Long-term exposure to the mixture of phthalates induced male reproductive toxicity in rats and the alleviative effects of quercetin

Toxicol Appl Pharmacol. 2024 Feb:483:116816. doi: 10.1016/j.taap.2024.116816. Epub 2024 Jan 11.

Abstract

Phthalates (PEs), such as di(2-ethylhexyl) phthalate (DEHP), dibutyl phthalate (DBP) and butyl benzyl phthalate (BBP) could cause reproductive and developmental toxicities, while human beings are increasingly exposed to them at low-doses. Phytochemical quercetin (Que) is a flavonoid that has estrogenic effect, anti-inflammatory and anti-oxidant effects. This study was conducted to assess the alleviative effect of Que. on male reproductive toxicity induced by the mixture of three commonly used PEs (MPEs) at low-dose in rats, and explore the underlying mechanism. Male rats were treated with MPEs (16 mg/kg/day) and/or Que. (50 mg/kg/d) for 91 days. The results showed that MPEs exposure caused male reproductive injuries, such as decreased serum sex hormones levels, abnormal testicular pathological structure, increased abnormal sperm rate and changed expressions of PIWIL1 and PIWIL2. Furthermore, MPEs also changed the expression of steroidogenic proteins in steroid hormone metabolism, including StAR, CYP11A1, CYP17A1, 17β-HSD, CYP19A1. However, the alterations of these parameters were reversed by Que. MPEs caused male reproductive injuries in rats; Que. inhibited MPEs' male reproductive toxicity, which might relate to the improvement of testosterone biosynthesis.

Keywords: Male reproductive toxicity; Phthalates; Quercetin; Steroid hormone metabolism.

MeSH terms

  • Animals
  • Argonaute Proteins / metabolism
  • Argonaute Proteins / pharmacology
  • Diethylhexyl Phthalate* / toxicity
  • Humans
  • Male
  • Phthalic Acids* / metabolism
  • Phthalic Acids* / toxicity
  • Quercetin / pharmacology
  • Rats
  • Rats, Sprague-Dawley
  • Semen / metabolism
  • Testis
  • Testosterone

Substances

  • phthalic acid
  • Quercetin
  • Testosterone
  • Phthalic Acids
  • Diethylhexyl Phthalate
  • PIWIL1 protein, human
  • Argonaute Proteins
  • PIWIL2 protein, human