ライフサイエンスコーパス: sensory afferent

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

2 nd calcium handling properties of trigeminal sensory afferents.

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

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

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

6 a major ion channel expressed in nociceptive sensory afferents.

7 organizing the projection pattern of spinal sensory afferents.

8 evelopment and survival of specific types of sensory afferents.

9 cription factors in the laminar targeting of sensory afferents.

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

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

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

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

14 al nervous system on peripheral unmyelinated sensory afferents.

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

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

17 tes robust regeneration of large, myelinated sensory afferents.

18 alin can exert presynaptic inhibition of the sensory afferents.

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

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

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

22 verse mechanisms, including an activation of sensory afferents.

23 enhanced release of Substance P from primary sensory afferents.

24 that is necessary for bifurcation of central sensory afferents.

25 ane permeable molecule Penetratin to injured sensory afferents.

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

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

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

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

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

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

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

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

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

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

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

37 Homonymous sensory afferents and motoneurons typically form monosyn

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

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

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

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

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

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

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

45 Primary sensory afferents and their neighboring host-defense cel

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

73 Although sensory afferents certainly establish the basic receptiv

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

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

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

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

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

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

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

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

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

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

84 Prostanoids sensitize sensory afferents during inflammation.

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

86 10 Hz) at C(5) also reduced the amplitude of sensory afferent evoked potentials in pectoralis produce

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

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

89 Leech sensory afferents express a mannose-containing epitope o

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

113 major reorganization of different stages of sensory afferent growth.

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

115 Sensory afferents have been incorporated in the model to

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

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

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

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

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

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

122 Sensory afferents in the leech are labeled with both con

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

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

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

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

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

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

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

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

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

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

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

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

135 Esophageal sensory afferent inputs terminate principally in the cen

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

137 ojections from dorsal horn neurons receiving sensory afferent inputs.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

162 Rat sensory afferent neurons were ablated by capsaicin treat

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

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

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

166 ustained hyperemic response mediated through sensory afferent neurons.

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

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

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

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

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

172 The sensory afferents of the redirected nerves reinnervate t

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

191 Optically silencing nociceptive sensory afferents significantly blunted the evoked visce

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

230 Physiological activation of sensory afferents within single glomeruli evoked diverse