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Article Publish Status: FREE
Abstract Title:

Chronic exposure to low dose of bisphenol A impacts on the first round of spermatogenesis via SIRT1 modulation.

Abstract Source:

Sci Rep. 2018 Feb 13 ;8(1):2961. Epub 2018 Feb 13. PMID: 29440646

Abstract Author(s):

Rosanna Chianese, Andrea Viggiano, Konrad Urbanek, Donato Cappetta, Jacopo Troisi, Marika Scafuro, Maurizio Guida, Grazia Esposito, Loreta Pia Ciuffreda, Francesco Rossi, Liberato Berrino, Silvia Fasano, Riccardo Pierantoni, Antonella De Angelis, Rosaria Meccariello

Article Affiliation:

Rosanna Chianese

Abstract:

Spermatogenesis depends on endocrine, autocrine and paracrine communications along the hypothalamus-pituitary-gonad axis. Bisphenol A (BPA), an estrogen-mimic endocrine disrupting chemical, is an environmental contaminant used to manufacture polycarbonate plastics and epoxy resins with toxic effects for male reproduction. Here we investigated whether the chronic exposure to low BPA doses affects spermatogenesis through the modulation of SIRT1, a NAD-dependent deacetylase involved in the progression of spermatogenesis, with outcomes on apoptosis, oxidative stress, metabolism and energy homeostasis. BPA exposure via placenta first, and lactation and drinking water later, affected the body weight gain in male offspring at 45 postnatal days and the first round of spermatogenesis, with impairment of blood testis barrier, reactive oxygen species production, DNA damage and decreased expression of SIRT1. The analysis of SIRT1 downstream molecular pathways revealed the increase of acetyl-p53,γH2AX foci, the decrease of oxidative stress defenses and the higher apoptotic rate in the testis of treated animals, with partial rescue at sex maturation. In conclusion, SIRT1 pathways disruption after BPA exposure can have serious consequences on the first round of spermatogenesis.

Study Type : Animal Study

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Sayer Ji
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