# Impact of Heavy Metals on Human Male Fertility—An Overview

**Authors:** Andrea López-Botella, Irene Velasco, Maribel Acién, Paula Sáez-Espinosa, José-Luis Todolí-Torró, Raquel Sánchez-Romero, María José Gómez-Torres

PMC · DOI: 10.3390/antiox10091473 · Antioxidants · 2021-09-15

## TL;DR

This paper reviews how heavy metals disrupt hormones and affect male fertility, highlighting the need for more research and better diagnostic tools.

## Contribution

The study compiles existing human research on heavy metals and male infertility, emphasizing the need for clinical trials and improved assessment methods.

## Key findings

- Heavy metals act as endocrine disruptors, negatively affecting male fertility.
- Only 144 relevant studies were identified after screening 636 articles from three databases.
- Better diagnostic tools and clinical trials are needed to confirm heavy metals' role in male infertility.

## Abstract

Heavy metals are endocrine disruptors which interfere with processes mediated by endogenous hormones of the organism, negatively affecting endocrine functions. Some studies have correlated heavy metal exposure with male infertility. However, the number of studies conducted on humans are limited. Therefore, the aim of this study is to summarize the current knowledge on how heavy metals influence human male fertility. Hence, three distinct databases were consulted—PubMed, Scopus and Web of Science—using single keywords and combinations of them. The total number of identified articles was 636. Nevertheless, by using the inclusion and exclusion criteria, 144 articles were finally included in this work. Results display that the development of adequate instruments for heavy metal assessment may play an important function in human male fertility diagnosis and treatment. Furthermore, clinical trials could be useful to confirm the role of heavy metals in human male fertility diagnosis. Overall, further research is required to fully understand the molecular and cellular basis of the influence of environmental and occupational exposure to heavy metals on human male infertility and reproductive outcomes.

## Linked entities

- **Diseases:** male infertility (MONDO:0005372)

## Full-text entities

- **Genes:** MRC1 (mannose receptor C-type 1) [NCBI Gene 4360] {aka CD206, CLEC13D, CLEC13DL, MMR, MRC1L1, bA541I19.1}, SFTPB (surfactant protein B) [NCBI Gene 6439] {aka PSP-B, SFTB3, SFTP3, SMDP1, SP-B}, PTK2 (protein tyrosine kinase 2) [NCBI Gene 5747] {aka FADK, FADK 1, FAK, FAK1, FRNK, PPP1R71}, SHBG (sex hormone binding globulin) [NCBI Gene 6462] {aka ABP, SBP, TEBG}, ALAD (aminolevulinate dehydratase) [NCBI Gene 210] {aka ALADH, PBGS}
- **Diseases:** Fertility (MESH:D007246), tract (MESH:D014570), inflammation (MESH:D007249), severe (MESH:D045169), obesity (MESH:D009765), Male Fertility (MESH:D007248), EDCs (MESH:D004700), infections (MESH:D007239), fragmentation (MESH:D012892), Pb poisoning (MESH:D011041), teratospermia (MESH:D000072660), oligospermia (MESH:D009845), testicular deterioration (MESH:D013733), impaired male reproductive function (MESH:D005832), abnormal progressive motility (MESH:C563515), COVID-19 (MESH:D000086382), necrotic (MESH:D009336), IVF (MESH:C566179), miscarriages (MESH:D000022), sperm abnormalities (MESH:C567467), azoospermia (MESH:D053713), spermatic abnormalities (MESH:D013086), reproductive disorders (MESH:D060737), cytotoxicity (MESH:D064420), defects (MESH:D000013), asthenoteratozoospermia (MESH:D053627), impaired prostate secretory (MESH:D011472)
- **Chemicals:** ascorbate (MESH:D001205), SZn (MESH:D013311), PbB (MESH:D011075), cAMP (MESH:D000242), Metal (MESH:D008670), folate (MESH:D005492), Bi (MESH:D001729), ROS (MESH:D017382), Chromium (MESH:D002857), Sr (MESH:D013324), Cesium (MESH:D002586), progesterone (MESH:D011374), Mo (MESH:D008982), V (MESH:D014639), HG (MESH:D008628), Be (MESH:D001608), SPCd (MESH:C536778), Thallium (MESH:D013793), graphite (MESH:D006108), Co (MESH:D003035), CdCl2 (MESH:D019256), lipid (MESH:D008055), Ag (MESH:D012834), dehydroascorbate (MESH:D003683), Sn (MESH:D014001), malondialdehyde (MESH:D008315), BP (MESH:C038809), bisphenol A (MESH:C006780), SP (MESH:C000604007), Ni (MESH:D009532), Arsenic (MESH:D001151), polychlorinated biphenyls (MESH:D011078), SE (MESH:D012643), In (MESH:D007204), phthalates (MESH:C032279), Platinum (MESH:D010984), Ca (MESH:D002118), Antimony (MESH:D000965), U (MESH:D014501), Al (MESH:D000535), Tungsten (MESH:D014414), Cadmium (MESH:D002104), estradiol (MESH:D004958), Lead (MESH:D007854), CuSO4 (MESH:D019327), Magnesium (MESH:D008274), dioxins (MESH:D004147), Te (MESH:D013691), carotenoids (MESH:D002338), S (MESH:D013455), Heavy Metals (MESH:D019216), testosterone (MESH:D013739), Cr Ni (MESH:C066018), BCd (-), Ti (MESH:D014025), B (MESH:D001895), Fe (MESH:D007501), SP, B (MESH:C042995), PAH (MESH:D011084), Zinc (MESH:D015032)
- **Species:** Oryza sativa (Asian cultivated rice, species) [taxon 4530], Cucumis sativus (cucumber, species) [taxon 3659], Spinacia oleracea (spinach, species) [taxon 3562], PX clade (clade) [taxon 569578], Homo sapiens (human, species) [taxon 9606], Nicotiana tabacum (American tobacco, species) [taxon 4097]
- **Cell lines:** S2 — Drosophila melanogaster (Fruit fly), Spontaneously immortalized cell line (CVCL_Z232)

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## References

121 references — full list in the complete paper: https://tomesphere.com/paper/PMC8468047/full.md

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Source: https://tomesphere.com/paper/PMC8468047