2017
The stochastic nature of action potential backpropagation in apical tuft dendrites
Short SM, Oikonomou KD, Zhou WL, Acker CD, Popovic MA, Zecevic D, Antic SD. The stochastic nature of action potential backpropagation in apical tuft dendrites. Journal Of Neurophysiology 2017, 118: 1394-1414. PMID: 28566465, PMCID: PMC5558024, DOI: 10.1152/jn.00800.2016.Peer-Reviewed Original ResearchConceptsDendritic CaPyramidal neuronsApical tuftCortical pyramidal neuronsAction potential backpropagationRat brain slicesSpontaneous synaptic inputsDifferent cortical layersVoltage-gated CaAP backpropagationAP burstsGlutamate iontophoresisSynaptic contactsSomatic APsApical trunkAP frequencyBrain slicesDendritic physiologySynaptic inputsCortical layersChannel inactivationLocal NaNeuronsSpike-timing dependent plasticityTrials
2015
Acetylcholine Acts through Nicotinic Receptors to Enhance the Firing Rate of a Subset of Hypocretin Neurons in the Mouse Hypothalamus through Distinct Presynaptic and Postsynaptic Mechanisms1,2
Zhou WL, Gao XB, Picciotto MR. Acetylcholine Acts through Nicotinic Receptors to Enhance the Firing Rate of a Subset of Hypocretin Neurons in the Mouse Hypothalamus through Distinct Presynaptic and Postsynaptic Mechanisms1,2. ENeuro 2015, 2: eneuro.0052-14.2015. PMID: 26322330, PMCID: PMC4551500, DOI: 10.1523/eneuro.0052-14.2015.Peer-Reviewed Original ResearchHypocretin neuronsMiniature EPSCsPostsynaptic nAChRsFiring rateHypocretin/orexin neuronsFrequency of mEPSCsAntagonism of nAChRsPhasic ACh releasePresence of atropineApplication of AChInternal calcium releaseNicotinic acetylcholine receptorsMouse brain slicesOne-thirdAddiction-related behaviorsPresynaptic AChPresynaptic nAChRsOrexin neuronsACh releaseGlutamatergic inputsPostsynaptic modulationPostsynaptic mechanismsMEPSC frequencyTonic activationBrain slices
2012
Physiological Properties of Human Fetal Cortex In Vitro
Moore A, Zhou W, Jakovcevski I, Zecevic N, Antic S. Physiological Properties of Human Fetal Cortex In Vitro. Neuromethods 2012, 73: 125-158. DOI: 10.1007/978-1-62703-020-5_3.Peer-Reviewed Original ResearchHuman fetal tissuesAnimal modelsWhole-cell patch-clamp recordingsFetal tissuesBrain developmentHuman cortical neuronsElectrical activityHuman fetal cortexAcute brain slicesSpontaneous electrical activityHuman cerebral cortexPatch-clamp recordingsNeuronal membrane excitabilityHuman cortical developmentNormal brain developmentEvolutionary changeBiophysical membrane propertiesCellular divisionCerebral cortexFetal cortexCortical neuronsBrain slicesCortical developmentPsychiatric diseasesFunctional maturation
2010
Brief dopaminergic stimulations produce transient physiological changes in prefrontal pyramidal neurons
Moore A, Zhou W, Potapenko E, Kim E, Antic S. Brief dopaminergic stimulations produce transient physiological changes in prefrontal pyramidal neurons. Brain Research 2010, 1370: 1-15. PMID: 21059342, PMCID: PMC3019254, DOI: 10.1016/j.brainres.2010.10.111.Peer-Reviewed Original ResearchConceptsPyramidal neuronsMidbrain dopaminergic neuronsPrefrontal cortexDopaminergic neuronsLayer 5 pyramidal neuronsRat medial prefrontal cortexAction potential firing ratePFC pyramidal neuronsPrefrontal pyramidal neuronsD1-like receptorsDirect synaptic contactsAction potential firingMedial prefrontal cortexDose-dependent responseDopaminergic stimulationIontophoretic pulsesCortical excitabilitySynaptic contactsDopaminergic agonistsSevere depressionPyramidal cellsTransient physiological changesBrain slicesAction potentialsCell bodies