| Literature DB >> 33803103 |
Filip Tirpák1, Hana Greifová2, Norbert Lukáč2, Robert Stawarz3, Peter Massányi2,3.
Abstract
Natural processes along with increased industrial production and the irresponsible behavior of mankind have resulted in environmental pollution. Environmental pollutants can be categorized based on their characteristics and appearance into the following groups: physical, biological, and chemical. Every single one of them represents a serious threat to the male reproductive tract despite the different modes of action. Male gonads and gametes are especially vulnerable to the effect of exogenous factors; therefore, they are considered a reliable indicator of environmental pollution. The impact of xenobiotics or radiation leads to an irreversible impairment of fertility displayed by histological changes, modulated androgen production, or compromised spermatozoa (or germ cells) quality. The present article reviews the exogenous threats, male reproductive system, the mode of action, and overall impact on the reproductive health of humans and animals.Entities:
Keywords: endocrine disruptors; heavy metals; mode of action; mycotoxins; oxidative stress; radiation; risk factors; seminal plasma; spermatozoa; testes
Year: 2021 PMID: 33803103 PMCID: PMC8001766 DOI: 10.3390/life11030213
Source DB: PubMed Journal: Life (Basel) ISSN: 2075-1729
The effect of non-ionizing and ionizing radiation on the most targeted sites in male reproduction.
| Radiation | The Site of the Effect | ||
|---|---|---|---|
| Testis | Epididymis | Spermatozoa | |
| Non-ionizing | dilatated and congested blood vessels in tunica albuginea and interstitium degenerated spermatogenic cells diminished Sertoli cells containing numerous vacuoles, swollen mitochondria, and broken organelles enhanced production of cytokines by Sertoli cells germ cells arrested in pre-meiotic stages induced generation of ROS | reduced weight of epididymis decreased sperm count morphological defects of spermatozoa increased lipid peroxidation diminished content of glutathione degeneration of epithelium cells | dose & frequency-dependent effect on motility spontaneous acrosome reaction sperm head malformations increased DNA damage |
| Ionizing | decreased testis weight damaged seminiferous tubules disorganized spermatogenic cells declined number of spermatocytes and spermatogonia induced apoptosis of spermatogenic cells degeneration of Sertoli cells the high appearance of swelling mitochondria extensive ROS generation | the lower weight of epididymis diminished luminal diameter high incidence of vacuoles in the epithelium impaired spermatogenesis reduced sperm count elevated apoptosis enhanced intracellular ROS decreased level of zinc | decreased motility and viability reduced sperm count morphological malformations elevated intracellular ROS down-regulated expression of tubulin decreased content of ATP |
The effect of selected (the most harmful) heavy metals on the most targeted sites in male reproduction.
| Heavy Metal | The Site of the Effect | ||
|---|---|---|---|
| Testis | Epididymis | Spermatozoa | |
| Cadmium | alterations in the number and structure of seminiferous tubules the increased volume of stroma the thinned layer of Sertoli and germ cells altered spermatogenesis | enhanced weight of epididymis thickened epithelia widened interstitium vacuolized Sertoli cells impaired spermatogenesis dilatated blood vessels induced apoptosis and inflammation interfered androgen production increased ROS production | reduction in sperm count decreased viability and motility altered morphology altered acrosome and mitochondrial segment changed DNA methylation |
| Lead | reduced testis weight disrupted testosterone production elevated ROS disorganization of seminiferous tubules interfered or even absent spermatogenesis enlarged spermatocytes inflamed tunica albuginea down-regulation of Catsper 1 and 2 | decreased weight of epididymis increased oxidative stress and lipid peroxidation diminished epididymal spermatozoa modulated enzymatic activity reduced quantity of stereocilia of epithelial cells lowered number of spermatozoa | decreased sperm count and motility excessive generation of ROS enhanced DNA damage morphological malformations decreased intracellular cAMP inhibition of sperm creatine kinase displacing zinc from its binding sites |
| Mercury | hypertrophy of seminiferous tubules with occlusions in the lumen vacuolated areas contained in the seminiferous tubules thinned tubules dilatated blood vessels the increased volume of the interstitium degeneration and disorganization of spermatogenic cells reduced number of spermatocytes down-regulation of Catsper 1 and 2 disruption of estrogen receptor | reduced weight of epididymis decreased sperm count morphological aberrations elevated levels of ROS and lipid peroxidation disruption of estrogen receptor | reduced sperm count higher incidence of immotile spermatozoa the damaged plasma membrane, axoneme elevated generation of ROS increased lipid peroxidation impaired fertilization ability altered DNA methylation decreased adenosine triphosphate inhibition of sperm creatine kinase |