Relationship between indicators of oxidative stress and idiopathic infertility in men
PDF (Українська)

Keywords

sperm plasma
malondialdehyde
glutathione peroxidase
NO-synthase
zinc
fructose

How to Cite

Melnyk , O., Vorobets , M., Оnufrovych O., Besedina , A., Fafula , R., & Vorobets, Z. (2022). Relationship between indicators of oxidative stress and idiopathic infertility in men. Experimental and Clinical Medicine, 91(2), 6-15. https://doi.org/10.35339/ekm.2022.91.2.mvo

Abstract

Male infertility is a major health problem worldwide. According to a study of the WHO and the European Association of Urologists, the incidence of infertility is increasing worldwide. The male factor causes up to 50% of all cases of infertility in married couples and approximately 7% of men worldwide suffer from infertility. No cause can be found in approximately 30% of infertile men, and these cases are called idiopathic infertility. In many such cases, oxidative stress is believed to be the main causative factor. Oxidative stress, which is characterized by an imbalance between the production of reactive oxygen species and the antioxidant defense system, which is responsible for their neutralization, leads to damage to many cellular structures, especially phospholipids of cell membranes. The study is aimed at studying the adverse effect of lipid peroxidation on spermatogenesis in idiopathic male infertility. The study was conducted on the sperm of 56 men with normozoospermia and 30 men with oligoasthenozoospermia. The levels of malondialdehyde, zinc, fructose, NO-synthase activity and glutathione peroxidase (GP) in seminal plasma were correlated with sperm count and motility. Ejaculate malondialdehyde and NO-synthase activity were significantly higher, while zinc, fructose and GP were significantly lower in oligoasthenospermic than in normospermic men (p<0.001). A 1.8-fold decrease in the level of fructose in the spermogram of patients of group oligoasthenospermia, compared to the data of normozoospermic men correlated with processes of impaired motility and viability of spermatozoa. This was confirmed by the data obtained in the scientific work, in the form of a statistically significant difference in the average indicator of the quantitative content of fructose in the studied groups of patients. In particular, we found a positive correlation between the fructose content in the ejaculate and sperm motility (r=0.69), as well as a positive correlation between fructose content and the number of spermatozoa in the ejaculate (r=0.53). There was a significant negative correlation between malondialdehyde and NO-synthase with sperm count and motility in oligoasthenospermia. Elevated levels of malondialdehyde, NO-synthase in sperm, and decreased levels of zinc and GP in oligoasthenospermia may be responsible for impaired sperm membrane integrity and play a role in sperm DNA damage. The positive correlation of zinc with sperm count and sperm motility indicates an important role of zinc in spermatogenesis. Thus, these parameters may be useful in determining the fertilization potential of sperm in the diagnosis, prognosis and treatment of male infertility, especially idiopathic infertility.

Keywords: sperm plasma, malondialdehyde, glutathione peroxidase, NO-synthase, zinc, fructose.

https://doi.org/10.35339/ekm.2022.91.2.mvo
PDF (Українська)

References

Salonia A, Bettocchi C, Boeri L, Capogrosso P, Carvalho J, Cilesiz NC, et al. Euro-pean Association of Urology Guidelines on Sexual and Reproductive Health-2021 Update: Male Sexual Dysfunction. Eur Urol. 2021;80(3):333-57. DOI: 10.1016/j.eururo.2021.06.007. PMID: 34183196.

Singh MP, Sinha MBK, Sinha R. Male infertility. Medicine Update. 2005;65:318-22. Available at: https://apiindia.org/uploads/pdf/medicine_update_2005/chapter_65.pdf

Campbell MJ, Lotti F, Baldi E, Schlatt S, Mario PR, Festin MPR, et al. Distribution of semen examination results 2020 – A follow up of data collated for the WHO semen analy-sis manual 2010. Andrology. 2021;9:817-22. DOI: 10.1111/andr.12983. PMID: 33528873.

Agarwal A, Henkel R, Sharma R, Tadros NN, Sabanegh E. Determination of seminal oxidation-reduction potential (ORP) as an easy and cost-effective clinical marker of male infertility. Andrologia. 2018;50(3):12914. DOI: 10.1111/and.12914. PMID: 29057493.

Agarwal A, Parekh N, Panner Selvam MK, Henkel R, Shah R, Homa ST, et al. Male oxidative stress infertility (MOSI): proposed terminology and clinical practice guidelines for management of idiopathic male infertility. World J. Mens. Health. 2019;37:296-312. DOI: 10.5534/wjmh.190055. PMCID: PMC6704307.

Tan J, Taskin O, Albert A, Bedaiwy MA. Association between sperm DNA fragmen-tation and idiopathic recurrent pregnancy loss: a systematic review and meta-analysis. Re-prod. Biomed. Online. 2019;3896:951-60. DOI: 10.1016/j.rbmo.2018.12.029. PMID: 30979611.

Aitken RJ. Reactive oxygen species as mediators of sperm capacitation and patho-logical damage. Mol. Reprod. Dev. 2017;84(10):1039-52. DOI: 10.1002/mrd.22871. PMID: 28749007.

Aitken RJ. Impact of oxidative stress on male and female germ cells: implications for fertility. Reproduction. 2020;159:R189-201. DOI: 10.1530/REP-19-0452. PMID: 31846434.

Alahmar AT. Role of oxidative stress in male infertility: an updated review. Hum. Reprod. Sci. 2019;12(1):4-18. DOI: 10.4103/jhrs.JHRS_150_18. PMID: 31007461.

Bisht S, Faiq M, Tolahunase M, Dada R. Oxidative stress and male infertility. Na-ture Reviews Urology. 2017;14:470-85. DOI: 10.1038/nrurol.2017.69. PMID: 28508879.

Fafula RV, Onufrovych OK, Iefremova UP, Vorobets MZ, Nakonechnyi IA, Mel-nyk OV, et al. Prooxidant/antioxidant balance in sperm cells of infertile men. World of Med-icine and Biology. 2018;4(66):120-4. DOI: 10.26724/2079-8334-2018-4-66-120-124.

Said TM, Agarwal A, Sharma RK, Thomas AJ Jr, Sikka SC. Impact of sperm mor-phology on DNA damage caused by oxidative stress induced by beta-nicotinamide adenine dinucleotide phosphate. Fertil. Steril. 2005;83:95-103. DOI: 10.1016/j.fertnstert.2004.06.056. PMID: 15652893.

Tremellen K. Oxidative stress and male infertility – a clinical perspective. Human Reproduction Update. 2008;14:243-58. DOI: 10.1093/humupd/dmn004. PMID: 18281241.

Vaughan DA, Tirado E, Garcia D, Datta V, Sakkas D. DNA fragmentation of sperm: a radical examination of the contribution of oxidative stress and age in 16945 semen samples. Human Reprod. 2020;35(10):2188-96. DOI: 10.1093/humrep/deaa159. PMID: 32976601.

Garrido N, Meseguer M, Simon C, Pellicer A, Remohi J. Prooxidative and antioxi-dative imbalance in human semen and its relation with male fertility. Asian J. Androl. 2004;6:59-65. PMID: 15064836.

WHO laboratory manual for the examination and processing of human semen. Sixth edition, 2021. 292 p. Available at: http://www.ivfcpd.com/PDF/WHO_6th_edition.pdf

Martins AD, Agarwal A. Oxidation reduction potential: a new biomarker of male infertility. Panminerva Med. 2019;61(2):108-17. DOI: 10.23736/S0031-0808.18.03529-2. PMID: 30990283.

Panner Selvam MK, Finelli R, Agarwal A, Henkel R. Evaluation of seminal oxida-tion-reduction potential in male infertility. Andrologia. 2021;53(2):e13610. DOI: 10.1111/ and.13610. PMID: 32399973.

Fafula RV, Оnufrovych ОK, Iefremova UP, Vorobets DZ, Melnyk OV, Vorobets ZD. The peculiarities of arginase pathway of L-arginine metabolism in spermatozoa of men with different forms of pathospermia. International Journal of Physiology and Pathophysiol-ogy. 2017;8(4):309-18. DOI: 10.1615/IntJPhysPathophys.v8.i4.30. PMID: 30204347.

Nasrin S, Iraj A, Rezvan N, Mohammad TG The correlation between total antioxi-dant capacity and Nitric Oxide concentration in seminal plasma with sperm DNA damage. Afr. J. of Biotech. 2010;9(35):5739-45. DOI: 10.5897/AJB10.429.

Colagar AH, Marzony ET, Chaichi J. Zinc levels in seminal plasma are associated with sperm quality in fertile and infertile men. Nutrition Research. 2009;29(2):82-8. DOI: 10.1016/j.nutres.2008.11.007. PMID: 19285597.

Limthong P, Thanida P. Zinc levels in seminal plasma of infertile Man. Srinagar Ind. Med. J. 2005;20(1):38-42. DOI: 10.1111/j.1439-0272.1990.tb01980.x. PMID: 2240624.

Creative Commons License

This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License.