Evidence map›Paper›PMID 42155080›Full record

ArticleArchives of endocrinology and metabolism2026

The essential role of the redox balance in adrenal steroidogenesis.

Juliana Lourenço Gebenlian, Aline Faccioli Bodoni, Fernanda Borchers Coeli-Lacchini, Margaret de Castro, Sonir Roberto Rauber Antonini

Abstract read
In one paragraph

Article in Archives of endocrinology and metabolism, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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.

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

5 authors.

Juliana Lourenço GebenlianUniversidade de São Paulo Faculdade de Medicina de Ribeirão Preto Departamento de Pediatria Ribeirão Preto SP Brasil Departamento de Pediatria, Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo, Ribeirão Preto, SP, Brasil.
Aline Faccioli BodoniUniversidade de São Paulo Faculdade de Medicina de Ribeirão Preto Departamento de Clínica Médica Ribeirão Preto SP Brasil Departamento de Clínica Médica, Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo, Ribeirão Preto, SP, Brasil.
Fernanda Borchers Coeli-LacchiniUniversidade de São Paulo Faculdade de Medicina de Ribeirão Preto Departamento de Clínica Médica Ribeirão Preto SP Brasil Departamento de Clínica Médica, Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo, Ribeirão Preto, SP, Brasil.
Margaret de CastroUniversidade de São Paulo Faculdade de Medicina de Ribeirão Preto Departamento de Clínica Médica Ribeirão Preto SP Brasil Departamento de Clínica Médica, Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo, Ribeirão Preto, SP, Brasil.
Sonir Roberto Rauber AntoniniUniversidade de São Paulo Faculdade de Medicina de Ribeirão Preto Departamento de Pediatria Ribeirão Preto SP Brasil Departamento de Pediatria, Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo, Ribeirão Preto, SP, Brasil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo analyze the impact of nicotinamide nucleotide transidrogenase (NNT) enzyme impairment on cortisol production, reactive oxygen species (ROS) formation, mitochondrial activity, and mitogen-activated protein kinase 8 (MAPK8) expression in the adrenocortical cell line. MATERIALS AND

methodssiRNA NNT knockdown was performed in H295R adrenocortical cells to evaluate the effects on cortisol secretion (RIA) and reactive oxygen species (ROS) intracellular production (DCFDA) in basal conditions and after stimulation with 10 uM forskolin. MAPK8 mRNA relative expression and protein localization were evaluated using quantitative PCR (qPCR) and immunofluorescence, respectively.

resultsNNT knockdown in the H295R adrenal cells specifically reduced NNT RNA and protein levels. Under basal conditions, no changes in ROS intracellular production or cortisol secretion were seen in NNT-depleted H295R cells. However, under forskolin (10 μM), a potent steroidogenesis agent, we observed a marked reduction in cortisol production (p < 0.0001) at the expense of normal ROS intracellular production and increased MAPK8 expression (p = 0.008).

conclusionNNT-deficient adrenocortical cells can maintain mitochondrial homeostasis and cortisol secretion in basal conditions. However, under stress, these cells seem to maintain the redox balance at the expense of impaired steroidogenesis. MAPK8 pathway activation appears to compensate for NNT deficiency.

Indexed as

Adrenal CortexAdrenal GlandsHydrocortisoneCell LineColforsinHumansMitochondriaOxidation-ReductionOxidative StressReactive Oxygen SpeciesRNA, Small InterferingColforsinHydrocortisoneReactive Oxygen SpeciesRNA, Small InterferingAdrenal steroidogenesesNNT geneoxidative stress

Identifiers

PMID42155080
PMCPMC13186557

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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.