HIGH DOSES OF BISPHENOL-A PROMOTE A REDUCTION IN THE NUMBER OF MYENTERIC NEURONS IN RATS

Bisphenol-A (BPA), found in plastics and food coatings, is known for its potential adverse health effects. While some studies have focused on BPA's endocrine effects, other research explores its impact on the myenteric plexus, which controls the motility of the digestive tract. The study investigated the effects of BPA on myenteric plexus neurons in rats. For the analysis of the effects on the myenteric plexus (MP), 32 male Wistar rats aged 40 days were divided into four groups (n=8) that received filtered water via gavage over 12 weeks for the control group (CG), dose group 1 (DG1) BPA solution at 0.05mg/kg, dose group 2 (DG2) BPA solution at 0.25mg/kg, and dose group 3 (DG3) BPA solution at 0.5mg/kg. The animals were weighed weekly to adjust the administered volume. At the end of the experimental period, a new weighing was performed, and the rats were euthanized. After laparotomy, the intestinal segments corresponding to the jejunum-ileum were collected to demonstrate the density of the population (Giemsa+), the subpopulations of active myenteric neurons (NADH-d+), and the nitrergic subpopulation (NADPH-d+). BPA exposure did not significantly affect the rats' weight gain, but, there was a reduction in the total density of myenteric neurons in DG3 (10.78mm²) compared to DG (18.88mm²) and DG1 (16.28mm²), and also a reduction in the NADH-d+ subpopulation between DG3 (8.50mm²) and the CG (14.45mm²) and DG1 (14.17mm²) groups. For the nitrergic subpopulation (NADPH-d+), there was no difference in the expression of these neurons. Based on the results obtained, it can be inferred that there was a reduction in cholinergic neurons (NADPH-d-), calculated from the total population of neurons. These findings suggest that BPA may compromise the neuronal function of the MP, possibly by inducing oxidative stress and apoptosis of subpopulations, acting as a xenoestrogen on the nuclear receptors of these neurons, and consequently affecting the regulation of gastrointestinal motility, interfering with cholinergic neuronal transmission and nitric oxide production, and also greater resistance of nitrergic neurons can be observed. Both studies highlight the importance of raising awareness about BPA, as well as the possible harmful effects on unique health. The need to understand the impacts of BPA on different biological systems is emphasized to better understand its effects on human health, especially considering its widespread presence in modern society.

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Publication Details

Journal
Aracê.
Published
2024-11-28
DOI
https://doi.org/10.56238/arev6n3-363
Primary Topic
Effects and risks of endocrine disrupting chemicals
Type
article
Field-Weighted Citation Impact
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article

HIGH DOSES OF BISPHENOL-A PROMOTE A REDUCTION IN THE NUMBER OF MYENTERIC NEURONS IN RATS

Edson Gerônimo, Ricardo de Melo Germano, Itaruã Machri Colla, Anna Furlan et al.
Aracê.
Effects and risks of endocrine disrupting chemicals
article

HIGH DOSES OF BISPHENOL-A PROMOTE A REDUCTION IN THE NUMBER OF MYENTERIC NEURONS IN RATS

Edson Gerônimo, Ricardo de Melo Germano, Itaruã Machri Colla, Anna Furlan, Wesley Alves Trindade, Andréia Assunção Soares, Luciana Kazue Otutumi, Paula Montanhini Favetta, Ana Laura Bosco Caetano, Maria Eduarda Lopes da Silva Vigo, Gabriel Henrique Oliveira de Souza
article en

Abstract

Bisphenol-A (BPA), found in plastics and food coatings, is known for its potential adverse health effects. While some studies have focused on BPA's endocrine effects, other research explores its impact on the myenteric plexus, which controls the motility of the digestive tract. The study investigated the effects of BPA on myenteric plexus neurons in rats. For the analysis of the effects on the myenteric plexus (MP), 32 male Wistar rats aged 40 days were divided into four groups (n=8) that received filtered water via gavage over 12 weeks for the control group (CG), dose group 1 (DG1) BPA solution at 0.05mg/kg, dose group 2 (DG2) BPA solution at 0.25mg/kg, and dose group 3 (DG3) BPA solution at 0.5mg/kg. The animals were weighed weekly to adjust the administered volume. At the end of the experimental period, a new weighing was performed, and the rats were euthanized. After laparotomy, the intestinal segments corresponding to the jejunum-ileum were collected to demonstrate the density of the population (Giemsa+), the subpopulations of active myenteric neurons (NADH-d+), and the nitrergic subpopulation (NADPH-d+). BPA exposure did not significantly affect the rats' weight gain, but, there was a reduction in the total density of myenteric neurons in DG3 (10.78mm²) compared to DG (18.88mm²) and DG1 (16.28mm²), and also a reduction in the NADH-d+ subpopulation between DG3 (8.50mm²) and the CG (14.45mm²) and DG1 (14.17mm²) groups. For the nitrergic subpopulation (NADPH-d+), there was no difference in the expression of these neurons. Based on the results obtained, it can be inferred that there was a reduction in cholinergic neurons (NADPH-d-), calculated from the total population of neurons. These findings suggest that BPA may compromise the neuronal function of the MP, possibly by inducing oxidative stress and apoptosis of subpopulations, acting as a xenoestrogen on the nuclear receptors of these neurons, and consequently affecting the regulation of gastrointestinal motility, interfering with cholinergic neuronal transmission and nitric oxide production, and also greater resistance of nitrergic neurons can be observed. Both studies highlight the importance of raising awareness about BPA, as well as the possible harmful effects on unique health. The need to understand the impacts of BPA on different biological systems is emphasized to better understand its effects on human health, especially considering its widespread presence in modern society.

Aracê.Vol. 6(3)
Coordenação de Aperfeiçoamento de Pessoal de Nível Superior, Universidade Paranaense
Openalex Percentile: Top 69%
Effects and risks of endocrine disrupting chemicals
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