Evidence map›Paper›PMID 39825167›Full record

ArticleGeroScience2025

5-HT

Nathan R Kerr, Anna R Dashtmian, Fereshteh B Darvishi, Charles D Brennan, Sindhuja N Ayyagari, Peter J Moore, Jose A Viteri, Meifang Wang, Mark M Rich, Brian C Clark and 1 more

Abstract read
In one paragraph

Article in GeroScience, 2025. 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
–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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Loss of 5-HTFrontiers in neural circuits · 2025
    Article
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.

Nathan R KerrDepartment of Physical Medicine and Rehabilitation, University of Missouri, Columbia, MO, USA.
Anna R DashtmianDepartment of Physical Medicine and Rehabilitation, University of Missouri, Columbia, MO, USA.
Fereshteh B DarvishiDepartment of Physical Medicine and Rehabilitation, University of Missouri, Columbia, MO, USA.
Charles D BrennanDepartment of Physical Medicine and Rehabilitation, University of Missouri, Columbia, MO, USA.
Sindhuja N AyyagariDepartment of Physical Medicine and Rehabilitation, University of Missouri, Columbia, MO, USA.
Peter J MooreDepartment of Physical Medicine and Rehabilitation, University of Missouri, Columbia, MO, USA.
Jose A ViteriDepartment of Physical Medicine and Rehabilitation, University of Missouri, Columbia, MO, USA.
Meifang WangDepartment of Physical Medicine and Rehabilitation, University of Missouri, Columbia, MO, USA.
Mark M RichDepartment of Neuroscience, Cell Biology and Physiology, Wright State University, Dayton, OH, 45435, USA.
Brian C ClarkOhio Musculoskeletal and Neurological Institute (OMNI), Ohio University, Athens, OH, USA.
W David ArnoldDepartment of Physical Medicine and Rehabilitation, University of Missouri, Columbia, MO, USA. wdavidarnold@health.missouri.edu.ORCID 0000-0001-9889-7036

Funding

Novel Approaches to Therapy of Muscle Ion ChannelopathiesR01AR074985 · NIAMS · WRIGHT STATE UNIVERSITY · PI MARK M RICH · 2019 to 2026
$3.9M
Neural mechanisms of age-related weaknessR01AG078129 · NIA · OHIO UNIVERSITY ATHENS · PI William David Arnold, Brian C Clark · 2023 to 2026
$2.5M
NIAMS NIH HHS R01 AR074985NIA NIH HHS R01 AG078129NIA NIH HHS R01AG078129
6 · The paper itself

Abstract

Sarcopenia, the pathological age-related loss of muscle mass and strength, contributes to physical decline, frailty, and diminished healthspan. The impact of sarcopenia is expected to rise as the aging population grows, and treatments remain limited. Therefore, novel approaches for enhancing physical function and strength in older adults are desperately needed. Recent evidence suggests that deficits in motor neuron excitability contribute significantly to age-related weakness. Accordingly, we hypothesized that enhancing motor neuron excitability could be a novel strategy for mitigating age-related declines in physical function and strength. To test this hypothesis, we targeted the 5-HT

Indexed as

SarcopeniaSerotonin 5-HT2 Receptor AgonistsAgingAnimalsDisease Models, AnimalEvoked Potentials, MotorMaleMiceMice, Inbred C57BLMotor NeuronsMuscle, SkeletalMuscle StrengthProof of Concept StudySerotonin 5-HT2 Receptor Agonists5-HT2C receptor agonismAge-related muscle weaknessLorcaserinMotor neuron excitabilityNeurotherapeuticsSarcopenia

Identifiers

PMID39825167
PMCPMC12181463

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.