Evidence mapPaperPMID 40806491Full record

ReviewInternational journal of molecular sciences2025

Unraveling the Translational Relevance of β-Hydroxybutyrate as an Intermediate Metabolite and Signaling Molecule.

Dwifrista Vani Pali, Sujin Kim, Keren Esther Kristina Mantik, Ju-Bi Lee, Chan-Young So, Sohee Moon, Dong-Ho Park, Hyo-Bum Kwak, Ju-Hee Kang

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed.

  1. Article
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  11. [Metabolomics study on anti-inflammatory effects of Guanjie Zhentong Babu plaster in collagen-induced arthritis rats].Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences · 2026
    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

9 authors.

Dwifrista Vani PaliDepartment of Pharmacology, College of Medicine, Inha University, Incheon 22212, Republic of Korea.
Sujin KimDepartment of Pharmacology, College of Medicine, Inha University, Incheon 22212, Republic of Korea.
Keren Esther Kristina MantikDepartment of Pharmacology, College of Medicine, Inha University, Incheon 22212, Republic of Korea.
Ju-Bi LeeDepartment of Pharmacology, College of Medicine, Inha University, Incheon 22212, Republic of Korea.
Chan-Young SoDepartment of Pharmacology, College of Medicine, Inha University, Incheon 22212, Republic of Korea.
Sohee MoonDepartment of Pharmacology, College of Medicine, Inha University, Incheon 22212, Republic of Korea.
Dong-Ho ParkProgram in Biomedical Science and Engineering, Inha University, Incheon 22212, Republic of Korea.ORCID 0000-0003-1863-0652
Hyo-Bum KwakProgram in Biomedical Science and Engineering, Inha University, Incheon 22212, Republic of Korea.ORCID 0000-0003-0451-4554
Ju-Hee KangDepartment of Pharmacology, College of Medicine, Inha University, Incheon 22212, Republic of Korea.ORCID 0000-0001-5235-8993

Funding

National Research Foundation of Korea 2022S1A5C2A03092407National Research Foundation of Korea NRF-2021R1A5A2031612National Research Foundation of Korea NRF-2023R1A2C1004370
6 · The paper itself

Abstract

β-hydroxybutyrate (BHB) is the most abundant ketone body produced during ketosis, a process initiated by glucose depletion and the β-oxidation of fatty acids in hepatocytes. Traditionally recognized as an alternative energy substrate during fasting, caloric restriction, and starvation, BHB has gained attention for its diverse signaling roles in various physiological processes. This review explores the emerging therapeutic potential of BHB in the context of sarcopenia, metabolic disorders, and neurodegenerative diseases. BHB influences gene expression, lipid metabolism, and inflammation through its inhibition of Class I Histone deacetylases (HDACs) and activation of G-protein-coupled receptors (GPCRs), specifically HCAR2 and FFAR3. These actions lead to enhanced mitochondrial function, reduced oxidative stress, and regulation of inflammatory pathways, with implication for muscle maintenance, neuroprotection, and metabolic regulation. Moreover, BHB's ability to modulate adipose tissue lipolysis and immune responses highlight its broader potential in managing chronic metabolic conditions and aging. While these findings show BHB as a promising therapeutic agent, further research is required to determine optimal dosing strategies, long-term effects, and its translational potential in clinical settings. Understanding BHB's mechanisms will facilitate its development as a novel therapeutic strategy for multiple organ systems affected by aging and disease.

Indexed as

3-Hydroxybutyric AcidSignal TransductionAnimalsHumansLipid MetabolismMetabolic Diseases3-Hydroxybutyric Acidinflammationlipolysisneurodegenerative diseasessarcopeniaβ-hydroxybutyrate

Identifiers

PMID40806491
PMCPMC12347605

What Socratic holds

Textmetadata
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.