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Influence of bisphenol A and its analog bisphenol S on cocaine- and amphetamine-regulated transcript peptide–positive enteric neurons in the mouse gastrointestinal tract

dc.contributor.authorMakowska, Krystyna
dc.contributor.authorFagundes, Kainã R. C. [UNESP]
dc.contributor.authorGonkowski, Sławomir
dc.contributor.institutionUniversity of Warmia and Mazury in Olsztyn
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.date.accessioned2025-04-29T20:06:01Z
dc.date.issued2023-01-01
dc.description.abstractIntroduction: Bisphenol A (BPA) is used in large quantities for the production of plastics and is present in various everyday objects. It penetrates living organisms and shows multidirectional adverse influence on many internal organs. For this reason, BPA is often replaced in plastic production by other substances. One of them is bisphenol S (BPS), whose effects on the enteric nervous system (ENS) have not been explained. Methods: Therefore, the present study compares the influence of BPA and BPS on the number of enteric neurons immunoreactive to cocaine-and amphetamine-regulated transcript (CART) peptide located in the ENS of the stomach, jejunum and colon with the use of double immunofluorescence method. Results: The obtained results have shown that both bisphenols studied induced an increase in the number of CART-positive enteric neurons, and the severity of changes depended on the type of enteric ganglion, the dose of bisphenols and the segment of the digestive tract. The most visible changes were noted in the myenteric ganglia in the colon. Moreover, in the colon, the changes submitted by BPS are more noticeable than those observed after BPA administration. In the stomach and jejunum, bisphenol-induced changes were less visible, and changes caused by BPS were similar or less pronounced than those noted under the impact of BPA, depending on the segment of the gastrointestinal tract and ganglion type studied. Discussion: The results show that BPS affects the enteric neurons containing CART in a similar way to BPA, and the BPS impact is even stronger in the colon. Therefore, BPS is not neutral for the gastrointestinal tract and ENS.en
dc.description.affiliationDepartment of Clinical Diagnostics Faculty of Veterinary Medicine University of Warmia and Mazury in Olsztyn
dc.description.affiliationLaboratório de Morfofisiologia Animal Instituto de Biociências Universidade Estadual Paulista
dc.description.affiliationDepartment of Clinical Physiology Faculty of Veterinary Medicine University of Warmia and Mazury in Olsztyn
dc.description.affiliationUnespLaboratório de Morfofisiologia Animal Instituto de Biociências Universidade Estadual Paulista
dc.identifierhttp://dx.doi.org/10.3389/fnmol.2023.1234841
dc.identifier.citationFrontiers in Molecular Neuroscience, v. 16.
dc.identifier.doi10.3389/fnmol.2023.1234841
dc.identifier.issn1662-5099
dc.identifier.scopus2-s2.0-85169680165
dc.identifier.urihttps://hdl.handle.net/11449/306355
dc.language.isoeng
dc.relation.ispartofFrontiers in Molecular Neuroscience
dc.sourceScopus
dc.subjectbisphenol A
dc.subjectbisphenol S
dc.subjectdigestive tract
dc.subjectendocrine disruptors
dc.subjectenteric neurons
dc.subjectmouse
dc.titleInfluence of bisphenol A and its analog bisphenol S on cocaine- and amphetamine-regulated transcript peptide–positive enteric neurons in the mouse gastrointestinal tracten
dc.typeArtigopt
dspace.entity.typePublication

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