Bruce Bean

Bruce Palmer Bean, PhD

Robert Winthrop Professor of Neurobiology

Neuronal Excitability and Ion Channel Pharmacology

Neurons communicate with each other using electrical impulses. Information is encoded as patterns of “action potentials”, millisecond-long reversals of the voltage across the cell membrane. Different neurons in the brain fire action potentials with a variety of distinct patterns. The Bean lab seeks to understand these different patterns of firing in terms of the underlying molecular devices – tiny pores in the membrane known as ion channels.

In mammalian brains, each neuron possesses several dozen different types of ion channels. Most of these are closed when the neuron is at rest (electrically silent). It is the coordinated, transient opening, or “gating” of particular types of ion channels that underlies electrical signaling. To understand how different combinations of ion channels work together to generate the distinct patterns of action potential firing in different neurons, we make electrical recordings of these cells using patch clamp, voltage clamp and other electrophysiological approaches.

Our goal is to use knowledge of the particular ion channels in different kinds of neurons to find new drugs that can selectively inhibit or enhance electrical activity of specific type of neurons by targeting specific ion channels. In collaboration with Dr. Clifford Woolf’s laboratory, we are currently focused on finding new drugs to treat pain, itch, and cough. We are also seeking to identify new drugs to disrupt epileptic activity.

Publications View
Sidedness of carbamazepine accessibility to voltage-gated sodium channels.
Authors: Authors: Jo S, Bean BP.
Mol Pharmacol
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Bupivacaine-induced cellular entry of QX-314 and its contribution to differential nerve block.
Authors: Authors: Brenneis C, Kistner K, Puopolo M, Jo S, Roberson D, Sisignano M, Segal D, Cobos EJ, Wainger BJ, Labocha S, Ferreirós N, von Hehn C, Tran J, Geisslinger G, Reeh PW, Bean BP, Woolf CJ.
Br J Pharmacol
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Persistent sodium current drives conditional pacemaking in CA1 pyramidal neurons under muscarinic stimulation.
Authors: Authors: Yamada-Hanff J, Bean BP.
J Neurosci
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Activity-dependent silencing reveals functionally distinct itch-generating sensory neurons.
Authors: Authors: Roberson DP, Gudes S, Sprague JM, Patoski HA, Robson VK, Blasl F, Duan B, Oh SB, Bean BP, Ma Q, Binshtok AM, Woolf CJ.
Nat Neurosci
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Permeation and block of TRPV1 channels by the cationic lidocaine derivative QX-314.
Authors: Authors: Puopolo M, Binshtok AM, Yao GL, Oh SB, Woolf CJ, Bean BP.
J Neurophysiol
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Phenotyping the function of TRPV1-expressing sensory neurons by targeted axonal silencing.
Authors: Authors: Brenneis C, Kistner K, Puopolo M, Segal D, Roberson D, Sisignano M, Labocha S, Ferreirós N, Strominger A, Cobos EJ, Ghasemlou N, Geisslinger G, Reeh PW, Bean BP, Woolf CJ.
J Neurosci
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Transient sodium current at subthreshold voltages: activation by EPSP waveforms.
Authors: Authors: Carter BC, Giessel AJ, Sabatini BL, Bean BP.
Neuron
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Modulation of neuronal sodium channels by the sea anemone peptide BDS-I.
Authors: Authors: Liu P, Jo S, Bean BP.
J Neurophysiol
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Rapid and efficient generation of functional motor neurons from human pluripotent stem cells using gene delivered transcription factor codes.
Authors: Authors: Hester ME, Murtha MJ, Song S, Rao M, Miranda CJ, Meyer K, Tian J, Boulting G, Schaffer DV, Zhu MX, Pfaff SL, Gage FH, Kaspar BK.
Mol Ther
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Targeting of sodium channel blockers into nociceptors to produce long-duration analgesia: a systematic study and review.
Authors: Authors: Roberson DP, Binshtok AM, Blasl F, Bean BP, Woolf CJ.
Br J Pharmacol
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