2022
Muscarinic antagonists impair multiple aspects of operant discrimination learning and performance
Yousuf H, Girardi E, Crouse R, Picciotto M. Muscarinic antagonists impair multiple aspects of operant discrimination learning and performance. Neuroscience Letters 2022, 794: 137025. PMID: 36529388, PMCID: PMC9812939, DOI: 10.1016/j.neulet.2022.137025.Peer-Reviewed Original ResearchConceptsOperant discriminationOperant discrimination learningCue-reward associationsLong-term memoryMultiple training sessionsPost-session injectionsCue associationsReward-related respondingMemory processesDiscrimination learningMaladaptive formsImpaired consolidationFood rewardSuccessful learningNose pokesDifferent learningPre-session injectionsTraining sessionsRewardTaskMemoryLearningMultiple aspectsEnvironmental cuesMuscarinic acetylcholine receptor family
2019
The role of acetylcholine in negative encoding bias: Too much of a good thing?
Mineur YS, Picciotto MR. The role of acetylcholine in negative encoding bias: Too much of a good thing? European Journal Of Neuroscience 2019, 53: 114-125. PMID: 31821620, PMCID: PMC7282966, DOI: 10.1111/ejn.14641.Peer-Reviewed Original ResearchConceptsPotential neural pathwaysSymptoms of anxietyAffective processesSustained attentionStressful eventsCore symptomsFacilitate learningAppropriate learningNeural pathwaysRole of acetylcholineGood thingLevels of AChLearningDepressionBiasDepressive episodeNeuromodulatory roleCholinergic signalingAnimal studiesAnxietyMemoryAcetylcholine SignalingHigh levelsEncodingACh
2016
CaMKII Phosphorylation of TARPγ-8 Is a Mediator of LTP and Learning and Memory
Park J, Chávez AE, Mineur YS, Morimoto-Tomita M, Lutzu S, Kim KS, Picciotto MR, Castillo PE, Tomita S. CaMKII Phosphorylation of TARPγ-8 Is a Mediator of LTP and Learning and Memory. Neuron 2016, 92: 75-83. PMID: 27667007, PMCID: PMC5059846, DOI: 10.1016/j.neuron.2016.09.002.Peer-Reviewed Original ResearchConceptsCaMKII phosphorylation siteCaMKII substratePhosphorylation sitesDependent protein kinase IIProtein kinase IIReceptor-dependent activationNMDA receptor-dependent activationProtein phosphorylationAMPAR-mediated transmissionKinase IICaMKII-dependent enhancementLong-term potentiationCaMKII phosphorylationCellular mechanismsPhosphorylationMolecular targetsAMPA receptorsCrucial mediatorSynaptic plasticityMemory formationSynaptic insertionEssential stepSynaptic transmissionActivity-dependent strengtheningBasal transmission
2011
Striatal‐enriched protein tyrosine phosphatase (STEP) knockout mice have enhanced hippocampal memory
Venkitaramani DV, Moura PJ, Picciotto MR, Lombroso PJ. Striatal‐enriched protein tyrosine phosphatase (STEP) knockout mice have enhanced hippocampal memory. European Journal Of Neuroscience 2011, 33: 2288-2298. PMID: 21501258, PMCID: PMC3118976, DOI: 10.1111/j.1460-9568.2011.07687.x.Peer-Reviewed Original ResearchMeSH KeywordsAnimalsBehavior, AnimalFocal Adhesion Kinase 2HippocampusMemoryMiceMice, Inbred C57BLMice, KnockoutMitogen-Activated Protein Kinase 1Mitogen-Activated Protein Kinase 3PhosphorylationProtein Tyrosine Phosphatases, Non-ReceptorReceptors, AMPAReceptors, N-Methyl-D-AspartateSynaptic TransmissionConceptsStriatal-enriched protein tyrosine phosphataseSTEP KO miceProtein tyrosine phosphataseBrain-specific phosphataseProline-rich tyrosine kinaseEffect of deletionN-methyl-D-aspartate receptorsERK1/2 substratesNR1/NR2B N‐Methyl‐d‐Aspartate ReceptorsPotential molecular mechanismsTyrosine phosphataseSignaling proteinsTyrosine phosphorylationDownstream effectorsKinase 1/2Molecular mechanismsTyrosine kinaseFunctional importanceKnockout micePhosphorylationSTEP knockout miceSynaptic strengtheningIsoxazole propionic acid (AMPA) receptorsSynaptosomal expressionRegulation
2001
Neuronal nicotinic acetylcholine receptor subunit knockout mice: physiological and behavioral phenotypes and possible clinical implications
Picciotto M, Caldarone B, Brunzell D, Zachariou V, Stevens T, King S. Neuronal nicotinic acetylcholine receptor subunit knockout mice: physiological and behavioral phenotypes and possible clinical implications. Pharmacology & Therapeutics 2001, 92: 89-108. PMID: 11916531, DOI: 10.1016/s0163-7258(01)00161-9.Peer-Reviewed Reviews, Practice Guidelines, Standards, and Consensus StatementsConceptsSignal transduction pathwaysHomologous recombinationTransduction pathwaysGenetic manipulationMolecular basisBehavioral phenotypesInactivation of nAChRsNicotinic acetylcholine receptorsSubunit compositionSubunitsNeuronal nicotinic receptorsPersistent activationNeurotransmitter releaseRelevant mutationsModel systemPossible clinical implicationsPhysiological propertiesAcetylcholine receptorsPhenotypeAutonomic gangliaNicotinic receptorsDisease statesDrug developmentPharmacological actionsNAChRs
2000
Brain Localization and Behavioral Impact of the G-Protein-Gated K+ Channel Subunit GIRK4
Wickman K, Karschin C, Karschin A, Picciotto M, Clapham D. Brain Localization and Behavioral Impact of the G-Protein-Gated K+ Channel Subunit GIRK4. Journal Of Neuroscience 2000, 20: 5608-5615. PMID: 10908597, PMCID: PMC6772558, DOI: 10.1523/jneurosci.20-15-05608.2000.Peer-Reviewed Original ResearchMeSH KeywordsAnimalsAvoidance LearningBehavior, AnimalBrain ChemistryChick EmbryoFemaleG Protein-Coupled Inwardly-Rectifying Potassium ChannelsGene ExpressionIn Situ HybridizationIon Channel GatingLocomotionMaleMaze LearningMemoryMiceMice, Inbred C57BLMice, KnockoutPotassium ChannelsPotassium Channels, Inwardly RectifyingRNA, MessengerConceptsGIRK4 mRNAG-protein-gated potassium (GIRK) channelsCortical pyramidal neuronsVentromedial hypothalamic nucleusParaventricular thalamic nucleusMorris water mazeG-Protein-GatedPassive avoidance paradigmMammalian nervous systemWild-type controlsEndopiriform nucleusPyramidal neuronsGlobus pallidusSynaptic inhibitionBrainstem nucleiHypothalamic nucleiPain perceptionThalamic nucleiInsular cortexNervous systemNeuronal populationsWater mazeLocomotor activityMouse brainGIRK subunits