Evidence map›Paper›PMID 38007051›Full record

ArticleMechanisms of ageing and development2024

Protective effects of apigenin on the brain transcriptome with aging.

Alyssa N Cavalier, Zachary S Clayton, Devin Wahl, David A Hutton, Cali M McEntee, Douglas R Seals, Thomas J LaRocca

Open access · greenAbstract read
In one paragraph

Article in Mechanisms of ageing and development, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

15 citing papers in PubMed, 16 citations in OpenAlex.

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  6. Multiorgan transcriptomics in mice identifies immunoglobulin heavy constant mu (Proceedings of the National Academy of Sciences of the United States of America · 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

7 authors at 2 institutions in 1 country.

Alyssa N CavalierDepartment of Health and Exercise Science, Colorado State University, Fort Collins, CO, United States; Columbine Health Systems Center for Healthy Aging, Colorado State University, Fort Collins, CO, United States.
Zachary S ClaytonDepartment of Integrative Physiology, University of Colorado Boulder, Boulder, CO, United States.
Devin WahlDepartment of Health and Exercise Science, Colorado State University, Fort Collins, CO, United States; Columbine Health Systems Center for Healthy Aging, Colorado State University, Fort Collins, CO, United States.
David A HuttonDepartment of Integrative Physiology, University of Colorado Boulder, Boulder, CO, United States.
Cali M McEnteeDepartment of Health and Exercise Science, Colorado State University, Fort Collins, CO, United States; Columbine Health Systems Center for Healthy Aging, Colorado State University, Fort Collins, CO, United States.
Douglas R SealsDepartment of Integrative Physiology, University of Colorado Boulder, Boulder, CO, United States.
Thomas J LaRoccaDepartment of Health and Exercise Science, Colorado State University, Fort Collins, CO, United States; Columbine Health Systems Center for Healthy Aging, Colorado State University, Fort Collins, CO, United States. Electronic address: Tom.LaRocca@Colostate.edu.
Colorado State University · USUniversity of Colorado Boulder · US

Funding

TRAINING IN RENAL &ELECTROLYTE DISEASE &HYPERTENSIONT32DK007135 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI JOHNSON, RICHARD JOSEPH, KENDRICK, JESSICA B · 1986 to 2024
$5.3M
Role of cellular senescence in cardiovascular agingR01AG055822 · NIA · BUCK INSTITUTE FOR RESEARCH ON AGING · PI CAMPISI, JUDITH, MELOV, SIMON · 2018 to 2022
$4.9M
Inclusive Transcriptomics to Uncover Molecular Mechanisms Underlying HealthspanR21AG060302 · NIA · COLORADO STATE UNIVERSITY · PI LAROCCA, THOMAS · 2019 to 2020
$765k
Translational studies of cellular senescence as a regulator of doxorubicin-mediated arterial dysfunctionK99HL159241 · NHLBI · UNIVERSITY OF COLORADO · PI CLAYTON, ZACHARY S. · 2022 to 2023
$350k
Role of repetitive element transcripts in brain aging and Alzheimer's diseaseF32AG069361 · NIA · COLORADO STATE UNIVERSITY · PI WAHL, DEVIN · 2021 to 2023
$210k
Mitochondrial oxidative stress: a target for treatment of doxorubicin-associated vascular endothelial dysfunctionF32HL151022 · NHLBI · UNIVERSITY OF COLORADO · PI CLAYTON, ZACHARY S. · 2020 to 2021
$89k
Role of ADAR1 and dsRNA in age-related neuroinflammation and Alzheimers diseaseF31AG084330 · NIA · COLORADO STATE UNIVERSITY · PI MCENTEE, CALI MADISON · 2023 to 2024
$81k
Role of age-associated epigenetic repetitive element derepression in Alzheimer's DiseaseF31AG079594 · NIA · COLORADO STATE UNIVERSITY · PI CAVALIER, ALYSSA NICOLE · 2022 to 2023
$58k
NHLBI NIH HHS F32 HL151022NHLBI NIH HHS K99 HL159241NIA NIH HHS F31 AG079594NIA NIH HHS F31 AG084330NIA NIH HHS F32 AG069361NIA NIH HHS R01 AG055822NIA NIH HHS R21 AG060302NIDDK NIH HHS T32 DK007135
6 · The paper itself

Abstract

Brain aging is associated with reduced cognitive function that increases the risk for dementia. Apigenin is a bioactive plant compound that inhibits cellular aging processes and could protect against age-related cognitive dysfunction, but its mechanisms of action in the brain have not been comprehensively studied. We characterized brain transcriptome changes in young and old mice treated with apigenin in drinking water. We observed improved learning/memory in old treated mice, and our transcriptome analyses indicated that differentially expressed genes with aging and apigenin were primarily related to immune responses, inflammation, and cytokine regulation. Moreover, we found that genes/transcripts that were increased in old vs. young mice but downregulated with apigenin treatment in old animals were associated with immune activation/inflammation, whereas transcripts that were reduced with aging but increased with apigenin were related neuronal function and signaling. We also found that these transcriptome differences with aging and apigenin treatment were driven in part by glial cells. To follow up on these in vivo transcriptome findings, we studied aged astrocytes in vitro, and we found that apigenin reduced markers of inflammation and cellular senescence in these cells. Collectively, our data suggest that apigenin may protect against age-related cognitive dysfunction by suppressing neuro-inflammatory processes.

Indexed as

ApigeninBrainTranscriptomeAgingAnimalsInflammationMiceApigeninAstrocytesBrain agingCognitive declineNeuroinflammationTranscriptomics

Identifiers

PMID38007051
PMCPMC10843586
OpenAlexW4388979167

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.