Evidence map›Paper›PMID 35371607›Full record

ArticleAging and disease2022

Juvenile Plasma Factors Improve Organ Function and Survival following Injury by Promoting Antioxidant Response.

Xiaogang Chu, Kumar Subramani, Bobby Thomas, Alvin V Terry, Sadanand Fulzele, Raghavan Pillai Raju

Open access · goldAbstract read
In one paragraph

Article in Aging and disease, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.0field-weighted citation impact, top 26% 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

12 citing papers in PubMed, 12 citations in OpenAlex.

  1. Research progress on blood therapy for anti-aging.Journal of advanced research · 2026
    Review
  2. Male germ cell-specific deletion ofZoological research · 2026
    Article
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  5. 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

6 authors at 1 institution in 1 country.

Xiaogang Chu1Department of Pharmacology and Toxicology, Medical College of Georgia, Augusta, GA 30912, USA.
Kumar Subramani1Department of Pharmacology and Toxicology, Medical College of Georgia, Augusta, GA 30912, USA.
Bobby Thomas2Departments of Pediatrics, Neuroscience and Drug Discovery, Darby Children's Research Institute, Medical University of South Carolina, Charleston, SC 29425, USA.
Alvin V Terry1Department of Pharmacology and Toxicology, Medical College of Georgia, Augusta, GA 30912, USA.
Sadanand Fulzele3Department of Medicine, Medical College of Georgia, Augusta, GA 30912, USA.
Raghavan Pillai Raju1Department of Pharmacology and Toxicology, Medical College of Georgia, Augusta, GA 30912, USA.
Augusta University · US

Funding

Reparative effect of juvenile factors in aging and injuryR01AG073338 · NIA · AUGUSTA UNIVERSITY · PI Raghavan Pillai Raju · 2022 to 2026
$2.8M
Metabolic alterations in hemorrhagic shockR01GM122059 · NIGMS · AUGUSTA UNIVERSITY · PI RAJU, RAGHAVAN PILLAI · 2017 to 2020
$1.2M
Reparative effect of juvenile factors in aging and injuryR56AG073338 · NIA · AUGUSTA UNIVERSITY · PI RAJU, RAGHAVAN PILLAI · 2021 to 2021
$316k
NIA NIH HHS R01 AG073338NIA NIH HHS R56 AG073338NIGMS NIH HHS R01 GM122059
6 · The paper itself

Abstract

Studies have shown that factors in the blood of young organisms can rejuvenate the old ones. Studies using heterochronic parabiosis models further reinforced the hypothesis that juvenile factors can rejuvenate aged systems. We sought to determine the effect of juvenile plasma-derived factors on the outcome following hemorrhagic shock injury in aged mice. We discovered that pre-pubertal (young) mice subjected to hemorrhagic shock survived for a prolonged period, in the absence of fluid resuscitation, compared to mature or aged mice. To further understand the mechanism of maturational dependence of injury resolution, extracellular vesicles isolated from the plasma of young mice were administered to aged mice subjected to hemorrhagic shock. The extracellular vesicle treatment prolonged life in the aged mice. The treatment resulted in reduced oxidative stress in the liver and in the circulation, along with an enhanced expression of the nuclear factor erythroid factor 2-related factor 2 (Nrf2) and its target genes, and a reduction in the expression of the transcription factor BTB and CNC homology 1 (Bach1). We propose that plasma factors in the juvenile mice have a reparative effect in the aged mice in injury resolution by modulating the Nrf2/Bach1 axis in the antioxidant response pathway.

Indexed as

agingexosomesextracellular vesiclesjuvenile factorsshock

Identifiers

PMID35371607
PMCPMC8947827
OpenAlexW4225764998

What OpenQuestion holds

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LicenceCC BY
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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.