruption of cell components were demonstrated by microarray analysis, with up-regulation of TGM4, TGFB1, COL1A1 and MMP2 confirmed. In conclusion, in utero and lactational exposure to TCDD induced dose-related prostatic fibrosis, indicating prostatic dysfunction and inducible semen quality reduction in second-generation rhesus monkeys. Copyright 2010 Elsevier Inc. All rights reserved.

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Year:  2010        PMID: 20067830     DOI: 10.1016/j.reprotox.2009.12.007

Source DB:  PubMed          Journal:  Reprod Toxicol        ISSN: 0890-6238            Impact factor:   3.143


  5 in total

Review 1.  Potential protective mechanisms of aryl hydrocarbon receptor (AHR) signaling in benign prostatic hyperplasia.

Authors:  Vatsal Mehta; Chad M Vezina
Journal:  Differentiation       Date:  2011 Nov-Dec       Impact factor: 3.880

2.  In Utero and Lactational TCDD Exposure Increases Susceptibility to Lower Urinary Tract Dysfunction in Adulthood.

Authors:  William A Ricke; Calvin W Lee; Tyler R Clapper; Andrew J Schneider; Robert W Moore; Kimberly P Keil; Lisa L Abler; Jalissa L Wynder; Arnaldo López Alvarado; Isaac Beaubrun; Jenny Vo; Tyler M Bauman; Emily A Ricke; Richard E Peterson; Chad M Vezina
Journal:  Toxicol Sci       Date:  2016-02-09       Impact factor: 4.849

3.  In utero and lactational 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) exposure exacerbates urinary dysfunction in hormone-treated C57BL/6J mice through a non-malignant mechanism involving proteomic changes in the prostate that differ from those elicited by testosterone and estradiol.

Authors:  Anne E Turco; Samuel Thomas; LaTasha K Crawford; Weiping Tang; Richard E Peterson; Lingjun Li; William A Ricke; Chad M Vezina
Journal:  Am J Clin Exp Urol       Date:  2020-02-25

Review 4.  Intersection of AHR and Wnt signaling in development, health, and disease.

Authors:  Andrew J Schneider; Amanda M Branam; Richard E Peterson
Journal:  Int J Mol Sci       Date:  2014-10-03       Impact factor: 5.923

5.  A mechanism linking perinatal 2,3,7,8 tetrachlorodibenzo-p-dioxin exposure to lower urinary tract dysfunction in adulthood.

Authors:  Anne E Turco; Steven R Oakes; Kimberly P Keil Stietz; Cheryl L Dunham; Diya B Joseph; Thrishna S Chathurvedula; Nicholas M Girardi; Andrew J Schneider; Joseph Gawdzik; Celeste M Sheftel; Peiqing Wang; Zunyi Wang; Dale E Bjorling; William A Ricke; Weiping Tang; Laura L Hernandez; Janet R Keast; Adrian D Bonev; Matthew D Grimes; Douglas W Strand; Nathan R Tykocki; Robyn L Tanguay; Richard E Peterson; Chad M Vezina
Journal:  Dis Model Mech       Date:  2021-07-27       Impact factor: 5.732

  5 in total

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