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Toxicology ; 436: 152428, 2020 04 30.
Article in English | MEDLINE | ID: mdl-32151602

ABSTRACT

The increase in human infertility prevalence due to male reproductive disorders has been associated with extensive endocrine-disrupting chemical (EDC) exposure. Acrylamide (AA) is a compound formed spontaneously during heat processing of some foods that are mainly consumed by children and adolescents. In this study, we evaluated the prepubertal AA exposure effects on male adult reproductive physiology using a prepubertal experimental model to analyze the pubertal development, spermatogenesis hormones levels and genes expression involved in male reproductive function. This study is the first one to use the validated protocol to correlate the AA exposure with puberty development, as well as the AA-induced endocrine disrupting effects on reproductive axis. AA did not affect the age at puberty, the reproductive organ's weight and serum hormonal levels. AA reduces spermatogenesis, induces morphological and functional defects on sperm and alters transcript expression of sexual hormone receptors (Ar and Esr2), the transcript expression of Tnf, Egr2, Rhcg and Lrrc34. These findings suggest that excessive AA consumption may impair their reproductive capacity at adulthood, despite no changes in hormonal profile being observed.


Subject(s)
Acrylamide/toxicity , Endocrine Disruptors/toxicity , Food Contamination , Infertility, Male/chemically induced , Sexual Development/drug effects , Spermatogenesis/drug effects , Spermatozoa/drug effects , Age Factors , Animals , Cation Transport Proteins/genetics , Cation Transport Proteins/metabolism , Dose-Response Relationship, Drug , Early Growth Response Protein 2/genetics , Early Growth Response Protein 2/metabolism , Estrogen Receptor beta/genetics , Estrogen Receptor beta/metabolism , Infertility, Male/metabolism , Infertility, Male/pathology , Infertility, Male/physiopathology , Male , Membrane Glycoproteins/genetics , Membrane Glycoproteins/metabolism , Rats, Wistar , Receptors, Androgen/genetics , Receptors, Androgen/metabolism , Repressor Proteins/genetics , Repressor Proteins/metabolism , Risk Assessment , Spermatozoa/metabolism , Spermatozoa/pathology , Tumor Necrosis Factor-alpha/genetics , Tumor Necrosis Factor-alpha/metabolism
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