<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Rossano S</submitter><funding>NCRR NIH HHS</funding><funding>NHLBI NIH HHS</funding><funding>Foundation for the National Institutes of Health</funding><funding>NIMH NIH HHS</funding><funding>NIH HHS</funding><pagination>3679-3691</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9826644</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>49(11)</volume><pubmed_abstract>&lt;h4>Purpose&lt;/h4>Exploring synaptic density changes during brain growth is crucial to understanding brain development. Previous studies in nonhuman primates report a rapid increase in synapse number between the late gestational period and the early neonatal period, such that synaptic density approaches adult levels by birth. Prenatal synaptic development may have an enduring impact on postnatal brain development, but precisely how synaptic density changes in utero are unknown because current methods to quantify synaptic density are invasive and require post-mortem brain tissue.&lt;h4>Methods&lt;/h4>We used synaptic vesicle glycoprotein 2A (SV2A) positron emission tomography (PET) radioligands [&lt;sup>11&lt;/sup>C]UCB-J and [&lt;sup>18&lt;/sup>F]Syn-VesT-1 to conduct the first assessment of synaptic density </pubmed_abstract><journal>European journal of nuclear medicine and molecular imaging</journal><pubmed_title>Imaging the fetal nonhuman primate brain with SV2A positron emission tomography (PET).</pubmed_title><pmcid>PMC9826644</pmcid><funding_grant_id>S10 OD016261</funding_grant_id><funding_grant_id>U42 OD027094</funding_grant_id><funding_grant_id>R24 HL085794</funding_grant_id><funding_grant_id>S10 RR025063</funding_grant_id><funding_grant_id>R21 MH120615</funding_grant_id><funding_grant_id>P51 OD011107</funding_grant_id><funding_grant_id>S10 RR029245</funding_grant_id><pubmed_authors>Kukis D</pubmed_authors><pubmed_authors>Tarantal AF</pubmed_authors><pubmed_authors>Benveniste H</pubmed_authors><pubmed_authors>Lorence I</pubmed_authors><pubmed_authors>Ye Y</pubmed_authors><pubmed_authors>Fowles K</pubmed_authors><pubmed_authors>Toyonaga T</pubmed_authors><pubmed_authors>Ropchan J</pubmed_authors><pubmed_authors>Felchner Z</pubmed_authors><pubmed_authors>Li S</pubmed_authors><pubmed_authors>Huang Y</pubmed_authors><pubmed_authors>Nabulsi N</pubmed_authors><pubmed_authors>Groman S</pubmed_authors><pubmed_authors>Carson RE</pubmed_authors><pubmed_authors>Berg E</pubmed_authors><pubmed_authors>Rossano S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Imaging the fetal nonhuman primate brain with SV2A positron emission tomography (PET).</name><description>&lt;h4>Purpose&lt;/h4>Exploring synaptic density changes during brain growth is crucial to understanding brain development. Previous studies in nonhuman primates report a rapid increase in synapse number between the late gestational period and the early neonatal period, such that synaptic density approaches adult levels by birth. Prenatal synaptic development may have an enduring impact on postnatal brain development, but precisely how synaptic density changes in utero are unknown because current methods to quantify synaptic density are invasive and require post-mortem brain tissue.&lt;h4>Methods&lt;/h4>We used synaptic vesicle glycoprotein 2A (SV2A) positron emission tomography (PET) radioligands [&lt;sup>11&lt;/sup>C]UCB-J and [&lt;sup>18&lt;/sup>F]Syn-VesT-1 to conduct the first assessment of synaptic density </description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Sep</publication><modification>2025-04-05T10:27:06.328Z</modification><creation>2025-04-05T10:27:06.328Z</creation></dates><accession>S-EPMC9826644</accession><cross_references><pubmed>35633376</pubmed><doi>10.1007/s00259-022-05825-6</doi></cross_references></HashMap>