<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Momozawa K</submitter><funding>The Japan Society for Reproductive Medicine</funding><pagination>365-371</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7542018</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>19(4)</volume><pubmed_abstract>&lt;h4>Purpose&lt;/h4>In the present study, I evaluated the usefulness of Medium RD, with mixed RPMI1640 and Dulbecco's modified Eagle's medium (1:1, v/v), as a chemically defined medium for in vitro maturation (IVM) of bovine oocytes.&lt;h4>Methods&lt;/h4>In vitro maturation was performed in 10 mmol/L HEPES-buffered TCM199 (mTCM199), 10 mmol/L HEPES-buffered Medium RD (mRD), and mTCM199 supplemented with fetal bovine serum fraction (mTCM199 + FBS fraction) that served as control. Cumulus-oocyte complexes were matured for 24 hours in three different media supplemented with follicle-stimulating hormone, estradiol-17β, and polyvinylpyrrolidone. Nuclear maturation of oocytes, their developmental competence into blastocysts after in vitro fertilization (IVF) and mitochondrial distribution in oocytes were investigated.&lt;h4>Results&lt;/h4>There was no difference in the ratio of matured oocytes regardless of IVM media. The percentage of morula stage was higher in mRD than in mTCM199 group (&lt;i>P&lt;/i> &lt; .05) at 120-144 hours after IVF, although the blastocyst rates between groups were not significantly different at 168-216 hours. IVM in mRD increased the percentage of oocytes with diffused mitochondrial distribution compared with the immature and mTCM199 and had similar percentage of oocytes in mTCM199 + FBS fraction.&lt;h4>Conclusions&lt;/h4>Medium RD would be useful as a chemically defined medium for IVM of bovine oocytes.</pubmed_abstract><journal>Reproductive medicine and biology</journal><pubmed_title>Usefulness of modified Medium RD as a chemically defined medium for in vitro maturation of bovine oocytes.</pubmed_title><pmcid>PMC7542018</pmcid><funding_grant_id>RMB01</funding_grant_id><pubmed_authors>Momozawa K</pubmed_authors></additional><is_claimable>false</is_claimable><name>Usefulness of modified Medium RD as a chemically defined medium for in vitro maturation of bovine oocytes.</name><description>&lt;h4>Purpose&lt;/h4>In the present study, I evaluated the usefulness of Medium RD, with mixed RPMI1640 and Dulbecco's modified Eagle's medium (1:1, v/v), as a chemically defined medium for in vitro maturation (IVM) of bovine oocytes.&lt;h4>Methods&lt;/h4>In vitro maturation was performed in 10 mmol/L HEPES-buffered TCM199 (mTCM199), 10 mmol/L HEPES-buffered Medium RD (mRD), and mTCM199 supplemented with fetal bovine serum fraction (mTCM199 + FBS fraction) that served as control. Cumulus-oocyte complexes were matured for 24 hours in three different media supplemented with follicle-stimulating hormone, estradiol-17β, and polyvinylpyrrolidone. Nuclear maturation of oocytes, their developmental competence into blastocysts after in vitro fertilization (IVF) and mitochondrial distribution in oocytes were investigated.&lt;h4>Results&lt;/h4>There was no difference in the ratio of matured oocytes regardless of IVM media. The percentage of morula stage was higher in mRD than in mTCM199 group (&lt;i>P&lt;/i> &lt; .05) at 120-144 hours after IVF, although the blastocyst rates between groups were not significantly different at 168-216 hours. IVM in mRD increased the percentage of oocytes with diffused mitochondrial distribution compared with the immature and mTCM199 and had similar percentage of oocytes in mTCM199 + FBS fraction.&lt;h4>Conclusions&lt;/h4>Medium RD would be useful as a chemically defined medium for IVM of bovine oocytes.</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Oct</publication><modification>2025-04-06T19:30:18.644Z</modification><creation>2025-04-06T19:30:18.644Z</creation></dates><accession>S-EPMC7542018</accession><cross_references><pubmed>33071638</pubmed><doi>10.1002/rmb2.12337</doi></cross_references></HashMap>