<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>232(21-22)</volume><submitter>Loomis S</submitter><pubmed_abstract>While treatment options are available, excessive daytime sleepiness (EDS) remains a significant unmet medical need for many patients. Relatively little rodent behavioural pharmacology has been conducted in this context to assess potential pro-vigilant compounds for their ability to restore functional capacity following experimentally induced sleep loss. Male Wistar rats were prepared for electroencephalographic (EEG) recording and subject to 11 h of sleep restriction using a biofeedback-induced cage rotation protocol. A simple response latency task (SRLT) was used to behaviourally index sleep restriction and the effects of pro-vigilant compounds: modafinil, D-amphetamine, caffeine, and the mGlu5-positive allosteric modulator LSN2814617. Sleep restriction resulted in a consistent, quantifie</pubmed_abstract><journal>Psychopharmacology</journal><pagination>3977-89</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4600478</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Distinct pro-vigilant profile induced in rats by the mGluR5 potentiator LSN2814617.</pubmed_title><pmcid>PMC4600478</pmcid><pubmed_authors>Tricklebank M</pubmed_authors><pubmed_authors>Kellett DO</pubmed_authors><pubmed_authors>Loomis S</pubmed_authors><pubmed_authors>Baxter C</pubmed_authors><pubmed_authors>Gilmour G</pubmed_authors><pubmed_authors>McCarthy A</pubmed_authors><pubmed_authors>Edgar DM</pubmed_authors></additional><is_claimable>false</is_claimable><name>Distinct pro-vigilant profile induced in rats by the mGluR5 potentiator LSN2814617.</name><description>While treatment options are available, excessive daytime sleepiness (EDS) remains a significant unmet medical need for many patients. Relatively little rodent behavioural pharmacology has been conducted in this context to assess potential pro-vigilant compounds for their ability to restore functional capacity following experimentally induced sleep loss. Male Wistar rats were prepared for electroencephalographic (EEG) recording and subject to 11 h of sleep restriction using a biofeedback-induced cage rotation protocol. A simple response latency task (SRLT) was used to behaviourally index sleep restriction and the effects of pro-vigilant compounds: modafinil, D-amphetamine, caffeine, and the mGlu5-positive allosteric modulator LSN2814617. Sleep restriction resulted in a consistent, quantifie</description><dates><release>2015-01-01T00:00:00Z</release><publication>2015 Nov</publication><modification>2025-06-01T12:02:19.29Z</modification><creation>2025-06-01T12:02:19.29Z</creation></dates><accession>S-EPMC4600478</accession><cross_references><pubmed>25902875</pubmed><doi>10.1007/s00213-015-3936-8</doi></cross_references></HashMap>