<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Sanchez-Cardenas C</submitter><funding>Eunice Kennedy Shriver National Institute of Child Health and Human Development</funding><funding>Consejo Nacional de Ciencia y Tecnología</funding><funding>NICHD NIH HHS</funding><pagination>e21528</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8441833</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>35(4)</volume><pubmed_abstract>We have recently reported two different methodologies that improve sperm functionality. The first method involved transient exposure to the Ca&lt;sup>2+&lt;/sup> ionophore A&lt;sub>23187&lt;/sub> , and the second required sperm incubation in the absence of energy nutrients (starvation). Both methods were associated with an initial loss of motility followed by a rescue step involving ionophore removal or addition of energy metabolites, respectively. In this work, we show that starvation is accompanied by an increase in intracellular Ca&lt;sup>2+&lt;/sup> ([Ca&lt;sup>2+&lt;/sup> ]&lt;sub>i&lt;/sub> ). Additionally, the starved cells acquire a significantly enhanced capacity to undergo a progesterone-induced acrosome reaction. Electrophysiological measurements show that CatSper channel remains active in starvation conditi</pubmed_abstract><journal>FASEB journal : official publication of the Federation of American Societies for Experimental Biology</journal><pubmed_title>Starvation induces an increase in intracellular calcium and potentiates the progesterone-induced mouse sperm acrosome reaction.</pubmed_title><pmcid>PMC8441833</pmcid><funding_grant_id>R01 HD088571</funding_grant_id><funding_grant_id>HD‐038082, HD‐088571</funding_grant_id><funding_grant_id>314839 and Fronteras 71</funding_grant_id><funding_grant_id>R01 HD038082</funding_grant_id><pubmed_authors>Darszon A</pubmed_authors><pubmed_authors>Sanchez-Cardenas C</pubmed_authors><pubmed_authors>De la Vega-Beltran JL</pubmed_authors><pubmed_authors>Hernandez-Cruz A</pubmed_authors><pubmed_authors>Martin-Hidalgo D</pubmed_authors><pubmed_authors>Orta G</pubmed_authors><pubmed_authors>Romarowski A</pubmed_authors><pubmed_authors>Visconti PE</pubmed_authors></additional><is_claimable>false</is_claimable><name>Starvation induces an increase in intracellular calcium and potentiates the progesterone-induced mouse sperm acrosome reaction.</name><description>We have recently reported two different methodologies that improve sperm functionality. The first method involved transient exposure to the Ca&lt;sup>2+&lt;/sup> ionophore A&lt;sub>23187&lt;/sub> , and the second required sperm incubation in the absence of energy nutrients (starvation). Both methods were associated with an initial loss of motility followed by a rescue step involving ionophore removal or addition of energy metabolites, respectively. In this work, we show that starvation is accompanied by an increase in intracellular Ca&lt;sup>2+&lt;/sup> ([Ca&lt;sup>2+&lt;/sup> ]&lt;sub>i&lt;/sub> ). Additionally, the starved cells acquire a significantly enhanced capacity to undergo a progesterone-induced acrosome reaction. Electrophysiological measurements show that CatSper channel remains active in starvation conditi</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Apr</publication><modification>2025-04-22T09:20:25.792Z</modification><creation>2025-04-05T22:59:28.423Z</creation></dates><accession>S-EPMC8441833</accession><cross_references><pubmed>33742713</pubmed><doi>10.1096/fj.202100122R</doi><doi>10.1096/fj.202100122r</doi></cross_references></HashMap>