Evidence map›Paper›PMID 39922530›Full record

ArticleNeuroscience letters2025

Changes in adropin levels in brain and peripheral tissues with aging.

Changjun Yang, John Aaron Howell, Lei Liu, Rachel E Gunraj, Eduardo Candelario-Jalil

Abstract read
In one paragraph

Article in Neuroscience letters, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  1. Article
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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

5 authors.

Changjun YangDepartment of Neuroscience, McKnight Brain Institute, University of Florida, Gainesville, FL, USA.
John Aaron HowellDepartment of Neuroscience, McKnight Brain Institute, University of Florida, Gainesville, FL, USA.
Lei LiuDepartment of Neuroscience, McKnight Brain Institute, University of Florida, Gainesville, FL, USA.
Rachel E GunrajDepartment of Neuroscience, McKnight Brain Institute, University of Florida, Gainesville, FL, USA.
Eduardo Candelario-JalilDepartment of Neuroscience, McKnight Brain Institute, University of Florida, Gainesville, FL, USA. Electronic address: ecandelario@ufl.edu.

Funding

Neurovascular Protection by Adropin in Ischemic StrokeR01NS103094 · NINDS · UNIVERSITY OF FLORIDA · PI CANDELARIO-JALIL, EDUARDO JESUS · 2018 to 2021
$1.5M
Neurovascular Protection by Adropin in Ischemic StrokeR56NS103094 · NINDS · UNIVERSITY OF FLORIDA · PI CANDELARIO-JALIL, EDUARDO JESUS · 2017 to 2017
$427k
NINDS NIH HHS R01 NS103094NINDS NIH HHS R56 NS103094
6 · The paper itself

Abstract

Adropin is a bioactive peptide found in the brain and various peripheral tissues. Evidence suggests that aging significantly decreases brain adropin levels, and interventions that elevate adropin may help alleviate age-related neurological disorders such as ischemic stroke and cognitive decline. However, the impact of aging on peripheral tissue adropin levels and its relationship with the neural recognition molecule NB-3/contactin-6 in the brain remains unclear. In this study, we quantified adropin using immunoblotting in brain and peripheral tissues (liver, lung, kidney, spleen, ileum, colon) from young (8-10 weeks) and aged (18-20 months) male mice. Results indicated a significant decrease in brain adropin levels in aged mice, while peripheral tissues showed no significant changes compared to young controls. Additionally, levels of NB-3/contactin-6, a potential adropin receptor and Notch1 ligand, were lower in aged brains. Co-immunoprecipitation demonstrated that adropin physically associates with brain NB-3. Notably, the age-related reduction in brain adropin correlates with increased oxidative stress markers (gp91

Indexed as

AgingBrainIntercellular Signaling Peptides and ProteinsAnimalsMaleMiceMice, Inbred C57BLOxidative StressEnho protein, mouseIntercellular Signaling Peptides and ProteinsAdropinAgingBrainNB-3Oxidative stress markersPeripheral tissue

Identifiers

PMID39922530
PMCPMC13417443

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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.