Morphine hyperalgesia gated through microglia-mediated disruption of neuronal Cl⁻ homeostasis.
about
Neurobiology of opioid dependence in creating addiction vulnerabilityGlia as drivers of abnormal neuronal activityPain and Poppies: The Good, the Bad, and the Ugly of Opioid AnalgesicsOpioid-induced central immune signaling: implications for opioid analgesiaEmerging targets in neuroinflammation-driven chronic painMu opioid receptors on primary afferent nav1.8 neurons contribute to opiate-induced analgesia: insight from conditional knockout miceActivation of mu opioid receptors sensitizes transient receptor potential vanilloid type 1 (TRPV1) via β-arrestin-2-mediated cross-talkOpioid receptor-triggered spinal mTORC1 activation contributes to morphine tolerance and hyperalgesiaNeuroinflammation-a co-occurring phenomenon linking chronic pain and opioid dependence.Toll-like receptor 4 mutant and null mice retain morphine-induced tolerance, hyperalgesia, and physical dependence.The Netrin-1 receptor DCC is a regulator of maladaptive responses to chronic morphine administrationBrain-derived neurotrophic factor involved epigenetic repression of UGT2B7 in colorectal carcinoma: A mechanism to alter morphine glucuronidation in tumor.P2X4 Receptor Function in the Nervous System and Current Breakthroughs in Pharmacology.Biphalin, a Dimeric Enkephalin, Alleviates LPS-Induced Activation in Rat Primary Microglial Cultures in Opioid Receptor-Dependent and Receptor-Independent Manners.Targeting brain-derived neurotrophic factor in the medial thalamus for the treatment of central poststroke pain in a rodent model.β-arrestin-2 regulates NMDA receptor function in spinal lamina II neurons and duration of persistent pain.Pain regulation by non-neuronal cells and inflammation.Pathological pain and the neuroimmune interface.β-arrestin-2-biased agonism of delta opioid receptors sensitizes transient receptor potential vanilloid type 1 (TRPV1) in primary sensory neurons.Erythropoietin attenuates loss of potassium chloride co-transporters following prenatal brain injury.Epigenetic regulation of spinal cord gene expression controls opioid-induced hyperalgesia.NADPH-oxidase 2 activation promotes opioid-induced antinociceptive tolerance in mice.Glial TLR4 signaling does not contribute to opioid-induced depression of respiration.Chloride extrusion enhancers as novel therapeutics for neurological diseasesToward a systematic approach to opioid rotation.Prevalence of narcotic bowel syndrome in opioid abusers in iran.A spinal analog of memory reconsolidation enables reversal of hyperalgesia.Evidence for brain glial activation in chronic pain patients.The pain interactome: connecting pain-specific protein interactions.Activation of adult rat CNS endothelial cells by opioid-induced toll-like receptor 4 (TLR4) signaling induces proinflammatory, biochemical, morphological, and behavioral sequelaeCation-chloride cotransporters in neuronal development, plasticity and diseaseReactive astrogliosis causes the development of spontaneous seizures.Role of the outer pore domain in transient receptor potential vanilloid 1 dynamic permeability to large cationsEngagement of the GABA to KCC2 signaling pathway contributes to the analgesic effects of A3AR agonists in neuropathic painMicroglia disrupt mesolimbic reward circuitry in chronic pain.Therapeutic restoration of spinal inhibition via druggable enhancement of potassium-chloride cotransporter KCC2-mediated chloride extrusion in peripheral neuropathic painIntrathecal rapamycin attenuates morphine-induced analgesic tolerance and hyperalgesia in rats with neuropathic pain.High salt intake increases blood pressure via BDNF-mediated downregulation of KCC2 and impaired baroreflex inhibition of vasopressin neuronsAssessment of morphine-induced hyperalgesia and analgesic tolerance in mice using thermal and mechanical nociceptive modalities.Neuroimmune Regulation of GABAergic Neurons Within the Ventral Tegmental Area During Withdrawal from Chronic Morphine.
P2860
Q26742048-BB08C1D6-D37A-4150-90F1-70304F61048AQ26771699-44640C00-5C6F-4414-92C4-D2DCCED8AC8CQ26782928-34391ABF-F625-4FE8-AD36-DFF6B950D029Q27021477-0E7945B0-CC29-45BD-A969-EEAC1A2CC374Q28242435-260983E5-03B6-47DB-9177-BDD6A68F57DEQ28533332-EC4D080D-CF91-42D0-B0DB-F833CA98BC72Q28541771-762DBE20-4352-43E7-A9CB-2E143C750CBBQ28576512-3711B8E9-7782-4DA5-8D6B-BEC5057DC485Q33602197-64AF453D-BC6B-4283-8862-B4D360F8734DQ33604982-3659AD5C-3385-4EB1-BDDF-64A79349E575Q33686637-8BCDEBD1-3820-44A7-B0E4-8F9604AFC6D5Q33710042-8FACA04D-6DB2-4F3A-AD41-1B7906C0CA2DQ33718454-4D69BB23-D8D3-4EED-AF01-561214446C46Q33721292-A3B8FC65-4296-4F5B-BFF9-11251DAECD4BQ33802458-A2854759-A2C9-4FB6-BE35-B0E499B43B53Q33814944-1B995111-BCD8-4310-AA23-2EFD98D8B034Q33846188-E7B1152A-2E67-4442-94AC-B98C42C7EDF3Q33925677-8F2DF173-7E7D-4D0C-9A79-33657E0B6661Q34039598-B085AF56-148F-4549-95F2-023A8D7CC642Q34053756-8566F7D4-8A1F-46CC-8184-5A6CDB59F174Q34227122-27E15064-0C6F-4123-93AA-B88006A3458BQ34285878-E10AA488-40B2-4338-9328-B110E5F07B25Q34353901-FAE6007B-B41E-4AAB-A0B1-620623A908BFQ34375595-18CF0057-3583-4A1B-BC89-37F892972A0EQ34394425-F673D2D6-437C-4DB8-A731-53977154941EQ34401446-872468F5-9FF1-4068-9A85-D51731F11585Q34428052-BC9DF2E6-EAF9-4149-ADD2-46F815DF4BDAQ34457857-1AA31224-BB4A-4453-B254-39F0C9FE7CD1Q34585717-3E0BACA3-581A-4E2A-B596-10933BC18AACQ34603199-EF8C4504-10E3-4B2B-8876-F4710DBAB76FQ34959293-8A55EC07-5A76-42EC-AA00-52D5D35A6242Q35117565-7C9AED16-B57E-450D-9416-D0768DD1DFF3Q35126683-C4E75A8F-5BBB-4B49-9C0B-603406CC3888Q35423661-134BF04B-985B-4622-B278-A715D450057CQ35675189-D20FCB67-A2C9-48F2-94FC-611765DB9A62Q35737356-1DB9AD1A-0F8F-4DDA-8208-1F4EA59139B1Q36016302-AC42BFBE-062E-4104-8E9F-882FD503B48CQ36078821-A8DF3167-8517-4E92-B093-B2275A2F9E6AQ36407701-38283417-631A-4A05-A120-9B1B930904C8Q36565595-845DF592-CB21-45B6-A686-C5A905363922
P2860
Morphine hyperalgesia gated through microglia-mediated disruption of neuronal Cl⁻ homeostasis.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on 06 January 2013
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Morphine hyperalgesia gated th ...... n of neuronal Cl⁻ homeostasis.
@en
Morphine hyperalgesia gated th ...... n of neuronal Cl⁻ homeostasis.
@nl
type
label
Morphine hyperalgesia gated th ...... n of neuronal Cl⁻ homeostasis.
@en
Morphine hyperalgesia gated th ...... n of neuronal Cl⁻ homeostasis.
@nl
prefLabel
Morphine hyperalgesia gated th ...... n of neuronal Cl⁻ homeostasis.
@en
Morphine hyperalgesia gated th ...... n of neuronal Cl⁻ homeostasis.
@nl
P2093
P2860
P50
P356
P1433
P1476
Morphine hyperalgesia gated th ...... n of neuronal Cl⁻ homeostasis.
@en
P2093
Antoine G Godin
Catherine M Cahill
Karen Vandal
Louis-Etienne Lorenzo
Michael W Salter
Nicolas Doyon
Simon Beggs
Sophie Laffray
Theresa-Alexandra M Mattioli
Tuan Trang
P2860
P2888
P304
P356
10.1038/NN.3295
P407
P50
P577
2013-01-06T00:00:00Z