| First Author | Villar-Pazos S | Year | 2017 |
| Journal | Sci Rep | Volume | 7 |
| Issue | 1 | Pages | 11770 |
| PubMed ID | 28924161 | Mgi Jnum | J:255771 |
| Mgi Id | MGI:6109950 | Doi | 10.1038/s41598-017-11995-3 |
| Citation | Villar-Pazos S, et al. (2017) Molecular mechanisms involved in the non-monotonic effect of bisphenol-a on ca2+ entry in mouse pancreatic beta-cells. Sci Rep 7(1):11770 |
| abstractText | 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 beta-cells from wild-type and oestrogen receptor ERbeta-/- mice, we found that exposure to increasing doses of BPA affected Ca(2+) entry in an NMDR manner. Low doses decreased plasma membrane Ca(2+) currents after downregulation of Cav2.3 ion channel expression, in a process involving ERbeta. High doses decreased Ca(2+) currents through an ERbeta-mediated mechanism and simultaneously increased Ca(2+) currents via oestrogen receptor ERalpha. The outcome of both molecular mechanisms explains the NMDR relationship between BPA and Ca(2+) entry in beta-cells. |
