Affiliation:
1. Reproductive Toxicology Laboratory, Department of Pharmacology Federal University of Paraná (UFPR) Curitiba Brazil
2. Animal Endocrine and Reproductive Physiology Laboratory, Department of Physiology Federal University of Paraná (UFPR) Curitiba Brazil
3. Reproductive Toxicology Laboratory, Department of Pharmacy State University of Centro‐Oeste Guarapuava Brazil
Abstract
ABSTRACTSeveral phthalates, mainly used as plasticizers, are known for their adverse effects on the male genital system. Previously, we demonstrated that an environmentally relevant mixture of six antiandrogenic phthalates (PMix), derived from a biomonitoring study in pregnant Brazilian women, was able to disrupt the reproductive development in male rats. Experimental groups (control, 0.1, 0.5, and 500 mg PMix/kg/day) were established starting from the extrapolated human dose (0.1 mg/kg/day), followed by doses 5 times and 5000 times higher. Pregnant rats received daily oral gavage administration of either vehicle (control) or PMix from gestational day 13 to postnatal day 10. Here, we examined male and female offspring regarding changes in gene expression of key reproductive factors in the hypothalamus and pituitary gland at adulthood and conducted a battery of behavioral tests in males, including partner preference, sexual behavior, and male attractiveness tests. PMix induced some changes in mating‐related behavior in males, as demonstrated by the absence of preference for females against males and a higher number of penetrations up to ejaculation in the 0.5 dose group. PMix decreased Esr2 expression in the male hypothalamus across all three doses, and in females at mid and high doses in both the hypothalamus and pituitary. In male hypothalamus, we also observed decreased Kiss1 transcripts in these groups and a reduction in AR at the 0.5 dose group. In summary, our results provide further evidence that phthalates in a mixture, even at low doses, may exert cumulative effects on the structures underlying sexual behavior, which seems to be more sensitive than reproductive endpoints for the same experimental design.
Funder
Coordenação de Aperfeiçoamento de Pessoal de Nível Superior
Conselho Nacional de Desenvolvimento Científico e Tecnológico
Reference63 articles.
1. Perinatal Exposure to the Phthalates DEHP, BBP, and DINP, but Not DEP, DMP, or DOTP, Alters Sexual Differentiation of the Male Rat;Gray L. E.;Toxicological Sciences,2000
2. Reproductive Toxicity of Phthalate Esters;Martino‐Andrade A. J.;Molecular Nutrition & Food Research,2010
3. Pathogenesis of Male Reproductive Tract Lesions From Gestation Through Adulthood Following in Utero Exposure to Di(n‐Butyl) Phthalate;Barlow N. J.;Toxicologic Pathology,2003
4. Dose‐Dependent Alterations in Gene Expression and Testosterone Synthesis in the Fetal Testes of Male Rats Exposed to Di (n‐Butyl) Phthalate;Lehmann K. P.;Toxicological Sciences,2004
5. In Utero and Lactational Exposure to Diisopentyl Phthalate Induces Fetal Toxicity and Antiandrogenic Effects in Rats;Curi T. Z.;Toxicological Sciences,2019