<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Santos RP</submitter><funding>Coordenação de Aperfeicoamento de Pessoal de Nível Superior</funding><funding>National Council for the Scientific Development</funding><funding>Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (Coordination for the Improvement of Higher Education Personnel) (CAPES) Brazil</funding><funding>National Council for Scientific and Technological Development</funding><pagination>934</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10967266</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>14(6)</volume><pubmed_abstract>We verified the possibility of cooling peccary semen for 4, 24, and 48 h before cryopreservation, using different dilution media (TRIS + egg yolk (20%) and PRIMXcell Ultra). Ten ejaculates were divided equally into six aliquots and then diluted. Two aliquots were stored in a biological incubator (4 h), and the remaining aliquots were stored in a commercial container, the Botutainer&lt;sup>®&lt;/sup> (24 and 48 h), both at 5 °C. The samples were cryopreserved and then evaluated for kinetic parameters, functionality, integrity, mitochondrial activity, morphology, and sperm binding capacity. After thawing, samples diluted in TRIS showed total motility of 43.4 ± 6.8%, 48.4 ± 6.2%, and 38.6 ± 5.0% after cooling for 4, 24, and 48 h before cryopreservation, respectively. Such results are significantly greater than those achieved with the use of PRIMXcell diluent for 4 (8.3 ± 2.8%), 24 (4.7 ± 1.4%), and 48 h (4.8 ± 2.9%) storage (&lt;i>p&lt;/i> &lt; 0.05). Furthermore, TRIS provided better preservation of sperm membrane integrity when samples were cooled for 24 h (44.5 ± 4.7%) before cryopreservation compared to those samples diluted in PRIMXcell Ultra stored for 24 (25.7 ± 4.0%) and 48 h (25.2 ± 4.0%) before freezing (&lt;i>p&lt;/i> &lt; 0.05). In summary, we suggest TRIS diluent + egg yolk (20%) as an effective option to allow semen to cool for 24 or 48 h in a transport container before cryopreservation.</pubmed_abstract><journal>Animals : an open access journal from MDPI</journal><pubmed_title>Effect of Diluents and Storage Time on the Cryopreservation of Collared Peccary (&lt;i>Pecari tajacu&lt;/i>) Semen after Cooling Storage in a Transport Container at 5 °C.</pubmed_title><pmcid>PMC10967266</pmcid><funding_grant_id>001</funding_grant_id><funding_grant_id>Financial Code 001</funding_grant_id><funding_grant_id>306409/2022-4</funding_grant_id><pubmed_authors>Matos YG</pubmed_authors><pubmed_authors>Dantas LL</pubmed_authors><pubmed_authors>Bezerra GSC</pubmed_authors><pubmed_authors>Santos RP</pubmed_authors><pubmed_authors>Silva AR</pubmed_authors><pubmed_authors>Pereira AG</pubmed_authors><pubmed_authors>Cavalcante YCS</pubmed_authors><pubmed_authors>Silva AM</pubmed_authors></additional><is_claimable>false</is_claimable><name>Effect of Diluents and Storage Time on the Cryopreservation of Collared Peccary (&lt;i>Pecari tajacu&lt;/i>) Semen after Cooling Storage in a Transport Container at 5 °C.</name><description>We verified the possibility of cooling peccary semen for 4, 24, and 48 h before cryopreservation, using different dilution media (TRIS + egg yolk (20%) and PRIMXcell Ultra). Ten ejaculates were divided equally into six aliquots and then diluted. Two aliquots were stored in a biological incubator (4 h), and the remaining aliquots were stored in a commercial container, the Botutainer&lt;sup>®&lt;/sup> (24 and 48 h), both at 5 °C. The samples were cryopreserved and then evaluated for kinetic parameters, functionality, integrity, mitochondrial activity, morphology, and sperm binding capacity. After thawing, samples diluted in TRIS showed total motility of 43.4 ± 6.8%, 48.4 ± 6.2%, and 38.6 ± 5.0% after cooling for 4, 24, and 48 h before cryopreservation, respectively. Such results are significantly greater than those achieved with the use of PRIMXcell diluent for 4 (8.3 ± 2.8%), 24 (4.7 ± 1.4%), and 48 h (4.8 ± 2.9%) storage (&lt;i>p&lt;/i> &lt; 0.05). Furthermore, TRIS provided better preservation of sperm membrane integrity when samples were cooled for 24 h (44.5 ± 4.7%) before cryopreservation compared to those samples diluted in PRIMXcell Ultra stored for 24 (25.7 ± 4.0%) and 48 h (25.2 ± 4.0%) before freezing (&lt;i>p&lt;/i> &lt; 0.05). In summary, we suggest TRIS diluent + egg yolk (20%) as an effective option to allow semen to cool for 24 or 48 h in a transport container before cryopreservation.</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Mar</publication><modification>2025-04-21T21:31:39.375Z</modification><creation>2025-04-05T18:21:43.564Z</creation></dates><accession>S-EPMC10967266</accession><cross_references><pubmed>38540032</pubmed><doi>10.3390/ani14060934</doi></cross_references></HashMap>