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Open AccessJournal ArticleDOI

Evaluation of human sperm function after repeated freezing and thawing.

Enoka Bandularatne, +1 more
- 04 Mar 2002 - 
- Vol. 23, Iss: 2, pp 242-249
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TLDR
The numbers of normal vital motile sperm after 3 serial freeze-thaw cycles are adequate for bringing about fertilization via intracytoplasmic sperm injection in ART programs.
Abstract
Sperm storage via freezing has been useful for men who have difficulty masturbating during assisted reproductive technology (ART) programs and before impotency caused by chemotherapy, vasectomy, and other procedures. Studies were undertaken to evaluate the extent of cryoinjury to sperm after repeated freezing and thawing. The results showed that normozoospermic and oligozoospermic sperm survived after 3 repeated freeze-thaw cycles. The inclusion of seminal plasma did not seem to protect human sperm during freezing and thawing. There were no significant differences in recovery percentages for motile, vital, and morphologically normal sperm between slow and rapid freezing methods in thaws 1, 2, and 3 of normozoospermic and oligozoospermic unwashed (u), washed (w), and washed + seminal plasma (ws) samples. However, there were significant percentage drops in the recovery of motile and vital sperm between each thaw (ie, first to second thaw, and second to third thaw) using both slow and rapid freezing for u, w, and ws samples (P < .01). There were also no significant differences in percentage recovery of motile, vital, and morphologically normal sperm between u, w, and ws samples during thaws 1 to 3 in the normozoospermic and oligozoospermic groups. Sperm were capable of fertilizing hamster oocytes microinjected with single sperms after 3 freeze-thaw cycles as evidenced by the formation of 2 distinct pronuclei and 2 polar bodies in 22.2% and 17.2% of normozoospermic and oligozoospermic samples, respectively. The numbers of normal vital motile sperm after 3 serial freeze-thaw cycles are adequate for bringing about fertilization via intracytoplasmic sperm injection in ART programs. Thus, leftover washed sperm in laboratories that perform in vitro fertilization can be frozen, thawed, and refrozen several times without loss of the sperms' ability to fertilize. This approach has tremendous benefits for men who have difficulty producing sperm and for those with low and declining sperm counts.

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Citations
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An Update on Oxidative Damage to Spermatozoa and Oocytes

TL;DR: Possible correctable measures include foremost lifestyle changes, but also supplementation with antioxidants to scavenge excessive ROS, but this should only be done after careful examination of the patient and establishment of the individual bodily antioxidant needs.
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Equine blastocyst development after intracytoplasmic injection of sperm subjected to two freeze-thaw cycles

TL;DR: Frozen stallion semen may be thawed, diluted, and refrozen without effect on the ability of motile spermatozoa to initiate embryo development after ICSI.
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Directional freezing of equine semen in large volumes

TL;DR: The results indicate that freezing stallion semen by MTG is superior to CRCM, and the differences according to all the evaluation methods were highly significant.
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Vitrification and conventional freezing methods in sperm cryopreservation: A systematic review and meta-analysis.

TL;DR: Vitrification is superior to conventional freezing methods in preservation of spermatozoa, regarding total and progressive motility and the efficacy of vitrification is influence by using different vitrification protocol and cryopreservation of different quality spermatozosa, according to the results of meta-analysis.
Journal ArticleDOI

The effect of repeated freezing and thawing on human sperm DNA fragmentation

TL;DR: Both motility and vitality decreased steadily following each cycle but cell survival was significantly greater in the unwashed samples; however, samples that were not washed and to which fresh cryoprotectant was not added after each cycle fared significantly better than their washed counterparts.
References
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Journal ArticleDOI

Sperm surface components involved in the control of the acrosome reaction

TL;DR: It is concluded that with the purification of a macromolecule involved in capacitation, specific proposals on the mechanism of capacitate, and new tools to evaluate the capacitation process, it is likely that another decade will not pass without emergence of a unifying molecular theory of sperm capacitation.
Journal ArticleDOI

Effect of seminal plasma on capacitation and hyperactivation in human spermatozoa.

TL;DR: The processes leading to hyperactivation and to the membrane changes associated with capacitation are not tightly interlinked and this finding is considered to be due to hyperactivated motility being associated with flagellar movement, while the CTC assay assesses changes in the Ca2+ levels of the sperm head plasma membrane.
Journal ArticleDOI

Variability in the human-hamster in vitro assay for fertility evaluation *

TL;DR: In this paper, the authors evaluated the sources of variability in the zona-free hamster egg penetration assay and found that the average difference in the percentage of fertilization between the replicates was 3.9%.
Journal ArticleDOI

Acrosomal status in fresh and capacitated human ejaculated sperm.

TL;DR: These studies may provide a basis for evaluating capacitation and ultimately fertility potential in the human male and the correlation of acrosomal loss with changes in motility and viability suggested that sperm senescence was not necessarily coupled to acrosome loss.
Journal ArticleDOI

Stress and semen quality in an in vitro fertilization program.

TL;DR: In this paper, the authors evaluated two semen profiles for each of 500 couples on IVF treatment and found that sperm density, total sperm count, and both quantitative and qualitative sperm motility were significantly lower in the second sample presented for IVF.
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This approach has tremendous benefits for men who have difficulty producing sperm and for those with low and declining sperm counts.