# Microplastics and male reproductive system: A comprehensive review based on cellular and molecular effects

**Authors:** Mohammad Karimian, Sahar Yaqubi

PMC · DOI: 10.1016/j.toxrep.2026.102226 · Toxicology Reports · 2026-02-19

## TL;DR

This paper reviews how microplastics negatively impact the male reproductive system by disrupting cellular and molecular processes.

## Contribution

The study provides a comprehensive review of microplastic effects on male reproduction, focusing on cellular and molecular mechanisms.

## Key findings

- Microplastics can damage testicular structure and function, leading to infertility issues.
- They trigger inflammation, oxidative stress, and aging in the testes.
- Microplastics disrupt spermatogenesis and impair sperm parameters.

## Abstract

Microplastics (MPs) have emerged as an important environmental challenge and can threaten human health. These particles can enter the human body through food consumption, breathing and even skin absorption and cause disruption in the functioning of various organs. In addition, MPs also have an effect on reproduction and can have a negative effect on various stages of reproduction, including gametogenesis and fertilization to embryo formation, and as a result, aggravate infertility problems. This research has investigated the effects of MPs on the male reproductive system, focusing on cellular and molecular processes and approaches to deal with this issue. This review conducted a comprehensive literature search across multiple scientific databases. Searches were performed in Google Scholar, Scopus, PubMed, and Web of Science to identify relevant publications. The search terms used included a combination of MPs, male infertility, sperm, toxicity, and related keywords. The final set of selected articles provides a comprehensive overview of the effects of MPs on cellular and molecular processes in the male reproductive system. In men, MPs can affect the structure and function of the testis and induce the aging process and the inflammatory signaling pathway, oxidative stress, and testicular malignancy. Also, these particles affect the process of spermatogenesis and disrupt sperm parameters. MPs activate different cell signaling pathways and have effects including reducing ATP production, reducing sperm DNA integrity, impairing sperm function and reducing sperm survival. On the other hand, MPs may have destructive effects on the production and balance of male hormones through interaction with the endocrine system. It is evident that proactive measures need to be implemented to address this issue and enhance reproductive health parameters.

•Microplastics influence reproductive health by affecting vital processes such as gametogenesis.•Specifically, in men, microplastics can negatively affect testicular structure and function.•Microplastics accelerate aging, trigger inflammation, and provoke oxidative stress in the testes.

Microplastics influence reproductive health by affecting vital processes such as gametogenesis.

Specifically, in men, microplastics can negatively affect testicular structure and function.

Microplastics accelerate aging, trigger inflammation, and provoke oxidative stress in the testes.

## Full-text entities

- **Genes:** Star (steroidogenic acute regulatory protein) [NCBI Gene 20845] {aka D8Ertd419e, stARD1}, Mcpt1 (mast cell protease 1) [NCBI Gene 17224] {aka Mcp-1}, Rela (Rela proto-oncogene, NFKB subunit) [NCBI Gene 19697] {aka p65, p65 NF-kappa B, p65 NFkB}, Cxcl15 (C-X-C motif chemokine ligand 15) [NCBI Gene 20309] {aka Il8, Scyb15, lungkine, weche}, Rps6 (ribosomal protein S6) [NCBI Gene 20104] {aka S6R}, Il6 (interleukin 6) [NCBI Gene 16193] {aka Il-6}, Prkca (protein kinase C, alpha) [NCBI Gene 18750] {aka Pkca}, Mmp9 (matrix metallopeptidase 9) [NCBI Gene 17395] {aka B/MMP9, Clg4b, Gel B, MMP-9, pro-MMP-9}, Nfe2l2 (NFE2 like bZIP transcription factor 2) [NCBI Gene 83619], Lhcgr (luteinizing hormone/choriogonadotropin receptor) [NCBI Gene 25477] {aka LH/CG-R, LSH-R, LSHR, Lhr}, TP53 (tumor protein p53) [NCBI Gene 7157] {aka BCC7, BMFS5, LFS1, P53, TRP53}, Epas1 (endothelial PAS domain protein 1) [NCBI Gene 13819] {aka HIF-2alpha, HIF2A, HLF, HRF, MOP2, bHLHe73}, Pink1 (PTEN induced putative kinase 1) [NCBI Gene 68943] {aka 1190006F07Rik, BRPK, mFLJ00387}, Gsr (glutathione-disulfide reductase) [NCBI Gene 116686], COX2 (cytochrome c oxidase subunit II) [NCBI Gene 17709], Ptk2 (PTK2 protein tyrosine kinase 2) [NCBI Gene 14083] {aka FADK 1, FAK, FRNK, Fadk, p125FAK}, Hsd17b4 (hydroxysteroid (17-beta) dehydrogenase 4) [NCBI Gene 15488] {aka 17-beta-HSD, 17[b]-HSD, DBP, MFE-2, MFP2, MPF-2}, Akt1 (Akt serine/threonine kinase 1) [NCBI Gene 11651] {aka Akt, LTR-akt, PKB, PKB/Akt, PKBalpha, Rac}, Rac1 (Rac family small GTPase 1) [NCBI Gene 19353] {aka D5Ertd559e}, Ar (androgen receptor) [NCBI Gene 11835] {aka Tfm}, NFE2L2 (NFE2 like bZIP transcription factor 2) [NCBI Gene 4780] {aka IMDDHH, NRF2, Nrf-2}, Star (steroidogenic acute regulatory protein) [NCBI Gene 25557], Mtor (mechanistic target of rapamycin kinase) [NCBI Gene 56717] {aka 2610315D21Rik, FRAP, FRAP2, Frap1, RAFT1, RAPT1}, Il10 (interleukin 10) [NCBI Gene 16153] {aka CSIF, If2a, Il-10}, Camp (cathelicidin antimicrobial peptide) [NCBI Gene 316010] {aka CRAMP}, Cat (catalase) [NCBI Gene 24248] {aka CS1, Cas1, Cat01, Catl, Cs-1}, Rictor (RPTOR independent companion of MTOR, complex 2) [NCBI Gene 78757] {aka 4921505C17Rik, 6030405M08Rik, AVO3, D530039E11Rik}, TGFB1 (transforming growth factor beta 1) [NCBI Gene 7040] {aka CAEND1, CED, DPD1, IBDIMDE, LAP, TGF-beta1}, Il1b (interleukin 1 beta) [NCBI Gene 16176] {aka IL-1beta, Il-1b}, Tnf (tumor necrosis factor) [NCBI Gene 21926] {aka DIF, TNF-a, TNF-alpha, TNFSF2, TNFalpha, Tnfa}, MAPK8 (mitogen-activated protein kinase 8) [NCBI Gene 5599] {aka JNK, JNK-46, JNK1, JNK1A2, JNK21B1/2, PRKM8}, Hmox1 (heme oxygenase 1) [NCBI Gene 24451] {aka HEOXG, Heox, Hmox, Ho-1, Ho1, hsp32}, Nfkb1 (nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105) [NCBI Gene 18033] {aka NF-KB1, NF-kappaB, NF-kappaB1, p105, p50, p50/p105}, AKT1 (AKT serine/threonine kinase 1) [NCBI Gene 207] {aka AKT, PKB, PKB-ALPHA, PRKBA, RAC, RAC-ALPHA}, Tgfb1 (transforming growth factor, beta 1) [NCBI Gene 21803] {aka TGF-beta1, TGFbeta1, Tgfb, Tgfb-1}, Crtc2 (CREB regulated transcription coactivator 2) [NCBI Gene 74343] {aka 4632407F12Rik, Torc2}
- **Diseases:** cryptorchidism (MESH:D003456), cardiotoxicity (MESH:D066126), problems (MESH:D019973), neurological abnormalities (MESH:D009461), reproductive disorders (MESH:D060737), occupational disorder (MESH:D009784), male infertility (MESH:D007248), Testicular cancer (MESH:D013736), endoplasmic reticulum (MESH:D008228), oligospermia (MESH:D009845), pregnancy loss (MESH:D000022), renal toxicity (MESH:D007674), seminoma (MESH:D018239), cytotoxicity (MESH:D064420), teratospermia (MESH:D000072660), orchitis (MESH:D009920), edema (MESH:D004487), implantation failure (MESH:D051437), PVC (MESH:C536210), neurotoxicity (MESH:D020258), gastrointestinal disorders (MESH:D005767), abortion (MESH:D000026), pulmonary toxicity (MESH:D008171), fertility impairment (MESH:D007246), EDCs (MESH:D004700), cancer (MESH:D009369), carcinogenic (MESH:D011230), mitochondrial dysfunction (MESH:D028361), spermatogenic dysfunction (MESH:C564030), inflammation (MESH:D007249), fibrosis (MESH:D005355), testicular damage (MESH:D013733), fetal growth retardation (MESH:D005317), endotoxemia (MESH:D019446)
- **Chemicals:** nitric oxide (MESH:D009569), polyethylene (MESH:D020959), hydroxyl radical (MESH:D017665), heavy metals (MESH:D019216), calcium (MESH:D002118), MP (MESH:D000080545), ROS (MESH:D017382), lead (MESH:D007854), LH (MESH:D007986), cadmium (MESH:D002104), vinyl chloride (MESH:D014752), polyurethane (MESH:D011140), PET (MESH:D011093), biochar (MESH:C540010), PLA (MESH:C033616), lipid (MESH:D008055), testosterone (MESH:D013739), iron (MESH:D007501), polypropylene (MESH:D011126), aluminum oxide (MESH:D000537), CCK-8 (MESH:D012844), water (MESH:D014867), ATP (MESH:D000255), AlCl3 (MESH:D000077410), Polystyrene (MESH:D011137), talc (MESH:D013627), cobalt (MESH:D003035), chitin (MESH:D002686), chlorine (MESH:D002713), PVC (MESH:D011143), polymer (MESH:D011108), malondialdehyde (MESH:D008315), polyester (MESH:D011091), polyaluminum chloride (MESH:C016213), fluorescein (MESH:D019793), graphene oxide (MESH:C000628730), mercury (MESH:D008628), silica (MESH:D012822), PS (MESH:D010758), oxygen (MESH:D010100), Rhamnetin (MESH:C063423), PE (-), superoxide (MESH:D013481), Hydrogen peroxide (MESH:D006861), nylon (MESH:D009757), aluminum (MESH:D000535)
- **Species:** PX clade (clade) [taxon 569578], Palaemon pugio (species) [taxon 221654], Perinereis aibuhitensis (species) [taxon 126650], Homo sapiens (human, species) [taxon 9606], Rattus norvegicus (brown rat, species) [taxon 10116], Mus musculus (house mouse, species) [taxon 10090], Tegillarca granosa (species) [taxon 220873]
- **Cell lines:** Balb/c — Mus musculus (Mouse), Spontaneously immortalized cell line (CVCL_0184), GC-2 — Mus musculus (Mouse), Conditionally immortalized cell line (CVCL_6633), TM3 — Mus musculus (Mouse), Spontaneously immortalized cell line (CVCL_4326), TM4 — Mus musculus (Mouse), Spontaneously immortalized cell line (CVCL_4327)

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12937021/full.md

## References

145 references — full list in the complete paper: https://tomesphere.com/paper/PMC12937021/full.md

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Source: https://tomesphere.com/paper/PMC12937021