ライフサイエンスコーパス: sensory afferent

1 easing the mechanosensitivity of nociceptive sensory afferent.

2 y-specific labeled lines at the level of the sensory afferent.

3 that is necessary for bifurcation of central sensory afferents.

4 ane permeable molecule Penetratin to injured sensory afferents.

5 nd calcium handling properties of trigeminal sensory afferents.

6 nes at receptors located in the periphery on sensory afferents.

7 iscrete receptive fields (RFs) of peripheral sensory afferents.

8 ues of the body, is innervated by trigeminal sensory afferents.

9 a major ion channel expressed in nociceptive sensory afferents.

10 organizing the projection pattern of spinal sensory afferents.

11 evelopment and survival of specific types of sensory afferents.

12 cription factors in the laminar targeting of sensory afferents.

13 s the main input station of the amygdala for sensory afferents.

14 hat the majority of these fibers are primary sensory afferents.

15 s of solitary tract, the target for visceral sensory afferents.

16 erior to the one measured for single primary sensory afferents.

17 al nervous system on peripheral unmyelinated sensory afferents.

18 f established A-delta and C fiber trigeminal sensory afferents.

19 e of a loss of excitatory input from primary sensory afferents.

20 where they are innervated by high-threshold sensory afferents.

21 tes robust regeneration of large, myelinated sensory afferents.

22 alin can exert presynaptic inhibition of the sensory afferents.

23 ected in the hindbrain at the entry zones of sensory afferents.

24 in levels to direct fine-scale topography of sensory afferents.

25 s of NGF-sensitive sympathetic efferents and sensory afferents.

26 verse mechanisms, including an activation of sensory afferents.

27 enhanced release of Substance P from primary sensory afferents.

28 ese channels are highly expressed in primary sensory afferents, accumulating evidence indicates that

29 motor efferents; MRs are secondary to type-I sensory afferent activation and LRs result from the enga

30 creases this high-fidelity inhibition, while sensory afferent activation combined with single-cell si

31 Primed DPSC-CM increased human pulp sensory afferent activity as compared with control DPSC-

32 ubsequent to persistent stimulation of small sensory afferents after tissue injury, may contribute to

33 ctional characteristics of several groups of sensory afferent and autonomic efferent fibres in the ca

34 flammatory reflex pathway, which consists of sensory afferent and motor efferent arcs.

35 ons receive monosynaptic input from TRPM8(+) sensory afferents and are selectively activated by innoc

36 roup 4 neurons receive contacts from primary sensory afferents and are therefore proprioceptive inter

37 ements at successively higher levels between sensory afferents and area 3b.

38 skin modulates gene expression in cutaneous sensory afferents and behavioral sensitivity to thermal,

39 al cells receive sensory signals via primary sensory afferents and cortical signals via corticothalam

40 Silent synapses form between some primary sensory afferents and dorsal horn neurons in the spinal

41 Combined tracing of ankle flexor sensory afferents and interneurons monosynaptically conn

42 nel that is expressed by capsaicin-sensitive sensory afferents and is activated by noxious heat, acid

43 e adult olfactory bulb network in which both sensory afferents and local microcircuits are continuous

44 ts, MRs are elicited by activation of type-I sensory afferents and LRs result from the engagement of

45 te complexes are touch receptors composed of sensory afferents and Merkel cells.

46 interneuronal network is interposed between sensory afferents and MNs.

47 Homonymous sensory afferents and motoneurons typically form monosyn

48 nsported to peripheral tissues by both vagal sensory afferents and motor efferents, which allowed us

49 tion in evoked synaptic transmission between sensory afferents and NTS second-order cells.

50 These neurons are largely controlled by sensory afferents and premotor neurons of the reticular

51 or elements and their controllers, including sensory afferents and serotonergic modulation.

52 Functional responses of primary sensory afferents and spinal cord were monitored in swin

53 AP firing in nociceptive as well as tactile sensory afferents and suggest a significantly expanded r

54 arget-derived neurotrophic factor for muscle sensory afferents and suggest that pharmacological doses

55 ted with peripheral sensitization of primary sensory afferents and the development of inflammation at

56 Primary sensory afferents and their neighboring host-defense cel

57 in the establishment of connections between sensory afferents and those motor pools that have synerg

58 spillover' from synapses between excitatory sensory afferents and VB neurones that can lead to a red

59 eveloping PrV requires incoming activity via sensory afferents and/or enhanced AMPA receptor exocytos

60 neurons mediated by the direct activation of sensory afferents, and that muscle responses to EES are

61 ons within the SDH are activated by distinct sensory afferents, and their interplay determines the ne

62 erves, the motor efferents form prior to the sensory afferents, and their pathfinding show no depende

63 containing epitope common to the full set of sensory afferents; and dye injections.

64 ivity in this circuit changes over time when sensory afferents are chronically removed in vivo.

65 The pathways taken by developing sensory afferents are compatible with the idea that cell

66 ural response properties that typify primary sensory afferents are critical to fully appreciate becau

67 on neural cells, peripheral nerves, and fine sensory afferents are dispensable for the lipopolysaccha

68 ormation is based on the Vth nerve, in which sensory afferents are formed first and must enter the hi

69 Fast excitation and stimulation of sensory afferents are mediated by 5-HT3 serotonergic rec

70 asticity effects when behaviorally important sensory afferents are redirected from their original loc

71 regenerated muscle and cutaneous myelinated sensory afferents are restricted to the correct spinal s

72 of neuronal networks was studied using leech sensory afferents as a model.

73 neuropeptides from activated small diameter sensory afferents at topographically distinct body surfa

74 repulsion mediates the early restriction of sensory afferents away from midline structures.

75 a single and Brn3a;Brn3b double mutant mice, sensory afferent axons from the DRG fail to form normal

76 evelopment of central projections of primary sensory afferent axons that express calcitonin gene-rela

77 ions and subsequent targeting of chordotonal sensory afferent axons to these same longitudinal connec

78 th the induction of spindle morphogenesis by sensory afferent axons.

79 neurons have a unique role relative to other sensory afferents because, as a single population, they

80 ion in response to electrical stimulation of sensory afferents, both single stimulus pulses as well a

81 eived direct projections from high-threshold sensory afferents but transmitted nociceptive signals wi

82 l sprouting and that an absence of p75NTR by sensory afferents (but not by sympathetic efferents) lea

83 esponses in MCs to electrical stimulation of sensory afferents, but only during latter stages of the

84 in 2 mice to selectively stimulate VGluT3(+) sensory afferents by blue light, and to assess light-evo

85 mechanisms involved in activation of airway sensory afferents by DEPs.

86 the peripheral releasing function of primary sensory afferents by sensitizing the terminals and facil

87 Photoreceptors differ from other types of sensory afferents by their abundant expression of galect

88 T2 content in the central synapses of spinal sensory afferents by using confocal and electron microsc

89 med DPSCs (primed DPSC-CM) were evaluated on sensory afferents by using primary cultures of mouse tri

90 hat motor neuron pools and subsets of muscle sensory afferents can be defined by the expression of ET

91 Although sensory afferents certainly establish the basic receptiv

92 Following the loss of large sensory afferents, changes in these muscle-activation pa

93 The formation of proper sensory afferent connections during development is essen

94 Inner ear sensory afferent connections establish sensory maps betw

95 positioning does not seem to be required for sensory afferent connectivity with motor neurons.

96 eceptors since it is known that many primary sensory afferents contain SP.

97 is presently largely unknown which types of sensory afferents contribute to various forms of neuropa

98 However, rapid peripheral action of NIC on sensory afferents could be an important factor in trigge

99 y that optogenetic inhibition of nociceptive sensory afferents could be used to modulate bladder pain

100 this loss with electrical stimulation of the sensory afferents could improve motoneuron function.

101 changes in breathing patterns via increased sensory afferent discharge to the brain stem.

102 of the dorsal spinal cord, but unmyelinated sensory afferents do not regenerate.

103 ceptors directly contribute to low-threshold sensory afferent drive into the dorsal horn, and can med

104 Prostanoids sensitize sensory afferents during inflammation.

105 solectin B4 (IB4)-binding, but not TRPV1(+), sensory afferents eliminated movement-induced BTP, sugge

106 10 Hz) at C(5) also reduced the amplitude of sensory afferent evoked potentials in pectoralis produce

107 evidence that M-currents modulate peripheral sensory afferent excitability and that altered M-current

108 xonic contacts with the central terminals of sensory afferents, exerting presynaptic inhibitory contr

109 Leech sensory afferents express a mannose-containing epitope o

110 These findings demonstrate that sensory afferent feedback from the contralateral hip adj

111 the spatio-temporal patterning of cutaneous sensory afferent fiber projections to the dorsal, but no

112 This ATP excites primary sensory afferent fibers and also stimulates neighboring

113 in at a dose inducing functional ablation of sensory afferent fibers and by devazepide, a CCK-A recep

114 t spinal synapses, including those formed by sensory afferent fibers and by intrinsic interneurons.

115 arinic receptors have been found on both the sensory afferent fibers and on the GCs.

116 ns both receive primary inputs from vibrissa sensory afferent fibers and send monosynaptic connection

117 r (NT)-containing glomus cells (GCs) and the sensory afferent fibers synapsing onto the GCs.

118 transmitter from glomus cells activates the sensory afferent fibers to transmit information to the n

119 between gustatory receptor cells and primary sensory afferent fibers transmit the output signal from

120 neural cells, on peripheral nerves, on fine sensory afferent fibers, and on brain endothelial cells,

121 rocircuits, and (4) excitation of intestinal sensory afferent fibers.

122 a,beta-meATP preferentially activate general sensory afferent fibres (LN) but not taste fibres (CT).

123 ynaptically evoked by stimulation of primary sensory afferent fibres in the tractus solitarius (ts) a

124 mbar ES is mediated via direct activation of sensory afferent fibres.

125 expression of PIEZO1 is critical for normal sensory afferent firing and behavioral responses to mech

126 niculate ganglion neurons, which provide the sensory afferents for taste buds of the anterior tongue

127 cral spinal cord horn that receives visceral sensory afferents from the bladder and distal colon, a p

128 cral spinal cord horn that receives visceral sensory afferents from the bladder and distal colon, a p

129 ere that in the blow fly, Calliphora vicina, sensory afferents from the campaniform fields project to

130 Here we investigated effects of 5-HT on sensory afferents from the colon and the expression of 5

131 d at the time corresponding to projection of sensory afferents from the dorsal root ganglion (DRG) in

132 After loss of the sensory afferents from the forelimb in monkeys because o

133 l fasciculation and for segregation of these sensory afferents from the main olfactory system; howeve

134 ic output of weakly activated populations of sensory afferents from the nose, thus demonstrating a ch

135 ctory (piriform) cortex depend on excitatory sensory afferents from the olfactory bulb.

136 f developing myotubes (type I) by peripheral sensory afferents (group Ia) is a critical event for ind

137 major reorganization of different stages of sensory afferent growth.

138 The diversity of cutaneous sensory afferents has been studied by many investigators

139 Sensory afferents have been incorporated in the model to

140 rotein, gephyrin, on terminals of rat spinal sensory afferents identified by Calcitonin-Gene-Related-

141 motoneurons of the muscles as descending and sensory afferents impose different states on the spinal

142 in cells may be modulated by the peptidergic sensory afferents in addition to the cholinergic sympath

143 To study of the role of nociceptive sensory afferents in freely behaving mice, we developed

144 rmined the effects of linaclotide on colonic sensory afferents in healthy mice and those with chronic

145 for artemin-responsive GFRalpha3/TRPV1/TRPA1 sensory afferents in mediating sensitivity associated wi

146 n population-level recordings of the haltere sensory afferents in specific fields of sensilla.

147 Sensory arbors were abolished by perturbing sensory afferents in the intact nervous system with Lan3

148 Sensory afferents in the leech are labeled with both con

149 elective innervation of hindbrain regions by sensory afferents in the zebrafish embryo, we mapped the

150 ng ion channels (ASICs) because treatment of sensory afferents in vitro with IL1beta-upregulated ASIC

151 4 induced neuroplastic changes in trigeminal sensory afferents, increasing calcitonin gene-related pe

152 ctivity in boutons identified as vagus nerve sensory afferents indicate that glutamate may be a trans

153 However, transmission of sensory afferent information through NTS CA neurons crit

154 It is well established that sensory afferents innervating muscle are more effective

155 Most vagal sensory afferents innervating the lower airways are acti

156 pulation of longitudinal and circumferential sensory afferents innervating the piloneural collar.

157 he transduction of mechanical information in sensory afferents innervating the skin and viscera.

158 nerve stimulation (VNS), which activates the sensory afferents innervating the stomach that convey st

159 eurites, and in vivo is required for correct sensory afferent innervation and other aspects of develo

160 uction of commissural neurons, and disrupted sensory afferent innervation of the dorsal horn.

161 g connectivity, particularly with respect to sensory afferent innervation of the spinal cord.

162 glutamatergic dorsal horn neurons, abnormal sensory afferent innervations, and reduced spinofugal in

163 n and other behaviors.SIGNIFICANCE STATEMENT Sensory afferent input is modulated according to state.

164 Overall, SCI alters sensory afferent input pathways to Shox2 INs and 5-HT mo

165 sity, and, in contrast, absent or diminished sensory afferent inputs correlate with increased densiti

166 evious data suggested that somatic and vagal sensory afferent inputs may converge in the rostral vent

167 Esophageal sensory afferent inputs terminate principally in the cen

168 compare inputs from locomotor circuits with sensory afferent inputs to compute sensory prediction er

169 ojections from dorsal horn neurons receiving sensory afferent inputs.

170 ual cortex and the SC, differently integrate sensory afferent inputs.

171 olitarii (nTS) is the first site of visceral sensory afferent integration, and thus is critical for c

172 k for the brain's core homeostatic functions-sensory/afferent, integration/processing, and motor/effe

173 A characteristic signature of a normal sensory afferent is its profuse collateral branching, wh

174 We conclude that: brief activity in a few sensory afferents is amplified by recruitment of many tI

175 he presynaptic NMDAR activity in the primary sensory afferents is an effective approach to attenuate

176 ion and reinnervation of muscle by motor and sensory afferents is completed in the periphery.

177 ate that the organization of the vomeronasal sensory afferents is dramatically different from that of

178 Electrical stimulation of primary sensory afferents is known to have an antinociceptive ef

179 ts suggest that stimulus encoding by primary sensory afferents is transformed into feature extraction

180 Although the role of kainate receptors on sensory afferents is unknown, it has been hypothesized t

181 ein associated with signaling in nociceptive sensory afferents, leads to insensitivity to pain withou

182 least in the neonate, convergent inputs from sensory afferents (likely Ia) and motor axons, raising t

183 se findings demonstrate directly that mature sensory afferents maintain their responsiveness to semap

184 uggesting that glutamatergic and peptidergic sensory afferents may be distinct populations.

185 ical regulation of presynaptic inhibition of sensory afferents may focus the central motor command by

186 To examine the possibility that sensory afferents modulate synaptic maturation on develo

187 urons and receives direct input from cranial sensory afferents, motor cortex, and satiation related n

188 Sensory afferent nerve fiber growth into the interverteb

189 stical fluctuations in the spike activity of sensory afferent nerve fibers.

190 hat sangre de grado is a potent inhibitor of sensory afferent nerve mechanisms and supports its ethno

191 elial permeability, mast cell activation and sensory afferent nerve upregulation play critical roles.

192 ontrol of lung function rely upon the airway sensory afferent nerves and the subsequent airway vagal

193 ernational finds selective ablation of renal sensory afferent nerves diminishes self-directed saline

194 Information about the activity of airway sensory afferent nerves in vivo can be obtained electrop

195 lized on peripheral and central processes of sensory afferent nerves, and activation of these channel

196 ers benefit by suppressing the activation of sensory afferent nerves.

197 enrichment of adrenergic (TH(+)) and CGRP(+) sensory-afferent nerves correlated with poorer swallowin

198 The kidney is also innervated by sensory (afferent) nerves that relay information to the

199 nd activation of gut FFA3 directly regulates sensory afferent neuronal firing.

200 re believed to depend on activation of vagal sensory afferent neurones, the mechanisms involved in ex

201 Protection of the stomach by sensory afferent neurons occurs by mechanisms also unrel

202 Spiral ganglion neurons (SGNs) are primary sensory afferent neurons that relay acoustic information

203 However, the ability of sensory afferent neurons to accurately reinnervate termi

204 mediated at least in part by the response of sensory afferent neurons to hydrogen ions.

205 Rat sensory afferent neurons were ablated by capsaicin treat

206 In spinal cord dorsal horn and in sensory afferent neurons, adenosine acts as a neuromodul

207 elieved to exist in both the dorsal horn and sensory afferent neurons, the expression profile of spec

208 t receptor potential A1 (TRPA1) expressed in sensory afferent neurons.

209 ustained hyperemic response mediated through sensory afferent neurons.

210 anatomical and functional associations with sensory afferent neurons.

211 te buds and transmitted to the hindbrain via sensory afferent neurons.

212 for survival and synaptogenesis in auditory sensory afferent neurons.

213 -loop optogenetic neuromodulation of bladder sensory afferents normalizes bladder function.

214 e spinal cord and central targets of primary sensory afferents (nucleus of the solitary tract, spinal

215 to beta3-AR stimulation are mediated by the sensory afferents of BAT, we tested the effects of CL-31

216 These responses suggest that depriving sensory afferents of mannose-specific recognition aborts

217 In control mice, sensory afferents of SAG neurons terminate at the vestib

218 Primary sensory afferents of the dorsal root ganglion (DRG) that

219 The sensory afferents of the redirected nerves reinnervate t

220 e of inputs from the reticular formation and sensory afferents on presynaptic inhibitory pathways and

221 However, if the synaptic strength from sensory afferents onto interneurons projecting to the tw

222 ence of reactive synaptogenesis of surviving sensory afferents or of inhibitory synapses.

223 s in flight, the central organization of the sensory afferents originating from the different field c

224 N-methyl-D-aspartate (NMDA) receptors in sensory afferents participate in chronic pain by mediati

225 However, SCI induces plasticity in both sensory afferent pathways and serotonergic modulation, e

226 tional synaptic connectivity from the 4 main sensory afferent pathways onto the three known classes o

227 These data indicate that control of sensory afferent polarity may involve two 5-HT receptor

228 idence of specificity during regeneration of sensory afferent projections to muscle.

229 DRG sensory neuron diversity and regulating sensory afferent projections to the central targets.

230 In addition, a subset of TrkA(+) sensory afferents projects to ectopic ventral positions.

231 ferences in behavioral, neuroanatomical, and sensory afferent properties suggest that the sensorimoto

232 dopaminergic modulation of primary olfactory sensory afferents, rather than a broader effect on cogni

233 d that optogenetic inhibition of nociceptive sensory afferents reduced both ongoing pain and evoked c

234 In addition, the accuracy of sensory afferent regeneration was highly correlated with

235 capsaicin to examine if common hepatic vagal sensory afferents regulate lard intake.

236 brief (0.1 ms, 1-100 V) stimulation of their sensory afferents remained transient regardless of stimu

237 ose ganglion, where the cell bodies of vagal sensory afferents reside.

238 present the main targets for supraspinal and sensory afferent signals adjusting gait.

239 Yet, sensory afferent signals may not directly provide such i

240 Optically silencing nociceptive sensory afferents significantly blunted the evoked visce

241 only on nerve growth factor (NGF)-responsive sensory afferents (small-diameter A-delta and C fibers s

242 s, firing patterns, or synaptic responses to sensory afferent stimulation.

243 act independently, depending on the type of sensory afferents studied.

244 ters, plays a critical role in two stages of sensory afferent synaptogenesis.

245 urbation at the ultrastructural level in the sensory afferent target region.

246 pression, and its level of activity, control sensory afferent targeting in the developing spinal cord

247 s not well understood, inhibition of bladder sensory afferents temporarily relieves pain.

248 avalpha2delta1 subunit (Cavalpha2delta1), on sensory afferent terminals in dorsal spinal cord to prom

249 erneurones localized to SG or indirectly via sensory afferent terminals.

250 I, II, and V of the dorsal horn, where pain-sensory afferents terminate.

251 utamate is a neurotransmitter in vagus nerve sensory afferents terminating in the nucleus tractus sol

252 the inappropriate recruitment of a cutaneous sensory afferent that originally innervated skin.

253 ouse receives major projections from primary sensory afferents that bind the plant lectin isolectin B

254 here was prominent immunostaining of primary sensory afferents that could be seen coursing through th

255 pattern of circumferential and longitudinal sensory afferents that innervate primary and secondary p

256 e activation and sensitization of trigeminal sensory afferents that innervate the cranial meninges.

257 While not explored, primary peripheral sensory afferents that innervate the epidermis may requi

258 The AL and/or the sensory afferents that project into them show staining p

259 tomical relationships between an ensemble of sensory afferents that represented the entire range of r

260 ed the possibility that stimulation of vagal sensory afferents, the major sensory input into the NST,

261 In sensory afferents, the number of dense core vesicles inc

262 We characterized a subset of leech sensory afferents, the photoreceptors, in terms of their

263 n at the central synapses of crushed primary sensory afferents through a mechanism that can be modula

264 tive synaptic transmission between a primary sensory afferent to a secondary neuron in the spinal cor

265 either an appropriate return of an original sensory afferent to muscle stretch receptors or the inap

266 assess contributions of sympathetic flow and sensory afferent to the ACC-induced vascular change.

267 Statoacoustic ganglion (SAG) neurons project sensory afferents to appropriate targets in the inner ea

268 ) threat evaluation, producing threat-imbued sensory afferents to elicit network-wide threat response

269 hat early life injury weakens the ability of sensory afferents to evoke feedforward inhibition of adu

270 ignaling from lower limb muscle group III/IV sensory afferents to the central motor command could be

271 sion of TRPV1 in an identified population of sensory afferents to the mouse L3-L5 DRG that innervate

272 genic inflammation enhances the responses of sensory afferents to the needling of acupoints and trigg

273 While molecular guidance of sensory afferents to the periphery has been well studied

274 These results show that both major sensory afferents to the superficial layers of cat SC co

275 ingrowth of trkA+ nociceptive/thermoceptive sensory afferents to their central targets.

276 information for muscle length and activity (sensory afferent), to modify motoneuron output to achiev

277 al static stimuli, such as pressure, whereas sensory afferents transduce dynamic stimuli, such as mov

278 temperature-sensing properties across human sensory afferent types.

279 e cerebellar cortex that receives trigeminal sensory afferents, was activated by stimulation of the u

280 occur secondary to damage to large diameter sensory afferents, we sought to determine whether vincri

281 ess the function of these AChRs, single unit sensory afferents were recorded from an isolated mouse e

282 By 24-27 weeks postconceptional age, sensory afferents were still immunoreactive, as were man

283 ry or disease can result from dysfunction of sensory afferents whereby the threshold for activation o

284 cord, and whether destruction of a subset of sensory afferents which are essential to alpha2-AR analg

285 indicate that SP can have a direct effect on sensory afferents with activation of these receptors res

286 ation between inputs from reticulospinal and sensory afferents with DRPs or PADs, indicating an absen

287 cells respond to a single stimulation of the sensory afferents with unusually long EPSPs, lasting sev

288 Physiological activation of sensory afferents within single glomeruli evoked diverse