Evidence mapPaperPMID 42121908Full record

ReviewCells2026

Targeting AMPK Networks for Male Reproductive Health: Mechanisms and Emerging Therapies.

Md Ataur Rahman, Abdel Halim Harrath, Maroua Jalouli, Jinwon Choi, Min Choi, Sohyun Park, Hyo Jeong Kim, Amama Rani, Salima Akter, Moon Nyeo Park and 1 more

Abstract readReview
In one paragraph

Review in Cells, 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

11 authors.

Md Ataur RahmanDepartment of Oncology, Karmanos Cancer Institute, Wayne State University, Detroit, MI 48201, USA.ORCID 0000-0001-6649-3694
Abdel Halim HarrathZoology Department, College of Science, King Saud University, Riyadh 11451, Saudi Arabia.ORCID 0000-0002-2170-1303
Maroua JalouliDepartment of Biology, College of Science, Imam Mohammad Ibn Saud Islamic University (IMSIU), Riyadh 11623, Saudi Arabia.
Jinwon ChoiDepartment of Pathology, College of Korean Medicine, Kyung Hee University, Seoul 02447, Republic of Korea.ORCID 0009-0009-7569-6480
Min ChoiDepartment of Pathology, College of Korean Medicine, Kyung Hee University, Seoul 02447, Republic of Korea.
Sohyun ParkDepartment of Pathology, College of Korean Medicine, Kyung Hee University, Seoul 02447, Republic of Korea.ORCID 0009-0005-2470-4613
Hyo Jeong KimDepartment of Pathology, College of Korean Medicine, Kyung Hee University, Seoul 02447, Republic of Korea.
Amama RaniDepartment of Pathology, College of Korean Medicine, Kyung Hee University, Seoul 02447, Republic of Korea.ORCID 0009-0008-7916-5743
Salima AkterDepartment of Pathology, College of Korean Medicine, Kyung Hee University, Seoul 02447, Republic of Korea.ORCID 0000-0002-1769-5879
Moon Nyeo ParkDepartment of Pathology, College of Korean Medicine, Kyung Hee University, Seoul 02447, Republic of Korea.ORCID 0000-0002-9276-3894
Bonglee KimDepartment of Pathology, College of Korean Medicine, Kyung Hee University, Seoul 02447, Republic of Korea.ORCID 0000-0002-8678-156X

Funding

National Research Foundation of Korea RS-2020-NR049559
6 · The paper itself

Abstract

Male infertility is an escalating global health issue, frequently associated with metabolic problems like obesity, diabetes, and age. Recent evidence designates AMP-activated protein kinase (AMPK) as a pivotal regulator linking energy balance to male reproductive function. AMPK regulates essential activities such as spermatogenesis, metabolic support of Sertoli cells, and steroidogenesis in Leydig cells, as well as sperm motility, capacitation, and the acrosome reaction. At the molecular level, AMPK coordinates signaling networks that include mTOR, SIRT1, PGC-1α, and FOXO to modulate mitochondrial function, oxidative stress, and autophagy-related quality control. Dysregulation of AMPK during metabolic and environmental stress results in compromised spermatogenesis, diminished sperm quality, mitochondrial malfunction, and reduced testosterone synthesis. Targeting AMPK signaling constitutes a possible therapeutic approach for enhancing male reproductive health. Pharmacological agents like metformin and AICAR, together with natural bioactive substances, lifestyle modifications, and exercise mimetics, have shown promise in reestablishing metabolic equilibrium and improving reproductive results. Moreover, combinatorial strategies that integrate antioxidants and autophagy modulators may yield synergistic advantages. Nonetheless, obstacles concerning tissue selectivity, optimum dose, and clinical translation persist. Future perspectives highlight precision medicine, biomarker-directed therapies, and the incorporation of metabolic health into fertility treatment. AMPK-targeted treatments collectively provide a novel and mechanistically sound method for addressing male infertility.

Indexed as

AMP-Activated Protein KinasesInfertility, MaleReproductive HealthAnimalsHumansMaleSignal TransductionSpermatogenesisAMP-Activated Protein KinasesAMPK signalingmale infertilitymetabolic infertilitymetabolic regulationsperm mitochondrial functiontestis

Identifiers

PMID42121908
PMCPMC13162928

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.