Neuralgia
|
0.400 |
Biomarker
|
phenotype |
BEFREE |
PERSPECTIVE: This study demonstrates that a MOR-DOR dual agonist given chronically in chronic neuropathic pain models has enhanced efficacy with strongly reduced tolerance and dependence, with a further anti-inflammatory effect in the spinal cord.
|
31201990 |
2019 |
Neuralgia
|
0.400 |
Biomarker
|
phenotype |
BEFREE |
We further show that the inhibitory function of MOR is impaired during neuropathic pain.
|
31316354 |
2019 |
Neuralgia
|
0.400 |
PosttranslationalModification
|
phenotype |
BEFREE |
These findings indicate that OCT1 may participate in neuropathic pain at least in part by transcriptionally activating Dnmt3a and subsequently epigenetic silencing of Oprm1 and Kcan2 in the DRG.
|
30247265 |
2019 |
Neuralgia
|
0.400 |
AlteredExpression
|
phenotype |
BEFREE |
These findings suggest that DRG TET1 overexpression mitigated neuropathic pain likely through rescue of MOR and Kv1.2 expression in the ipsilateral DRG.
|
30515739 |
2019 |
Neuralgia
|
0.400 |
Biomarker
|
phenotype |
BEFREE |
Moreover, evidences of neuroplastic changes that may underlie the low efficacy of MOR agonists under neuropathic pain conditions are reviewed and discussed.
|
30318675 |
2019 |
Neuralgia
|
0.400 |
Biomarker
|
phenotype |
BEFREE |
Agonists selectively acting at NOP, MOP, DOP and KOP receptors as well as mixed opioid receptor agonists are known to exert anti-hypersensitive efficacy in the rat spinal nerve ligation (SNL) model of neuropathic pain.
|
29524385 |
2018 |
Neuralgia
|
0.400 |
GeneticVariation
|
phenotype |
BEFREE |
In the meta-analysis, polymorphisms in HLA-DRB1*13 (odds ratio [OR], 2.96; confidence interval [CI], 1.93-4.56), HLA-DRB1*04 (OR, 1.40; CI, 1.02-1.93), HLA-DQB1*03 (OR, 2.86; CI, 1.57-5.21), HLA-A*33 (OR, 2.32; CI, 1.42-3.80), and HLA-B*44 (OR, 3.17; CI, 2.22-4.55) were associated with significantly increased risk of developing NP, whereas HLA-A*02 (OR, 0.64; CI, 0.47-0.87) conferred reduced risk and neither rs1799971 in OPRM1 (OR, 0.55; CI, 0.27-1.11) nor rs4680 in COMT (OR, 0.95; CI, 0.81-1.13) were significantly associated with NP.
|
29351172 |
2018 |
Neuralgia
|
0.400 |
Biomarker
|
phenotype |
BEFREE |
Endomorphins (EMs, including EM-1 and EM-2), the most effective and specific endogenous agonists of the MOR, exert more potent analgesia in acute and neuropathic pain than other opiates, such as morphine.
|
28848403 |
2017 |
Neuralgia
|
0.400 |
Biomarker
|
phenotype |
BEFREE |
Bivalent ligand that activates mu opioid receptor and antagonizes mGluR5 receptor reduces neuropathic pain in mice.
|
28891868 |
2017 |
Neuralgia
|
0.400 |
AlteredExpression
|
phenotype |
BEFREE |
Inhibition of DNMT3a catalytic activity with DNMT inhibitor RG108 significantly blocked the increase in methylation of the MOR promoter, and then upregulated MOR expression and attenuated thermal hyperalgesia in neuropathic pain mice.
|
29075135 |
2017 |
Neuralgia
|
0.400 |
Biomarker
|
phenotype |
BEFREE |
Blocking this increase also prevented the nerve injury-induced increase in DNA methylation in the promoter and 5'-untranslated region of the Oprm1 gene in the injured DRG, restored morphine or loperamide (a peripheral acting MOR preferring agonist) analgesic effects, and attenuated the development of their analgesic tolerance under neuropathic pain conditions.
|
28267064 |
2017 |
Neuralgia
|
0.400 |
Biomarker
|
phenotype |
BEFREE |
Mimicking SNL-induced DRG miR-143 downregulation through DRG microinjection of miR143 inhibitors in naive rats increased the expression of Dnmt3a and reduced the expression of <i>Oprm1</i> mRNA and MOR in injected DRG and produced neuropathic pain-like symptoms.
|
29170626 |
2017 |
Neuralgia
|
0.400 |
GeneticVariation
|
phenotype |
BEFREE |
Effect of naltrexone on neuropathic pain in mice locally transfected with the mutant μ-opioid receptor gene in spinal cord.
|
24866991 |
2015 |
Neuralgia
|
0.400 |
AlteredExpression
|
phenotype |
BEFREE |
Our present data suggested a model that miR-134 participated in CFA-induced inflammatory pain by balancing the expression of MOR1 in DRGs, which implied that miR-134 may be a potential therapeutic target for the treatment of neuropathic pain including inflammation.
|
22865422 |
2013 |
Neuralgia
|
0.400 |
Biomarker
|
phenotype |
CTD_human |
Pharmacological characterization and gene expression profiling of an L5/L6 spinal nerve ligation model for neuropathic pain in mice.
|
18400411 |
2008 |
Neuralgia
|
0.400 |
Biomarker
|
phenotype |
BEFREE |
To assess whether MOP-R phosphorylation occurs following endogenous opioid release, we induced chronic neuropathic pain by partial sciatic nerve ligation (pSNL), which caused a significant increase in MOR-P2-IR in the striatum. pSNL also induced signs of mu opioid receptor tolerance demonstrated by a rightward shift in the morphine dose response in the tail withdrawal assay and by a reduction in morphine conditioned place preference (CPP).
|
17467916 |
2007 |
Neuralgia
|
0.400 |
Biomarker
|
phenotype |
CTD_human |
Loss of peripheral morphine analgesia contributes to the reduced effectiveness of systemic morphine in neuropathic pain.
|
14718584 |
2004 |
Neuralgia
|
0.400 |
AlteredExpression
|
phenotype |
BEFREE |
Plasticity of MuOR gene expression may contribute to variations in clinical responses to opioid analgesics in clinical states such as neuropathic pain.
|
9366465 |
1997 |