Evidence map›Paper›PMID 31494803›Full record

ArticleEndocrine2019

Age effect on thyroid hormone brain response in male mice.

Helena Kerp, Kathrin Engels, Frederike Kramer, Denica Doycheva, Georg Sebastian Hönes, Denise Zwanziger, Lars Christian Moeller, Heike Heuer, Dagmar Führer

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Article in Endocrine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.0field-weighted citation impact, top 23% 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

6 citing papers in PubMed, 9 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

9 authors at 2 institutions in 1 country.

Helena KerpDepartment of Endocrinology, Diabetes and Metabolism, University of Duisburg-Essen, 45122, Essen, Germany.
Kathrin EngelsDepartment of Endocrinology, Diabetes and Metabolism, University of Duisburg-Essen, 45122, Essen, Germany.
Frederike Kramer *Leibniz Institute on Aging/Fritz Lipmann Institute (FLI), 07745, Jena, Germany.
Denica Doycheva *Leibniz Institute on Aging/Fritz Lipmann Institute (FLI), 07745, Jena, Germany.
Georg Sebastian HönesDepartment of Endocrinology, Diabetes and Metabolism, University of Duisburg-Essen, 45122, Essen, Germany.
Denise ZwanzigerDepartment of Endocrinology, Diabetes and Metabolism, University of Duisburg-Essen, 45122, Essen, Germany.
Lars Christian MoellerDepartment of Endocrinology, Diabetes and Metabolism, University of Duisburg-Essen, 45122, Essen, Germany.
Heike HeuerDepartment of Endocrinology, Diabetes and Metabolism, University of Duisburg-Essen, 45122, Essen, Germany.
Dagmar FührerDepartment of Endocrinology, Diabetes and Metabolism, University of Duisburg-Essen, 45122, Essen, Germany. Dagmar.fuehrer@uk-essen.de.
University of Duisburg-Essen · DELeibniz Institute on Aging - Fritz Lipmann Institute (FLI) · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThyroid hormones (TH) are important for brain development and central nervous system (CNS) function. Disturbances of thyroid function occur with higher prevalence in the ageing population and may negatively impact brain function.

methodsWe investigated the age impact on behavior in young adult and old male mice (5 vs. 20 months) with chronic hypo- or hyper-thyroidism as well as in sham-treated controls. Expression of TH transporters and TH responsive genes was studied in CNS and pituitary by in situ hybridization and qRT-PCR, whereas TH serum concentrations were determined by immunoassay.

resultsSerum TH levels were lower in old compared with young hyperthyroid mice, suggesting a milder hyperthyroid phenotype in the aged group. Likewise, elevated plus maze activity was reduced in old hyperthyroid animals. Under hypothyroid conditions, thyroxine serum concentrations did not differ in young and old mice. Both groups showed a comparable decline in activity and elevated anxiety levels. However, an attenuated increase in hypothalamic thyrotropin releasing hormone and pituitary thyroid stimulating hormone transcript expression was found in old hypothyroid mice. Brain expression of monocarboxylate transporter 8 and organic anion transporting polypeptide 1c1 was not affected by age or TH status.

conclusionsIn summary, ageing attenuates neurological phenotypes in hyperthyroid but not hypothyroid mice, which fits with age effects on TH serum levels in the animals. In contrast no changes in TH transporter expression were found in aged mouse brains with hyper- or hypo-thyroid state.

Indexed as

AgingAnimalsBrainGene ExpressionHyperthyroidismHypothyroidismMaleMaze LearningMice, Inbred C57BLMonocarboxylic Acid TransportersOrganic Cation Transport ProteinsRotarod Performance TestSymportersThyroid HormonesThyrotropinThyrotropin-Releasing HormoneMonocarboxylic Acid TransportersOatp2 protein, mouseOrganic Cation Transport ProteinsSlc16a2 protein, mouseSymportersThyroid HormonesThyrotropinThyrotropin-Releasing HormoneAgeingHyperthyroidismHypothyroidismMale miceThyroid hormones

Identifiers

PMID31494803
OpenAlexW2971848034

What OpenQuestion holds

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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.