Evidence map›Paper›PMID 40444969›Full record

ArticlemSystems2025

Young gut microbiota transplantation improves the metabolic health of old mice.

Jiaojiao Xie, Taewan Kim, Zhongmao Liu, Hunter Panier, Suresh Bokoliya, Ming Xu, Yanjiao Zhou

Abstract read
In one paragraph

Article in mSystems, 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. Review
  2. Review
  3. Article
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  5. Review
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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.

Jiaojiao Xie *The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang, China.ORCID 0000-0002-0357-1410
Taewan Kim *Center of Aging, University of Connecticut Health Center, Farmington, Connecticut, USA.ORCID 0000-0002-9524-4993
Zhongmao LiuDepartment of Medicine, University of Connecticut Health Center, Farmington, Connecticut, USA.
Hunter PanierDepartment of Medicine, University of Connecticut Health Center, Farmington, Connecticut, USA.
Suresh BokoliyaDepartment of Medicine, University of Connecticut Health Center, Farmington, Connecticut, USA.
Ming XuCenter of Aging, University of Connecticut Health Center, Farmington, Connecticut, USA.ORCID 0000-0002-3920-8947
Yanjiao ZhouDepartment of Medicine, University of Connecticut Health Center, Farmington, Connecticut, USA.ORCID 0000-0001-6528-7039

Funding

Reciprocal Modulation of the Microbiome and Cellular Senescence in Metabolic DysfunctionR01AG068860 · NIA · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI XU, MING, ZHOU, YANJIAO · 2020 to 2024
$2.8M
NIA NIH HHS R01 AG068860
6 · The paper itself

Abstract

The gut microbiota evolves over a lifetime and significantly impacts the aging process. Targeting the gut microbiota represents a novel avenue to delay aging and aging-related physical and mental decline. However, the underlying mechanism by which the microbiota modulates the aging process, particularly age-related physical and behavioral changes is not completely understood. We conducted fecal microbiota transplantation (FMT) from young or old male donor mice to the old male recipients. Old recipients with young microbiota had a higher alpha diversity than the old recipients with old microbiota. Compared to FMT with old microbiota, FMT with young microbiota reduced body weight and prevented fat accumulation in the old recipients. FMT with young microbiota also lowered frailty, increased grip strength, and alleviated depression and anxiety-like behavior in the old recipients. Consistent with observed physical changes, untargeted metabolomic analysis of serum and stools revealed that FMT with young microbiota lowered age-related long-chain fatty acid levels and increased amino acid levels in the old recipients. Bulk RNAseq analysis of the amygdala of the brain showed that FMT with young microbiota downregulated inflammatory pathways and upregulated oxidative phosphorylation in the old recipients. Our results demonstrate that FMT with young microbiota has substantial positive influences on age-related body composition, frailty, and psychological behaviors. These effects are associated with changes in host lipid and amino acid metabolism in the periphery and transcriptional regulation of neuroinflammation and energy utilization in the brain. IMPORTANCE: The gut microbiome is a key hallmark of aging. Fecal microbiota transplantation (FMT) using young microbiota represents a novel rejuvenation strategy to delay aging. Our study provides compelling evidence that transplanting microbiota from young mice significantly improved grip strength, frailty, and body composition in aged recipient mice. At the molecular level, FMT improved aging-related metabolic markers in the gut and circulation. Additionally, FMT from young microbiota rejuvenated the amygdala of the aged brain by downregulating inflammatory pathways. This study highlights the importance of metabolic reprogramming via young microbiota FMT in improving physical and metabolic health in elderly recipients.

Indexed as

AgingFecal Microbiota TransplantationGastrointestinal MicrobiomeAnimalsBody CompositionMaleMiceMice, Inbred C57BLagingamino acidsanxietydepressionfecal microbiota transplantationgut microbiotalipid

Identifiers

PMID40444969
PMCPMC12172422

What Socratic holds

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LicenceCC BY
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 Socratic graph.