Molecular mechanisms involved in the non-monotonic effect of bisphenol-a on ca2+ entry in mouse pancreatic β-cells

Sci Rep. 2017 Sep 18;7(1):11770. doi: 10.1038/s41598-017-11995-3.


In regulatory toxicology, the dose-response relationship is a key element towards fulfilling safety assessments and satisfying regulatory authorities. Conventionally, the larger the dose, the greater the response, following the dogma "the dose makes the poison". Many endocrine disrupting chemicals, including bisphenol-A (BPA), induce non-monotonic dose response (NMDR) relationships, which are unconventional and have tremendous implications in risk assessment. Although several molecular mechanisms have been proposed to explain NMDR relationships, they are largely undemonstrated. Using mouse pancreatic β-cells from wild-type and oestrogen receptor ERβ-/- mice, we found that exposure to increasing doses of BPA affected Ca2+ entry in an NMDR manner. Low doses decreased plasma membrane Ca2+ currents after downregulation of Cav2.3 ion channel expression, in a process involving ERβ. High doses decreased Ca2+ currents through an ERβ-mediated mechanism and simultaneously increased Ca2+ currents via oestrogen receptor ERα. The outcome of both molecular mechanisms explains the NMDR relationship between BPA and Ca2+ entry in β-cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Benzhydryl Compounds / toxicity*
  • Calcium / metabolism*
  • Calcium Channels, R-Type / biosynthesis
  • Calcium Channels, R-Type / genetics
  • Calcium Signaling / drug effects*
  • Calcium Signaling / genetics
  • Cation Transport Proteins / biosynthesis
  • Cation Transport Proteins / genetics
  • Dose-Response Relationship, Drug
  • Estrogen Receptor beta / genetics
  • Estrogen Receptor beta / metabolism
  • Gene Expression Regulation / drug effects
  • Insulin-Secreting Cells / metabolism*
  • Insulin-Secreting Cells / pathology
  • Male
  • Mice
  • Mice, Knockout
  • Phenols / toxicity*


  • Benzhydryl Compounds
  • Cacna1e protein, mouse
  • Calcium Channels, R-Type
  • Cation Transport Proteins
  • Estrogen Receptor beta
  • Phenols
  • bisphenol A
  • Calcium