Evidence map›Paper›PMID 27036707›Full record

ArticleReproductive biology and endocrinology : RB&E2016

Flutamide induces alterations in the cell-cell junction ultrastructure and reduces the expression of Cx43 at the blood-testis barrier with no disturbance in the rat seminiferous tubule morphology.

Katarzyna Chojnacka, Anna Hejmej, Marta Zarzycka, Waclaw Tworzydlo, Szczepan Bilinski, Laura Pardyak, Alicja Kaminska, Barbara Bilinska

Open access · goldAbstract read
In one paragraph

Article in Reproductive biology and endocrinology : RB&E, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

4 citing papers in PubMed, 20 citations in OpenAlex.

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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

8 authors at 1 institution in 1 country.

Katarzyna ChojnackaDepartment of Endocrinology, Institute of Zoology, Jagiellonian University, Krakow, Poland.
Anna HejmejDepartment of Endocrinology, Institute of Zoology, Jagiellonian University, Krakow, Poland.
Marta ZarzyckaDepartment of Endocrinology, Institute of Zoology, Jagiellonian University, Krakow, Poland.
Waclaw TworzydloDepartment of Developmental Biology and Morphology of Invertebrates, Institute of Zoology, Jagiellonian University, Krakow, Poland.
Szczepan BilinskiDepartment of Developmental Biology and Morphology of Invertebrates, Institute of Zoology, Jagiellonian University, Krakow, Poland.
Laura PardyakDepartment of Endocrinology, Institute of Zoology, Jagiellonian University, Krakow, Poland.
Alicja KaminskaDepartment of Endocrinology, Institute of Zoology, Jagiellonian University, Krakow, Poland.
Barbara BilinskaDepartment of Endocrinology, Institute of Zoology, Jagiellonian University, Krakow, Poland. barbara.bilinska@uj.edu.pl.
Jagiellonian University · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPresent study was designed to establish a causal connection between changes in the cell-cell junction protein expression at the blood-testis barrier and alterations in the adult rat testis histology following an anti-androgen flutamide exposure. Particular emphasis was placed on the basal ectoplasmic specialization (ES) in the seminiferous epithelium and expression of gap junction protein, connexin 43 (Cx43).

methodsFlutamide (50 mg/kg body weight) was administered to male rats daily from 82 to 88 postnatal day. Testes from 90-day-old control and flutamide-exposed rats were used for all analyses. Testis morphology was analyzed using light and electron microscopy. Gene and protein expressions were analyzed by real-time RT-PCR and Western blotting, respectively, protein distribution by immunohistochemistry, and steroid hormone concentrations by radioimmunoassay.

resultsSeminiferous epithelium of both groups of rats displayed normal histology without any loss of germ cells. In accord, no difference in the apoptosis and proliferation level was found between control and treated groups. As shown by examination of semi-thin and ultrathin sections, cell surface occupied by the basal ES connecting neighboring Sertoli cells and the number of gap and tight junctions coexisting with the basal ES were apparently reduced in flutamide-treated rats. Moreover, the appearance of unconventional circular ES suggests enhanced internalization and degradation of the basal ES. These changes were accompanied by decreased Cx43 and ZO-1 expression (p < 0.01) and a loss of linear distribution of these proteins at the region of the blood-testis barrier. On the other hand, Cx43 expression in the interstitial tissue of flutamide-treated rats increased (p < 0.01), which could be associated with Leydig cell hypertrophy. Concomitantly, both intratesticular testosterone and estradiol concentrations were elevated (p < 0.01), but testosterone to estradiol ratio decreased significantly (p < 0.05) in flutamide-treated rats compared to the controls.

conclusionsShort-term treatment with flutamide applied to adult rats exerts its primary effect on the basal ES, coexisting junctional complexes and their constituent proteins Cx43 and ZO-1, without any apparent morphological alterations in the seminiferous epithelium. In the interstitial compartment, however, short-term exposure leads to both histological and functional changes of the Leydig cells.

Indexed as

Androgen AntagonistsAnimalsApoptosisCell ProliferationConnexin 43EstradiolFlutamideGene ExpressionImmunohistochemistryIn Situ Nick-End LabelingIntercellular JunctionsMaleRatsRats, WistarRNA, MessengerSeminiferous TubulesAndrogen AntagonistsConnexin 43EstradiolFlutamideGja1 protein, ratRNA, MessengerTestosteroneBasal ectoplasmic specializationCx43FlutamideRatTestisUltrastructure

Identifiers

PMID27036707
PMCPMC4818424
OpenAlexW2323492104

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LicenceCC BY
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Registered trials

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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.