<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Currie J</submitter><funding>NIA NIH HHS</funding><funding>National Institutes of Health</funding><funding>Alzheimer&amp;apos;s Association</funding><pagination>110219</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12940509</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>409</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Study of synaptic integrity using conventional electrophysiology is a gold standard for quantitative assessment of neurodegeneration. Fluorescence assisted single-synapse long-term potentiation (FASS-LTP) provides a high throughput method to assess the synaptic integrity of neurotransmission within and between different brain regions as a measure of pharmacological efficacy in translational models.&lt;h4>New method&lt;/h4>We adapted the existing method to our purpose by adding a step during the thawing of frozen samples, by an extra step of placing them on a rocker at room temperature for 30 minutes immediately following thawing with constant mixing on a shaker. This allowed for gradual, uniform thawing, effectively separating the synaptosomes. Our study demonstrates FASS-LTP </pubmed_abstract><journal>Journal of neuroscience methods</journal><pubmed_title>Using FASS-LTP in postmortem mice brain tissues to assess pathological synaptic function.</pubmed_title><pmcid>PMC12940509</pmcid><funding_grant_id>R01 AG063945</funding_grant_id><funding_grant_id>R21 AG059223</funding_grant_id><funding_grant_id>T32 AG067952</funding_grant_id><pubmed_authors>Budhwani S</pubmed_authors><pubmed_authors>Garza KH</pubmed_authors><pubmed_authors>Mallipudi M</pubmed_authors><pubmed_authors>Sreenivasamurthy SGS</pubmed_authors><pubmed_authors>Natarajan C</pubmed_authors><pubmed_authors>Currie J</pubmed_authors><pubmed_authors>Krishnan B</pubmed_authors></additional><is_claimable>false</is_claimable><name>Using FASS-LTP in postmortem mice brain tissues to assess pathological synaptic function.</name><description>&lt;h4>Background&lt;/h4>Study of synaptic integrity using conventional electrophysiology is a gold standard for quantitative assessment of neurodegeneration. Fluorescence assisted single-synapse long-term potentiation (FASS-LTP) provides a high throughput method to assess the synaptic integrity of neurotransmission within and between different brain regions as a measure of pharmacological efficacy in translational models.&lt;h4>New method&lt;/h4>We adapted the existing method to our purpose by adding a step during the thawing of frozen samples, by an extra step of placing them on a rocker at room temperature for 30 minutes immediately following thawing with constant mixing on a shaker. This allowed for gradual, uniform thawing, effectively separating the synaptosomes. Our study demonstrates FASS-LTP </description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Sep</publication><modification>2026-07-16T21:57:23.047Z</modification><creation>2026-07-11T03:08:31.142Z</creation></dates><accession>S-EPMC12940509</accession><cross_references><pubmed>39013526</pubmed><doi>10.1016/j.jneumeth.2024.110219</doi></cross_references></HashMap>