Cells and circuits for amygdala neuroplasticity in the transition to chronic pain

Maladaptive plasticity is linked to the chronification of diseases such as pain, but the transition from acute to chronic pain is not well understood mechanistically. Neuroplasticity in the central nucleus of the amygdala (CeA) has emerged as a mechanism for sensory and emotional-affective aspects of injury-induced pain, although evidence comes from studies conducted almost exclusively in acute pain conditions and agnostic to cell type specificity. Here, we report time-dependent changes in genetically distinct and projection-specific CeA neurons in neuropathic pain. Hyperexcitability of CRF projection neurons and synaptic plasticity of parabrachial (PB) input at the acute stage shifted to hyperexcitability without synaptic plasticity in non-CRF neurons at the chronic phase. Accordingly, chemogenetic inhibition of the PB→CeA pathway mitigated pain-related behaviors in acute, but not chronic, neuropathic pain. Cell-type-specific temporal changes in neuroplasticity provide neurobiological evidence for the clinical observation that chronic pain is not simply the prolonged persistence of acute pain.

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Publication Details

Journal
Cell Reports
Published
2024-08-23
DOI
https://doi.org/10.1016/j.celrep.2024.114669
Citations
33
Primary Topic
Pain Mechanisms and Treatments
Type
article
Field-Weighted Citation Impact
10.78

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article

Cells and circuits for amygdala neuroplasticity in the transition to chronic pain

Torri D. Wilson, Jeitzel M. Torres-Rodriguez, Benjamin Neugebauer, Jenny J. Lin et al.
33 citations
Cell Reports
Pain Mechanisms and Treatments
10.78
article

Cells and circuits for amygdala neuroplasticity in the transition to chronic pain

Torri D. Wilson, Jeitzel M. Torres-Rodriguez, Benjamin Neugebauer, Jenny J. Lin, Sudhuman Singh, Sarah Chaudhry, Volker Neugebauer, Yarimar Carrasquillo, Takaki Kiritoshi, Vadim Yakhnitsa
article en
33 citations

Abstract

Maladaptive plasticity is linked to the chronification of diseases such as pain, but the transition from acute to chronic pain is not well understood mechanistically. Neuroplasticity in the central nucleus of the amygdala (CeA) has emerged as a mechanism for sensory and emotional-affective aspects of injury-induced pain, although evidence comes from studies conducted almost exclusively in acute pain conditions and agnostic to cell type specificity. Here, we report time-dependent changes in genetically distinct and projection-specific CeA neurons in neuropathic pain. Hyperexcitability of CRF projection neurons and synaptic plasticity of parabrachial (PB) input at the acute stage shifted to hyperexcitability without synaptic plasticity in non-CRF neurons at the chronic phase. Accordingly, chemogenetic inhibition of the PB→CeA pathway mitigated pain-related behaviors in acute, but not chronic, neuropathic pain. Cell-type-specific temporal changes in neuroplasticity provide neurobiological evidence for the clinical observation that chronic pain is not simply the prolonged persistence of acute pain.

Cell ReportsVol. 43(9)
Texas Tech University (US), National Institutes of Health (US), National Center for Complementary and Integrative Health (US), Texas Tech University Health Sciences Center (US)
University of Washington, University of Texas at Austin, National Institutes of Health, National Institute of Neurological Disorders and Stroke, National Center for Complementary and Integrative Health
Good health and well-being, Zero hunger
Openalex Percentile: Top 1%
Pain Mechanisms and Treatments
10.78
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