Evidence map›Paper›PMID 28299639›Full record

ArticleGeroScience2017

Age-related changes in central effects of corticotropin-releasing factor (CRF) suggest a role for this mediator in aging anorexia and cachexia.

Judit Tenk, Ildikó Rostás, Nóra Füredi, Alexandra Mikó, Margit Solymár, Szilvia Soós, Balázs Gaszner, Diana Feller, Miklós Székely, Erika Pétervári and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in GeroScience, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.4field-weighted citation impact, top 22% 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

14 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Aging and Thymosin Alpha-1.International journal of molecular sciences · 2025
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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

11 authors at 1 institution in 1 country.

Judit TenkInstitute for Translational Medicine, Medical School, University of Pécs, 12 Szigeti str, Pécs, H-7624, Hungary.
Ildikó RostásInstitute for Translational Medicine, Medical School, University of Pécs, 12 Szigeti str, Pécs, H-7624, Hungary.
Nóra FürediInstitute for Translational Medicine, Medical School, University of Pécs, 12 Szigeti str, Pécs, H-7624, Hungary.
Alexandra MikóInstitute for Translational Medicine, Medical School, University of Pécs, 12 Szigeti str, Pécs, H-7624, Hungary.
Margit SolymárInstitute for Translational Medicine, Medical School, University of Pécs, 12 Szigeti str, Pécs, H-7624, Hungary.
Szilvia SoósInstitute for Translational Medicine, Medical School, University of Pécs, 12 Szigeti str, Pécs, H-7624, Hungary.
Balázs GasznerDepartment of Anatomy, Medical School, University of Pécs, 12 Szigeti str, Pécs, H-7624, Hungary.
Diana FellerDepartment of Pharmaceutical Biotechnology, Medical School, University of Pecs, 12 Szigeti str, Pécs, H-7624, Hungary.
Miklós SzékelyInstitute for Translational Medicine, Medical School, University of Pécs, 12 Szigeti str, Pécs, H-7624, Hungary.
Erika PéterváriInstitute for Translational Medicine, Medical School, University of Pécs, 12 Szigeti str, Pécs, H-7624, Hungary.
Márta BalaskóInstitute for Translational Medicine, Medical School, University of Pécs, 12 Szigeti str, Pécs, H-7624, Hungary. marta.balasko@aok.pte.hu.
University of Pecs · HU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hypothalamic corticotropin-releasing factor (CRF) lays downstream to catabolic melanocortins and at least partly mediates their catabolic effects. Age-related changes in the melanocortin system (weak responsiveness in middle-aged and a strong one in old rats) have been shown to contribute to middle-aged obesity and later to aging anorexia and cachexia of old age groups. We hypothesized that catabolic (anorexigenic and hypermetabolic) CRF effects vary with aging similarly to those of melanocortins. Thus, we aimed to test whether age-related variations of CRF effects may also contribute to middle-aged obesity and aging anorexia leading to weight loss of old age groups. Food intake, body weight, core temperature, heart rate, and activity were recorded in male Wistar rats of young, middle-aged, aging, and old age groups (from 3 to 24 months) during a 7-day intracerebroventricular CRF infusion (0.2 μg/μl/h) in a biotelemetric system. In addition, CRF gene expression was also assessed by quantitative RT-PCR in the paraventricular nucleus (PVN) of intact animals of the same age groups. The infusion suppressed body weight in the young, aging, and old rats, but not in middle-aged animals. Weak anorexigenic and hypermetabolic effects were detected in the young, whereas strong anorexia (without hypermetabolism) developed in the oldest age groups in which post mortem analysis showed also a reduction of retroperitoneal fat mass. CRF gene expression in the PVN increased with aging. Our results support the potential contribution of age-related changes in CRF effects to aging anorexia and cachexia. The role of the peptide in middle-aged obesity cannot be confirmed.

Indexed as

Age FactorsAgingAnimalsAnorexiaBody WeightCachexiaCorticotropin-Releasing HormoneEatingEnergy MetabolismHumansInfusions, ParenteralLeptinMaleModels, AnimalRatsRats, WistarCorticotropin-Releasing HormoneLeptinRNAAgingCore temperatureCorticotropin-releasing factor (CRF)Energy homeostasisFood intakeWistar rat

Identifiers

PMID28299639
PMCPMC5352590
OpenAlexW2572059016

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.