Brian Tanaka, PhD
Associate Research ScientistCards
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Center for Neuroscience and Regeneration Research
950 Campbell Ave., Bldg 34
West Haven, CT 06516
United States
About
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Associate Research Scientist
Biography
Brian S. Tanaka, PhD is an Associate Research Scientist studying voltage-gated sodium channels as therapeutic targets for pain. His current work centers on sodium channel pharmacology and nociceptor excitability, contributing to efforts developing non-addictive analgesic strategies for chronic pain.
Dr. Tanaka’s work has centered on defining how sodium channel mutations and pharmacological agents shape neuronal excitability in pain and seizure disorders. His doctoral work at the University of California, Irvine established the role of Nav1.6 in seizure resistance, including a collaboration with Allergan applying high-throughput two-electrode voltage-clamp screening to identify sodium channel blockers.
He then completed postdoctoral training with Stephen Waxman, MD, PhD at Yale School of Medicine, where he led electrophysiology efforts characterizing patient-derived iPSC sensory neuron models of pain, and demonstrated patient-specific, mechanism-based efficacy of lacosamide in a rare monogenic pain disorder.
Dr. Tanaka subsequently spent five years as a Research Scientist at Arvinas, where he built multi-electrode array and high-content imaging infrastructure for iPSC and primary neuron assays for target validation and compound screening for Huntington’s and other neurodegenerative diseases. His industry experience connects mechanistic ion channel biology to scalable assay development and therapeutic candidate de-risking, a perspective he now brings to pain drug discovery at Yale.
His research has produced more than 15 peer-reviewed publications in journals including Brain, Nature, The Journal of Physiology, The Journal of Neuroscience, and Neuron, along with numerous national and international conference presentations.
Departments & Organizations
Education & Training
- Associate Research Scientist
- Yale School of Medicine (2020)
- Postdoctoral Associate
- Yale School of Medicine (2019)
- PhD
- University of California, Irvine (2013)
- BS
- University of California, Irvine (2002)
Research
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Overview
Medical Research Interests
ORCID
0000-0002-6678-6478
Research at a Glance
Yale Co-Authors
Publications Timeline
Research Interests
Shujun Liu
Betsy Schulman, PhD
Sulayman Dib-Hajj, PhD
Carolina Gomis Perez, PhD
Mark Estacion, PhD
Matthew Alsaloum, PhD
Publications
2025
Correction of sodium channel mutations in sensory neurons reverses aberrant properties
Shim J, Tanaka B, Taub D, Mis M, Schulman B, Snavely A, Cheng Y, Laedermann C, Buttermore E, Ren A, Hermawan C, Dou D, Kawaguchi R, Geschwind D, Dib-Hajj S, Waxman S, Woolf C. Correction of sodium channel mutations in sensory neurons reverses aberrant properties. Brain 2025, 148: 3718-3726. PMID: 40279376, PMCID: PMC13369953, DOI: 10.1093/brain/awaf155.Peer-Reviewed Original ResearchCitationsAltmetricConceptsGain-of-function mutationsSensory neuronsElectrophysiological propertiesDisease presentationVoltage gated sodium channel Nav1.7Paroxysmal extreme pain disorderSmall fiber neuropathySodium channel Nav1.7Rodent sensory neuronsPain-related disordersCell linesSodium channel mutationsInherited ErythromelalgiaEffects of gain-of-function mutationsFiber neuropathyPain disordersChannel mutationsControl iPSCsPatient samplesG mutationIPSCsIon channelsNeuronsPersonalized medicineNav1.7
2021
Lacosamide Inhibition of NaV1.7 Channels Depends on its Interaction With the Voltage Sensor Domain and the Channel Pore
Labau JIR, Alsaloum M, Estacion M, Tanaka B, Dib-Hajj FB, Lauria G, Smeets HJM, Faber CG, Dib-Hajj S, Waxman SG. Lacosamide Inhibition of NaV1.7 Channels Depends on its Interaction With the Voltage Sensor Domain and the Channel Pore. Frontiers In Pharmacology 2021, 12: 791740. PMID: 34992539, PMCID: PMC8724789, DOI: 10.3389/fphar.2021.791740.Peer-Reviewed Original ResearchCitationsAltmetricKCNQ variants and pain modulation: a missense variant in Kv7.3 contributes to pain resilience
Yuan JH, Estacion M, Mis MA, Tanaka BS, Schulman BR, Chen L, Liu S, Dib-Hajj FB, Dib-Hajj SD, Waxman SG. KCNQ variants and pain modulation: a missense variant in Kv7.3 contributes to pain resilience. Brain Communications 2021, 3: fcab212-. PMID: 34557669, PMCID: PMC8454204, DOI: 10.1093/braincomms/fcab212.Peer-Reviewed Original ResearchCitationsAltmetricConceptsPluripotent stem cell-derived sensory neuronsNav1.7 mutationSensory neuronsPain ProfilePain phenotypesPain resilienceDorsal root ganglion neuronsDaily pain diaryPeripheral sensory neuronsMissense variantsVoltage-clamp recordingsSodium channel Nav1.7Different pain experiencesPotential genetic factorsWhole-exome sequencingLarger M-currentsErythromelalgia patientsNeuropathic painPain episodesModerate painPain diaryPain modulationSevere painInter-individual variabilityGanglion neurons
2020
Pharmacological activity and NMR solution structure of the leech peptide HSTX-I
McMahon KL, Tay B, Deuis JR, Tanaka BS, Peigneur S, Jin AH, Tytgat J, Waxman SG, Dib-Hajj SD, Vetter I, Schroeder CI. Pharmacological activity and NMR solution structure of the leech peptide HSTX-I. Biochemical Pharmacology 2020, 181: 114082. PMID: 32524995, PMCID: PMC8494138, DOI: 10.1016/j.bcp.2020.114082.Peer-Reviewed Original ResearchCitationsAltmetricMeSH Keywords and ConceptsConceptsNMR solution spectroscopyOne-pot oxidationSolution structureLow micromolar activitySolution spectroscopyThree-dimensional solution structureSingle-step purificationMicromolar activityNMR solution structureHydrophobic peptidesIon channel subtypesHigh yieldsPeptide toxinsStep purificationPharmacological activitiesDisulfide bondsTetrodotoxin-resistant isoformsTetrodotoxin-resistant NaPathogenesis of painVoltage-gated sodium channelsNaSubAnalgesic efficacyInflammatory painSpectroscopyDifferential effect of lacosamide on Nav1.7 variants from responsive and non-responsive patients with small fibre neuropathy
Labau J, Estacion M, Tanaka BS, de Greef B, Hoeijmakers J, Geerts M, Gerrits MM, Smeets H, Faber CG, Merkies I, Lauria G, Dib-Hajj SD, Waxman SG. Differential effect of lacosamide on Nav1.7 variants from responsive and non-responsive patients with small fibre neuropathy. Brain 2020, 143: 771-782. PMID: 32011655, PMCID: PMC7089662, DOI: 10.1093/brain/awaa016.Peer-Reviewed Original ResearchCitationsAltmetricMeSH Keywords and ConceptsConceptsSmall fiber neuropathyEffects of lacosamideNon-responsive patientsSubset of patientsCommon pain disordersRecent clinical studiesUse-dependent inhibitionUse-dependent mannerVoltage-clamp recordingsPotent sodium channel inhibitorSlow inactivationSodium channel inhibitorsNeuronal hyperexcitabilityResponsive patientsPain disordersNav1.7 mutationClinical studiesAchievable concentrationsPatientsLacosamideNeuropathyChannel inhibitorsSodium channelsPainFunction mutations
2019
Dexpramipexole blocks Nav1.8 sodium channels and provides analgesia in multiple nociceptive and neuropathic pain models.
Urru M, Muzzi M, Coppi E, Ranieri G, Buonvicino D, Camaioni E, Coppini R, Pugliese AM, Tanaka B, Estacion M, Waxman SG, Dib-Hajj SD, Chiarugi A. Dexpramipexole blocks Nav1.8 sodium channels and provides analgesia in multiple nociceptive and neuropathic pain models. Pain 2019, 161: 831-841. PMID: 31815915, DOI: 10.1097/j.pain.0000000000001774.Peer-Reviewed Original ResearchCitationsMeSH Keywords and ConceptsConceptsDorsal root ganglion neuronsNeuropathic pain modelPain modelGanglion neuronsClinical trialsCultured rat dorsal root ganglion neuronsRat dorsal root ganglion neuronsEffects of dexpramipexoleMouse pain modelsCentral side effectsTreatment of painGood safety profileNav1.8 sodium channelsSodium channel blockersPotent sodium channel blockerSelective targetingNav1.8-null miceSodium conductanceNerve constrictionNeuropathic painPain reductionPeripheral nociceptorsPain indicationsExcellent tolerabilitySafety profileBuilding sensory axons: Delivery and distribution of NaV1.7 channels and effects of inflammatory mediators
Akin EJ, Higerd-Rusli GP, Mis MA, Tanaka BS, Adi T, Liu S, Dib-Hajj FB, Waxman SG, Dib-Hajj SD. Building sensory axons: Delivery and distribution of NaV1.7 channels and effects of inflammatory mediators. Science Advances 2019, 5: eaax4755. PMID: 31681845, PMCID: PMC6810356, DOI: 10.1126/sciadv.aax4755.Peer-Reviewed Original ResearchCitationsAltmetricMeSH Keywords and ConceptsConceptsMicrotubule-dependent vesicular transportSingle-molecule resolutionVesicular traffickingVesicular transportSurface deliveryPlasma membraneMembrane distributionFunctional studiesAxon terminiSodium channel NaLive visualizationSensory axonsVesiclesTraffickingNew insightsChannel NaContribution of NaDisease statesRab6ANav1.7 channelsDorsal root ganglion neuronsTerminusThreefold increaseGanglion neuronsMembraneNaV1.6 regulates excitability of mechanosensitive sensory neurons
Israel MR, Tanaka BS, Castro J, Thongyoo P, Robinson SD, Zhao P, Deuis JR, Craik DJ, Durek T, Brierley SM, Waxman SG, Dib‐Hajj S, Vetter I. NaV1.6 regulates excitability of mechanosensitive sensory neurons. The Journal Of Physiology 2019, 597: 3751-3768. PMID: 31087362, DOI: 10.1113/jp278148.Peer-Reviewed Original ResearchCitationsAltmetricMeSH Keywords and ConceptsConceptsPeripheral sensory neuronsPeripheral nervous systemDorsal root ganglion neuronsSensory neuronsVoltage-gated sodium channelsGanglion neuronsSodium channelsLarge-diameter dorsal root ganglion neuronsTonic action potential firingWhole-cell patch-clamp recordingsMultiple voltage-gated sodium channelsIntra-plantar injectionMechanosensitive sensory neuronsVivo behavioral assessmentsAction potential firingChannel activationPatch-clamp recordingsPotential therapeutic targetMechanical stimuliΒ-scorpion toxinSodium channel isoformsPain pathwaysThermal allodyniaPain generationSensory afferentsRestoration of brain circulation and cellular functions hours post-mortem
Vrselja Z, Daniele SG, Silbereis J, Talpo F, Morozov YM, Sousa AMM, Tanaka BS, Skarica M, Pletikos M, Kaur N, Zhuang ZW, Liu Z, Alkawadri R, Sinusas AJ, Latham SR, Waxman SG, Sestan N. Restoration of brain circulation and cellular functions hours post-mortem. Nature 2019, 568: 336-343. PMID: 30996318, PMCID: PMC6844189, DOI: 10.1038/s41586-019-1099-1.Peer-Reviewed Original ResearchCitationsAltmetricMeSH Keywords and ConceptsConceptsGlial inflammatory responsesMaintenance of microcirculationRestoration of microcirculationSpontaneous synaptic activityPulsatile perfusion systemBrains of humansCerebral metabolismReperfusion injuryElectrocorticographic activityInflammatory responseSynaptic activityNormothermic conditionsBlood flowMammalian brainPrevents edemaPig brainBrainBrain circulationMicrocirculationCell deathLarge mammalian brainsHoursEdemaPost-mortem intervalEchogenic
2018
Resilience to Pain: A Peripheral Component Identified Using Induced Pluripotent Stem Cells and Dynamic Clamp
Mis MA, Yang Y, Tanaka BS, Gomis-Perez C, Liu S, Dib-Hajj F, Adi T, Garcia-Milian R, Schulman BR, Dib-Hajj SD, Waxman SG. Resilience to Pain: A Peripheral Component Identified Using Induced Pluripotent Stem Cells and Dynamic Clamp. Journal Of Neuroscience 2018, 39: 382-392. PMID: 30459225, PMCID: PMC6335750, DOI: 10.1523/jneurosci.2433-18.2018.Peer-Reviewed Original ResearchCitationsAltmetricMeSH Keywords and ConceptsMeSH KeywordsAdultChildChronic PainErythromelalgiaExcitatory Postsynaptic PotentialsExomeFemaleGanglia, SpinalHumansImmunohistochemistryIndividualityInduced Pluripotent Stem CellsKCNQ Potassium ChannelsMaleMembrane PotentialsNAV1.7 Voltage-Gated Sodium ChannelPain MeasurementPatch-Clamp TechniquesResilience, PsychologicalSensory Receptor CellsConceptsWhole-exome sequencingPeripheral sensory neuronsSensory neuronsSpecific gene variantsGene variantsPluripotent stem cell-derived sensory neuronsInterindividual differencesDorsal root ganglion neuronsExome sequencingDifferent pain profilesDRG neuron excitabilityDynamic clampPeripheral nervous systemStem cellsPain ProfilePluripotent stem cellsChronic painPeripheral mechanismsGanglion neuronsNeuron excitabilityPainNervous systemHuman genetic modelsNeuronsDifferent gene variants
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950 Campbell Ave., Bldg 34
West Haven, CT 06516
United States
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