Repository of Research and Investigative Information

Repository of Research and Investigative Information

Shahid Sadoughi University of Medical Sciences

Prolonged incubation of processed human spermatozoa will increase DNA fragmentation

(2014) Prolonged incubation of processed human spermatozoa will increase DNA fragmentation. Andrologia. pp. 374-379.

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Abstract

Summary: One of the causes of failure in ART is sperm DNA fragmentation which may be associated with long period of spermatozoa incubation at 37 °C. The objective was to evaluate the rate of sperm DNA fragmentation using the sperm chromatin dispersion (SCD) test after swim-up at different time intervals prior to use. In this prospective study, 21 normozoospermic specimens were analysed. The samples were incubated at 37 °C after preparation by direct swim-up. DNA fragmentation was assessed at different time intervals (0, 1, 2 and 3 h) using SCD test. Spermatozoa with no DNA fragmentation showed large- or medium-sized halos, and sperm cells with DNA fragmentation showed either a small halo or no halo. The rates of normal morphology and progressive motility after sperm processing were 72.33 ± 2.53 and 90 ± 1.02, respectively. The rate of sperm DNA fragmentation was significantly higher after 2 h (8.81 ± 0.93, P = 0.004) and 3 h (10.76 ± 0.89, P < 0.0001) of incubation compared to 0 h (4.38 ± 0.8). A positive correlation was found between the incubation time and sperm DNA damage (P < 0.0001). Prolonged incubation of prepared normozoospermic samples at 37 °C is associated with higher rates of sperm DNA fragmentation. Therefore, sperm samples intended for ART procedures should be used within 2 h of incubation at 37 °C. © 2013 Blackwell Verlag GmbH.

Item Type: Article
Keywords: DNA; chromatin, article; cell structure; cell viability; chromatin; DNA damage; DNA fragmentation; human; human cell; incubation time; male; normal human; prospective study; reproductive procedure; spermatozoon; spermatozoon count; spermatozoon incubation; spermatozoon motility; genetic procedures; isolation and purification; procedures; semen analysis; sperm preservation; temperature, Chromatin; DNA Fragmentation; Genetic Techniques; Humans; Male; Semen Analysis; Semen Preservation; Spermatozoa; Temperature
Page Range: pp. 374-379
Journal or Publication Title: Andrologia
Volume: 46
Number: 4
Publisher: Blackwell Publishing Ltd
Depositing User: ms soheila Bazm
URI: http://eprints.ssu.ac.ir/id/eprint/9110

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