Sperm chromatin immaturity observed in short abstinence ejaculates affects DNA integrity and longevity in vitro

Uppangala, Shubhashree and Mathai, Sherine Eliza and Salian, Sujith Raj and Kumar, Dayanidhi and Singh, Vikram Jeet and D’souza, Fiona and Kalthur, Guruprasad and Kamath, Asha and Adiga, Satish Kumar (2016) Sperm chromatin immaturity observed in short abstinence ejaculates affects DNA integrity and longevity in vitro. PLos One, 11 (4). pp. 1-11. ISSN 1932-6203

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Background: The influence of ejaculatory abstinence (EA) on semen parameters and subsequent reproductive outcome is still debatable; hence understanding the impact of EA on sperm structural and functional integrity may provide a valuable information on predicting successful clinical outcome. Objective: To understand the influence of EA on sperm chromatin maturity, integrity, longevity and global methylation status. Methods: This experimental prospective study included 76 ejaculates from 19 healthy volunteers who provided ejaculates after observing 1, 3, 5 and 7 days of abstinence. Sperm chromatin maturity, DNA integrity and global methylation status were assessed in the neat ejaculate. Sperm motility, DNA integrity and longevity were assessed in the processed fraction of the fresh and frozen-thawed ejaculates to determine their association with the length of EA. Results: Spermatozoa from 1 day ejaculatory abstinence (EA-1) displayed significantly higher level of sperm chromatin immaturity in comparison to EA-3 (P < 0.05) and EA-5 (P < 0.01) whereas; the number of 5-methyl cytosine immunostained spermatozoa did not vary significantly across groups. On the other hand, in vitro incubation of processed ejaculate from EA-1 resulted in approximately 20 and 40 fold increase in the DNA fragmented spermatozoa at the end of 6 and 24h respectively (P < 0.01–0.001). Conclusion: Use of short-term EA for therapeutic fertilization would be a clinically valuable strategy to improve the DNA quality. However, use of such spermatozoa after prolonged incubation in vitro should be avoided as it can carry a substantial risk of transmitting DNA fragmentation to the oocytes.

Item Type: Article
Subjects: Medicine > KMC Manipal > Clinical Embryology
Medicine > KMC Manipal > Community Medicine
Depositing User: KMC Library
Date Deposited: 24 May 2016 09:08
Last Modified: 17 Aug 2021 09:24
URI: http://eprints.manipal.edu/id/eprint/146110

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