Addition of zinc to human ejaculate prior to cryopreservation prevents freeze-thaw-induced DNA damage and preserves sperm function

Aditi P. Kotdawala, Sangeetha Kumar, Sujith R. Salian, Prashanth Thankachan, Kaushik Govindraj, Pratap Kumar, Guruprasad Kalthur, Satish K. Adiga

Research output: Contribution to journalArticle

21 Citations (Scopus)

Abstract

Purpose: To study the effect of addition of zinc to human semen sample prior to cryopreservation on post-thaw sperm quality and function. Methods: Semen samples were collected from men attending university infertility clinic for semen analysis (n=109). Liquefied semen samples were cryopreserved in glycerol-egg yolk- citrate medium with or without the prior addition of zinc (100 μM) and stored in liquid nitrogen. After 10 days, the semen samples were thawed to assess the outcome. Sperm motility, DNA integrity, mitochondrial potential and the ability of spermatozoa to undergo capacitation and acrosome reaction was assessed in post-thaw samples. Results: Semen samples cryopreserved after addition of zinc had a significantly higher percentage of sperm with intact DNA (p<0.001), mitochondrial function (p<0.001) and progressive motility (p<0.01) compared to the semen samples cryopreserved without zinc supplementation. Apart from this, ability to undergo capacitation and acrosome reaction in vitro was significantly higher in semen samples cryopreserved with zinc (p<0.0001 and p<0.001 respectively). Conclusions: Addition of zinc to semen samples prior to cryopreservation helps in preventing the freeze-thaw-induced sperm DNA damage and loss of sperm function.

Original languageEnglish
Pages (from-to)1447-1453
Number of pages7
JournalJournal of Assisted Reproduction and Genetics
Volume29
Issue number12
DOIs
Publication statusPublished - 12-2012

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Cryopreservation
Semen
DNA Damage
Spermatozoa
Zinc
Acrosome Reaction
Egg Yolk
Semen Analysis
Sperm Motility
Mitochondrial DNA
Citric Acid
Glycerol
Infertility
Nitrogen
DNA

All Science Journal Classification (ASJC) codes

  • Obstetrics and Gynaecology
  • Reproductive Medicine
  • Developmental Biology
  • Genetics
  • Genetics(clinical)

Cite this

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title = "Addition of zinc to human ejaculate prior to cryopreservation prevents freeze-thaw-induced DNA damage and preserves sperm function",
abstract = "Purpose: To study the effect of addition of zinc to human semen sample prior to cryopreservation on post-thaw sperm quality and function. Methods: Semen samples were collected from men attending university infertility clinic for semen analysis (n=109). Liquefied semen samples were cryopreserved in glycerol-egg yolk- citrate medium with or without the prior addition of zinc (100 μM) and stored in liquid nitrogen. After 10 days, the semen samples were thawed to assess the outcome. Sperm motility, DNA integrity, mitochondrial potential and the ability of spermatozoa to undergo capacitation and acrosome reaction was assessed in post-thaw samples. Results: Semen samples cryopreserved after addition of zinc had a significantly higher percentage of sperm with intact DNA (p<0.001), mitochondrial function (p<0.001) and progressive motility (p<0.01) compared to the semen samples cryopreserved without zinc supplementation. Apart from this, ability to undergo capacitation and acrosome reaction in vitro was significantly higher in semen samples cryopreserved with zinc (p<0.0001 and p<0.001 respectively). Conclusions: Addition of zinc to semen samples prior to cryopreservation helps in preventing the freeze-thaw-induced sperm DNA damage and loss of sperm function.",
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Addition of zinc to human ejaculate prior to cryopreservation prevents freeze-thaw-induced DNA damage and preserves sperm function. / Kotdawala, Aditi P.; Kumar, Sangeetha; Salian, Sujith R.; Thankachan, Prashanth; Govindraj, Kaushik; Kumar, Pratap; Kalthur, Guruprasad; Adiga, Satish K.

In: Journal of Assisted Reproduction and Genetics, Vol. 29, No. 12, 12.2012, p. 1447-1453.

Research output: Contribution to journalArticle

TY - JOUR

T1 - Addition of zinc to human ejaculate prior to cryopreservation prevents freeze-thaw-induced DNA damage and preserves sperm function

AU - Kotdawala, Aditi P.

AU - Kumar, Sangeetha

AU - Salian, Sujith R.

AU - Thankachan, Prashanth

AU - Govindraj, Kaushik

AU - Kumar, Pratap

AU - Kalthur, Guruprasad

AU - Adiga, Satish K.

PY - 2012/12

Y1 - 2012/12

N2 - Purpose: To study the effect of addition of zinc to human semen sample prior to cryopreservation on post-thaw sperm quality and function. Methods: Semen samples were collected from men attending university infertility clinic for semen analysis (n=109). Liquefied semen samples were cryopreserved in glycerol-egg yolk- citrate medium with or without the prior addition of zinc (100 μM) and stored in liquid nitrogen. After 10 days, the semen samples were thawed to assess the outcome. Sperm motility, DNA integrity, mitochondrial potential and the ability of spermatozoa to undergo capacitation and acrosome reaction was assessed in post-thaw samples. Results: Semen samples cryopreserved after addition of zinc had a significantly higher percentage of sperm with intact DNA (p<0.001), mitochondrial function (p<0.001) and progressive motility (p<0.01) compared to the semen samples cryopreserved without zinc supplementation. Apart from this, ability to undergo capacitation and acrosome reaction in vitro was significantly higher in semen samples cryopreserved with zinc (p<0.0001 and p<0.001 respectively). Conclusions: Addition of zinc to semen samples prior to cryopreservation helps in preventing the freeze-thaw-induced sperm DNA damage and loss of sperm function.

AB - Purpose: To study the effect of addition of zinc to human semen sample prior to cryopreservation on post-thaw sperm quality and function. Methods: Semen samples were collected from men attending university infertility clinic for semen analysis (n=109). Liquefied semen samples were cryopreserved in glycerol-egg yolk- citrate medium with or without the prior addition of zinc (100 μM) and stored in liquid nitrogen. After 10 days, the semen samples were thawed to assess the outcome. Sperm motility, DNA integrity, mitochondrial potential and the ability of spermatozoa to undergo capacitation and acrosome reaction was assessed in post-thaw samples. Results: Semen samples cryopreserved after addition of zinc had a significantly higher percentage of sperm with intact DNA (p<0.001), mitochondrial function (p<0.001) and progressive motility (p<0.01) compared to the semen samples cryopreserved without zinc supplementation. Apart from this, ability to undergo capacitation and acrosome reaction in vitro was significantly higher in semen samples cryopreserved with zinc (p<0.0001 and p<0.001 respectively). Conclusions: Addition of zinc to semen samples prior to cryopreservation helps in preventing the freeze-thaw-induced sperm DNA damage and loss of sperm function.

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