Literature DB >> 12324652

Developing a laboratory animal model for perinatal endocrine disruption: the hamster chronicles.

William J Hendry1, Daniel M Sheehan, Shafiq A Khan, Jeffrey V May.   

Abstract

At the biomedical, regulatory, and public level, considerable concern surrounds the concept that inappropriate exposure to endocrine-disrupting chemicals, especially during the prenatal and/or neonatal period, may disrupt normal reproductive tract development and adult function. The intent of this review was to 1. Describe some unique advantages of the hamster for perinatal endocrine disruptor (ED) studies, 2. Summarize the morphological and molecular consequences of exposure to the established perinatal ED, diethylstilbestrol, in the female and male hamster, 3. Present some new, histomorphological insight into the process of neonatal diethylstilbestrol-induced disruption in the hamster uterus, and 4. Introduce recent efforts and future plans to evaluate the potency and mechanism of action of other putative EDs in the hamster experimental system. Taken together, the findings indicate that the hamster represents a unique and sensitive in vivo system to probe the phenomenon of endocrine disruption. The spectrum of candidate endpoints includes developmental toxicity, neoplasia, and more subtle endpoints of reproductive dysfunction.

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Year:  2002        PMID: 12324652     DOI: 10.1177/153537020222700904

Source DB:  PubMed          Journal:  Exp Biol Med (Maywood)        ISSN: 1535-3699


  7 in total

1.  Neonatal diethylstilbestrol exposure disrupts female reproductive tract structure/function via both direct and indirect mechanisms in the hamster.

Authors:  Imala D Alwis; Dulce M Maroni; Isabel R Hendry; Shyamal K Roy; Jeffrey V May; Wendell W Leavitt; William J Hendry
Journal:  Reprod Toxicol       Date:  2011-09-24       Impact factor: 3.143

2.  Altered microRNA expression patterns during the initiation and promotion stages of neonatal diethylstilbestrol-induced dysplasia/neoplasia in the hamster (Mesocricetus auratus) uterus.

Authors:  Ramesh Padmanabhan; Isabel R Hendry; Jennifer R Knapp; Bin Shuai; William J Hendry
Journal:  Cell Biol Toxicol       Date:  2017-03-06       Impact factor: 6.691

3.  Epigenetic transgenerational actions of endocrine disruptors.

Authors:  Michael K Skinner; Mohan Manikkam; Carlos Guerrero-Bosagna
Journal:  Reprod Toxicol       Date:  2010-11-03       Impact factor: 3.143

4.  Developmental exposure to diethylstilbestrol alters uterine gene expression that may be associated with uterine neoplasia later in life.

Authors:  Retha R Newbold; Wendy N Jefferson; Sherry F Grissom; Elizabeth Padilla-Banks; Ryan J Snyder; Edward K Lobenhofer
Journal:  Mol Carcinog       Date:  2007-09       Impact factor: 4.784

Review 5.  Epigenetic transgenerational actions of environmental factors in disease etiology.

Authors:  Michael K Skinner; Mohan Manikkam; Carlos Guerrero-Bosagna
Journal:  Trends Endocrinol Metab       Date:  2010-01-14       Impact factor: 12.015

6.  Altered gene expression patterns during the initiation and promotion stages of neonatally diethylstilbestrol-induced hyperplasia/dysplasia/neoplasia in the hamster uterus.

Authors:  William J Hendry; Hussam Y Hariri; Imala D Alwis; Sumedha S Gunewardena; Isabel R Hendry
Journal:  Reprod Toxicol       Date:  2014-09-19       Impact factor: 3.143

7.  In Vivo Study of The Oestrogenic Activity of Milk.

Authors:  Lidia Radko; Andrzej Posyniak
Journal:  J Vet Res       Date:  2021-09-23       Impact factor: 1.744

  7 in total

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