Literature DB >> 19710361

Characterization of the hypothalamic-pituitary-adrenal axis response to atrazine and metabolites in the female rat.

Melanie J P Fraites1, Ralph L Cooper, Angela Buckalew, Saro Jayaraman, Lesley Mills, Susan C Laws.   

Abstract

Atrazine (ATR) has recently been shown to activate the hypothalamic-pituitary-adrenal (HPA) axis in rodents. The current study investigated the effect of ATR and two of its chlorinated metabolites, desisopropylatrazine (DIA) and diamino-s-chlorotriazine (DACT), on the HPA axis in the Long-Evans female rat. A single oral gavage administration of 75 mg/kg ATR or 60.2 mg/kg DIA (a dose equimolar to the applied ATR dose) during the morning of proestrus resulted in significant, acute increases in circulating adrenocorticotropic hormone (ACTH), corticosterone, and progesterone. Oral doses of ATR or DIA were given daily over the course of the 4-day ovarian cycle starting on the day of vaginal estrus, resulted in a similar, dose-responsive activation of the HPA axis. The increase in ACTH, corticosterone, and progesterone by these compounds was of a similar magnitude to that produced by 5-min restraint stress. Single or multiple oral exposures to DACT, on the other hand, did not significantly alter pituitary-adrenal hormone release. These results were observed despite plasma levels of DACT being higher than any other metabolite at the time of hormone measurement. Overall, circulating metabolite concentrations following equimolar dosing were much higher than those observed after ATR administration. Additional studies indicated that the activation of the HPA axis by oral exposure to ATR and DIA was not due simply to the stimulation of gastrointestinal afferents. Similar responses were observed in rats which received an oral dose of ATR following bilateral subdiaphramatic vagotomy and following intravenous administration of DIA in jugular vein catheterized animals. We conclude that ATR and the metabolite DIA significantly activate the HPA axis following oral exposure in the female rat. Activation of this endocrine axis by these chlorotriazines could contribute to the induced changes of female reproductive function reported previously.

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Year:  2009        PMID: 19710361     DOI: 10.1093/toxsci/kfp194

Source DB:  PubMed          Journal:  Toxicol Sci        ISSN: 1096-0929            Impact factor:   4.849


  29 in total

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Journal:  Endocr Rev       Date:  2012-03-14       Impact factor: 19.871

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Review 3.  Contributions of nonhematopoietic cells and mediators to immune responses: implications for immunotoxicology.

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Journal:  Toxicol Sci       Date:  2015-06       Impact factor: 4.849

4.  Embryonic Atrazine Exposure Elicits Alterations in Genes Associated with Neuroendocrine Function in Adult Male Zebrafish.

Authors:  Sara E Wirbisky; Maria S Sepúlveda; Gregory J Weber; Amber S Jannasch; Katharine A Horzmann; Jennifer L Freeman
Journal:  Toxicol Sci       Date:  2016-07-13       Impact factor: 4.849

5.  Atrazine acts as an endocrine disrupter by inhibiting cAMP-specific phosphodiesterase-4.

Authors:  Marek Kucka; Kristina Pogrmic-Majkic; Svetlana Fa; Stanko S Stojilkovic; Radmila Kovacevic
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6.  Developmental origins of neurotransmitter and transcriptome alterations in adult female zebrafish exposed to atrazine during embryogenesis.

Authors:  Sara E Wirbisky; Gregory J Weber; Maria S Sepúlveda; Changhe Xiao; Jason R Cannon; Jennifer L Freeman
Journal:  Toxicology       Date:  2015-04-27       Impact factor: 4.221

7.  Are the adverse effects of stressors on amphibians mediated by their effects on stress hormones?

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Review 8.  Exposure to endocrine disruptors during adulthood: consequences for female fertility.

Authors:  Saniya Rattan; Changqing Zhou; Catheryne Chiang; Sharada Mahalingam; Emily Brehm; Jodi A Flaws
Journal:  J Endocrinol       Date:  2017-03-29       Impact factor: 4.286

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Journal:  Physiol Behav       Date:  2015-09-25

10.  The effects of gestational and chronic atrazine exposure on motor behaviors and striatal dopamine in male Sprague-Dawley rats.

Authors:  Jennifer L Walters; Theresa A Lansdell; Keith J Lookingland; Lisa E Baker
Journal:  Toxicol Appl Pharmacol       Date:  2015-10-09       Impact factor: 4.219

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