Search results for "TRPV Cation Channels"

showing 5 items of 15 documents

TRPV1 channels in nitric oxide-mediated signalling: insight on excitatory transmission in rat CA1 pyramidal neurons

2022

Nitric oxide (NO) is a fascinating signalling molecule implicated in a plethora of biological functions, especially at the synaptic level. Exploring neurotransmission in the hippocampus could be instrumental in the individuation of putative targets for nitric-oxide mediated neuromodulation, especially in terms of the potential repercussions on fundamental processes i.e. synaptic plasticity and excitability-related phenomena. Among these targets, endovanilloid signalling constitutes an object of study since Transient Receptors Vanilloid type 1 (TRPV1) channels possess a NO-sensitive gate modulating its activation. Also, NO has been referred to as a mediator for numerous endocannabinoid effec…

Pyramidal CellsTRPV Cation ChannelsNitric oxideNitric Oxide Synthase Type IAnandamideLigandsBiochemistrySynaptic TransmissionCA1RatsTRPV1mEPSCPhysiology (medical)Animals[SDV.NEU]Life Sciences [q-bio]/Neurons and Cognition [q-bio.NC]CapsaicinPatch-clampEndocannabinoids
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Phenotypic spectrum and incidence of TRPV4 mutations in patients with inherited axonal neuropathy.

2014

Objective: To clarify the phenotypic spectrum and incidence of TRPV4 mutations in patients with inherited axonal neuropathies. Methods: We screened for TRPV4 mutations in 169 French unrelated patients with inherited axonal peripheral neuropathy. Ninety-five patients had dominant Charcot-Marie-Tooth type 2 (CMT2) disease, and 74 patients, including 39 patients with distal hereditary motor neuropathy, 14 with congenital spinal muscular atrophy and arthrogryposis, 13 with CMT2, and 8 with scapuloperoneal spinal muscular atrophy, presented with additional vocal cord paralysis and/or skeletal dysplasia. Results: No deleterious TRPV4 mutation was identified in the 95 patients with “pure” CMT2 (0/…

TRPV4AdultMalePathologymedicine.medical_specialtyAdolescentTRPV Cation ChannelsYoung AdultMedicineMissense mutationHumansVocal cord paralysisHereditary Sensory and Autonomic NeuropathiesChildKyphoscoliosisAgedArthrogryposisbusiness.industryMusclesSpinal muscular atrophyMiddle Agedmedicine.diseasePhenotypeDysplasiaMutationFemaleNeurology (clinical)Francemedicine.symptomBone DiseasesbusinessAsymptomatic carrierNeurology
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How much potential for transient receptor potential channels in the bladder?

2015

Transient receptor potential channelbusiness.industryUrologyCystitisUrinary BladderBiophysicsAnimalsTRPV Cation ChannelsMedicineFemalebusinessBJU International
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'TRPing' synaptic ribbon function in the rat pineal gland: neuroendocrine regulation involves the capsaicin receptor TRPV1.

2009

Synaptic ribbons (SRs) are presynaptic structures thought to regulate and facilitate multivesicular release. In the pineal gland, they display a circadian rhythm with higher levels at night paralleling melatonin synthesis. To gain more insight into the processes involved and the possible functions of these structures, a series of experiments were conducted in rodents. We studied the regional distribution of a molecular marker of pineal SRs, the kinesin motor KIF3A in the gland. Respective immunoreactivity was abundant in central regions of the gland where sympathetic fibers were less dense, and vice versa, revealing that intercellular communication between adjacent pinealocytes is enhanced …

endocrine systemmedicine.medical_specialtyEndocrinology Diabetes and MetabolismTRPV1KinesinsTRPV Cation ChannelsBiologyBradykininPineal GlandCalcium in biologyPinealocyteMembrane PotentialsMelatoninRats Sprague-DawleyCellular and Molecular Neurosciencechemistry.chemical_compoundPineal glandNorepinephrineEndocrinologyInternal medicinemedicineAnimalsMelatoninSynaptic ribbonEndocrine and Autonomic SystemsRatsEndocrinologymedicine.anatomical_structurenervous systemchemistrySynapseslipids (amino acids peptides and proteins)CalciumCapsaicinCapsazepineEndocrine glandmedicine.drugNeuroendocrinology
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The identification of peroxisome proliferator-activated receptor alpha-independent effects of oleoylethanolamide on intestinal transit in mice

2009

Oleoylethanolamide (OEA) is an endogenous lipid produced in the intestine that mediates satiety by activation of peroxisome proliferator-activated receptor alpha (PPARalpha). OEA inhibits gastric emptying and intestinal motility, but the mechanism of action remains to be determined. We investigated whether OEA inhibits intestinal motility by activation of PPARalpha. PPARalpha immunoreactivity was examined in whole mount preparations of mouse gastrointestinal (GI) tract. The effect of OEA on motility was assessed in wildtype, PPARalpha, cannabinoid CB(1) receptor and CB(2) receptor gene-deficient mice and in a model of accelerated GI transit. In addition, the effect of OEA on motility was as…

medicine.medical_specialtyPhysiologymedicine.medical_treatmentTRPV Cation ChannelsMotilityOleic AcidsBiologydigestive systemReceptor Cannabinoid CB2MiceOleoylethanolamidechemistry.chemical_compoundReceptor Cannabinoid CB1Glucagon-Like Peptide 1Internal medicinemedicineAnimalsPPAR alphaReceptorMice KnockoutGastric emptyingEndocrine and Autonomic Systemsdigestive oral and skin physiologyGastroenterologyImmunohistochemistryEndocannabinoid systemEndocrinologyMechanism of actionchemistrylipids (amino acids peptides and proteins)CannabinoidPeroxisome proliferator-activated receptor alphamedicine.symptomGastrointestinal MotilityEndocannabinoids
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