Evaluation of telomere length, reactive oxygen species, and apoptosis in spermatozoa of patients with oligospermia

Author:

Margiana Ria1234ORCID,Gupta Reena5,Al‐Jewari Watheq Mohammed6,Hjazi Ahmed7,Alsaab Hashem O.8,Mustafa Yasser Fakri9ORCID,Singh Rajesh10,Thaibt Ruiscul11,Alkhayyat Safa12,Ibrahim Ahmed Jaber13

Affiliation:

1. Department of Anatomy, Faculty of Medicine Universitas Indonesia Jakarta Indonesia

2. Master's Programme Biomedical Sciences, Faculty of Medicine Universitas Indonesia Jakarta Indonesia

3. Andrology Program, Faculty of Medicine Universitas Airlangga Surabaya Indonesia

4. Dr. Soetomo General Academic Hospital Surabaya Indonesia

5. Institute of Pharmaceutical Research GLA University Bharthia India

6. Department of Medical Technology Al Rafidain University College Bagdad Iraq

7. Department of Medical Laboratory Sciences, College of Applied Medical Sciences Prince Sattam bin Abdulaziz University Al‐Kharj Saudi Arabia

8. Pharmaceutics and Pharmaceutical Technology Taif University Taif Saudi Arabia

9. Department of Pharmaceutical Chemistry University of Mosul Mosul Iraq

10. Uttaranchal Institute of Technology Uttaranchal University Dehradun India

11. Medical Technical College Al‐Farahidi University Baghdad Iraq

12. College of Pharmacy The Islamic University Najaf Iraq

13. Scientific Research Center Al‐Ayen University Nasiriyah Iraq

Abstract

Abstract50% of cases of infertility are caused by male factor, which acquired or congenital problems may bring on. Male infertility can be caused by oligospermia and asthenozoospermia, which are common. Since the same mutations that cause azoospermia in some people also cause oligozoospermia in others, oligozoospermia may be thought of as a less severe form of azoospermia. Studies have demonstrated telomere length, catalase activity, super oxide dismutase (SOD), and DNA fragmentation can be influential factors for male infertility. The amount of apoptosis, oxidative stress factors, telomere length, and DNA fragmentation were some aspects of healthy sperm that we chose to look into in this study and compare to oligospermia individuals. Oligospermia patients (n = 24) and fertile men (n = 27) semen samples were collected, and the apoptosis rate of sperms in both groups was analyzed (Flow cytometry). Also, gene expression of apoptotic and antiapoptotic markers and telomere length were examined (real‐time polymerase chain reaction). The sperm DNA fragmentation kit was used to determine DNA fragmentation and to evaluate catalase and SOD activity; the specific kits and methods were utilized. Higher expression levels of caspase3 (p = .0042), caspase8 (p = .0145), caspase9 (p = .0275), and BAX (p = .0202) mRNA were observed in patients who had oligospermia. In contrast, lower mRNA expression of BCL‐2 (p = .0009) was detected in this group. In addition, telomere length was decreased in the oligospermia group (p < .0001) compared to the health group. Moreover, the frequency of apoptosis is induced in patients (p = .0026). The catalase activity is low (p = .0008), but the SOD activity is high (p = .0015) in the patient group. As a result of our findings, we may list the sperm cell apoptosis rate, telomere length, the degree of sperm DNA fragmentation, and lastly, the measurement of significant and efficient oxidative stress markers like SOD and catalase in semen plasma among the principal diagnostic characteristics for oligospermia. Future studies will be better able to treat oligospermia by showing whether these indicators are rising or falling.

Publisher

Wiley

Subject

Cell Biology,Clinical Biochemistry,General Medicine,Biochemistry

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