Evidence map›Paper›PMID 40671822›Full record

ArticleFrontiers in veterinary science2025

Characterization of the vitrification parameters for oviduct aggregates in

Mohamed M M El-Sokary, Hamad A Albreiki, Seham F Shehata, Karima Gh M Mahmoud

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Article in Frontiers in veterinary science, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Mohamed M M El-SokaryDepartment of Theriogenology, Faculty of Veterinary Medicine, Benha University, Benha, Egypt.
Hamad A AlbreikiFaculty of Health Sciences, Higher Colleges of Technology, Abu Dhabi, United Arab Emirates.
Seham F ShehataDepartment of Animal Wealth Development, Faculty of Veterinary Medicine, Benha University, Benha, Egypt.
Karima Gh M MahmoudDepartment of Animal Reproduction and Artificial Insemination, Veterinary Research Institute, National Research Centre, Giza, Egypt.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Camel oviductal isthmus aggregates provide a novel and promising model for studying sperm attachment and longevity, offering a potential alternative for short-to mid-term sperm preservation and transport under non-cryogenic conditions. Effective cryopreservation of the aggregates for later use can contribute to addressing challenges associated with camel semen preservation by potentially extending sperm lifespan and facilitating semen transport to remote areas without cryogenic facilities. Challenges in preserving the structural integrity and viability of camel oviductal aggregates remain a key critical gap during cryopreservation. This study evaluated the efficiency of vitrification protocols for camel oviductal isthmus aggregates, focusing on the effects of aggregate size, cryoprotectants (CPA), cryodevices, post-thaw viability, and sperm-binding capacity. Methods: Aggregates retrieved from the oviductal isthmus were classified into four size groups (50, 100, 150, and 200 μm) and vitrified to determine the influence of size on post-thaw outcomes. CPA concentrations (3, 5, and 7 M) of DMSO and EG in a 1:1 ratio were tested for their impact on structural integrity and viability. The performance of cryodevices, including cryovials, 0.5 mL straws, and 0.25 mL straws, was also assessed. Results and discussion: The results indicated that aggregates sized 150 μm and 200 μm demonstrated superior post-thaw viability, with intactness rates of 78 ± 2.0% and 83 ± 2.8%, respectively. Among the tested CPA concentrations, 7 M showed the highest post-vitrification viability (69 ± 1.9%). Additionally, 0.25 mL straw cryodevice achieved significantly better post-thaw viability (67 ± 2.7%) compared to 0.5 mL straws (32 ± 2.1%) and cryovials (10 ± 1.1%). Regarding sperm-binding capacity post-thaw, aggregates treated with 5 M (69 sperm) and 7 M (74) CPAs showed the highest binding rates, with no significant difference between these concentrations. Further studies are required to optimize vitrification protocols to enhance the aggregate's post-vitrification viability and structural integrity.

Indexed as

camelcryodevicecryoprotectantisthmusreproductive biotechnology

Identifiers

PMID40671822
PMCPMC12263357

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.