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Centralization of noxious stimulus-induced analgesia (NSIA) is related to activity at inhibitory synapses in the spinal cord

https://doi.org/10.1016/j.pain.2009.03.005
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What this work says

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

inferredcites →https://doi.org/10.1007/bf01244705openalex-snapshot
Neuroprotectant effects of LY 274614, a structurally novel systemically active competitive NMDA receptor antagonist
inferredcites →https://doi.org/10.1016/0006-8993(90)90599-7openalex-snapshot
Role of anterior pretectal nucleus in somatosensory cortical descending modulation of jaw-opening reflex in rats
inferredcites →https://doi.org/10.1016/0006-8993(91)90886-zopenalex-snapshot
Periaqueductal gray matter and nucleus raphe magnus involvement in anterior pretectal nucleus-induced inhibition of jaw-opening reflex in rats
inferredcites →https://doi.org/10.1016/0006-8993(92)90520-jopenalex-snapshot
Effects of lesions of locus coeruleus/subcoeruleus on diffuse noxious inhibitory controls in the rat
inferredcites →https://doi.org/10.1016/0006-8993(92)90888-gopenalex-snapshot
Immunohistochemical evidence that Met-enkephalin and GABA coexist in some neurones in rat dorsal horn
inferredcites →https://doi.org/10.1016/0006-8993(92)91071-lopenalex-snapshot
Involvement of the subnucleus reticularis dorsalis in diffuse noxious inhibitory controls in the rat
inferredcites →https://doi.org/10.1016/0014-2999(90)90337-6openalex-snapshot
CGP 35348: a centrally active blocker of GABAB receptors
inferredcites →https://doi.org/10.1016/0031-9384(76)90029-9openalex-snapshot
Chronic catheterization of the spinal subarachnoid space
inferredcites →https://doi.org/10.1016/0165-0173(85)90003-7openalex-snapshot
Is the jaw-opening reflex a valid model of pain?
inferredcites →https://doi.org/10.1016/0165-6147(96)10038-9openalex-snapshot
GABAC receptors: relatively simple transmitter-gated ion channels?
inferredcites →https://doi.org/10.1016/0301-0082(93)90045-topenalex-snapshot
The localization of classical transmitters and neuropeptides within neurons in laminae I–III of the mammalian spinal dorsal horn
inferredcites →https://doi.org/10.1016/0304-3959(79)90049-6openalex-snapshot
Diffuse noxious inhibitory controls (DNIC). I. Effects on dorsal horn convergent neurones in the rat
inferredcites →https://doi.org/10.1016/c2009-0-63235-9openalex-snapshot
The Rat Brain in Stereotaxic Coordinates
inferredcites →https://doi.org/10.1016/s0006-8993(00)03184-xopenalex-snapshot
Striatal modulation of the jaw opening reflex
inferredcites →https://doi.org/10.1016/s0006-8993(98)01050-6openalex-snapshot
Inhibitory effects of electrical stimulation of ventrolateral orbital cortex on the rat jaw-opening reflex
inferredcites →https://doi.org/10.1016/s0022-3565(25)23430-9openalex-snapshot
Novel peptidic mu opioid antagonists: pharmacologic characterization in vitro and in vivo.
inferredcites →https://doi.org/10.1016/s0028-3908(99)00082-9openalex-snapshot
2-Methyl-6-(phenylethynyl)-pyridine (MPEP), a potent, selective and systemically active mGlu5 receptor antagonist
inferredcites →https://doi.org/10.1016/s0028-3908(99)00167-7openalex-snapshot
Mobilisation of intracellular Ca2+ by mGluR5 metabotropic glutamate receptor activation in neonatal rat cultured dorsal root ganglia neurones
inferredcites →https://doi.org/10.1016/s0304-3940(98)00099-8openalex-snapshot
Central NO is involved in the antinociceptive action of intracisternal antidepressants in freely moving rats
inferredcites →https://doi.org/10.1016/s0304-3959(03)00332-4openalex-snapshot
Contribution of spinal glutamatergic mechanisms in heterosegmental antinociception induced by noxious stimulation
inferredcites →https://doi.org/10.1016/s0304-3959(99)00278-xopenalex-snapshot
Prolonged ovarian sex steroid treatment of male rats produces antinociception: identification of sex-based divergent analgesic mechanisms
inferredcites →https://doi.org/10.1016/s0306-4522(01)00175-0openalex-snapshot
NMDA or non-NMDA receptor antagonists attenuate increased Fos expression in spinal dorsal horn GABAergic neurons after intradermal injection of capsaicin in rats
inferredcites →https://doi.org/10.1016/s0306-4522(01)00264-0openalex-snapshot
Nicotine withdrawal hyperalgesia and opioid-mediated analgesia depend on nicotine receptors in nucleus accumbens
inferredcites →https://doi.org/10.1016/s0306-4522(99)00062-7openalex-snapshot
Electrically-evoked inhibitory effects of the nucleus submedius on the jaw-opening reflex are mediated by ventrolateral orbital cortex and periaqueductal gray matter in the rat
inferredcites →https://doi.org/10.1016/s0361-9230(98)00059-8openalex-snapshot
Suppressive effect of vagal afferents on the activity of the trigeminal spinal neurons related to the jaw-opening reflex in rats: involvement of the endogenous opioid system
inferredcites →https://doi.org/10.1046/j.1460-9568.2002.01915.xopenalex-snapshot
µ/δ Cooperativity and opposing κ‐opioid effects in nucleus accumbens‐mediated antinociception in the rat
inferredcites →https://doi.org/10.1046/j.1460-9568.2002.02204.xopenalex-snapshot
Inhibition of tonic spinal glutamatergic activity induces antinociception in the rat
inferredcites →https://doi.org/10.1111/j.1460-9568.2003.03031.xopenalex-snapshot
Contribution of spinal inhibitory receptors in heterosegmental antinociception induced by noxious stimulation
inferredcites →https://doi.org/10.1111/j.1476-5381.1991.tb12121.xopenalex-snapshot
Phosphinic acid analogues of GABA are antagonists at the GABAB receptor in the rat anococcygeus
inferredcites →https://doi.org/10.1113/expphysiol.1992.sp003593openalex-snapshot
Modulation by peripheral conditioning stimuli of the responses of trigeminal brain stem neurones and of the jaw opening reflex to tooth pulp stimulation in chronically prepared, anaesthetized cats
inferredcites →https://doi.org/10.1113/jphysiol.1993.sp019616openalex-snapshot
Studies of brain structures involved in diffuse noxious inhibitory controls in the rat: the rostral ventromedial medulla.
inferredcites →https://doi.org/10.1126/science.281.5375.419openalex-snapshot
Corelease of Two Fast Neurotransmitters at a Central Synapse
inferredcites →https://doi.org/10.1136/bmj.38042.506748.eeopenalex-snapshot
Systematic review of topical capsaicin for the treatment of chronic pain
inferredcites →https://doi.org/10.1152/jn.1990.64.6.1712openalex-snapshot
Studies of the brain structures involved in diffuse noxious inhibitory controls: the mesencephalon
inferredcites →https://doi.org/10.1523/jneurosci.15-04-03154.1995openalex-snapshot
Antinociception produced by an ascending spino-supraspinal pathway
inferredcites →https://doi.org/10.1523/jneurosci.19-16-07175.1999openalex-snapshot
Pain-Induced Analgesia Mediated by Mesolimbic Reward Circuits
inferredcites →https://doi.org/10.1523/jneurosci.22-15-06773.2002openalex-snapshot
Altered Nucleus Accumbens Circuitry Mediates Pain-Induced Antinociception in Morphine-Tolerant Rats

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.4468455openalex-extracted
Impact of Endogenous Analgesia Triggered by Acupuncture, Stress or Noxious Stimulation on the Pronociceptive Effect of Rem Sleep Deprivation
inferred← citeshttps://doi.org/10.1007/7854_2014_351openalex-snapshot
Endogenous Analgesia, Dependence, and Latent Pain Sensitization
inferred← citeshttps://doi.org/10.1007/s12035-018-1116-7openalex-snapshot
Pain Inhibits Pain: an Ascending-Descending Pain Modulation Pathway Linking Mesolimbic and Classical Descending Mechanisms
inferred← citeshttps://doi.org/10.1016/b978-0-12-802838-4.00028-5openalex-snapshot
Functional MRI Advances to Reveal the Hidden Networks Behind the Cerebral Processing of Itch
inferred← citeshttps://doi.org/10.1016/j.brainres.2012.05.010openalex-snapshot
The functional role of ascending nociceptive control in defensive behavior
inferred← citeshttps://doi.org/10.1016/j.jpain.2013.12.008openalex-snapshot
Ascending Nociceptive Control Contributes to the Antinociceptive Effect of Acupuncture in a Rat Model of Acute Pain
inferred← citeshttps://doi.org/10.1016/j.neuroscience.2014.10.049openalex-snapshot
Effect of pain chronification and chronic pain on an endogenous pain modulation circuit in rats
inferred← citeshttps://doi.org/10.1016/j.peptides.2010.09.016openalex-snapshot
Endogenous opiates and behavior: 2009
inferred← citeshttps://doi.org/10.1037/bne0000255openalex-snapshot
Pain chronification and chronic pain impair a defensive behavior, but not the ability of acute pain to facilitate it, through the activation of an endogenous analgesia circuit.
inferred← citeshttps://doi.org/10.1038/s41598-023-32512-9openalex-snapshot
Rat model of attention-deficit hyperactivity disorder exhibits delayed recovery from acute incisional pain due to impaired descending noradrenergic inhibition
inferred← citeshttps://doi.org/10.1039/9781782629276-00194openalex-snapshot
Positive Allosteric Modulators of Opioid Receptors
inferred← citeshttps://doi.org/10.1097/fbp.0000000000000529openalex-snapshot
Pain and stress: functional evidence that supra-spinal mechanisms involved in pain-induced analgesia mediate stress-induced analgesia
inferred← citeshttps://doi.org/10.1097/j.pain.0000000000004048openalex-snapshot
Cortical disinhibition in peripheral neuropathy unveiled by exploratory analysis of spectral alterations in contact heat–evoked potential
inferred← citeshttps://doi.org/10.1111/ejn.12688openalex-snapshot
Activation of transient receptor potential vanilloid 2‐expressing primary afferents stimulates synaptic transmission in the deep dorsal horn of the rat spinal cord and elicits mechanical hyperalgesia
inferred← citeshttps://doi.org/10.1126/science.1239403openalex-snapshot
Constitutive μ-Opioid Receptor Activity Leads to Long-Term Endogenous Analgesia and Dependence
inferred← citeshttps://doi.org/10.1152/ajpregu.00401.2016openalex-snapshot
Sex difference in the contribution of GABAB receptors to tibial neuromodulation of bladder overactivity in cats
inferred← citeshttps://doi.org/10.1186/1472-6882-14-96openalex-snapshot
Abundant expression and functional participation of TRPV1 at Zusanli acupoint (ST36) in mice: mechanosensitive TRPV1 as an “acupuncture-responding channel”
inferred← citeshttps://doi.org/10.1186/s12894-021-00899-0openalex-snapshot
Systemic and intrathecal baclofen produce bladder antinociception in rats
inferred← citeshttps://doi.org/10.1213/ane.0000000000001301openalex-snapshot
Amitriptyline, but Not Pregabalin, Reverses the Attenuation of Noxious Stimulus–Induced Analgesia After Nerve Injury in Rats
inferred← citeshttps://doi.org/10.1213/ane.0000000000002380openalex-snapshot
Repeated Administration of Duloxetine Suppresses Neuropathic Pain by Accumulating Effects of Noradrenaline in the Spinal Cord
inferred← citeshttps://doi.org/10.1556/2060.2023.00273openalex-snapshot
Impact of endogenous analgesia triggered by acupuncture, stress, or noxious stimulation on REM sleep-deprived rats
inferred← citeshttps://doi.org/10.3389/fphar.2025.1500313openalex-snapshot
Innovative therapeutic strategies using ADHD medications tailored to the behavioral characteristics of patients with chronic pain
inferred← citeshttps://doi.org/10.3390/molecules21070844openalex-snapshot
Capsaicin: Current Understanding of Its Mechanisms and Therapy of Pain and Other Pre-Clinical and Clinical Uses
inferred← citeshttps://doi.org/10.47749/t/unicamp.2013.907913openalex-snapshot
Efeito da hiperalgesia persistente no comportamento defensivo de ratos e na capacidade de um circuito de analgesia endógeno em modulá-lo
inferred← citeshttps://doi.org/10.47749/t/unicamp.2014.932732openalex-snapshot
Envolvimento de mediadores inflamatórios na hiperalgesia muscular induzida por contração isométrica sustentada em ratos
inferred← citeshttps://doi.org/10.47749/t/unicamp.2018.1062977openalex-snapshot
Efeito dos beta-adrenoceptores na redução da atividade do controle nociceptivo ascendente induzida pela hiperalgesia persistente
inferred← citeshttps://doi.org/10.47749/t/unicamp.2018.1096905openalex-snapshot
Estudo do efeito modulatório do exercício fisico sobre a antinocicepção induzida por estimulo nocivo em camundongos
inferred← citeshttps://doi.org/10.7759/cureus.64235openalex-snapshot
Use of Baclofen Premedication as an Analgesic Adjuvant in Patients Undergoing Percutaneous Nephrolithotripsy: A Placebo-Controlled, Double-Blind Randomized Trial
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