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1 sts the existence of distinct classes of the vanilloid receptor ().
2 that also expressed substance P and the VR1 vanilloid receptor.
3 stances is a recent acquisition of mammalian vanilloid receptors.
4 ing they do not arise from the activation of vanilloid receptors.
5 data provide strong evidence for subtypes of vanilloid receptors.
6 ain plays its role in the heat activation of vanilloid receptors.
7 ain plays its role in the heat activation of vanilloid receptors.
8 xpression of the heat and capsaicin receptor vanilloid receptor 1 (TRPV1 or VR1) was changed in recta
10 ., capsaicin, a transient receptor potential vanilloid receptor 1 (TRPV1) agonist] stimuli and becaus
12 s an agonist at transient receptor potential vanilloid receptor 1 (TRPV1) in nociceptive sensory neur
15 IX, XII, and XIV and cytosolic CA II and the vanilloid receptor 1 (TRPV1) were expressed in duodenum
16 ermined whether transient receptor potential vanilloid receptor 1 (TRPV1), a cation channel activated
21 es the neuronal transient receptor potential vanilloid receptor 1 (TRPV1), expressed on sensory C-fib
22 ensitization of transient receptor potential vanilloid receptor 1 (TRPV1), which is gated by capsaici
24 vity of the bronchopulmonary C-fibres to the vanilloid receptor 1 (VR1) agonist capsaicin was depende
26 ely 3 s acid treatment was not affected by a vanilloid receptor 1 (VR1) antagonist, capsazepine (10 m
27 ous studies demonstrate an important role of vanilloid receptor 1 (VR1) in inflammation and injury-in
32 identifying " peptide-rich" neurons; or the vanilloid receptor 1 (VR1), identifying neurons activate
33 minals of cranial visceral afferents express vanilloid receptor 1 (VR1), little is known about their
34 of Gr28 neurons by expressing the mammalian Vanilloid Receptor 1 (VR1), which is activated by capsai
35 d immunofluorescence labelling revealed that vanilloid receptor 1 (VR1)-containing afferent nerve fib
37 In horizontal brainstem slices, we used the vanilloid receptor 1 agonist capsaicin (CAP; 100 nm) to
38 2+ transients were completely blocked by the vanilloid receptor 1 antagonist capsazepine (100 microm)
40 unofluorescence labeling showed a diminished vanilloid receptor 1 immunoreactivity in dorsal root gan
41 tion channel subfamily V member 1 (TRPV1) or vanilloid receptor 1 is a nonselective cation channel th
42 ctivation of endoplasmic reticulum-localized vanilloid receptor 1 triggered store operated calcium en
43 against proteinase-activated receptor 2 and vanilloid receptor 1, a marker for primary nociceptive n
44 t receptor potential vanilloid 1 (TRPV1), or vanilloid receptor 1, is the founding member of the vani
46 tent agonist of transient receptor potential vanilloid receptor-1 (TRPV1), abolished DD responses and
51 the activation of afferent central terminal vanilloid receptor-1 (VR1) receptors and P2X receptors.
54 minor role for transient receptor potential vanilloid receptor-1 as mediators of cutaneous acid-indu
55 spective TRPV1 (transient receptor potential vanilloid receptor-1) and TrkA receptors on nociceptor s
56 Vr1, stretch-inactivated channel (SIC), and vanilloid receptor 5' splice variant (VR.5'sv) have been
58 lose, glucose, caffeine, denatonium, and the vanilloid receptor activator capsaicin all stimulated se
60 molecular characterization of the capsaicin (vanilloid) receptor, an excitatory ion channel expressed
63 atively impermeant CA inhibitor benzolamide, vanilloid receptor antagonist capsazepine, or sodium-hyd
64 ese responses were also not inhibited by the vanilloid receptor antagonist, capsazepine, suggesting t
65 show that the engagement of the cannabinoid/vanilloid receptors augments the number and immune suppr
67 enhance the piperine current by altering the vanilloid receptor/channel complex or increasing the len
68 and cytokines) and relevant receptors (e.g., vanilloid receptor channels and proteinase-activated, ca
71 ed calcium-induced calcium release in either vanilloid receptor-expressing neurons or heterologous ex
75 Furthermore, NADA potently activates native vanilloid receptors in neurons from rat dorsal root gang
76 tor pharmacology in the PNS, the function of vanilloid receptors in the brain has remained elusive.
77 The transient receptor potential TRPV1 or vanilloid receptor is a nonselective ligand-gated channe
81 peptide (CGRP) and substance P; the related vanilloid receptor-like protein (VRL) 2; glial markers S
82 r of the vanilloid receptor/TRP gene family, vanilloid receptor-like protein 3 (VRL3, also known as T
83 annel with mechanosensitive properties and a vanilloid receptor-like protein that is responsive to hi
85 In this context, the recent cloning of the vanilloid receptor may be a useful target for drug disco
89 f the rapid advances in our understanding of vanilloid-receptor pharmacology in the PNS, the function
91 between the endoplasmic reticulum-localized vanilloid receptor regulated stores and thapsigargin-sen
92 f ion channels, we cloned cDNAs encoding the vanilloid receptor-related osmotically activated channel
94 ge- and time-dependent properties of the rat vanilloid receptor (rVR1) stably expressed in human embr
97 ously found that a Drosophila protein in the vanilloid receptor subfamily (TRPV) channel subunit, Nan
98 ly (transient receptor potential superfamily-vanilloid receptor subfamily) of channel genes have been
101 capsaicin stimulates muscle metabosensitive vanilloid receptor subtype 1 (VR1), inducing a neurally
102 cloned capsaicin receptor, also known as the vanilloid receptor subtype 1 (VR1), is a heat-gated ion
103 enes neighboring CTNS (human ortholog of rat vanilloid receptor subtype 1 gene, CARKL, TIP-1, P2X5, a
104 s positive for the nociceptive neuron marker vanilloid receptor subtype 1, the small peptidergic neur
109 provide further support for the existence of vanilloid receptor subtypes on DRG neurons with distinct
110 n channel but it may represent an additional vanilloid receptor subunit involved in the formation of
111 response by identifying a domain of the rat vanilloid receptor that confers sensitivity to capsaicin
113 emperature-sensitive cationic channels (e.g. vanilloid receptor TRP channels) constitute the underlyi
120 Phosphorylation-dependent modulation of the vanilloid receptor TRPV1 is one of the key mechanisms me
121 tion of the conformational trajectory of the vanilloid receptor TRPV1 with resiniferatoxin (RTx) boun
124 s AEA; however, CP acts by engagement of the vanilloid receptor TRPV1, causing local production of AE
127 n embryonic kidney 293T cells expressing the vanilloid receptor (TRPV1) or a purinergic receptor (P2X
129 was attributable to stimulation of neuronal vanilloid receptor, TRPV1, because blockers of this chan
131 expressing a calcium-permeable ion channel, vanilloid receptor type 1 (the capsaicin receptor), and
133 This study investigated the contribution of vanilloid receptor type 1 (VR-1) containing fibers to SC
139 edge of the distribution and function of the vanilloid receptor (VR-1 or TRPV1) in the CNS lacks the
140 nals in the rat spinal cord that express the vanilloid receptor VR1 are from small and medium dorsal
146 ately 2%) IB4-positive neurons expressed the vanilloid receptor VR1, a heat-sensitive receptor expres
147 ns colocalized with immunoreactivity for the vanilloid receptor VR1, another protein associated prima
157 family V, member 1 (TRPV1; also known as the vanilloid receptor, VR1) in nociceptive neurons of the d
161 h non-CB1, SR141716A-sensitive site, the VR1 vanilloid receptor, was tested by administering SR141716