2020
DOI: 10.1007/s12031-020-01626-4
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TRPV1, Targeted by miR-338-3p, Induces Neuropathic Pain by Interacting with NECAB2

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Cited by 17 publications
(14 citation statements)
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References 26 publications
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“…Recently, a study found that the expression of TRPV1 mRNA and protein was significantly up-regulated in the dorsal spinal cord tissues in a rat model of chronic constriction injury [28] . TRPV1 up-regulation apparently increased mechanical allodynia and thermal hyperalgesia as well as the expression of inflammationassociated genes (COX-2, TNF-α, and IL-6).…”
Section: Trpv1 Channelmentioning
confidence: 99%
See 1 more Smart Citation
“…Recently, a study found that the expression of TRPV1 mRNA and protein was significantly up-regulated in the dorsal spinal cord tissues in a rat model of chronic constriction injury [28] . TRPV1 up-regulation apparently increased mechanical allodynia and thermal hyperalgesia as well as the expression of inflammationassociated genes (COX-2, TNF-α, and IL-6).…”
Section: Trpv1 Channelmentioning
confidence: 99%
“…Moreover, TRPV1 was identified as a downstream target of miR-338-3p and overexpression of TRPV1 restrained the inhibitory effect of miR-338-3p on neuropathic. It appears that TRPV1 has the potential to be a target for the treatment of neuropathic [28] . Clearly, further studies on this pathway may yield desirable results for the development of novel therapeutic strategy of migraine, a typical neuroinflammatory disease.…”
Section: Trpv1 Channelmentioning
confidence: 99%
“…More recently, several studies examined the regulatory role played by microRNAs (miRNAs) in posttranscriptional regulation of TRPV1. For instance, it was demonstrated that miR-338-3p directly targets TRPV1, increasing mechanical allodynia and thermal hyperalgesia as well as the expression of inflammation-associated genes (COX-2, TNF-α, and IL-6) [80]. Regarding the spermatozoa, dysregulation of miRNAs has been correlated to male infertility [170], allowing to hypothesize a correlation between miRNAs and TRPV1 receptor also in spermatozoa.…”
Section: Sperm Chemotaxis Trpv1 and The Endocannabinoid System (Ecs)mentioning
confidence: 99%
“…According to the position of the first double bond present in their structures, this big family can be divided into n-3 (α-linolenic acid (ALA) and its products eicosapentanoic acid (EPA), docosahexaenoic acid (DHA), 20-hydroxyeicosapentaenoic acid (20-HEPE) and 22-hydroxyeicosapentaenoic acid (22-HDoHE)), and n-6 linoleic acid (LA) and its products γ-linoleic acid, arachidonic acid (AA) [ 69 ] (which produces hepoxylin, HXA-3, 14,15-epoxyeicosatrienoic acid, 14,15-EET, and 20-hydroxyeicosatetranoic acid, 20-HETE), 9- and 13-hydroxyoctadecadienoic acids (9-HODE and 13-HODE). Other agonists endogenously secreted are oxytocin [ 70 ], adenosine [ 71 ], nitric oxide [ 72 ], hydrogen sulfide (H 2 S) [ 73 ], lysophosphatidic acid (LPA) [ 74 ] and its derivative diacylglycerol [ 75 ], pH variations [ 76 , 77 ], vitamin D [ 78 ], N-acyl amino acids/neurotransmitters [ 79 ], miRNAs [ 80 , 81 ], prostaglandins, nerve growth factors and the endocannabinoids family, including N-Acyl amides [ 82 ] (N-acyl GABAS [ 83 , 84 ] derived then in D-GABAs, L-GABA and A-GABA) and N-acylethanolamines (NAEs) [ 85 ], such as anandamide (AEA) *** [ 86 ], oleylethanolamine (OEA) [ 87 ] and palmitoylethanolamine (PEA) [ 88 ]. * Product from arachidonic acid.…”
Section: Figurementioning
confidence: 99%
“…NECAB2 has been reported to interact with two G-protein coupled receptors in the human embryonic kidney cells in a calcium-regulated manner ( Canela et al, 2007 , 2009 ). At the spinal level, necab2 is down-regulated by the peripheral nerve injury ( Zhang et al, 2014 ) and functions as a critical determinant of pro-nociceptive neurotransmission ( Zhang et al, 2018 ; Ma et al, 2021 ). A proteomic study involving yeast two-hybrid screening showed that NECAB2 interacts with five autism-risk genes ( FMR1 , FXR1 , FXR2 , SMARCA2 , and TSC1 ) ( Sakai et al, 2011 ).…”
Section: Introductionmentioning
confidence: 99%