Literature DB >> 26827910

Impairment of object recognition memory by maternal bisphenol A exposure is associated with inhibition of Akt and ERK/CREB/BDNF pathway in the male offspring hippocampus.

Chong Wang1, Zhihui Li2, Haijun Han3, Guangying Luo4, Bingrui Zhou2, Shaolin Wang5, Jundong Wang6.   

Abstract

Bisphenol A (BPA) is a commonly used endocrine-disrupting chemical used as a component of polycarbonates plastics that has potential adverse effects on human health. Exposure to BPA during development has been implicated in memory deficits, but the mechanism of action underlying the effect is not fully understood. In this study, we investigated the effect of maternal exposure to BPA on object recognition memory and the expressions of proteins important for memory, especially focusing on the ERK/CREB/BDNF pathway. Pregnant Sprague-Dawley female rats were orally treated with either vehicle or BPA (0.05, 0.5, 5 or 50 mg/kg BW/day) during days 9-20 of gestation. Male offspring were tested on postnatal day 21 with the object recognition task. Recognition memory was assessed using the object recognition index (index=the time spent exploring the novel object/(the time spent exploring the novel object+the time spent exploring the familiar object)). In the test session performed 90 min after the training session, BPA-exposed male offspring not only spent more time in exploring the familiar object at the highest dose than the control, but also displayed a significantly decreased the object recognition index at the doses of 0.5, 5 and 50 mg/kg BW/day. During the test session performed 24h after the training session, BPA-treated males did not change the time spent exploring the familiar object, but had a decreased object recognition index at 5 and 50 mg/kg BW/day, when compared to control group. These findings indicate that object recognition memory was susceptible to maternal BPA exposure. Western blot analysis of hippocampi from BPA-treated male offspring revealed a decrease in Akt, phospho-Akt, p44/42 MAPK and phospho-p44/42 MAPK protein levels, compared to controls. In addition, BPA significantly inhibited the levels of phosphorylation of CREB and BDNF in the hippocampus. Our results show that maternal BPA exposure may full impair object recognition memory, and that impairment may be related to a decrease in Akt activation and an inhibition of the ERK/CREB/BDNF pathway in the hippocampus. This study also adds new evidence that suggests BPA has an antagonistic effect on the action of estrogen in the brain.
Copyright © 2016 Elsevier Ireland Ltd. All rights reserved.

Entities:  

Keywords:  Akt; Bisphenol A; ERK/CREB/BDNF pathway; Maternal; Object recognition memory

Mesh:

Substances:

Year:  2016        PMID: 26827910     DOI: 10.1016/j.tox.2016.01.010

Source DB:  PubMed          Journal:  Toxicology        ISSN: 0300-483X            Impact factor:   4.221


  17 in total

1.  Bisphenol A (BPA) induces progesterone receptor expression in an estrogen receptor α-dependent manner in perinatal brain.

Authors:  Allyssa Fahrenkopf; Christine K Wagner
Journal:  Neurotoxicol Teratol       Date:  2020-01-09       Impact factor: 3.763

Review 2.  Estrogenic Endocrine Disrupting Chemicals Influencing NRF1 Regulated Gene Networks in the Development of Complex Human Brain Diseases.

Authors:  Mark Preciados; Changwon Yoo; Deodutta Roy
Journal:  Int J Mol Sci       Date:  2016-12-13       Impact factor: 5.923

3.  Developmental toxicity of bisphenol S in Caenorhabditis elegans and NODEF mice.

Authors:  Callie M McDonough; Daniel J Guo; Tai L Guo
Journal:  Neurotoxicology       Date:  2021-09-28       Impact factor: 4.294

4.  Gene expression and DNA methylation changes in the hypothalamus and hippocampus of adult rats developmentally exposed to bisphenol A or ethinyl estradiol: a CLARITY-BPA consortium study.

Authors:  Ana Cheong; Sarah A Johnson; Emily C Howald; Mark R Ellersieck; Luísa Camacho; Sherry M Lewis; Michelle M Vanlandingham; Jun Ying; Shuk-Mei Ho; Cheryl S Rosenfeld
Journal:  Epigenetics       Date:  2018-08-15       Impact factor: 4.528

5.  Early life bisphenol A exposure and neurobehavior at 8years of age: Identifying windows of heightened vulnerability.

Authors:  Shaina L Stacy; George D Papandonatos; Antonia M Calafat; Aimin Chen; Kimberly Yolton; Bruce P Lanphear; Joseph M Braun
Journal:  Environ Int       Date:  2017-07-29       Impact factor: 9.621

6.  Reversible Changes in BDNF Expression in MK-801-Induced Hippocampal Astrocytes Through NMDAR/PI3K/ERK Signaling.

Authors:  Wenjuan Yu; Hongwei Fang; Lei Zhang; Miaowen Hu; Sidi He; Huafang Li; Hao Zhu
Journal:  Front Cell Neurosci       Date:  2021-05-14       Impact factor: 5.505

7.  Therapeutic effects of astragaloside IV and Astragalus spinosus saponins against bisphenol A-induced neurotoxicity and DNA damage in rats.

Authors:  Amina E Essawy; Heba-Tallah Abd Elrahim Abd Elkader; Omaima A Khamiss; Saber Mohamed Eweda; Heba Mohamed Abdou
Journal:  PeerJ       Date:  2021-08-09       Impact factor: 2.984

8.  Alcohol amplifies ketamine-induced apoptosis in primary cultured cortical neurons and PC12 cells through down-regulating CREB-related signaling pathways.

Authors:  Daiying Zuo; Feng Sun; Jiahui Cui; Yumiao Liu; Zi Liu; Xuejiao Zhou; Zengqiang Li; Yingliang Wu
Journal:  Sci Rep       Date:  2017-09-05       Impact factor: 4.379

9.  Fetal Bisphenol-A Induced Changes in Murine Behavior and Brain Gene Expression Persisted in Adult-aged Offspring.

Authors:  Zhihao Wang; Myles H Alderman; Cyrus Asgari; Hugh S Taylor
Journal:  Endocrinology       Date:  2020-12-01       Impact factor: 4.736

10.  Behavioral changes and hyperglycemia in NODEF mice following bisphenol S exposure are affected by diets.

Authors:  Callie M McDonough; Joella Xu; Tai L Guo
Journal:  Neurotoxicology       Date:  2021-06-08       Impact factor: 4.398

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.