Book contents
- Manual of Sperm Function Testing in Human Assisted Reproduction
- Cambridge Laboratory Manuals in Assisted Reproductive Technology
- Manual of Sperm Function Testing in Human Assisted Reproduction
- Copyright page
- Dedication
- Contents
- Contributors
- Short Biography
- Foreword
- Preface
- Introduction
- Chapter 1 Standard Semen Examination: Manual Semen Analysis
- Chapter 2 Standard Semen Analysis: Computer-Assisted Semen Analysis
- Chapter 3 Standard Semen Analysis: Home Sperm Testing
- Chapter 4 Standard Semen Analysis: Leukocytospermia
- Chapter 5 Standard Semen Analysis: Morphology
- Chapter 6 Sperm Vitality: Eosin-Nigrosin Dye Exclusion
- Chapter 7 Sperm Vitality: Hypo-Osmotic Swelling Test
- Chapter 8 Determination of Mitochondrial Membrane Potential by Flow Cytometry in Human Sperm Cells
- Chapter 9 Capacitation and Acrosome Reaction: Fluorescence Techniques to Determine Acrosome Reaction
- Chapter 10 Capacitation and Acrosome Reaction: Histochemical Techniques to Determine Acrosome Reaction
- Chapter 11 Zona Binding: Competitive Sperm-Binding Assay
- Chapter 12 Zona Binding: Hemizona Assay
- Chapter 13 Oolemma Binding: Sperm Penetration Assay
- Chapter 14 Oxidative Stress Testing: Direct Tests
- Chapter 15 Oxidative Stress Testing: Indirect Tests
- Chapter 16 Chromatin Condensation: Aniline Blue Stain
- Chapter 17 Chromatin Condensation: Chromomycin A3 (CMA3) Stain
- Chapter 18 Sperm Chromatin Structure: Toluidine Blue Staining
- Chapter 19 DNA Damage: TdT-Mediated dUTP Nick-End-Labelling Assay
- Chapter 20 DNA Damage: Sperm Chromatin Structure Assay
- Chapter 21 DNA Damage: COMET Assay
- Chapter 22 DNA Damage: Halo Sperm Test
- Chapter 23 DNA Damage: Fluorescent In-Situ Hybridization
- Chapter 24 Clinical Value of Sperm Function Tests
- Chapter 25 Future Developments: Sperm Proteomics
- Conclusion
- Index
- References
Chapter 6 - Sperm Vitality: Eosin-Nigrosin Dye Exclusion
Published online by Cambridge University Press: 05 April 2021
- Manual of Sperm Function Testing in Human Assisted Reproduction
- Cambridge Laboratory Manuals in Assisted Reproductive Technology
- Manual of Sperm Function Testing in Human Assisted Reproduction
- Copyright page
- Dedication
- Contents
- Contributors
- Short Biography
- Foreword
- Preface
- Introduction
- Chapter 1 Standard Semen Examination: Manual Semen Analysis
- Chapter 2 Standard Semen Analysis: Computer-Assisted Semen Analysis
- Chapter 3 Standard Semen Analysis: Home Sperm Testing
- Chapter 4 Standard Semen Analysis: Leukocytospermia
- Chapter 5 Standard Semen Analysis: Morphology
- Chapter 6 Sperm Vitality: Eosin-Nigrosin Dye Exclusion
- Chapter 7 Sperm Vitality: Hypo-Osmotic Swelling Test
- Chapter 8 Determination of Mitochondrial Membrane Potential by Flow Cytometry in Human Sperm Cells
- Chapter 9 Capacitation and Acrosome Reaction: Fluorescence Techniques to Determine Acrosome Reaction
- Chapter 10 Capacitation and Acrosome Reaction: Histochemical Techniques to Determine Acrosome Reaction
- Chapter 11 Zona Binding: Competitive Sperm-Binding Assay
- Chapter 12 Zona Binding: Hemizona Assay
- Chapter 13 Oolemma Binding: Sperm Penetration Assay
- Chapter 14 Oxidative Stress Testing: Direct Tests
- Chapter 15 Oxidative Stress Testing: Indirect Tests
- Chapter 16 Chromatin Condensation: Aniline Blue Stain
- Chapter 17 Chromatin Condensation: Chromomycin A3 (CMA3) Stain
- Chapter 18 Sperm Chromatin Structure: Toluidine Blue Staining
- Chapter 19 DNA Damage: TdT-Mediated dUTP Nick-End-Labelling Assay
- Chapter 20 DNA Damage: Sperm Chromatin Structure Assay
- Chapter 21 DNA Damage: COMET Assay
- Chapter 22 DNA Damage: Halo Sperm Test
- Chapter 23 DNA Damage: Fluorescent In-Situ Hybridization
- Chapter 24 Clinical Value of Sperm Function Tests
- Chapter 25 Future Developments: Sperm Proteomics
- Conclusion
- Index
- References
Summary
Assessment of sperm vitality is an important component of semen analysis. It helps to distinguish spermatozoa that are alive and immotile from those that are dead. Sperm vitality can be assessed routinely on all semen samples by assessing the membrane integrity of the cell by identifying the spermatozoa with an intact cell membrane. This can be done by using 1) the dye exclusion test or 2) the hypotonic or hypoosmotic swelling test. Sperm vitality can therefore provide a good comparison with the motility of the sample. Eosin is used as a marker for dead cells because eosin can penetrate the cells when the membrane is damaged, while cells that have an intact membrane remain unstained. Nigrosin is a background stain that increases the contrast to the otherwise faintly stained cells [1, 2, 3, 4]. Both the single step and two-step staining using eosin and nigrosin have been used to assess sperm vitality. Both the wet preparation and the air-dried methods have been compared to study the correlation with motility [5, 6, 7]. The wet preparations evaluated by using either positive or negative phase-contrast microscopy consistently showed higher percentage of nonviable cells compared to the air-dried eosin-nigrosin smears. The air-dried smears have consistently shown that the sum of the motile (viable) and stained (presumed dead) preparations never exceeded 100 percent indicating that the air-dried method is the method of choice for determining vitality. In this chapter, we describe the staining protocols for vitality, the cut-off of motility when vitality must be tested, indications for poor motility and quality control recommended for performing sperm vitality in conjunction with basic semen analysis.
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- Publisher: Cambridge University PressPrint publication year: 2021
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