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Related Concept Videos

Spermatogenesis01:41

Spermatogenesis

Spermatogenesis is the process by which haploid sperm cells are produced in the male testes. It starts with stem cells located close to the outer rim of seminiferous tubules. These spermatogonial stem cells divide asymmetrically to give rise to additional stem cells (meaning that these structures “self-renew”), as well as sperm progenitors, called spermatocytes. Importantly, this method of asymmetric mitotic division maintains a population of spermatogonial stem cells in the male reproductive...
Sperm Structure and Semen Composition01:22

Sperm Structure and Semen Composition

During ejaculation, males release around 2-5 milliliters of semen, which is a complex mixture of mature sperm and various fluids produced by accessory glands. The mature sperm cells measure approximately 60 micrometers in length and consist of a head, neck, midpiece, and tail. The head is flattened and tapered, measuring about 4 to 5 micrometers in length. It contains a nucleus with condensed chromosomes and an acrosome, a cap-like structure filled with enzymes essential for penetrating the...
Sperm Transport01:15

Sperm Transport

The journey of sperm from its origin to the point of ejaculation begins within the seminiferous tubules of the testis. Here, Sertoli cells produce fluid that propels non-motile sperm through a series of conduits, starting with the straight tubules leading to the rete testis. This interconnected network of tubules acts as the initial pathway for sperm, guiding them into the efferent ductules and then into the epididymis for maturation.
The maturation phase occurs in the epididymis, where sperm...

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Related Experiment Video

Updated: May 8, 2026

Using an Extracellular Flux Analyzer to Measure Changes in Glycolysis and Oxidative Phosphorylation during Mouse Sperm Capacitation
08:22

Using an Extracellular Flux Analyzer to Measure Changes in Glycolysis and Oxidative Phosphorylation during Mouse Sperm Capacitation

Published on: January 22, 2020

Response to capacitating stimuli indicates extender-related differences in boar sperm function.

S Schmid1, H Henning, A M Petrunkina

  • 1Unit for Reproductive Medicine, Clinic for Pigs and Small Ruminants, University of Veterinary Medicine Hannover, Foundation, Hannover, Germany.

Journal of Animal Science
|August 31, 2013
PubMed
Summary
This summary is machine-generated.

Boar sperm are sensitive to chilling; a new test measuring their response to capacitation stimuli can detect differences in semen extenders. This method helps identify better preservation strategies for boar semen quality.

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Last Updated: May 8, 2026

Using an Extracellular Flux Analyzer to Measure Changes in Glycolysis and Oxidative Phosphorylation during Mouse Sperm Capacitation
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Published on: May 24, 2013

Area of Science:

  • Reproductive Biology
  • Animal Science
  • Sperm Preservation

Background:

  • Porcine spermatozoa are vulnerable to chilling and aging in vitro.
  • Developing effective semen extenders is crucial for boar sperm preservation.
  • Sensitive functional assays are needed to evaluate new preservation strategies.

Purpose of the Study:

  • To assess if the specific response to capacitation stimuli can detect differences in boar sperm preservation by extenders.
  • To compare the efficacy of Beltsville Thawing Solution (BTS) and Androstar Plus during hypothermic storage.

Main Methods:

  • Boar semen was stored in BTS and Androstar Plus at various temperatures (5°C, 10°C, 17°C, 22°C).
  • Sperm function was assessed using flow cytometry to measure intracellular calcium and plasma membrane integrity after incubation in capacitating and control media.
  • The specific response to capacitation stimuli was determined by analyzing the loss of low-calcium live cells.

Main Results:

  • Sperm motility and membrane integrity remained high, except in BTS at 5°C.
  • Semen stored in BTS showed a greater loss of response to capacitation stimuli compared to Androstar Plus.
  • Phospholipid disorder showed no significant extender-related differences.
  • Field insemination trials showed no fertility differences for semen stored up to 48h at 10°C in Androstar Plus versus BTS at 17°C.

Conclusions:

  • Assessing the specific reactivity to capacitation stimuli is a sensitive method for detecting extender-dependent changes in chilled boar sperm functionality.
  • Androstar Plus may offer better protection for boar spermatozoa during hypothermic storage compared to BTS.
  • This functional assay can aid in selecting optimal semen extenders for boar fertility preservation.