ライフサイエンスコーパス: tractus solitarius

1 the NK-1 receptor antagonist in the nucleus tractus solitarius.

2 ive constant-latency synaptic input from the tractus solitarius.

3 d in the subnucleus centralis of the nucleus tractus solitarius.

4 cuneate nucleus, area postrema, and nucleus tractus solitarius.

5 , infected neurons were found in the nucleus tractus solitarius.

6 of premotor neurons localized in the nucleus tractus solitarius.

7 orsomedial subnucleus of the rostral nucleus tractus solitarius.

8 termediate and rostral levels of the nucleus tractus solitarius.

9 , medial and dorsal subnuclei of the nucleus tractus solitarius.

10 parabrachial nuclei, and commissural nucleus tractus solitarius.

11 ctivity in the trigeminal nuclei and nucleus tractus solitarius.

12 aventricular nucleus, but not in the nucleus tractus solitarius.

13 rainstem, with high abundance in the nucleus tractus solitarius.

14 ubnuclei of the trigeminal nerve and nucleus tractus solitarius.

15 ynapse of lung afferent neurons, the nucleus tractus solitarius.

16 by an NK-1 receptor mechanism in the nucleus tractus solitarius.

17 old), area postrema (7-fold) and the nucleus tractus solitarius (4-fold).

18 of the noradrenergic neurons in the nucleus tractus solitarius, A5 and A7, was also observed.

19 he baroreceptor center of the nucleus of the tractus solitarius accounts for these actions.

20 upraoptic nucleus, central amygdala, nucleus tractus solitarius and area postrema compared with vehic

21 ial nucleus, intermediate and caudal nucleus tractus solitarius and area postrema), reward (the shell

22 the synaptic connections between the nucleus tractus solitarius and dorsal motor nucleus of the vagus

23 in dorsal medulla that includes the nucleus tractus solitarius and dorsal reticular nucleus.

24 the airway sensory receptors to the nucleus tractus solitarius and from this site to airway-related

25 re observed in the gustatory rostral nucleus tractus solitarius and in areas involved in vestibulo-oc

26 al and intermediate subnuclei of the nucleus tractus solitarius and in other medullary, pontine, midb

27 tocellular reticular nucleus, nucleus of the tractus solitarius and locus coeruleus also exhibited al

28 of the ITR have connections with the nucleus tractus solitarius and projections to the ventrolateral

29 ression; and oxidative stress in the nucleus tractus solitarius and rostral ventrolateral medulla as

30 on neurons whose connections to the nucleus tractus solitarius and rostral ventrolateral medulla res

31 eathing control circuitry within the nucleus tractus solitarius and the caudal part of ventral respir

32 l and medial subnuclei of the caudal nucleus tractus solitarius and the dorsolateral, dorsomedial and

33 DMH increased Fos expression in the nucleus tractus solitarius and the ventrolateral medulla bilater

34 ently evoked upon stimulation of the nucleus tractus solitarius and these responses were also blocked

35 tract, a caudolateral region of the nucleus tractus solitarius, and a lateral band of the principal

36 rsal horn (laminae I and II) and the nucleus tractus solitarius, and both PB subnuclei send projectio

37 X was also found in the medial portion of n. tractus solitarius, and both the rostral and caudal vent

38 and hippocampus, habenula, amygdala, nucleus tractus solitarius, and circumventricular organs such as

39 erve plexi, the medial subnucleus of nucleus tractus solitarius, and the dorsal motor nucleus of the

40 whether the infected neurons in the nucleus tractus solitarius are part of sympathetic or parasympat

41 arabrachial nucleus, and commissural nucleus tractus solitarius, as previously observed in chronic mo

42 implanted bilaterally in the medial nucleus tractus solitarius at a site that produced apnea in resp

43 restoration of DBH expression in the nucleus tractus solitarius, but not in the locus coeruleus, rest

44 after electrical stimulation of the nucleus tractus solitarius, but the effect was slower than for t

45 or and increased Fos labeling in the nucleus tractus solitarius caudal region, which receives vagal c

46 principally in the central subnucleus of the tractus solitarius (cNTS).

47 The dorsolateral subnucleus of the nucleus tractus solitarius (dlNTS) was processed for the histoch

48 The dorsal medial nucleus tractus solitarius (dmNTS) has long been appreciated as

49 Electrical stimulation of the nucleus of the tractus solitarius evoked EPSCs and IPSCs.

50 Constant latency tractus solitarius-evoked EPSCs were decreased in amplit

51 A novel group of neurons in the nucleus tractus solitarius expresses the enzyme 11-beta-hydroxys

52 control distribution of cells in the nucleus tractus solitarius expressing c-fos in response to physi

53 ed with low-sucrose beverages in the nucleus tractus solitarius for both groups.

54 ed an increase in trigeminal but not nucleus tractus solitarius Fos labeling, and no behavioral avoid

55 the caudal ventrolateral medulla and nucleus tractus solitarius, Fos-positive neurons projected to th

56 pothalamus) and two hindbrain sites (nucleus tractus solitarius, fourth ventricle).

57 GABA(A) receptors on neurons in the nucleus tractus solitarius, hypoglossal nucleus, and dorsal moto

58 iety - one region which includes the nucleus tractus solitarius in the hindbrain, and another more di

59 em cardiorespiratory-related region (nucleus tractus solitarius) in vitro.

60 rrents (eEPSCs) evoked by stimulation of the tractus solitarius, in a concentration-dependent manner.

61 t NTS neurones, including neurones receiving tractus solitarius input (i.e. viscerosensory) and those

62 The contiguous nucleus tractus solitarius, involved in integrating sensory inpu

63 This neural circuitry within the nucleus tractus solitarius is consistent with a complex central

64 ata suggest that NE signaling by the nucleus tractus solitarius is necessary for morphine reward.

65 ed c-Fos-ir expression mainly in the nucleus tractus solitarius, lateral reticular nucleus, lateral t

66 lateral subnucleus), area postrema, nucleus tractus solitarius, locus coeruleus, paraventricular nuc

67 long-term synaptic plasticity in the nucleus tractus solitarius may play a role in the homeostatic re

68 jun and c-fos mRNA expression in the nucleus tractus solitarius (middle, mNTS, and rostral, rNTS) and

69 kade of GABA receptors in the medial nucleus tractus solitarius (mNTS) also attenuated the PVN-induce

70 nts on neurones in the medial nucleus of the tractus solitarius (mNTS) and in the dorsal motor nucleu

71 ne-containing portions of the medial nucleus tractus solitarius (mNTS) at both intermediate (NTSi) an

72 nd contralateral sides of the medial nucleus tractus solitarius (mNTS) in rats receiving EA ST 36 com

73 hormone leptin signals in the medial nucleus tractus solitarius (mNTS) to suppress food intake, in pa

74 lateral parabrachial nucleus (LPB), nucleus tractus solitarius (NST), frontal cerebral cortex and th

75 ssion was similarly increased in the nucleus tractus solitarius (NTS) A2 region in virgin and pregnan

76 icant increase in AEA content in the nucleus tractus solitarius (NTS) after an increase in blood pres

77 revealed axonal degeneration of the nucleus tractus solitarius (NTS) and area postrema (AP) of the m

78 ow that glutamatergic neurons in the nucleus tractus solitarius (NTS) and caudal serotonergic neurons

79 ptic transmission between the nucleus of the tractus solitarius (NTS) and dorsal motor nucleus of the

80 The nucleus tractus solitarius (NTS) and dorsal motor nucleus of the

81 ell bodies within the area postrema, nucleus tractus solitarius (NTS) and nodose ganglion.

82 ell bodies within the area postrema, nucleus tractus solitarius (NTS) and nodose ganglion.

83 i of the dorsal motor nucleus (DMN), nucleus tractus solitarius (NTS) and nucleus ambiguus (NA) with

84 signals that are transmitted to the nucleus tractus solitarius (NTS) and parabrachial nucleus (PB).

85 pression in two brainstem areas, the nucleus tractus solitarius (NTS) and the rostral ventrolateral m

86 s from the area postrema (AP) to the nucleus tractus solitarius (NTS) and to examine the synaptic int

87 lateral hypothalamic area (LHA), and nucleus tractus solitarius (NTS) are co-linked to these two site

88 A subset of neurons in the nucleus tractus solitarius (NTS) are uniquely sensitive to the a

89 ical studies highlight the hindbrain nucleus tractus solitarius (NTS) as a brain region important for

90 2 enzyme) containing neurons of the nucleus tractus solitarius (NTS) become activated during low-sod

91 ked by electrical stimulation of the nucleus tractus solitarius (NTS) but not evoked EPSCs.

92 NE to the limbic system, such as the nucleus tractus solitarius (NTS) contribute to this process.

93 he dorsal vagal complex (DVC; nucleus of the tractus solitarius (NTS) dorsal motor nucleus of the vag

94 e P (SP) is released from the feline nucleus tractus solitarius (NTS) in response to activation of sk

95 to quantify NO concentration in the nucleus tractus solitarius (NTS) in vitro in brain slices and in

96 lpha1-noradrenergic receptors in the nucleus tractus solitarius (NTS) influences neural processes tha

97 The nucleus of the tractus solitarius (NTS) is a primary termination zone f

98 The nucleus tractus solitarius (NTS) is essential for orchestrating

99 tween baroreceptor afferents and the nucleus tractus solitarius (NTS) is essential for reflex regulat

100 Here, we show that the hindbrain nucleus tractus solitarius (NTS) is essential for vocalization i

101 nl; n=12) in rats with contralateral nucleus tractus solitarius (NTS) lesion.

102 excitatory amino acid (EAA) induced nucleus tractus solitarius (NTS) neuronal activity were investig

103 ng vagal afferent evoked activity of nucleus tractus solitarius (NTS) neurones.

104 ral afferents innervate second-order nucleus tractus solitarius (NTS) neurons via myelinated (A-type)

105 ies and synaptic transmission in the nucleus tractus solitarius (NTS) neurons, the first synaptic sta

106 duced in the small intestines and in nucleus tractus solitarius (NTS) neurons.

107 c-Fos expression in the nucleus tractus solitarius (NTS) of the rat has been found to fo

108 of other neurons ramified within the nucleus tractus solitarius (NTS) or DMV.

109 ic acid-A (GABA(A)) receptors in the nucleus tractus solitarius (NTS) participate in autonomic regula

110 Neurons in the rat nucleus tractus solitarius (NTS) possess morphologic characteris

111 In rats, cisplatin activates nucleus tractus solitarius (NTS) projections to the lateral para

112 The nucleus tractus solitarius (NTS) receives dense terminations fro

113 in baroreceptor transmission in the nucleus tractus solitarius (NTS) remains an area of active resea

114 A subset of neurons within the nucleus tractus solitarius (NTS) shows c-Fos activation during p

115 d rat, electrical stimulation of the nucleus tractus solitarius (NTS) synchronizes the EEG by increas

116 h concentration may have reached the nucleus tractus solitarius (nTS) to elicit depressor and bradyca

117 cond-order neurons within the caudal nucleus tractus solitarius (NTS) to initiate autonomic reflexes.

118 esponses of gustatory neurons in the nucleus tractus solitarius (NTS) to tastant stimuli were recorde

119 ectively, while Fos labelling in the nucleus tractus solitarius (NTS) was increased by 5-fold compare

120 llary depressor area (CVLM), and the nucleus tractus solitarius (nTS) were also included for comparis

121 put originating from neurones in the nucleus tractus solitarius (NTS) were determined by evoking acti

122 brain segments containing primarily nucleus tractus solitarius (NTS) were employed for slice superfu

123 within astrocytes and neurons in the nucleus tractus solitarius (NTS), a hindbrain nucleus critical f

124 ates GLP-1-expressing neurons in the nucleus tractus solitarius (NTS), a hindbrain nucleus that proje

125 POMC neurons are also found in the nucleus tractus solitarius (NTS), a region regulating satiety.

126 racteristics of CCK receptors in the nucleus tractus solitarius (NTS), a region that contains central

127 dissociated neurons of the brainstem nucleus tractus solitarius (nTS), a region that receives massive

128 undance in the caudal portion of the nucleus tractus solitarius (NTS), an area which together with th

129 fferent vagal fibers, neurons of the nucleus tractus solitarius (NTS), and the efferent fibers origin

130 r nucleus of the hypothalamus (PVN), nucleus tractus solitarius (NTS), and the parasympathetic nucleu

131 leus (DMN), and all subnuclei of the nucleus tractus solitarius (NTS), but one.

132 echolamine (CA) neurons found in the nucleus tractus solitarius (NTS), dorsal motor nucleus of the va

133 The nucleus tractus solitarius (NTS), especially its ventrolateral,

134 1beta, TNFalpha and IL6 mRNAs in the nucleus tractus solitarius (NTS), hypothalamus, hippocampus and

135 involve vagal afferent input to the nucleus tractus solitarius (NTS), including cardiopulmonary resp

136 the brainstem, in particular, in the nucleus tractus solitarius (NTS), is well established.

137 neurons are found bilaterally within nucleus tractus solitarius (nTS), lateral to the commissural sub

138 estradiol increased Fos abundance in nucleus tractus solitarius (NTS), rostral ventrolateral medulla

139 lots of protein equivalents from the nucleus tractus solitarius (NTS), the first central relay for pe

140 l neuroanatomical hub connecting the nucleus tractus solitarius (NTS), the major central source of GL

141 d synaptic function in the brainstem nucleus tractus solitarius (nTS), the principal site for integra

142 r, TrkB, are highly expressed in the nucleus tractus solitarius (nTS), the principal target of cardio

143 a region in the medial subnucleus of nucleus tractus solitarius (nTS), the reticular formation just v

144 ticity in this reflex pathway in the nucleus tractus solitarius (NTS), the site of termination of the

145 ral spinal trigeminal nucleus (VSP), nucleus tractus solitarius (NTS), ventrolateral medulla (VLM) an

146 ations functionally expressed in the nucleus tractus solitarius (NTS), we conducted several physiolog

147 nvolve glutamatergic synapses in the nucleus tractus solitarius (NTS), where afferent endings from ar

148 paraventricular nucleus (PVN) to the nucleus tractus solitarius (NTS), where cells that respond to pe

149 In nucleus tractus solitarius (NTS)-A2 and NTS-C2, both NPY+ and TH

150 food has been strongly implicated in nucleus tractus solitarius (NTS)-mediated satiation, but the exa

151 receptors, has been reported in the nucleus tractus solitarius (nTS).

152 central autonomic nuclei such as the nucleus tractus solitarius (NTS).

153 autonomic signal transmission in the nucleus tractus solitarius (NTS).

154 ies at this first synapse within the nucleus tractus solitarius (NTS).

155 evoked by stimulation of the nucleus of the tractus solitarius (NTS).

156 fects of hypoxia at the level of the nucleus tractus solitarius (NTS).

157 eus of the amygdala (CeA) and nucleus of the tractus solitarius (NTS).

158 xtran amine were made into the LC or nucleus tractus solitarius (NTS).

159 agal neurons upon stimulation of the nucleus tractus solitarius (NTS).

160 4 to the central terminal field, the nucleus tractus solitarius (NTS).

161 h regards to their dependence on the nucleus tractus solitarius (NTS).

162 preganglionic neurons and/or to the nucleus tractus solitarius (NTS).

163 in cardiorespiratory regions of the nucleus tractus solitarius (nTS).

164 entrally projecting neurons from the nucleus tractus solitarius (NTS).

165 fic subpopulations of neurons in the nucleus tractus solitarius (NTS).

166 vasopressin (AVP) released in medial nucleus tractus solitarius (NTS).

167 ike peptide-1 (GLP-1) neurons in the nucleus tractus solitarius (NTS).

168 rsal vagal complex (DVC, i.e. nucleus of the tractus solitarius, NTS, and dorsal motor nucleus of the

169 t the level of the solitary nucleus (nucleus tractus solitarius; NTS), their involvement in the trans

170 ventricular nuclei in the forebrain, and the tractus solitarius nuclei, lateral parabrachial nuclei i

171 like sensation when delivered to the nucleus tractus solitarius of behaving rats.

172 ) and rostral (rNTS) portions of the nucleus tractus solitarius of SHRs and WKY rats.

173 st, SR 140333, was injected into the nucleus tractus solitarius of the conscious guinea pigs who were

174 vagal afferent fibers synapse in the nucleus tractus solitarius of the medulla and then descend to ex

175 napses of the medial and commissural nucleus tractus solitarius of the medulla.

176 exclusively in the area postrema and nucleus tractus solitarius of the mouse brainstem.

177 sural and medial subdivisions of the nucleus tractus solitarius of wild-type F344.Cck1r(+/+) rats, wh

178 diagonal band of Broca, hippocampus, nucleus tractus solitarius, parabrachial nucleus, paraventricula

179 urons receive GLP-1 innervation from nucleus tractus solitarius preproglucagon neurons that were acti

180 that GLP-1-producing neurons in the nucleus tractus solitarius project monosynaptically to the lPBN,

181 pathways from the spinal trigeminal, nucleus tractus solitarius, raphe magnus, raphe pallidus, and th

182 was also found in the area postrema/nucleus tractus solitarius region by RT-PCR.

183 s, cerebellum, posterior cortex, and nucleus tractus solitarius regions.

184 ion (5 Hz) of primary afferent fibers in the tractus solitarius resulted in a phasic depression (acco

185 egmental area, parabrachial nucleus, nucleus tractus solitarius, rostral/caudal ventrolateral medulla

186 e number of CFLI cells in the caudal Nucleus Tractus Solitarius significantly more than preloads of m

187 -ir expression in the area postrema, nucleus tractus solitarius, solitary tract, and spinal trigemina

188 on caused c-Fos-ir expression in the nucleus tractus solitarius, spinal trigeminal tract, solitary tr

189 micked by endogenous release of glutamate by tractus solitarius stimulation, and was prevented by a g

190 n of sympathetic activity, including nucleus tractus solitarius, the lateral tegmental field rostral

191 se CRCs are the medullary raphe, the nucleus tractus solitarius, the ventrolateral medulla, the fasti

192 othalamus, dorsomedial hypothalamus, nucleus tractus solitarius), there appeared to be no significant

193 sensory afferents terminating in the nucleus tractus solitarius, these terminals were identified by t

194 nch of the glossopharyngeal nerve to nucleus tractus solitarius; this precipitates an impressive arra

195 ones were predominantly located close to the tractus solitarius (TS) and could be GABAergic or glutam

196 on of primary sensory afferent fibres in the tractus solitarius (ts) and currents postsynaptically ev

197 2 s, 25 Hz trains of stimuli applied to the tractus solitarius (TS), induced a small (10%) but signi

198 r cardiovascular afferent signaling (nucleus tractus solitarius, ventrolateral medulla) in both cell

199 , substantia nigra, locus coeruleus, nucleus tractus solitarius, ventrolateral medulla, pontine nucle

200 urons of the ventrolateral subnucleus of the tractus solitarius (vlNTS) act as an inspiratory off-swi

201 rvation to cardiac vagal neurons the nucleus tractus solitarius was electrically stimulated.

202 ely, GK message was not found in the nucleus tractus solitarius, which contains glucosensing neurons,