Evidence map›Paper›PMID 34158080›Full record

ArticleReproductive biology and endocrinology : RB&E2021

Prolactin promotes a partial recovery from the atrophy of both male and female gerbil prostates caused by castration.

Marianna Zanatelli, Simone Jacovaci Colleta, Luiz Henrique Alves Guerra, Fernanda Cristina Alcântara Santos, Rejane Maira Góes, Patricia Simone Leite Vilamaior, Sebastião Roberto Taboga

Open access · goldAbstract read
In one paragraph

Article in Reproductive biology and endocrinology : RB&E, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.3field-weighted citation impact, top 41% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed, 3 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 3 institutions in 1 country.

Marianna ZanatelliDepartment of Structural and Functional Biology, Institute of Biology, State University of Campinas - UNICAMP, SP, Campinas, Brazil.
Simone Jacovaci ColletaLaboratory of Microscopy and Microanalysis, Department of Biology, São Paulo State University - UNESP/IBILCE, Rua Cristóvão Colombo, 2265, Jardim Nazareth, SP, 15054-000, São José do Rio Preto, Brasil.
Luiz Henrique Alves GuerraLaboratory of Microscopy and Microanalysis, Department of Biology, São Paulo State University - UNESP/IBILCE, Rua Cristóvão Colombo, 2265, Jardim Nazareth, SP, 15054-000, São José do Rio Preto, Brasil.
Fernanda Cristina Alcântara SantosDepartment of Morphology, Federal University of Goiás -UFG , GO, Goiânia, Brazil.
Rejane Maira GóesDepartment of Structural and Functional Biology, Institute of Biology, State University of Campinas - UNICAMP, SP, Campinas, Brazil.
Patricia Simone Leite VilamaiorLaboratory of Microscopy and Microanalysis, Department of Biology, São Paulo State University - UNESP/IBILCE, Rua Cristóvão Colombo, 2265, Jardim Nazareth, SP, 15054-000, São José do Rio Preto, Brasil.
Sebastião Roberto TabogaDepartment of Structural and Functional Biology, Institute of Biology, State University of Campinas - UNICAMP, SP, Campinas, Brazil. sebastiao.taboga@unesp.br.ORCID http://orcid.org/0000-0002-0970-4288
Universidade Estadual de Campinas (UNICAMP) · BRUniversidade Estadual Paulista (Unesp) · BRUniversidade Federal de Goiás · BR

Funding

Conselho Nacional de Desenvolvimento Científico e Tecnológico 301596/2011-5Conselho Nacional de Desenvolvimento Científico e Tecnológico 442630/2014-0Fundação de Amparo à Pesquisa do Estado de São Paulo 2012/00695-6
6 · The paper itself

Abstract

backgroundThe male and female prostates are controlled by steroid hormones, suffering important morphological and physiological changes after castration. Prolactin is involved in the regulation of the male prostate, having already been identified in the tissue, acting through its receptor PRLR. In the Mongolian gerbil, in addition to the male prostate, the female prostate is also well developed and active in its secretion processes. The aim of the present study was to evaluate the effects of exposure to exogenous prolactin in the prostate of both intact and castrated male and female gerbils in order to establish if prolactin administration can sustain prostate cell activity in conditions of sexual hormone deprivation.

methodsThe morphological analyses were performed by biometric analysis, lesion histological analysis and morphometric-stereological aspects. In addition, immune-cytochemical tests were performed for prolactin and its receptor, as well as for the receptors of androgen and oestrogen and serum prolactin dosage. All data were submitted to ANOVA or Kruskal-Wallis tests for comparison between groups. P < 0.05 was considered to be statistically significant.

resultsThe results showed a strong influence of prolactin on the morphology of the prostate, with the development of important epithelial alterations, after only 3 days of administration, and an expressive epithelial cell discard process after 30 days of administration. Prolactin acts in synergy with testosterone in males and mainly with oestrogens in females, establishing different steroid hormonal receptor immunoreactivity according to sex. It was also demonstrated that prolactin can assist in the recovery from some atrophic effects caused in the gland after castration, without causing additional tissue damage.

conclusionsThe prolactin and its receptor are involved in the maintenance of the homeostasis of male and female gerbils, and also cause distinct histological alterations after exogenous exposure for 3 and 30 days. The effects of prolactin are related to its joint action on androgens and oestrogens and it can also assist in the recovery from the atrophic effects of castration.

Indexed as

AnimalsAtrophyFemaleGerbillinaeMaleOrchiectomyOvariectomyProlactinProstateReceptors, ProlactinRecovery of FunctionProlactinReceptors, ProlactinCastrationFemale prostateGerbilProlactinProlactin receptorProstate

Identifiers

PMID34158080
PMCPMC8218528
OpenAlexW3173392710

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.