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Vertebrate reproductive science and technology
RESEARCH ARTICLE (Open Access)

Efficiency of the zinc chelator 1,10-phenanthroline for assisted oocyte activation following ICSI in pigs

Olinda Briski A B , Juan P. Cabeza https://orcid.org/0000-0003-4117-2610 A , Daniel F. Salamone https://orcid.org/0000-0003-0858-0313 A B , Rafael Fernández-Martin A B and Andrés Gambini https://orcid.org/0000-0002-3652-2068 C D *
+ Author Affiliations
- Author Affiliations

A Facultad de Agronomía, Universidad de Buenos Aires, Ciudad Autónoma de Buenos Aires, Buenos Aires C1417DSE, Argentina.

B CONICET-Universidad de Buenos Aires, Instituto de Investigaciones en Producción Animal (INPA), Ciudad Autónoma de Buenos Aires, Buenos Aires C1417DSE, Argentina.

C School of Agriculture and Food Sustainability, The University of Queensland, Gatton, Qld 4343, Australia.

D School of Veterinary Sciences, The University of Queensland, Gatton, Qld 4343, Australia.

* Correspondence to: a.gambini@uq.edu.au

Handling Editor: Ye Yuan

Reproduction, Fertility and Development 36, RD24129 https://doi.org/10.1071/RD24129
Submitted: 6 June 2024  Accepted: 21 August 2024  Published online: 13 September 2024

© 2024 The Author(s) (or their employer(s)). Published by CSIRO Publishing. This is an open access article distributed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (CC BY-NC-ND)

Abstract

Context

In vitro embryo production in pigs is an important tool for advancing biomedical research. Intracytoplasmic sperm injection (ICSI) circumvents the polyspermy problems associated with conventional IVF in porcine. However, the suboptimal efficiency for ICSI in pigs requires new strategies to increase blastocyst formation rates.

Aim

To investigate novel methods for assisted activation using the zinc chelator 1,10-phenanthroline (PHEN), and to improve embryo developmental competence and quality of ICSI porcine blastocyst.

Methods

ICSI embryos were treated with PHEN after or before sperm injection, recording pronuclear formation, blastocyst rate and the expression of SMARCA4, OCT4, SOX2 and CDX2.

Key results

Neither electrical nor PHEN significantly improves pronuclear formation rates before or after ICSI. Following in vitro culture to the blastocyst stage, no significant differences were observed in developmental rates among the groups. Moreover, the use of PHEN did not alter the total cell number or the expression of OCT4, SOX2 and CDX2 in pig ICSI blastocysts.

Conclusions

Assisted oocyte activation with PHEN does not affect the preimplantation development of ICSI-derived pig embryos.

Implications

These results hold significance in refining and advancing the application of assisted oocyte activation techniques. They offer insights into addressing fertility issues and propelling advancements in human and animal reproductive medicine.

Keywords: assisted oocyte activation, chelating agent, in vitro breeding, pluripotency, preimplantation embryo development, swine.

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