TRPV1 in GABAergic Interneurons Mediates Neuropathic Mechanical Allodynia and Disinhibition of the Nociceptive Circuitry in the Spinal Cord

Yong Ho Kim, Seung Keun Back, Alexander J. Davies, Heejin Jeong, Hyun Jung Jo, Geehoon Chung, Heung Sik Na, Yong Chul Bae, Sangjeong Kim, Joong Soo Kim, Sung Jun Jung, Seog Bae Oh

Research output: Contribution to journalArticle

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Abstract

Neuropathic pain and allodynia may arise from sensitization of central circuits. We report a mechanism of disinhibition-based central sensitization resulting from long-term depression (LTD) of GABAergic interneurons as a consequence of TRPV1 activation in the spinal cord. Intrathecal administration of TRPV1 agonists led to mechanical allodynia that was not dependent on peripheral TRPV1 neurons. TRPV1 was functionally expressed in GABAergic spinal interneurons and activation of spinal TRPV1 resulted in LTD of excitatory inputs and a reduction of inhibitory signaling to spinothalamic tract (STT) projection neurons. Mechanical hypersensitivity after peripheral nerve injury was attenuated in TRPV1-/- mice but not in mice lacking TRPV1-expressing peripheral neurons. Mechanical pain was reversed by a spinally applied TRPV1 antagonist while avoiding the hyperthermic side effect of systemic treatment. Our results demonstrate that spinal TRPV1 plays a critical role as a synaptic regulator and suggest the utility of central nervous system-specific TRPV1 antagonists for treating neuropathic pain.

Original languageEnglish
Pages (from-to)640-647
Number of pages8
JournalNeuron
Volume74
Issue number4
DOIs
StatePublished - 24 May 2012

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Hyperalgesia
Interneurons
Central Nervous System Sensitization
Spinal Cord
Neuralgia
Neurons
Spinothalamic Tracts
Peripheral Nerve Injuries
Hypersensitivity
Central Nervous System
Pain
Therapeutics

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Kim, Yong Ho ; Back, Seung Keun ; Davies, Alexander J. ; Jeong, Heejin ; Jo, Hyun Jung ; Chung, Geehoon ; Na, Heung Sik ; Bae, Yong Chul ; Kim, Sangjeong ; Kim, Joong Soo ; Jung, Sung Jun ; Oh, Seog Bae. / TRPV1 in GABAergic Interneurons Mediates Neuropathic Mechanical Allodynia and Disinhibition of the Nociceptive Circuitry in the Spinal Cord. In: Neuron. 2012 ; Vol. 74, No. 4. pp. 640-647.
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abstract = "Neuropathic pain and allodynia may arise from sensitization of central circuits. We report a mechanism of disinhibition-based central sensitization resulting from long-term depression (LTD) of GABAergic interneurons as a consequence of TRPV1 activation in the spinal cord. Intrathecal administration of TRPV1 agonists led to mechanical allodynia that was not dependent on peripheral TRPV1 neurons. TRPV1 was functionally expressed in GABAergic spinal interneurons and activation of spinal TRPV1 resulted in LTD of excitatory inputs and a reduction of inhibitory signaling to spinothalamic tract (STT) projection neurons. Mechanical hypersensitivity after peripheral nerve injury was attenuated in TRPV1-/- mice but not in mice lacking TRPV1-expressing peripheral neurons. Mechanical pain was reversed by a spinally applied TRPV1 antagonist while avoiding the hyperthermic side effect of systemic treatment. Our results demonstrate that spinal TRPV1 plays a critical role as a synaptic regulator and suggest the utility of central nervous system-specific TRPV1 antagonists for treating neuropathic pain.",
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Kim, YH, Back, SK, Davies, AJ, Jeong, H, Jo, HJ, Chung, G, Na, HS, Bae, YC, Kim, S, Kim, JS, Jung, SJ & Oh, SB 2012, 'TRPV1 in GABAergic Interneurons Mediates Neuropathic Mechanical Allodynia and Disinhibition of the Nociceptive Circuitry in the Spinal Cord', Neuron, vol. 74, no. 4, pp. 640-647. https://doi.org/10.1016/j.neuron.2012.02.039

TRPV1 in GABAergic Interneurons Mediates Neuropathic Mechanical Allodynia and Disinhibition of the Nociceptive Circuitry in the Spinal Cord. / Kim, Yong Ho; Back, Seung Keun; Davies, Alexander J.; Jeong, Heejin; Jo, Hyun Jung; Chung, Geehoon; Na, Heung Sik; Bae, Yong Chul; Kim, Sangjeong; Kim, Joong Soo; Jung, Sung Jun; Oh, Seog Bae.

In: Neuron, Vol. 74, No. 4, 24.05.2012, p. 640-647.

Research output: Contribution to journalArticle

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