Evidence map›Paper›PMID 42533568›Full record

ArticleFASEB journal : official publication of the Federation of American Societies for Experimental Biology2026

From Collapse to Active Self-Repair: Integrative Multi-Omics and Machine Learning Analysis Map the Hepatic Metabolic Adaption in Response to Simulated Spaceflight Stress.

Han Zhang, Boyang Li, Yufan Zou, Feng Yao, Weijun Su, Bo Li

Abstract read
In one paragraph

Article in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Han ZhangSchool of Interdisciplinary Science, Beijing Institute of Technology, Beijing, China.ORCID https://orcid.org/0009-0002-6564-4977
Boyang LiSchool of Interdisciplinary Science, Beijing Institute of Technology, Beijing, China.ORCID https://orcid.org/0000-0002-0184-5633
Yufan ZouSchool of Medicine, Nankai University, Tianjin, China.
Feng YaoSchool of Interdisciplinary Science, Beijing Institute of Technology, Beijing, China.
Weijun SuSchool of Medicine, Nankai University, Tianjin, China.ORCID https://orcid.org/0000-0002-2836-5445
Bo LiSchool of Interdisciplinary Science, Beijing Institute of Technology, Beijing, China.ORCID https://orcid.org/0000-0001-5669-1785

Funding

MOST | National Natural Science Foundation of China (NSFC) 32471197MOST | National Natural Science Foundation of China (NSFC) 82202072
6 · The paper itself

Abstract

Long-term spaceflight poses substantial challenges to human physiology, with the liver being highly susceptible due to its central metabolic role. To determine whether hepatic alterations represent transient stress or sustained remodeling, we performed an integrated multi-omics analysis in a rat model simulating chronic space radiation and microgravity. Herein, we applied an integrated multi-omics and AI-driven analytical framework combining histopathology, cytokine and miRNA profiling, proteomics, metabolomics and Western blot validation. After 21 days of simulated space conditions, rats exhibited significant hepatic atrophy, histopathological injury, and metabolic dysfunction resembling a NAFLD-like phenotype, accompanied by multi-omics signatures of impaired oxidative phosphorylation, disrupted TCA cycle activity, altered lipid-metabolic regulation, and inflammatory remodeling. During a 14-day recovery phase, hepatic atrophy and histological lesions were incompletely improved, with omics changes suggesting partial restoration of mitochondrial related energy metabolism, PPAR associated lipid regulation, and fatty acid β-oxidation. Machine learning-based proteomics identified a panel of energy-related and lipid-metabolic proteins that robustly distinguished injury from recovery states. External validation with NASA GeneLab transcriptomic datasets supported the suppression of extracellular matrix programs and structural repair during injury. Together, these findings organize the hepatic response to simulated spaceflight into (1) AMPK/PPAR-γ/PGC-1α-centered energy-related lipid/mitochondrial regulation, (2) ACSM5/CRAT-associated fatty-acid utilization and carnitine-shuttle remodeling, and (3) TGF-β/IGF1-related structural repair and anabolic signaling. This study provides a comprehensive organ-level overview for understanding hepatic adaptation to extreme spaceflight environments and identifies potential targets for mitigating astronaut health risks during long-duration missions.

Indexed as

Adaptation, PhysiologicalLiverMachine LearningSpace FlightStress, PhysiologicalWeightlessness SimulationAnimalsEnergy MetabolismLipid MetabolismMaleMetabolomicsMultiomicsProteomicsRatsRats, Sprague-DawleyAI‐driven multi‐omics integrationenergy‐metabolic regulationfatty‐acid utilizationsimulated space environmentstructural repair

Identifiers

PMID42533568
PMCPMC13424968

What Socratic 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 Socratic graph.