In vivo evaluation of the potential protective effects of prolactin against damage caused by methylmercury

Non-biodegradable metals such as mercury accumulate in living organisms during life (bioaccumulation) and also within trophic webs (biomagnification) and may reach high concentrations in humans. The contamination of humans by mercury in drinking water and food may be common, in particular in riversi...

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Main Authors: L. Cunha, L. Bonfim, G. Lima, R. Silva, L. Silva, P. Lima, V. Oliveira-Bahia, J. Freitas, R. Burbano, C. Rocha
Format: Article
Language:English
Published: Associação Brasileira de Divulgação Científica 2022-07-01
Series:Brazilian Journal of Medical and Biological Research
Subjects:
Online Access:http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2022000100647&tlng=en
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author L. Cunha
L. Bonfim
G. Lima
R. Silva
L. Silva
P. Lima
V. Oliveira-Bahia
J. Freitas
R. Burbano
C. Rocha
author_facet L. Cunha
L. Bonfim
G. Lima
R. Silva
L. Silva
P. Lima
V. Oliveira-Bahia
J. Freitas
R. Burbano
C. Rocha
author_sort L. Cunha
collection DOAJ
description Non-biodegradable metals such as mercury accumulate in living organisms during life (bioaccumulation) and also within trophic webs (biomagnification) and may reach high concentrations in humans. The contamination of humans by mercury in drinking water and food may be common, in particular in riverside communities that have a diet rich in fish. In vitro studies of human cell lines exposed to the cytotoxic and mutagenic effects of methylmercury have shown that prolactin has potential cytoprotective properties and may act as a co-mitogenic factor and inhibitor of apoptosis. The present in vivo study investigated the protective potential of prolactin against the toxic effects of methylmercury in the mammal Mus musculus. Histological and biochemical analyses, together with biomarker of genotoxicity, were used to verify the protective potential of prolactin in mice exposed to methylmercury. The reduction in kidney and liver tissue damage was not significant. However, results of biochemical and genotoxic analyses were excellent. After prolactin treatment, a significant reduction was observed in biochemical parameters and mutagenic effects of methylmercury. The study results therefore indicated that prolactin has protective effects against the toxicity of methylmercury and allowed us to suggest the continuation of research to propose prolactin in the future, as an alternative to prevent the damage caused by mercury, especially in populations that are more exposed.
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spelling doaj.art-efcf2adf25ed445b862ca7266b2a62392022-12-22T03:37:08ZengAssociação Brasileira de Divulgação CientíficaBrazilian Journal of Medical and Biological Research1414-431X2022-07-015510.1590/1414-431x2022e11976In vivo evaluation of the potential protective effects of prolactin against damage caused by methylmercuryL. Cunhahttps://orcid.org/0000-0002-1085-3635L. Bonfimhttps://orcid.org/0000-0001-6542-6641G. Limahttps://orcid.org/0000-0002-9168-2881R. Silvahttps://orcid.org/0000-0002-6056-7880L. Silvahttps://orcid.org/0000-0002-4417-7401P. Limahttps://orcid.org/0000-0002-1068-2813V. Oliveira-Bahiahttps://orcid.org/0000-0002-5439-4223J. Freitashttps://orcid.org/0000-0002-0568-7177R. Burbanohttps://orcid.org/0000-0002-4872-234XC. Rochahttps://orcid.org/0000-0003-3037-1323Non-biodegradable metals such as mercury accumulate in living organisms during life (bioaccumulation) and also within trophic webs (biomagnification) and may reach high concentrations in humans. The contamination of humans by mercury in drinking water and food may be common, in particular in riverside communities that have a diet rich in fish. In vitro studies of human cell lines exposed to the cytotoxic and mutagenic effects of methylmercury have shown that prolactin has potential cytoprotective properties and may act as a co-mitogenic factor and inhibitor of apoptosis. The present in vivo study investigated the protective potential of prolactin against the toxic effects of methylmercury in the mammal Mus musculus. Histological and biochemical analyses, together with biomarker of genotoxicity, were used to verify the protective potential of prolactin in mice exposed to methylmercury. The reduction in kidney and liver tissue damage was not significant. However, results of biochemical and genotoxic analyses were excellent. After prolactin treatment, a significant reduction was observed in biochemical parameters and mutagenic effects of methylmercury. The study results therefore indicated that prolactin has protective effects against the toxicity of methylmercury and allowed us to suggest the continuation of research to propose prolactin in the future, as an alternative to prevent the damage caused by mercury, especially in populations that are more exposed.http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2022000100647&tlng=enMercuryProlactinHistological evaluationBiochemical parametersGenotoxicity
spellingShingle L. Cunha
L. Bonfim
G. Lima
R. Silva
L. Silva
P. Lima
V. Oliveira-Bahia
J. Freitas
R. Burbano
C. Rocha
In vivo evaluation of the potential protective effects of prolactin against damage caused by methylmercury
Brazilian Journal of Medical and Biological Research
Mercury
Prolactin
Histological evaluation
Biochemical parameters
Genotoxicity
title In vivo evaluation of the potential protective effects of prolactin against damage caused by methylmercury
title_full In vivo evaluation of the potential protective effects of prolactin against damage caused by methylmercury
title_fullStr In vivo evaluation of the potential protective effects of prolactin against damage caused by methylmercury
title_full_unstemmed In vivo evaluation of the potential protective effects of prolactin against damage caused by methylmercury
title_short In vivo evaluation of the potential protective effects of prolactin against damage caused by methylmercury
title_sort in vivo evaluation of the potential protective effects of prolactin against damage caused by methylmercury
topic Mercury
Prolactin
Histological evaluation
Biochemical parameters
Genotoxicity
url http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2022000100647&tlng=en
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