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Sperm cryopreservation and biobanking are emerging as tools for supporting genetic management of small and threatened populations in amphibian conservation programs. However, there is little to no evidence demonstrating reproductive maturity and viability of offspring generated with cryopreserved sperm, potentially limiting widespread integration of these technologies. The purpose of this report is to demonstrate that amphibian sperm can be cryopreserved and thawed to successfully produce individuals of an F1 generation that can reach adulthood and reproductive maturity, to generating viable gametes and an F2 generation. Species-specific exogenous hormones were administered to both F0 and F1 adults to stimulate spermiation and oviposition in the eastern tiger salamander (), dusky gopher frog (), and Puerto Rican crested toad (). Sperm cells collected non-lethally from F0 adults were cryopreserved, thawed, and used for in vitro fertilization (IVF) to produce F1 offspring. Individuals of the F1 generation are shown to reach adulthood, express viable gametes, and produce offspring through facilitated breeding, or IVF. The production of amphibian F2 generations shown here demonstrates that amphibian sperm collected non-lethally can be banked and used to generate reproductively viable animals of subsequent generations, thus maintaining valuable genetic linages and diversity in threatened amphibian species. The incredible value that cryopreservation of sperm has for long-term genetic management aids in the sustainability of both in situ and ex situ conservation efforts for this taxon.
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http://dx.doi.org/10.3390/ani13010053 | DOI Listing |
Cryobiology
September 2025
Laboratory of Teaching and Research in Pathology of Reproduction, Center of Biotechnology in Animal Reproduction, Department of Animal Reproduction, School of Veterinary Medicine and Animal Science, University of São Paulo (USP), Pirassununga, SP, Brazil. Electronic address:
Sperm capacitation is a critical process for successful fertilization, involving multiple regulated cellular changes. On the other hand, cryopreservation induces membrane changes that can mimic capacitation, potentially leading to misinterpretation of sperm function. Distinguishing true capacitation from cryoinjury remains challenging, as both share surface markers despite involving distinct mechanisms and impacts on fertilization.
View Article and Find Full Text PDFFr J Urol
September 2025
Service d'urologie, Hopital La Conception, Marseille, France. Electronic address:
Introduction: After spinal cord injury, most men cannot conceive without medical help. Therefore, this systematic review aimed to provide updated, high-quality recommendations up on fertility preservation (FP) in patients with spinal cord injury to urologists/andrologists, neuro-urologists, laboratory physicians, endocrinologists and other healthcare professionals.
Methods: These guidelines were based on a systematic review of studies published between January 1990 and June 2024 performed following the Preferred Reporting Items for Systematic Reviews and Meta-Analyses criteria.
Anim Reprod Sci
September 2025
College of Animal Science and Technology, Qingdao Agricultural University, Qingdao 266109, China. Electronic address:
Due to the current limitations of boar semen cryopreservation systems, the effective restoration of sperm quality following thawing remains a significant challenge. This study investigates whether post-thaw boar sperm can uptake exogenous long-chain fatty acids (LCFAs) and utilize them for ATP generation, thereby sustaining linear motility and enhancing sperm vitality. Boar semen was diluted in extender solutions supplemented with varying concentrations of a lipid mixture (0, 0.
View Article and Find Full Text PDFZhonghua Nan Ke Xue
August 2025
The Sun Yat-sen University Cancer Center, Guangzhou, Guangdong 510060, China.
Objective: The aim of this study is to explore the influencing factors of fertility preservation decision-making in testicular cancer patient and provide a basis for clinical decision.
Methods: A descriptive qualitative study was conducted using purposive sampling in 18 testicular cancer patients. Semi-structured interviews were performed, and data were analyzed through content analysis.
Reprod Domest Anim
September 2025
Institute for Reproduction of Farm Animals Schönow, Bernau, Germany.
Extended bull sperm for artificial insemination is routinely cryopreserved and stored in liquid nitrogen (LN, -196°C) tanks to maintain semen quality for extended periods. Bacterial contamination impairs sperm quality; however, hygienic conditions of LN tanks are monitored insufficiently. This study aimed to assess the hygienic situation in routinely used LN tanks under field conditions.
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