Aquaporin expression in cryopreserved human sperm: exploring the capabilities of natural deep eutectic solvents (NADEs).

Autor:	Jahanseir F; Department of Biology, Faculty of Sciences, University of Guilan, Rasht, Iran. jahanseir76@gmail.com., Ghasemian F; Department of Biology, Faculty of Sciences, University of Guilan, Rasht, Iran. ghasemian@guilan.ac.ir., Zahiri Z; Reproductive Health Research Center, Department of Obstetrics and Gynecology, Alzahra Hospital, School of Medicine; Mehr Fertility, Research Center, Guilan University of Medical Sciences, Rasht, Iran. drzibazahiri@yahoo.com.
Jazyk:	angličtina
Zdroj:	Cryo letters [Cryo Letters] 2024 May-Jun; Vol. 45 (3), pp. 158-167.
Abstrakt:	Background: Aquaporins (AQPs) are essential proteins that facilitate the rapid movement of water and cryoprotective agents (CPAs) during the cryopreservation process, and ensure the cryo-tolerance of sperm cells. Objective: This study evaluated the preservation of aquaporin levels in human sperm after undergoing freezing using natural deep eutectic solvents (NADES) as CPAs for cryoprotection. Materials and Methods: From June 2021 to October 2022, 35 semen samples with normal sperm parameters were acquired from the Mehr Infertility Treatment Institute in Rasht, Iran. The samples were divided into several groups for analysis: control group (not frozen), group frozen with SpermFreeze Solution, and groups frozen with different NADESs, including ChS, ChX, ChU, ChG, GlyP, and EtP. After thawing, various aspects for each group were assessed, including the integrity and condensation of sperm chromatin, viability, motility, integrity of acrosome, and the expression of AQP1, AQP3, AQP7, AQP8, and AQP9 genes. Results: The analysis of gene expression revealed that freezing with ChS and GlyP preserved the expression of the AQP1 and AQP3 genes compared to the control group. Regarding AQP7 and AQP8, significant differences were not observed in expression levels between certain NADES groups (e.g., ChS, ChU, and GlyP) and the control group. Additionally, samples frozen with specific NADESs, such as ChS, ChG, EtP, and GlyP, exhibited preserved levels of AQP9 expression when compared to the control group. Conclusion: These findings emphasize the importance of NADES in preserving the expression of aquaporins in cryopreserved human sperm and their important fertility parameters. Doi.org/10.54680/fr24310110512.
Databáze:	MEDLINE
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