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The central amygdala to periaqueductal gray pathway comprises intrinsically distinct neurons differentially affected in a model of inflammatory pain

https://doi.org/10.1113/jp276935
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Outgoing claims: the papers this work cites, builds on, or argues with.

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Intrinsic connections of the rat amygdaloid complex: Projections originating in the central nucleus
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Characterization of the electrophysiological and morphological properties of rat central amygdala neurons in vitro
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Characterization of neurons in the rat central nucleus of the amygdala: Cellular physiology, morphology, and opioid sensitivity
inferredcites →https://doi.org/10.1002/cne.902080409openalex-snapshot
Cytoarchitecture of the central amygdaloid nucleus of the rat
inferredcites →https://doi.org/10.1002/cne.902460406openalex-snapshot
Neuronal architecture in the rat central nucleus of the amygdala: A cytological, hodological, and immunocytochemical study
inferredcites →https://doi.org/10.1002/cne.903030111openalex-snapshot
Connections between the central nucleus of the amygdala and the midbrain periaqueductal gray: Topography and reciprocity
inferredcites →https://doi.org/10.1002/cne.903290205openalex-snapshot
The organization of the efferent projections from the pontine parabrachial area to the amygdaloid complex: A phaseolus vulgaris leucoagglutinin (PHA‐L) study in the rat
inferredcites →https://doi.org/10.1002/cne.903610211openalex-snapshot
Intrinsic connections of the rat amygdaloid complex: Projections originating in the basal nucleus
inferredcites →https://doi.org/10.1007/978-3-662-46450-2_13openalex-snapshot
Amygdala Pain Mechanisms
inferredcites →https://doi.org/10.1007/bf00239551openalex-snapshot
Amygdaloid projections to the mesencephalon, pons and medulla oblongata in the cat
inferredcites →https://doi.org/10.1016/0006-8993(84)90360-3openalex-snapshot
A reinvestigation of the analgesic effects induced by stimulation of the periaqueductal gray matter in the rat. I. The production of behavioral side effects together with analgesia
inferredcites →https://doi.org/10.1016/0006-8993(88)91465-5openalex-snapshot
Integrated defence reaction elicited by excitatory amino acid microinjection in the midbrain periaqueductal grey region of the unrestrained cat
inferredcites →https://doi.org/10.1016/0006-8993(95)00525-uopenalex-snapshot
An electrophysiological characterization of the projection from the central nucleus of the amygdala to the periaqueductal gray of the rat: the role of opioid receptors
inferredcites →https://doi.org/10.1016/0166-2236(94)90047-7openalex-snapshot
Columnar organization in the midbrain periaqueductal gray: modules for emotional expression?
inferredcites →https://doi.org/10.1016/0301-0082(95)00009-kopenalex-snapshot
Functional characteristics of the midbrain periaqueductal gray
inferredcites →https://doi.org/10.1016/0304-3940(88)90226-1openalex-snapshot
Elicitation of intraspecific defence reactions in the rat from midbrain periaqueductal grey by microinjection of kainic acid, without neurotoxic effects
inferredcites →https://doi.org/10.1016/j.neulet.2017.09.025openalex-snapshot
Distinct neuronal populations in the basolateral and central amygdala are activated with acute pain, conditioned fear, and fear-conditioned analgesia
inferredcites →https://doi.org/10.1016/j.neuron.2014.04.042openalex-snapshot
Amygdala Microcircuits Controlling Learned Fear
inferredcites →https://doi.org/10.1016/j.pain.2004.03.015openalex-snapshot
Block of NMDA and non-NMDA receptor activation results in reduced background and evoked activity of central amygdala neurons in a model of arthritic pain
inferredcites →https://doi.org/10.1016/j.pain.2006.09.003openalex-snapshot
NMDA receptor-independent synaptic plasticity in the central amygdala in the rat model of neuropathic pain
inferredcites →https://doi.org/10.1016/j.tins.2011.03.005openalex-snapshot
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inferredcites →https://doi.org/10.1016/s0149-7634(01)00049-5openalex-snapshot
Parallel circuits mediating distinct emotional coping reactions to different types of stress
inferredcites →https://doi.org/10.1016/s0169-328x(00)00194-7openalex-snapshot
Regional expression of a gene encoding a neuron-specific Na+-dependent inorganic phosphate cotransporter (DNPI) in the rat forebrain
inferredcites →https://doi.org/10.1016/s0361-9230(00)00313-0openalex-snapshot
Central circuits mediating patterned autonomic activity during active vs. passive emotional coping
inferredcites →https://doi.org/10.1038/nature09553openalex-snapshot
Genetic dissection of an amygdala microcircuit that gates conditioned fear
inferredcites →https://doi.org/10.1038/nature09559openalex-snapshot
Encoding of conditioned fear in central amygdala inhibitory circuits
inferredcites →https://doi.org/10.1038/nature17996openalex-snapshot
Midbrain circuits for defensive behaviour
inferredcites →https://doi.org/10.1046/j.0953-816x.2001.01879.xopenalex-snapshot
Physiological properties of central amygdala neurons: species differences
inferredcites →https://doi.org/10.1093/cercor/bhl127openalex-snapshot
Morphological, Electrophysiological, and Synaptic Properties of Corticocallosal Pyramidal Cells in the Neonatal Rat Neocortex
inferredcites →https://doi.org/10.1111/j.1460-9568.2012.08235.xopenalex-snapshot
Asymmetric time‐dependent activation of right central amygdala neurones in rats with peripheral neuropathy and pregabalin modulation
inferredcites →https://doi.org/10.1113/eph8702357openalex-snapshot
Pain Pathways and Parabrachial Circuits in the Rat
inferredcites →https://doi.org/10.1124/jpet.104.074633openalex-snapshot
Effect of the μ Opioid on Excitatory and Inhibitory Synaptic Inputs to Periaqueductal Gray-Projecting Neurons in the Amygdala
inferredcites →https://doi.org/10.1126/science.1239403openalex-snapshot
Constitutive μ-Opioid Receptor Activity Leads to Long-Term Endogenous Analgesia and Dependence
inferredcites →https://doi.org/10.1152/jn.00135.2007openalex-snapshot
Differential Effects of CRF1 and CRF2 Receptor Antagonists on Pain-Related Sensitization of Neurons in the Central Nucleus of the Amygdala
inferredcites →https://doi.org/10.1152/jn.00211.2004openalex-snapshot
Firing Properties and Connectivity of Neurons in the Rat Lateral Central Nucleus of the Amygdala
inferredcites →https://doi.org/10.1152/jn.00232.2011openalex-snapshot
Corticospinal-specific HCN expression in mouse motor cortex: Ih-dependent synaptic integration as a candidate microcircuit mechanism involved in motor control
inferredcites →https://doi.org/10.1152/jn.00485.2003openalex-snapshot
Differential Roles of mGluR1 and mGluR5 in Brief and Prolonged Nociceptive Processing in Central Amygdala Neurons
inferredcites →https://doi.org/10.1152/jn.00495.2006openalex-snapshot
Differential Changes of Group II and Group III mGluR Function in Central Amygdala Neurons in a Model of Arthritic Pain
inferredcites →https://doi.org/10.1152/jn.00514.2012openalex-snapshot
Morphology, PKCδ expression, and synaptic responsiveness of different types of rat central lateral amygdala neurons
inferredcites →https://doi.org/10.1152/jn.00799.2002openalex-snapshot
Differential Sensitization of Amygdala Neurons to Afferent Inputs in a Model of Arthritic Pain
inferredcites →https://doi.org/10.1152/physrev.00037.2009openalex-snapshot
Plastic Synaptic Networks of the Amygdala for the Acquisition, Expression, and Extinction of Conditioned Fear
inferredcites →https://doi.org/10.1177/1073858403261077openalex-snapshot
The Amygdala and Persistent Pain
inferredcites →https://doi.org/10.1186/1744-8069-10-26openalex-snapshot
A Simplified Up-Down Method (SUDO) for Measuring Mechanical Nociception in Rodents Using von Frey Filaments
inferredcites →https://doi.org/10.1186/1744-8069-5-21openalex-snapshot
NR2B Receptor Blockade Inhibits Pain-Related Sensitization of Amygdala Neurons
inferredcites →https://doi.org/10.1523/eneuro.0010-18.2018openalex-snapshot
Quantified Coexpression Analysis of Central Amygdala Subpopulations
inferredcites →https://doi.org/10.1523/eneuro.0367-16.2017openalex-snapshot
Intrinsic Circuits in the Lateral Central Amygdala
inferredcites →https://doi.org/10.1523/jneurosci.08-07-02517.1988openalex-snapshot
Different projections of the central amygdaloid nucleus mediate autonomic and behavioral correlates of conditioned fear
inferredcites →https://doi.org/10.1523/jneurosci.18-09-03426.1998openalex-snapshot
Distinct Regions of the Periaqueductal Gray Are Involved in the Acquisition and Expression of Defensive Responses
inferredcites →https://doi.org/10.1523/jneurosci.23-01-00052.2003openalex-snapshot
Synaptic Plasticity in the Amygdala in a Model of Arthritic Pain: Differential Roles of Metabotropic Glutamate Receptors 1 and 5
inferredcites →https://doi.org/10.1523/jneurosci.3309-15.2016openalex-snapshot
Wiring Specificity and Synaptic Diversity in the Mouse Lateral Central Amygdala
inferredcites →https://doi.org/10.1523/jneurosci.3536-06.2007openalex-snapshot
Activation of the Extracellular Signal-Regulated Kinase in the Amygdala Modulates Pain Perception
inferredcites →https://doi.org/10.1523/jneurosci.3644-10.2010openalex-snapshot
Projection-Specific Neuromodulation of Medial Prefrontal Cortex Neurons
inferredcites →https://doi.org/10.1523/jneurosci.4166-13.2014openalex-snapshot
Fear Conditioning Potentiates Synaptic Transmission onto Long-Range Projection Neurons in the Lateral Subdivision of Central Amygdala
inferredcites →https://doi.org/10.3389/fncel.2015.00161openalex-snapshot
Highly differentiated cellular and circuit properties of infralimbic pyramidal neurons projecting to the periaqueductal gray and amygdala
inferredcites →https://doi.org/10.3389/fncir.2010.00100openalex-snapshot
Ephus: multipurpose data acquisition software for neuroscience experiments
inferredcites →https://doi.org/10.3791/51212openalex-snapshot
Measuring Changes in Tactile Sensitivity in the Hind Paw of Mice Using an Electronic von Frey Apparatus
inferredcites →https://doi.org/10.3791/51212-vopenalex-snapshot
Measuring Changes in Tactile Sensitivity in the Hind Paw of Mice Using an Electronic von Frey Apparatus

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Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Persistent inflammation selectively activates opioid-sensitive phasic-firing neurons within the vlPAG
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Chronic inflammatory pain and chronic THC vapor inhalation alter midbrain neuronal activity
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Kappa opioid receptors in the central amygdala modulate spinal nociceptive processing through an action on amygdala CRF neurons
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Agent-based modeling of the central amygdala and pain using cell-type specific physiological parameters
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mWAKE in the Central Amygdala Regulates Fear Learning and Memory
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inferred← citeshttps://doi.org/10.3389/fncel.2022.999509openalex-snapshot
NMDARs mediate peripheral and central sensitization contributing to chronic orofacial pain
inferred← citeshttps://doi.org/10.3389/fnsys.2022.1044686openalex-snapshot
The role of endogenous opioid neuropeptides in neurostimulation-driven analgesia
inferred← citeshttps://doi.org/10.3389/fnsys.2022.963812openalex-snapshot
Cellular and circuit diversity determines the impact of endogenous opioids in the descending pain modulatory pathway
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Developing a 3-D computational model of neurons in the central amygdala to understand pharmacological targets for pain
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Inhibitory Effects of Columbianadin on Nociceptive Behaviors in a Neuropathic Pain Model, and on Voltage-Gated Calcium Currents in Dorsal Root Ganglion Neurons in Mice
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Neural Plasticity in the Brain during Neuropathic Pain
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Dysfunction of Small-Conductance Ca2+-Activated Potassium (SK) Channels Drives Amygdala Hyperexcitability and Neuropathic Pain Behaviors: Involvement of Epigenetic Mechanisms
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Multiple Posterior Insula Projections to the Brainstem Descending Pain Modulatory System
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Stress-induced analgesia: The role of the HPA axis hormones
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Forebrain-Midbrain Circuits and Peptides Involved in Hyperalgesia After Chronic Alcohol Exposure
inferred← citeshttps://doi.org/10.7554/elife.68130openalex-snapshot
Cellular, circuit and transcriptional framework for modulation of itch in the central amygdala
inferred← citeshttps://doi.org/10.7554/elife.84262openalex-snapshot
Multimodal mapping of cell types and projections in the central nucleus of the amygdala
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