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Descending pain modulation and chronification of pain

https://doi.org/10.1097/spc.0000000000000055

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/(sici)1096-9861(19990315)405:3<359::aid-cne6>3.0.co;2-wopenalex-snapshot

Projections of neurons in the periaqueductal gray to pontine and medullary catecholamine cell groups involved in the modulation of nociception

inferredcites →https://doi.org/10.1002/ana.23922openalex-snapshot

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inferredcites →https://doi.org/10.1002/cne.23024openalex-snapshot

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Narcotic analgetics: CNS sites and mechanisms of action as revealed by intracerebral injection techniques

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Diffuse noxious inhibitory controls (DNIC). II. Lack of effect on non-convergent neurones, supraspinal involvement and theoretical implications

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Differential mediation of descending pain facilitation and inhibition by spinal 5HT-3 and 5HT-7 receptors

inferredcites →https://doi.org/10.1016/j.brainresrev.2004.07.004openalex-snapshot

Descending control of persistent pain: inhibitory or facilitatory?

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Descending control of nociception: Specificity, recruitment and plasticity

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Human brain mechanisms of pain perception and regulation in health and disease

inferredcites →https://doi.org/10.1016/j.ejphar.2008.06.087openalex-snapshot

Role of α2-adrenoceptors in enhancement of antinociceptive effect in diabetic mice

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Common Chronic Pain Conditions in Developed and Developing Countries: Gender and Age Differences and Comorbidity With Depression-Anxiety Disorders

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The Prevalence of Chronic Pain in United States Adults: Results of an Internet-Based Survey

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Persistent Pain After Breast Cancer Treatment: A Critical Review of Risk Factors and Strategies for Prevention

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Endogenous Inhibition of Somatic Pain Is Impaired in Girls With Irritable Bowel Syndrome Compared With Healthy Girls

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Persistent Postmastectomy Pain in Breast Cancer Survivors: Analysis of Clinical, Demographic, and Psychosocial Factors

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inferredcites →https://doi.org/10.1016/j.neuron.2009.07.014openalex-snapshot

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inferredcites →https://doi.org/10.1016/j.neuron.2010.03.002openalex-snapshot

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inferredcites →https://doi.org/10.1016/j.neuroscience.2007.05.004openalex-snapshot

Rostral ventromedial medulla control of spinal sensory processing in normal and pathophysiological states

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Spinal cord mechanisms mediating behavioral hyperalgesia induced by neurokinin-1 tachykinin receptor activation in the rostral ventromedial medulla

inferredcites →https://doi.org/10.1016/j.nurt.2009.07.009openalex-snapshot

Preclinical and Early Clinical Investigations Related to Monoaminergic Pain Modulation

inferredcites →https://doi.org/10.1016/j.pain.2006.01.021openalex-snapshot

Peripheral 5-HT2A receptor antagonism attenuates primary thermal hyperalgesia and secondary mechanical allodynia after thermal injury in rats

inferredcites →https://doi.org/10.1016/j.pain.2008.08.008openalex-snapshot

Descending facilitation from the brainstem determines behavioural and neuronal hypersensitivity following nerve injury and efficacy of pregabalin

inferredcites →https://doi.org/10.1016/j.pain.2008.09.009openalex-snapshot

Periaqueductal gray neurons project to spinally projecting GABAergic neurons in the rostral ventromedial medulla

inferredcites →https://doi.org/10.1016/j.pain.2008.11.009openalex-snapshot

5-HT7 receptor activation inhibits mechanical hypersensitivity secondary to capsaicin sensitization in mice

inferredcites →https://doi.org/10.1016/j.pain.2009.11.009openalex-snapshot

The pain matrix: Reloaded or reborn as we image tonic pain using arterial spin labelling

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Endogenous analgesic action of the pontospinal noradrenergic system spatially restricts and temporally delays the progression of neuropathic pain following tibial nerve injury

inferredcites →https://doi.org/10.1016/j.pneurobio.2006.08.001openalex-snapshot

Noradrenergic pain modulation

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Chronic constriction injury of sciatic nerve induces the up-regulation of descending inhibitory noradrenergic innervation to the lumbar dorsal horn of mice

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Inhibitory effects evoked from both the lateral and ventrolateral periaqueductal grey are selective for the nociceptive responses of rat dorsal horn neurones

inferredcites →https://doi.org/10.1016/s0006-8993(97)01104-9openalex-snapshot

Antinociception following opioid stimulation of the basolateral amygdala is expressed through the periaqueductal gray and rostral ventromedial medulla

inferredcites →https://doi.org/10.1016/s0014-2999(98)00910-8openalex-snapshot

Endogenous noradrenergic tone controls symptoms of allodynia in the spinal nerve ligation model of neuropathic pain

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An isobolographic analysis of the antinociceptive effect of systemically and intrathecally administered combinations of clonidine and opiates.

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inferredcites →https://doi.org/10.1016/s0304-3959(02)00368-8openalex-snapshot

Descending modulation in persistent pain: an update

inferredcites →https://doi.org/10.1016/s0304-3959(99)00139-6openalex-snapshot

Pain: An unpleasant topic

inferredcites →https://doi.org/10.1016/s0306-4522(97)00437-5openalex-snapshot

Enkephalin neurons that project to the A7 catecholamine cell group are located in nuclei that modulate nociception: ventromedial medulla

inferredcites →https://doi.org/10.1016/s0306-4522(98)00673-3openalex-snapshot

Microinjection of morphine in the A7 catecholamine cell group produces opposing effects on nociception that are mediated by α1- and α2-adrenoceptors

inferredcites →https://doi.org/10.1038/bjc.2012.445openalex-snapshot

Development of a screening instrument for risk factors of persistent pain after breast cancer surgery

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Primary sensory cortices contain distinguishable spatial patterns of activity for each sense

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inferredcites →https://doi.org/10.1038/nn.3153openalex-snapshot

Corticostriatal functional connectivity predicts transition to chronic back pain

inferredcites →https://doi.org/10.1038/nn.3628openalex-snapshot

Pain vulnerability: a neurobiological perspective

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A common neurobiology for pain and pleasure

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Neuropathic pain is maintained by brainstem neurons co-expressing opioid and cholecystokinin receptors

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Intrathecal, but Not Intravenous, Clonidine Reduces Experimental Thermal or Capsaicin-Induced Pain and Hyperalgesia in Normal Volunteers

inferredcites →https://doi.org/10.1097/00000542-199012000-00022openalex-snapshot

Antinociceptive Interaction Between Opioids and Medetomidine

inferredcites →https://doi.org/10.1097/00006123-197709000-00018openalex-snapshot

Long term results of periventricular gray self-stimulation

inferredcites →https://doi.org/10.1097/00132586-196512000-00023openalex-snapshot

STUDIES ON THE SITE OF ANALGESIC ACTION OF MORPHINE BY INTRACEREBRAL MICRO-INJECTION

inferredcites →https://doi.org/10.1097/aln.0b013e3181cf423dopenalex-snapshot

Persistent Postsurgical Pain

inferredcites →https://doi.org/10.1097/psy.0b013e318185c510openalex-snapshot

Association of Depression and Anxiety Alone and in Combination With Chronic Musculoskeletal Pain in Primary Care Patients

inferredcites →https://doi.org/10.1097/spc.0000000000000108openalex-snapshot

Improving the quality of end-of-life discussions

inferredcites →https://doi.org/10.1097/spc.0000000000000109openalex-snapshot

Desire for hastened death

inferredcites →https://doi.org/10.1097/spc.0000000000000114openalex-snapshot

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inferredcites →https://doi.org/10.1097/spc.0000000000000115openalex-snapshot

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inferredcites →https://doi.org/10.1097/spc.0000000000000116openalex-snapshot

Existential distress among healthcare providers caring for patients at the end of life

inferredcites →https://doi.org/10.1097/spc.0000000000000117openalex-snapshot

The central role of meaning in adjustment to the loss of a child to cancer

inferredcites →https://doi.org/10.1097/spc.0000000000000118openalex-snapshot

Understanding death with limited experience in life

inferredcites →https://doi.org/10.1097/spc.0000000000000119openalex-snapshot

The supportive roles of religion and spirituality in end-of-life and palliative care of patients with cancer in a culturally diverse context

inferredcites →https://doi.org/10.1111/j.1460-9568.2007.05623.xopenalex-snapshot

Fibromyalgia patients show an abnormal dopamine response to pain

inferredcites →https://doi.org/10.1111/j.1476-5381.2011.01820.xopenalex-snapshot

Activation of NK1receptors in the locus coeruleus induces analgesia through noradrenergic‐mediated descending inhibition in a rat model of neuropathic pain

inferredcites →https://doi.org/10.1111/j.1526-4637.2006.00178.xopenalex-snapshot

Duloxetine and Other Antidepressants in the Treatment of Patients with Fibromyalgia

inferredcites →https://doi.org/10.1111/j.1526-4637.2007.00280.xopenalex-snapshot

A Population in Pain: Report from the Olmsted County Health Study

inferredcites →https://doi.org/10.1111/j.1526-4637.2008.00425.xopenalex-snapshot

Prevalence of Chronic Pain in a Representative Sample in the United States

inferredcites →https://doi.org/10.1111/nyas.12095openalex-snapshot

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Endogenous Pain Modulation in Response to Exercise in Patients with Rheumatoid Arthritis, Patients with Chronic Fatigue Syndrome and Comorbid Fibromyalgia, and Healthy Controls: A Double‐Blind Randomized Controlled Trial

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Sex Differences in the Stability of Conditioned Pain Modulation (CPM) among Patients with Chronic Pain

inferredcites →https://doi.org/10.1113/eph8702354openalex-snapshot

The Caudal Medullary Ventrolateral Reticular Formation in Nociceptive‐Cardiovascular Integration. An Experimental Study in the Rat

inferredcites →https://doi.org/10.1113/eph8702357openalex-snapshot

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inferredcites →https://doi.org/10.1113/jphysiol.2010.196923openalex-snapshot

Endogenous descending modulation: spatiotemporal effect of dynamic imbalance between descending facilitation and inhibition of nociception

inferredcites →https://doi.org/10.1124/jpet.300.1.282openalex-snapshot

α2C-Adrenergic Receptors Mediate Spinal Analgesia and Adrenergic-Opioid Synergy

inferredcites →https://doi.org/10.1126/science.1067176openalex-snapshot

Placebo and Opioid Analgesia-- Imaging a Shared Neuronal Network

inferredcites →https://doi.org/10.1126/science.164.3878.444openalex-snapshot

Surgery in the Rat during Electrical Analgesia Induced by Focal Brain Stimulation

inferredcites →https://doi.org/10.1126/science.301658openalex-snapshot

Pain Relief by Electrical Stimulation of the Central Gray Matter in Humans and Its Reversal by Naloxone

inferredcites →https://doi.org/10.1152/jn.00676.2006openalex-snapshot

Kappa Opioid Receptor (KOR) and GAD67 Immunoreactivity Are Found in off and neutral Cells in the Rostral Ventromedial Medulla

inferredcites →https://doi.org/10.1152/jn.1998.80.5.2244openalex-snapshot

Midbrain Periaqueductal Gray (PAG) Inhibits Nociceptive Inputs to Sacral Dorsal Horn Nociceptive Neurons Through α2-Adrenergic Receptors

inferredcites →https://doi.org/10.1152/physiol.00024.2008openalex-snapshot

Imaging CNS Modulation of Pain in Humans

inferredcites →https://doi.org/10.1155/2012/610561openalex-snapshot

Reliability of the Conditioned Pain Modulation Paradigm to Assess Endogenous Inhibitory Pain Pathways

inferredcites →https://doi.org/10.1159/000321644openalex-snapshot

Pain-Associated Adaptive Cortical Reorganisation in Chronic Pancreatitis

inferredcites →https://doi.org/10.1177/1099800413520486openalex-snapshot

Conditioned Pain Modulation in Women With Irritable Bowel Syndrome

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Descending Serotonergic Facilitation and the Antinociceptive Effects of Pregabalin in a Rat Model of Osteoarthritic Pain

inferredcites →https://doi.org/10.1200/jco.2013.54.8149openalex-snapshot

Developing a Service Model That Integrates Palliative Care Throughout Cancer Care: The Time Is Now

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Distribution of Glycine/GABA Neurons in the Ventromedial Medulla with Descending Spinal Projections and Evidence for an Ascending Glycine/GABA Projection

inferredcites →https://doi.org/10.1371/journal.pone.0055460openalex-snapshot

Is Altered Central Pain Processing Related to Disease Stage in Chronic Pancreatitis Patients with Pain? An Exploratory Study

inferredcites →https://doi.org/10.1517/14656566.2012.696097openalex-snapshot

Mechanistic and functional differentiation of tapentadol and tramadol

inferredcites →https://doi.org/10.1523/jneurosci.17-09-03285.1997openalex-snapshot

SEROTONERGIC Pontomedullary Neurons Are Not Activated by Antinociceptive Stimulation in the Periaqueductal Gray

inferredcites →https://doi.org/10.1523/jneurosci.22-12-05129.2002openalex-snapshot

Time-Dependent Descending Facilitation from the Rostral Ventromedial Medulla Maintains, But Does Not Initiate, Neuropathic Pain

inferredcites →https://doi.org/10.1523/jneurosci.23-23-08370.2003openalex-snapshot

Enhanced Evoked Excitatory Transmitter Release in Experimental Neuropathy Requires Descending Facilitation

inferredcites →https://doi.org/10.1523/jneurosci.2541-04.2004openalex-snapshot

Chronic Back Pain Is Associated with Decreased Prefrontal and Thalamic Gray Matter Density

inferredcites →https://doi.org/10.1523/jneurosci.2638-08.2008openalex-snapshot

Identifying Brain Activity Specifically Related to the Maintenance and Perceptual Consequence of Central Sensitization in Humans

inferredcites →https://doi.org/10.1523/jneurosci.3623-09.2009openalex-snapshot

Sustained Morphine-Induced Sensitization and Loss of Diffuse Noxious Inhibitory Controls in Dura-Sensitive Medullary Dorsal Horn Neurons

inferredcites →https://doi.org/10.1523/jneurosci.3686-05.2006openalex-snapshot

Supraspinal Brain-Derived Neurotrophic Factor Signaling: A Novel Mechanism for Descending Pain Facilitation

inferredcites →https://doi.org/10.1523/jneurosci.4856-05.2006openalex-snapshot

Direct GABAergic and Glycinergic Inhibition of the Substantia Gelatinosa from the Rostral Ventromedial Medulla Revealed by In Vivo Patch-Clamp Analysis in Rats

inferredcites →https://doi.org/10.1523/jneurosci.5389-09.2010openalex-snapshot

Molecular Depletion of Descending Serotonin Unmasks Its Novel Facilitatory Role in the Development of Persistent Pain

inferredcites →https://doi.org/10.2337/dc11-1108openalex-snapshot

Prevalence and Characteristics of Painful Diabetic Neuropathy in a Large Community-Based Diabetic Population in the U.K.

inferredcites →https://doi.org/10.3109/9781420086805-5openalex-snapshot

The Pharmacological Treatment of Fibromyalgia

inferredcites →https://doi.org/10.3171/jns.1977.47.2.0178openalex-snapshot

Pain reduction by electrical brain stimulation in man

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Personalized Pain Medicine: The Clinical Value of Psychophysical Assessment of Pain Modulation Profile

What points at this work

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

inferred← citeshttps://doi.org/10.2139/ssrn.4581053openalex-extracted

Genetic Labeling of the Nucleus of Tractus Solitarius Neurons Associated with Electrical Stimulation of Cervical or Auricular Vagus Nerve in Mice

inferred← citeshttps://doi.org/10.1002/9781118967225.ch8openalex-snapshot

Central Circuits Promoting Chronification of Migraine

inferred← citeshttps://doi.org/10.1002/9781119747826.refsopenalex-snapshot

References

inferred← citeshttps://doi.org/10.1002/acr.24437openalex-snapshot

Association of Pain Sensitization and Conditioned Pain Modulation to Pain Patterns in Knee Osteoarthritis

inferred← citeshttps://doi.org/10.1002/acr.25104openalex-snapshot

Identifying and Managing Nociplastic Pain in Individuals With Rheumatic Diseases: A Narrative Review

inferred← citeshttps://doi.org/10.1002/art.40101openalex-snapshot

Effects of Treadmill Exercise on Advanced Osteoarthritis Pain in Rats

inferred← citeshttps://doi.org/10.1002/art.42429openalex-snapshot

The Biology of Pain: Through the Rheumatology Lens

inferred← citeshttps://doi.org/10.1002/brb3.70008openalex-snapshot

Hypoperfusion of periaqueductal gray as an imaging biomarker in chronic migraine beyond diagnosis: A 3D pseudocontinuous arterial spin labeling MR imaging

inferred← citeshttps://doi.org/10.1002/brb3.70541openalex-snapshot

Can EEG‐Neurofeedback Training Enhance Effective Connectivity in People With Chronic Secondary Musculoskeletal Pain? A Secondary Analysis of a Feasibility Randomized Controlled Clinical Trial

inferred← citeshttps://doi.org/10.1002/brb3.71614openalex-snapshot

Passive Oscillatory Body Motion Attenuates Pain‐Related Behaviors and Increases β‐Endorphin Immunoreactivity in a Murine Fracture Model: A Preliminary Study

inferred← citeshttps://doi.org/10.1002/ejp.1140openalex-snapshot

Assessment and manifestation of central sensitisation across different chronic pain conditions

inferred← citeshttps://doi.org/10.1002/ejp.1294openalex-snapshot

General versus pain‐specific cognitions: Pain catastrophizing but not optimism influences conditioned pain modulation

inferred← citeshttps://doi.org/10.1002/ejp.1435openalex-snapshot

Cornea nerve fibre state determines analgesic response to tapentadol in fibromyalgia patients without effective endogenous pain modulation

inferred← citeshttps://doi.org/10.1002/ejp.1504openalex-snapshot

Enhanced pain modulation capacity among individuals with borderline personality disorder: A possible mechanism underlying their hypoalgesia

inferred← citeshttps://doi.org/10.1002/ejp.1580openalex-snapshot

Activation of the descending pain modulatory system using cuff pressure algometry: Back translation from man to rat

inferred← citeshttps://doi.org/10.1002/ejp.1792openalex-snapshot

Pain referral area is reduced by remote pain

inferred← citeshttps://doi.org/10.1002/ejp.2170openalex-snapshot

Examining the role of mood in pain‐limited treadmill walking duration in young healthy individuals

inferred← citeshttps://doi.org/10.1002/ejp.2185openalex-snapshot

Subgrouping of facilitatory or inhibitory conditioned pain modulation responses in patients with chronic knee pain. Explorative analysis from a multicentre trial

inferred← citeshttps://doi.org/10.1002/ejp.70187openalex-snapshot

Exploring the Relationship Between Physical Activity and Pressure Pain Tolerance in the General Population. The Tromsø Study 2015–2016

inferred← citeshttps://doi.org/10.1002/ejp.70190openalex-snapshot

Reduced Descending Itch Inhibition in Peripheral Neuropathy Patients With Chronic Pruritus

inferred← citeshttps://doi.org/10.1002/ejp.70312openalex-snapshot

Associations Between Dynamic Quantitative Sensory Testing and Physical Therapy Outcomes in Chronic Low Back Pain: An Exploratory, Prospective Longitudinal Cohort Study

inferred← citeshttps://doi.org/10.1002/ejp.70332openalex-snapshot

The Meaning of Pain in the Clinical Management of Patients With Disorders of Consciousness: Is It a Neglected Issue?

inferred← citeshttps://doi.org/10.1002/ejp.70392openalex-snapshot

Effects of Low‐Dose Acetylsalicylic Acid on Spontaneous Pain, Pain Sensitivity, and Central Pain Modulation in Response to a Sleep Restriction Challenge in Healthy Individuals

inferred← citeshttps://doi.org/10.1002/ejp.806openalex-snapshot

Effects of insular stimulation on thermal nociception

inferred← citeshttps://doi.org/10.1002/hbm.24834openalex-snapshot

Sensorimotor and pain‐related alterations of the gray matter and white matter in Type 2 diabetic patients with peripheral neuropathy

inferred← citeshttps://doi.org/10.1002/hbm.25401openalex-snapshot

Supraspinal nociceptive networks in neuropathic pain after spinal cord injury

inferred← citeshttps://doi.org/10.1002/hbm.70291openalex-snapshot

A Novel Investigation of an In‐Scanner Alternative to the Cold Pressor Test in Healthy Individuals

inferred← citeshttps://doi.org/10.1002/jnr.24150openalex-snapshot

Circadian control of pain and neuroinflammation

inferred← citeshttps://doi.org/10.1002/jnr.25018openalex-snapshot

Associations between pain catastrophizing and resting‐state functional brain connectivity: Ethnic/race group differences in persons with chronic knee pain

inferred← citeshttps://doi.org/10.1002/jnr.70039openalex-snapshot

Sex and Strain Differences in Analgesic and Hyperlocomotor Effects of Morphine and μ‐Opioid Receptor Expression in Mice

inferred← citeshttps://doi.org/10.1002/mds.70004openalex-snapshot

Electrophysiological Evidence for Impaired Central Pain Modulation in Parkinson's Disease

inferred← citeshttps://doi.org/10.1002/pne2.12046openalex-snapshot

What is pain: Are cognitive and social features core components?

inferred← citeshttps://doi.org/10.1002/ptr.7968openalex-snapshot

Saffron (Crocus sativus) and its constituents for pain management: A review of current evidence

inferred← citeshttps://doi.org/10.1007/164_2019_205openalex-snapshot

Electrophysiological Actions of N/OFQ

inferred← citeshttps://doi.org/10.1007/174_2017_55openalex-snapshot

Irritable Bowel Syndrome and Dysphagia

inferred← citeshttps://doi.org/10.1007/978-3-030-01845-0_136openalex-snapshot

Targeting the Endogenous Pain Modulation System

inferred← citeshttps://doi.org/10.1007/978-3-030-02976-0_3openalex-snapshot

Mechanisms of Pain and Headache

inferred← citeshttps://doi.org/10.1007/978-3-030-21657-3_3openalex-snapshot

Pain Physiology and the Neurobiology of Nociception

inferred← citeshttps://doi.org/10.1007/978-3-030-21657-3_7openalex-snapshot

Low Back Pain

inferred← citeshttps://doi.org/10.1007/978-3-031-09936-6_10openalex-snapshot

Opioids in Pain

inferred← citeshttps://doi.org/10.1007/978-3-031-45493-6_10openalex-snapshot

The Roles of Endogenous Opioids in Placebo and Nocebo Effects: From Pain to Performance to Prozac

inferred← citeshttps://doi.org/10.1007/978-3-031-45493-6_6openalex-snapshot

Modulatory Processes in Craniofacial Pain States

inferred← citeshttps://doi.org/10.1007/978-3-031-69734-0_21openalex-snapshot

An Integrated Medical and Psychological Approach to Understanding and Assessing Chronic Pain

inferred← citeshttps://doi.org/10.1007/978-3-031-90347-2_27-1openalex-snapshot

Neuropathic-Nociceptive Pain in ENT Diseases-Persistent Idiopathic Facial Pain (PIFP), Trigeminal, Glossofaringeal Nevralji

inferred← citeshttps://doi.org/10.1007/978-3-031-90347-2_27-2openalex-snapshot

Neuropathic-Nociceptive Pain in ENT Diseases: Persistent Idiopathic Facial Pain (PIFP), Trigeminal Neuralgia, Glossopharyngeal Neuralgia

inferred← citeshttps://doi.org/10.1007/978-3-032-06268-0_27openalex-snapshot

Neuropathic-Nociceptive Pain in ENT Diseases: Persistent Idiopathic Facial Pain (PIFP), Trigeminal Neuralgia, Glossopharyngeal Neuralgia

inferred← citeshttps://doi.org/10.1007/978-3-032-07519-2_14openalex-snapshot

Pain Management of Spine Tumors

inferred← citeshttps://doi.org/10.1007/978-3-032-21675-5_2openalex-snapshot

Pathophysiology of Pain

inferred← citeshttps://doi.org/10.1007/978-3-319-28100-1_8-1openalex-snapshot

Neurophysiology of Orofacial Pain

inferred← citeshttps://doi.org/10.1007/978-3-319-28100-1_8-2openalex-snapshot

Neurophysiology of Orofacial Pain

inferred← citeshttps://doi.org/10.1007/978-3-319-28100-1_8-3openalex-snapshot

Neurophysiology of Orofacial Pain

inferred← citeshttps://doi.org/10.1007/978-3-319-39406-0_8openalex-snapshot

Novel Approaches to Apoptosis-Inducing Therapies

inferred← citeshttps://doi.org/10.1007/978-3-319-44348-5_15openalex-snapshot

A Comparison of Clinical Features and Mechanisms of Trigeminal Postherpetic Neuralgia and Trigeminal Neuralgia

inferred← citeshttps://doi.org/10.1007/978-3-319-71694-7_2openalex-snapshot

Pathophysiology of Pain

inferred← citeshttps://doi.org/10.1007/978-3-319-72303-7_8openalex-snapshot

Neurophysiology of Orofacial Pain

inferred← citeshttps://doi.org/10.1007/978-3-319-77432-9_10openalex-snapshot

Pain

inferred← citeshttps://doi.org/10.1007/978-3-662-47329-0_48-1openalex-snapshot

Anästhesie bei operativen Interventionen in der Gynäkologie

inferred← citeshttps://doi.org/10.1007/978-3-662-50512-0_5openalex-snapshot

Neurobiologisch e und psychobiologische Faktoren der Chronifizierung und Plastizität

inferred← citeshttps://doi.org/10.1007/978-3-662-66215-1_4openalex-snapshot

Schwerpunkte des Therapieprozesses, Anamnese, Befundung und Patientenbeispiel

inferred← citeshttps://doi.org/10.1007/978-90-368-2230-5_1openalex-snapshot

Neurofysiologie bij pijn

inferred← citeshttps://doi.org/10.1007/978-981-10-6577-4_12openalex-snapshot

Overlapping Chronic Pain and Depression: Pathophysiology and Management

inferred← citeshttps://doi.org/10.1007/978-981-95-6872-7_9openalex-snapshot

Chronic Pain and Major Depression: Shared Psychological and Neurobiological Mechanism

inferred← citeshttps://doi.org/10.1007/978-981-97-4087-1_53-1openalex-snapshot

Neuroplasticity and Chronic Pain Pathways in Low Backache

inferred← citeshttps://doi.org/10.1007/s00213-017-4686-6openalex-snapshot

5-HT modulation of pain perception in humans

inferred← citeshttps://doi.org/10.1007/s00221-025-07191-9openalex-snapshot

Reduced volume in the amygdala of trigeminal neuralgia patients: a neuroimaging study with clinical correlates

inferred← citeshttps://doi.org/10.1007/s00234-024-03286-2openalex-snapshot

Investigating the brain functional abnormalities underlying pain hypervigilance in chronic neck and shoulder pain: a resting-state fMRI study

inferred← citeshttps://doi.org/10.1007/s00429-020-02173-9openalex-snapshot

Supraspinal neural mechanisms of the analgesic effect produced by transcutaneous electrical nerve stimulation

inferred← citeshttps://doi.org/10.1007/s00484-026-03157-wopenalex-snapshot

Does the predominance of central sensitization alter the effect of balneotherapy combined with conventional physical therapy in patients with chronic low back and knee pain?

inferred← citeshttps://doi.org/10.1007/s00508-020-01798-4openalex-snapshot

Pain management in hemophilia: expert recommendations

inferred← citeshttps://doi.org/10.1007/s00772-017-0271-xopenalex-snapshot

Chronische Schmerzen

inferred← citeshttps://doi.org/10.1007/s10461-017-1856-9openalex-snapshot

Psychological Factors Associated With Painful Versus Non-Painful HIV-Associated Sensory Neuropathy

inferred← citeshttps://doi.org/10.1007/s10571-020-00967-3openalex-snapshot

Supraspinal Mechanisms of Intestinal Hypersensitivity

inferred← citeshttps://doi.org/10.1007/s10827-022-00826-8openalex-snapshot

Thalamocortical bistable switch as a theoretical model of fibromyalgia pathogenesis inferred from a literature survey

inferred← citeshttps://doi.org/10.1007/s11033-025-10888-3openalex-snapshot

The role of sesamin in alleviating acute and chronic pain: a focus on the TRL4-NF-KB-NLRP3 signaling pathway

inferred← citeshttps://doi.org/10.1007/s11064-016-1880-6openalex-snapshot

Role of the RVM in Descending Pain Regulation Originating from the Cerebrospinal Fluid-Contacting Nucleus

inferred← citeshttps://doi.org/10.1007/s11682-022-00652-7openalex-snapshot

Functional connectivity modulations during offset analgesia in chronic pain patients: an fMRI study

inferred← citeshttps://doi.org/10.1007/s11892-019-1150-5openalex-snapshot

Painful and Painless Diabetic Neuropathies: What Is the Difference?

inferred← citeshttps://doi.org/10.1007/s11910-020-01068-wopenalex-snapshot

Post-Traumatic Headache in Children and Adolescents: a Narrative Review with a Focus on Management

inferred← citeshttps://doi.org/10.1007/s11916-018-0666-8openalex-snapshot

Chronification of Pain: Mechanisms, Current Understanding, and Clinical Implications

inferred← citeshttps://doi.org/10.1007/s11916-019-0766-0openalex-snapshot

Pavlov’s Pain: the Effect of Classical Conditioning on Pain Perception and its Clinical Implications

inferred← citeshttps://doi.org/10.1007/s11916-024-01353-0openalex-snapshot

Pain and Perception: Exploring Psychedelics as Novel Therapeutic Agents in Chronic Pain Management

inferred← citeshttps://doi.org/10.1007/s11916-025-01426-8openalex-snapshot

The Mechanism of Action of Remote Electrical Neuromodulation (REN) in Treating Migraine and Potentially Other Idiopathic Pain Conditions

inferred← citeshttps://doi.org/10.1007/s11926-024-01159-4openalex-snapshot

How to Distinguish Non-Inflammatory from Inflammatory Pain in RA?

inferred← citeshttps://doi.org/10.1007/s12264-025-01519-9openalex-snapshot

Chemokine CCL2 Mediates Neuroglial Crosstalk and Drives Chronic Pain Pathogenesis

inferred← citeshttps://doi.org/10.1007/s12264-025-01553-7openalex-snapshot

A Novel Long-range Excitatory Neural Circuit from the Magnocellular Red Nucleus to Spinal Dorsal Horn Facilitates Neuropathic Pain-like Behaviors in Male Mice

inferred← citeshttps://doi.org/10.1007/s12671-017-0823-xopenalex-snapshot

Immediate and Lasting Chronic Pain Reduction Following a Brief Self-Implemented Mindfulness-Based Interoceptive Exposure Task: a Pilot Study

inferred← citeshttps://doi.org/10.1007/s13365-018-0686-5openalex-snapshot

Enhanced facilitation and diminished inhibition characterizes the pronociceptive endogenous pain modulatory balance of persons living with HIV and chronic pain

inferred← citeshttps://doi.org/10.1007/s15016-016-5547-yopenalex-snapshot

Thorakaler Diskusprolaps – oft falsch eingeschätzt?

inferred← citeshttps://doi.org/10.1007/s40122-024-00601-wopenalex-snapshot

Correlations of The Central Sensitization Inventory, conditioned pain modulation, cognitions and psychological factors in individuals with chronic neck pain: A cross-sectional study

inferred← citeshttps://doi.org/10.1007/s40263-016-0328-5openalex-snapshot

Unexplained Painful Physical Symptoms in Patients with Major Depressive Disorder: Prevalence, Pathophysiology and Management

inferred← citeshttps://doi.org/10.1007/s40263-024-01072-5openalex-snapshot

Pharmacological and Non-pharmacological Approaches for the Management of Neuropathic Pain in Multiple Sclerosis

inferred← citeshttps://doi.org/10.1007/s40265-018-1007-2openalex-snapshot

Tapentadol Prolonged Release: A Review in Pain Management

inferred← citeshttps://doi.org/10.1007/s40265-023-01927-zopenalex-snapshot

Pharmacological Management of Orofacial Pain

inferred← citeshttps://doi.org/10.1007/s40266-025-01225-1openalex-snapshot

Pain in Osteoporosis: Current and Future Strategies

inferred← citeshttps://doi.org/10.1007/s40429-024-00563-1openalex-snapshot

Managing Pain in Patients With Comorbid Alcohol Use Disorder and Chronic Pain

inferred← citeshttps://doi.org/10.1007/s40675-025-00326-yopenalex-snapshot

Inflammatory and Central Pain-Modulatory Pathways Linking Sleep Disturbances with Pain: The Role of Sex

inferred← citeshttps://doi.org/10.1007/s41204-025-00438-4openalex-snapshot

Nanomaterial derived electroceuticals for personalized pain and inflammation: technologies and patents

inferred← citeshttps://doi.org/10.1007/s42399-022-01268-0openalex-snapshot

Transcutaneous Vagus Nerve Stimulation: an Alternative Treatment of Chronic Migraine—a Systematic Review

inferred← citeshttps://doi.org/10.1016/b978-0-08-101012-9.00011-3openalex-snapshot

Pain in pigs

inferred← citeshttps://doi.org/10.1016/b978-0-12-805408-6.00035-xopenalex-snapshot

The Senses Fibromyalgia

inferred← citeshttps://doi.org/10.1016/b978-0-12-809324-5.24257-0openalex-snapshot

Neuropathic Pain: Mechanisms, Clinical Aspects and Treatment Options

inferred← citeshttps://doi.org/10.1016/b978-0-12-818988-7.00034-0openalex-snapshot

Phantom limb pain

inferred← citeshttps://doi.org/10.1016/b978-0-12-820589-1.00028-2openalex-snapshot

Neurocognition and placebo analgesia: Linking in functional magnetic resonance imaging

inferred← citeshttps://doi.org/10.1016/b978-0-12-820669-0.00010-4openalex-snapshot

Spinal cord involvement in diabetic neuropathy and neuropathic pain

inferred← citeshttps://doi.org/10.1016/b978-0-323-40196-8.00001-2openalex-snapshot

Anatomy and Physiology of the Pain Signaling Process

inferred← citeshttps://doi.org/10.1016/b978-0-323-48566-1.00002-4openalex-snapshot

Central Sensitization, Central Sensitization Syndromes, and Chronic Neuropathic Pain

inferred← citeshttps://doi.org/10.1016/b978-0-323-71317-7.00006-8openalex-snapshot

A Practical Approach to the Treatment of Painful Polyneuropathies

inferred← citeshttps://doi.org/10.1016/b978-0-323-88389-4.00063-4openalex-snapshot

Psychosocial recovery and reintegration of patients with burn injuries

inferred← citeshttps://doi.org/10.1016/b978-0-443-10583-8.00020-9openalex-snapshot

Surgical Pain Management

inferred← citeshttps://doi.org/10.1016/b978-0-443-15736-3.00003-2openalex-snapshot

Brainstem in pain control

inferred← citeshttps://doi.org/10.1016/b978-0-443-24705-7.00002-8openalex-snapshot

Neuroanatomy and neurophysiology of migraine

inferred← citeshttps://doi.org/10.1016/b978-0-444-63954-7.00039-2openalex-snapshot

Sport-related injury and pain classification

inferred← citeshttps://doi.org/10.1016/b978-0-444-64125-0.00017-7openalex-snapshot

Serotonin—pain modulation

inferred← citeshttps://doi.org/10.1016/bs.apha.2017.05.003openalex-snapshot

Cannabinoids and Pain: Sites and Mechanisms of Action

inferred← citeshttps://doi.org/10.1016/bs.irn.2024.10.005openalex-snapshot

Clinical neurophysiology of neuropathic pain

inferred← citeshttps://doi.org/10.1016/bs.irn.2024.10.008openalex-snapshot

Neuroanatomy of the nociceptive system: From nociceptors to brain networks

inferred← citeshttps://doi.org/10.1016/bs.irn.2025.02.002openalex-snapshot

Cognitive and affective models of psychedelics in rodents

inferred← citeshttps://doi.org/10.1016/j.adaj.2023.02.017openalex-snapshot

Insomnia is associated with symptoms of central sensitization in patients with painful temporomandibular disorders

inferred← citeshttps://doi.org/10.1016/j.addbeh.2026.108839openalex-snapshot

Bidirectional associations between pain and e-cigarette use among young adults using data from PATH Waves 7 and 7.5

inferred← citeshttps://doi.org/10.1016/j.anclin.2016.01.003openalex-snapshot

Advancing the Pain Agenda in the Veteran Population

inferred← citeshttps://doi.org/10.1016/j.archoralbio.2022.105570openalex-snapshot

Efficacy and mechanism of the antinociceptive effects of cannabidiol on acute orofacial nociception induced by Complete Freund’s Adjuvant in male Mus musculus mice

inferred← citeshttps://doi.org/10.1016/j.arr.2024.102249openalex-snapshot

Mechanisms of pain in aging and age-related conditions: Focus on caregivers

inferred← citeshttps://doi.org/10.1016/j.arth.2022.10.007openalex-snapshot

Significant Analgesic Benefits of Perioperative Duloxetine in Patients Who Have Depressive Symptoms Undergoing Total Hip Arthroplasty: A Randomized Controlled Trial

inferred← citeshttps://doi.org/10.1016/j.bbi.2023.08.018openalex-snapshot

Beyond biopsychosocial: The keystone mechanism theory of pain

inferred← citeshttps://doi.org/10.1016/j.bbi.2025.01.021openalex-snapshot

Neonatal exposure to morphine results in prolonged pain hypersensitivity during adolescence, driven by gut microbial dysbiosis and gut-brain axis-mediated inflammation

inferred← citeshttps://doi.org/10.1016/j.bbih.2026.101339openalex-snapshot

An explorative cross-sectional study on the association between immunological biomarkers in patients with chronic pain

inferred← citeshttps://doi.org/10.1016/j.bbr.2018.04.055openalex-snapshot

Diffuse noxious inhibitory controls and brain networks are modulated in a testosterone-dependent manner in Sprague Dawley rats

inferred← citeshttps://doi.org/10.1016/j.bbr.2024.115215openalex-snapshot

Inflammatory injury induces pain sensitization that is expressed beyond the site of injury in male (and not in female) mice

inferred← citeshttps://doi.org/10.1016/j.bbr.2026.116329openalex-snapshot

Fatty acid amide hydrolase (FAAH) inhibitor reduces persistent inflammatory pain in mice depending on μ- and δ-opioid receptors activity: Involvement of heme oxygenase-1

inferred← citeshttps://doi.org/10.1016/j.bbrc.2017.05.036openalex-snapshot

Inhibition of the high affinity choline transporter enhances hyperalgesia in a rat model of chronic pancreatitis

inferred← citeshttps://doi.org/10.1016/j.bbrc.2018.08.137openalex-snapshot

Norepinephrine-induced downregulation of GLT-1 mRNA in rat astrocytes

inferred← citeshttps://doi.org/10.1016/j.bbrc.2019.02.153openalex-snapshot

New nociceptive circuits to the hypothalamic perifornical area from the spinal cord and spinal trigeminal nucleus via the parabrachial nucleus

inferred← citeshttps://doi.org/10.1016/j.bcp.2024.116516openalex-snapshot

Ketamine – An Imperfect Wonder Drug?

inferred← citeshttps://doi.org/10.1016/j.biopha.2023.115360openalex-snapshot

The antidepressant drugs vortioxetine and duloxetine differentially and sex-dependently affect animal well-being, cognitive performance, cardiac redox status and histology in a model of osteoarthritis

inferred← citeshttps://doi.org/10.1016/j.biopsych.2021.11.023openalex-snapshot

The Role of the Locus Coeruleus in Pain and Associated Stress-Related Disorders

inferred← citeshttps://doi.org/10.1016/j.bja.2019.07.026openalex-snapshot

Pain regulation by gut microbiota: molecular mechanisms and therapeutic potential

inferred← citeshttps://doi.org/10.1016/j.bja.2026.03.069openalex-snapshot

Nucleus raphe magnus serotonin neurones bidirectionally control spinal nociceptive transmission in mice

inferred← citeshttps://doi.org/10.1016/j.brainres.2018.08.003openalex-snapshot

nNOS immunoreactivity co-localizes with GABAergic and cholinergic neurons, and associates with β-endorphinergic and met-enkephalinergic opioidergic fibers in rostral ventromedial medulla and A5 of the mouse

inferred← citeshttps://doi.org/10.1016/j.brainres.2019.03.018openalex-snapshot

The blockade of 5-HT1A receptors in the ventral tegmental area inhibited morphine/dextromethorphan-induced analgesia in pain rat models

inferred← citeshttps://doi.org/10.1016/j.brainres.2021.147539openalex-snapshot

Responses of neurons in rostral ventromedial medulla to nociceptive stimulation of craniofacial region and tail in rats

inferred← citeshttps://doi.org/10.1016/j.brainresbull.2022.02.002openalex-snapshot

Impaired visceral pain-related functions of the midbrain periaqueductal gray in rats with colitis

inferred← citeshttps://doi.org/10.1016/j.brainresbull.2025.111616openalex-snapshot

The D2-like dopamine and opioidergic receptors have interactions in the CA1 region of the hippocampus in modulating the formalin-induced inflammatory pain

inferred← citeshttps://doi.org/10.1016/j.brat.2025.104824openalex-snapshot

A randomized-controlled trial comparing relative effects of mindfulness-based interoceptive exposure focus versus distraction on cold-pressor induced pain

inferred← citeshttps://doi.org/10.1016/j.brs.2023.07.058openalex-snapshot

BurstDR spinal cord stimulation rebalances pain input and pain suppression in the brain in chronic neuropathic pain

inferred← citeshttps://doi.org/10.1016/j.brs.2024.08.007openalex-snapshot

Genetic labeling of the nucleus of tractus solitarius neurons associated with electrical stimulation of the cervical or auricular vagus nerve in mice

inferred← citeshttps://doi.org/10.1016/j.cct.2025.107947openalex-snapshot

Evaluating brain mechanisms of combined vagus nerve stimulation and mindfulness training for migraine: A randomized 2 × 2 factorial clinical trial protocol

inferred← citeshttps://doi.org/10.1016/j.clineuro.2023.108089openalex-snapshot

Volumetric alteration of brainstem in female migraineurs with and without aura

inferred← citeshttps://doi.org/10.1016/j.cophys.2019.03.008openalex-snapshot

Supraspinal neuroimmune crosstalk in chronic pain states

inferred← citeshttps://doi.org/10.1016/j.cophys.2019.06.001openalex-snapshot

Inflammatory pain neural plasticity

inferred← citeshttps://doi.org/10.1016/j.cub.2025.07.005openalex-snapshot

A history of injury enhances affective and sensory responses to predator threat by sensitizing corticosterone release through TRPA1 receptor signaling

inferred← citeshttps://doi.org/10.1016/j.douler.2021.01.003openalex-snapshot

La formation réticulée : anatomie, fonctions dans le contrôle de la douleur

inferred← citeshttps://doi.org/10.1016/j.drudis.2017.04.016openalex-snapshot

Animal models of pain and migraine in drug discovery

inferred← citeshttps://doi.org/10.1016/j.drugalcdep.2016.12.002openalex-snapshot

Providing chronic pain management in the “Fifth Vital Sign” Era: Historical and treatment perspectives on a modern-day medical dilemma

inferred← citeshttps://doi.org/10.1016/j.ejphar.2016.05.041openalex-snapshot

Preventive and alleviative effects of the dual enkephalinase inhibitor (Denki) PL265 in a murine model of neuropathic pain

inferred← citeshttps://doi.org/10.1016/j.ejphar.2019.172859openalex-snapshot

Histamine H4 receptor stimulation in the locus coeruleus attenuates neuropathic pain by promoting the coeruleospinal noradrenergic inhibitory pathway

inferred← citeshttps://doi.org/10.1016/j.ejphar.2023.175810openalex-snapshot

Targeting α7-nAChR by galantamine mitigates reserpine-induced fibromyalgia-like symptoms in rats: Involvement of cAMP/PKA, PI3K/AKT, and M1/M2 microglia polarization

inferred← citeshttps://doi.org/10.1016/j.eplepsyres.2026.107839openalex-snapshot

Maximal electroconvulsive shock-induced seizures elicit long-lasting analgesia and short-lasting hyperoxia in a sex dependent manner

inferred← citeshttps://doi.org/10.1016/j.expneurol.2016.06.019openalex-snapshot

Peripheral and central neuronal ATF3 precedes CD4+ T-cell infiltration in EAE

inferred← citeshttps://doi.org/10.1016/j.expneurol.2018.05.002openalex-snapshot

Ionic plasticity and pain: The loss of descending serotonergic fibers after spinal cord injury transforms how GABA affects pain

inferred← citeshttps://doi.org/10.1016/j.expneurol.2019.112976openalex-snapshot

Enhanced descending pain facilitation in acute traumatic brain injury

inferred← citeshttps://doi.org/10.1016/j.expneurol.2020.113428openalex-snapshot

Loss of diffuse noxious inhibitory control after traumatic brain injury in rats: A chronic issue

inferred← citeshttps://doi.org/10.1016/j.expneurol.2026.115690openalex-snapshot

Depleting non-resolving neuroinflammation in chronic spinal cord injury attenuates thermal hypersensitivity

inferred← citeshttps://doi.org/10.1016/j.gaitpost.2019.04.007openalex-snapshot

Gluteus medius activity during gait is altered in individuals with chronic ankle instability: An ultrasound imaging study

inferred← citeshttps://doi.org/10.1016/j.heliyon.2025.e43409openalex-snapshot

Effectiveness of sensorimotor training on pain, cervical joint position sense, range of motion, balance, and disability in chronic neck pain: A systematic review

inferred← citeshttps://doi.org/10.1016/j.ibneur.2022.12.007openalex-snapshot

Research progress on the mechanism of chronic neuropathic pain

inferred← citeshttps://doi.org/10.1016/j.ibror.2019.05.005openalex-snapshot

Acute nociceptive stimuli rapidly induce the activity of serotonin and noradrenalin neurons in the brain stem of awake mice

inferred← citeshttps://doi.org/10.1016/j.ibror.2020.01.003openalex-snapshot

Impaired hemodynamic activity in the right dorsolateral prefrontal cortex is associated with impairment of placebo analgesia and clinical symptoms in postherpetic neuralgia

inferred← citeshttps://doi.org/10.1016/j.ijosm.2017.05.002openalex-snapshot

Integrating osteopathic approaches based on biopsychosocial therapeutic mechanisms. Part 1: The mechanisms

inferred← citeshttps://doi.org/10.1016/j.isci.2026.117340openalex-snapshot

Green light exposure reduces central sensitization in cats with osteoarthritis-associated somatosensory impairment

inferred← citeshttps://doi.org/10.1016/j.jare.2025.02.037openalex-snapshot

Dual function of MrgprB2 receptor-dependent neural immune axis in chronic pain

inferred← citeshttps://doi.org/10.1016/j.jbmt.2023.12.005openalex-snapshot

Association between myofascial trigger point therapy and conditioned pain modulation

inferred← citeshttps://doi.org/10.1016/j.jep.2024.117710openalex-snapshot

Ayahuasca and its major component harmine promote antinociceptive effects in mouse models of acute and chronic pain

inferred← citeshttps://doi.org/10.1016/j.jneumeth.2020.108997openalex-snapshot

Animal models of pain: Diversity and benefits

inferred← citeshttps://doi.org/10.1016/j.jneuroim.2020.577198openalex-snapshot

Sepsis-induced encephalopathy impairs descending nociceptive pathways in rats

inferred← citeshttps://doi.org/10.1016/j.jpain.2015.01.007openalex-snapshot

Relationship Between Blood- and Cerebrospinal Fluid–Bound Neurotransmitter Concentrations and Conditioned Pain Modulation in Pain-Free and Chronic Pain Subjects

inferred← citeshttps://doi.org/10.1016/j.jpain.2015.12.001openalex-snapshot

Central Sensitization and Neuropathic Features of Ongoing Pain in a Rat Model of Advanced Osteoarthritis

inferred← citeshttps://doi.org/10.1016/j.jpain.2016.09.005openalex-snapshot

Dysfunctional Pain Modulation in Torture Survivors: The Mediating Effect of PTSD

inferred← citeshttps://doi.org/10.1016/j.jpain.2016.11.004openalex-snapshot

The Transition of Acute Postoperative Pain to Chronic Pain: An Integrative Overview of Research on Mechanisms

inferred← citeshttps://doi.org/10.1016/j.jpain.2017.07.002openalex-snapshot

Modulation of Itch by Conditioning Itch and Pain Stimulation in Healthy Humans

inferred← citeshttps://doi.org/10.1016/j.jpain.2017.11.004openalex-snapshot

Endogenous Pain Modulation Induced by Extrinsic and Intrinsic Psychological Threat in Healthy Individuals

inferred← citeshttps://doi.org/10.1016/j.jpain.2018.04.012openalex-snapshot

The Influence of Placebo Analgesia Manipulations on Pain Report, the Nociceptive Flexion Reflex, and Autonomic Responses to Pain

inferred← citeshttps://doi.org/10.1016/j.jpain.2018.06.004openalex-snapshot

Nociceptive and Cognitive Changes in a Murine Model of Polytrauma

inferred← citeshttps://doi.org/10.1016/j.jpain.2020.10.007openalex-snapshot

Transcranial Direct Current Stimulation of the Dorsolateral Prefrontal Cortex Alters Emotional Modulation of Spinal Nociception

inferred← citeshttps://doi.org/10.1016/j.jpain.2020.12.008openalex-snapshot

Serotonin Plays a Key Role in the Development of Opioid-Induced Hyperalgesia in Mice

inferred← citeshttps://doi.org/10.1016/j.jpain.2021.03.146openalex-snapshot

The Relationship Between Adverse Life Events and Endogenous Inhibition of Pain and Spinal Nociception: Findings From the Oklahoma Study of Native American Pain Risk (OK-SNAP)

inferred← citeshttps://doi.org/10.1016/j.jpain.2021.12.005openalex-snapshot

Family History of Alcohol Use Disorder as a Predictor of Endogenous Pain Modulation Among Moderate to Heavy Drinkers

inferred← citeshttps://doi.org/10.1016/j.jpain.2023.02.024openalex-snapshot

Mechanical and Heat Hyperalgesia upon Withdrawal From Chronic Intermittent Ethanol Vapor Depends on Sex, Exposure Duration, and Blood Alcohol Concentration in Mice

inferred← citeshttps://doi.org/10.1016/j.jpain.2023.03.009openalex-snapshot

Persistent Changes in Mechanical Nociception in Rats With Traumatic Brain Injury Involving Polytrauma

inferred← citeshttps://doi.org/10.1016/j.jpain.2023.08.005openalex-snapshot

Differential Effects of Thermal Stimuli in Eliciting Temporal Contrast Enhancement: A Psychophysical Study

inferred← citeshttps://doi.org/10.1016/j.jpain.2023.10.027openalex-snapshot

Gender Differences in Pain Threshold, Unpleasantness, and Descending Pain Modulatory Activation Across the Adult Life Span: A Cross Sectional Study

inferred← citeshttps://doi.org/10.1016/j.jpain.2023.11.012openalex-snapshot

EEG-Based Cortical Alterations in Individuals With Chronic Knee Pain Secondary to Osteoarthritis: A Cross-sectional Investigation

inferred← citeshttps://doi.org/10.1016/j.jpain.2024.104611openalex-snapshot

Assessing the Influence of Nonischemic A-Fiber Conduction Blockade on Offset Analgesia: An Experimental Study

inferred← citeshttps://doi.org/10.1016/j.jpain.2024.104691openalex-snapshot

High Body Mass Index Disrupts the Homeostatic Effects of Pain Inhibitory Control in the Symptomatology of Patients With Fibromyalgia

inferred← citeshttps://doi.org/10.1016/j.jpain.2026.106213openalex-snapshot

Thalamocortical and corticostriatal pathways in the progression from acute to chronic musculoskeletal pain: An fMRI study

inferred← citeshttps://doi.org/10.1016/j.jpain.2026.106281openalex-snapshot

Connectivity of neuropeptide Y-Cre spinal interneurons reveal monosynaptic inputs from pathways involved in pain and itch in mice

inferred← citeshttps://doi.org/10.1016/j.jpain.2026.106405openalex-snapshot

Bidirectional modulation of the R2 blink reflex using a lower limb cuff-pressure heterotopic conditioning stimulus across repeated sessions

inferred← citeshttps://doi.org/10.1016/j.jpsychires.2025.11.037openalex-snapshot

Electroacupuncture alleviates neuropathic pain and long-term cognitive impairment via the rACC-vlPAG neural circuit

inferred← citeshttps://doi.org/10.1016/j.jspd.2017.03.012openalex-snapshot

Preoperative Norepinephrine Levels in Cerebrospinal Fluid and Plasma Correlate With Pain Intensity After Pediatric Spine Surgery

inferred← citeshttps://doi.org/10.1016/j.jval.2024.07.022openalex-snapshot

Age and Gender Differences in the Relationship Between Chronic Pain and Dementia Among Older Australians

inferred← citeshttps://doi.org/10.1016/j.kine.2017.02.131openalex-snapshot

Modulation et dérèglements neurophysiologiques des voies de la douleur

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