» Articles » PMID: 22419778

Hormones and Endocrine-disrupting Chemicals: Low-dose Effects and Nonmonotonic Dose Responses

Overview
Journal Endocr Rev
Specialty Endocrinology
Date 2012 Mar 16
PMID 22419778
Citations 874
Authors
Affiliations
Soon will be listed here.
Abstract

For decades, studies of endocrine-disrupting chemicals (EDCs) have challenged traditional concepts in toxicology, in particular the dogma of "the dose makes the poison," because EDCs can have effects at low doses that are not predicted by effects at higher doses. Here, we review two major concepts in EDC studies: low dose and nonmonotonicity. Low-dose effects were defined by the National Toxicology Program as those that occur in the range of human exposures or effects observed at doses below those used for traditional toxicological studies. We review the mechanistic data for low-dose effects and use a weight-of-evidence approach to analyze five examples from the EDC literature. Additionally, we explore nonmonotonic dose-response curves, defined as a nonlinear relationship between dose and effect where the slope of the curve changes sign somewhere within the range of doses examined. We provide a detailed discussion of the mechanisms responsible for generating these phenomena, plus hundreds of examples from the cell culture, animal, and epidemiology literature. We illustrate that nonmonotonic responses and low-dose effects are remarkably common in studies of natural hormones and EDCs. Whether low doses of EDCs influence certain human disorders is no longer conjecture, because epidemiological studies show that environmental exposures to EDCs are associated with human diseases and disabilities. We conclude that when nonmonotonic dose-response curves occur, the effects of low doses cannot be predicted by the effects observed at high doses. Thus, fundamental changes in chemical testing and safety determination are needed to protect human health.

Citing Articles

Distribution of Environmental Phenols into Follicular Fluid and Urine of Women Attending Infertility Clinic.

Klimowska A, Jurewicz J, Radwan M, Radwan P, Pol P, Wielgomas B J Xenobiot. 2025; 15(1).

PMID: 39997360 PMC: 11856404. DOI: 10.3390/jox15010017.


Frequencies of enamel hypomineralisation in permanent and primary molars in a medieval and early-modern-age population (7th - 17th c.) in Sains-en-Gohelle (Pas de Calais, France).

Estivals J, Couture C, Rouas P, Manton D, Garot E Sci Rep. 2025; 15(1):5704.

PMID: 39962213 PMC: 11832890. DOI: 10.1038/s41598-025-87589-1.


Gestational exposure to environmental chemical mixtures and cognitive abilities in children: A pooled analysis of two North American birth cohorts.

Puvvula J, Hwang W, McCandless L, Xie C, Braun J, Vuong A Environ Int. 2025; 196:109298.

PMID: 39893913 PMC: 11896093. DOI: 10.1016/j.envint.2025.109298.


In Vivo Investigation of the Effects of Nonylphenol on the Pituitary-Adrenal Axis and Pineal Gland in Male Rats.

Inkaya E, Tokgoz E, Barlas N Basic Clin Pharmacol Toxicol. 2025; 136(3):e70003.

PMID: 39887640 PMC: 11783352. DOI: 10.1111/bcpt.70003.


Differential Gene Expression Analysis in a Lumbar Spinal Stenosis Rat Model via RNA Sequencing: Identification of Key Molecular Pathways and Therapeutic Insights.

Hong J, Jeon W, Kim H, Yeo C, Kim H, Lee Y Biomedicines. 2025; 13(1).

PMID: 39857775 PMC: 11762803. DOI: 10.3390/biomedicines13010192.


References
1.
. Hormonal Chaos: The Scientific and Social Origins of the Environmental Endocrine Hypothesis. Nat Med. 2000; 6(3):246-247. DOI: 10.1038/73073. View

2.
Asp V, Ulleras E, Lindstrom V, Bergstrom U, Oskarsson A, Brandt I . Biphasic hormonal responses to the adrenocorticolytic DDT metabolite 3-methylsulfonyl-DDE in human cells. Toxicol Appl Pharmacol. 2009; 242(3):281-9. DOI: 10.1016/j.taap.2009.10.018. View

3.
Kruger T, Long M, Bonefeld-Jorgensen E . Plastic components affect the activation of the aryl hydrocarbon and the androgen receptor. Toxicology. 2008; 246(2-3):112-23. DOI: 10.1016/j.tox.2007.12.028. View

4.
Ryan B, Hotchkiss A, Crofton K, Gray Jr L . In utero and lactational exposure to bisphenol A, in contrast to ethinyl estradiol, does not alter sexually dimorphic behavior, puberty, fertility, and anatomy of female LE rats. Toxicol Sci. 2009; 114(1):133-48. DOI: 10.1093/toxsci/kfp266. View

5.
Carr J, Gentles A, Smith E, Goleman W, Urquidi L, Thuett K . Response of larval Xenopus laevis to atrazine: assessment of growth, metamorphosis, and gonadal and laryngeal morphology. Environ Toxicol Chem. 2003; 22(2):396-405. View