Cited by 105Effects and risks of endocrine disrupting chemicalsPesticide Exposure and ToxicitySexual Differentiation and Disorders

Effects of Pesticides and Toxic Substances On Behavioral and Morphological Reproductive Development: Endocrine Versus Nonendocrine Mechanisms

Gray, Leon Earl, Ostby, Joseph·1998·Toxicology and Industrial Health

Abstract

Exposure to toxic substances or pesticides during critical perinatal developmental periods can alter reproductive and central nervous system (CNS) function in a manner that does not compromise the growth and viability of the fetus but causes functional alterations that become apparent later in life. While some "CNS/behavioral teratogens" are mutagenic or alter cell division, other chemicals produce alterations of CNS development via endocrine-mediated mechanisms. The following discussion will focus on studies conducted primarily in our laboratory that describe how pesticides and toxic substances alter development of the reproductive and central nervous systems as a consequence of organizational or activational exposures. Abnormal behavior and morphology can result from exposure to endocrine-disrupting toxicants by altering organization of the CNS during critical stages of life or activation of behavior after puberty. Some of the toxicants that alter rodent sexual differentiation include xenoestrogens, antiandrogenic pesticides, and dioxin-like toxic substances. Chemicals that alter sex-linked nonreproductive and reproductive CNS development via nonhormonal mechanisms are also discussed in order to demonstrate that multiple mechanisms of action are involved in the development of behavioral abnormalities in pre- and perinatally exposed offspring. The fact that reproductive function (behavioral, biochemical, and morphological) can be altered via such a wide variety of mechanisms…

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Crossref · 10.1177/074823379801400111

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  • The dose used in the Flynn study was lower (up to 60 mg/kg/day to pregnant female) than that used in the Hotchkiss et al. (200 mg/kg/day to neonatal pup) and Gray and Ostby studies (200 mg/kg/day to pregnant female).

    “Second, the dose used in the Flynn study was lower (up to 60 mg/kg/day to pregnant female) than that used in the Hotchkiss et al. (200 mg/kg/day to neonatal pup) and Gray and Ostby studies (200 mg/kg/day to pregnant female).”
  • In studies by Flynn et al. (2001) and Gray and Ostby (1998), neonatal exposure to the AR antagonist was through lactational exposure, whereas in Hotchkiss et al. (2001) the compound was administered directly to the pup.

    “First, in studies conducted by Flynn et al. (2001) and Gray and Ostby (1998), neonatal exposure to the AR antagonist was through lactational exposure. In the Hotchkiss et al. study (2001), the compound was administered directly to the pup.”
  • In both Flynn et al. (2001) and Gray and Ostby (1998) studies, no effect of perinatal vinclozolin was found on male play behavior.

    “In both of these studies, no effect of perinatal vinclo- zolin was found on male play behavior.”

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Authors
Gray, L. E., & Ostby, J.
Affiliations
Environmental Protection Agency (US)
Venue
Toxicology and Industrial Health
Published
1998-01
Volume
14
Issue
1-2
Pages
159-184
ISSN
  • 0748-2337 (ISSN-L)
  • 1477-0393
OpenAlex
W2162762716
Cited by
105
References
0
Citations by year
2026: 1 · 2025: 1 · 2024: 2 · 2023: 2 · 2022: 2 · 2021: 1 · 2019: 2 · 2018: 2 · 2017: 3 · 2016: 1 · 2015: 1 · 2014: 1 · 2013: 3 · 2012: 2
FWCI
8.93
Type
journal article
Language
en
Open access
closed
Locations
  • Toxicology and Industrial Health (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Physical Sciences › Environmental Science › Health, Toxicology and Mutagenesis › Effects and risks of endocrine disrupting chemicals
  • Life Sciences › Agricultural and Biological Sciences › Plant Science › Pesticide Exposure and Toxicity
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Sexual Differentiation and Disorders
Keywords
pesticides, endocrine disruptors, reproductive development, central nervous system development, sexual differentiation, xenoestrogens, organizational effects, activational effects, perinatal exposure, reproductive morphology, behavioral abnormalities, hazard identification
MeSH terms
Animals, Central Nervous System, Environmental Exposure, Female, Food Contamination, Genitalia, Humans, Male, Neurosecretory Systems, Pesticides, Puberty, Reproduction, Sexual Behavior, Gonadal Steroid Hormones, Mice, Rats

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