Tehran University of Medical Sciences

Science Communicator Platform

Stay connected! Follow us on X network (Twitter):
Share this content! On (X network) By
Leptin and Prolactin Reduce Cryodamage in Normozoospermic Human Semen Samples During Cryopreservation; [La Leptina Y La Prolactina Reducen El Criodano En Muestras De Semen Humano Normozoospermico Durante La Criopreservacion] Publisher Pubmed



Ebrahimi SM1 ; Shokri S2 ; Ziaeipour S3 ; Asa E4 ; Manesh MBM4 ; Qomi SRT4 ; Latifpour M5 ; Nejatbakhsh R6
Authors
Show Affiliations
Authors Affiliations
  1. 1. Department of Medical Surgical Nursing, Abhar School of Nursing, Zanjan University of Medical Sciences, Zanjan, Iran
  2. 2. School of Rural Health, Faculty of Medicine and Health, University of Sydney, Dubbo, NSW, Australia
  3. 3. Department of Anatomical Sciences, School of Medicine, Beheshti University of Medical Sciences, Tehran, Iran
  4. 4. Infertility Treatment Center of Academic Center of Education, Culture and Research (ACECR), Qom Branch, Qom, Iran
  5. 5. Department of Anatomical Sciences, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran
  6. 6. Department of Anatomical Sciences, School of Medicine, Zanjan University of Medical Sciences, Zanjan, Iran

Source: Revista Internacional de Andrologia Published:2023


Abstract

Objectives: Cryopreservation has destructive effects on the function and structure of spermatozoa. It is known that leptin and prolactin play an active role in decreasing the rates of reactive oxygen species and DNA fragmentation, as well as enhancing sperm motility. Hence, this experiment aimed to investigate the effects of leptin and prolactin as pro-survival factors on the normozoospermic human semen samples during cryopreservation. Material and methods: Semen samples were collected from 15 healthy, fertile men ranging from 25 to 40 years. Cryopreservation of the samples was performed in liquid nitrogen over a period of two weeks, using five varying concentrations of leptin/prolactin, 0, 10, 100, 500, and 1000 ng/ml respectively. Sperm motility, total caspase activity, and mitochondrial and cytosolic ROS were measured by flowcytometry, TUNEL, and other appropriate tests after thawing of the samples. Results: Both hormones were observed to have positive effects on the motility of the samples post-cryopreservation, the highest improvement being in the 100 ng/ml concentration leptin and prolactin in comparison to the control group (P = 0.01 and P = 0.041, respectively). A significant reduction of mitochondrial ROS was also observed in 100 and 1000 ng/ml of leptin (P = 0.042), and there was a considerable decrease in the cytosolic ROS in the 100 ng/ml of prolactin in comparison to the control group (P = 0.048). Total caspase activity was also highly reduced in the 100, 500, and 1000 ng/ml of leptin compared to the control group (P = 0.039). Interestingly, both hormones also significantly decreased DNA fragmentation in 1000 ng/ml compared to the control group (P = 0.042). Conclusion: It can be concluded that leptin and prolactin act as protective agents against cryodamage to spermatozoa during cryopreservation. © 2022