ライフサイエンスコーパス: tractus

1 ucleus ovoidalis and from the nucleus of the tractus ovoidalis.

2 late food intake e.g. area postrema, nucleus tractus solitaries and dorsal motor nucleus of the vagus

3 ective inhibition of the commissural nucleus tractus solitarii (cNTS) significantly reduced tSNA.

4 m the commissural subdivision of the nucleus tractus solitarii (cNTS) using in vivo microdialysis dur

5 n of neurones within the commissural nucleus tractus solitarii (commNTS) with glycine (40 nmol/80 nl)

6 d by infusions of lidocaine into the nucleus tractus solitarii (NTS) and by propranolol infused into

7 nuclei comprising the DVC, i.e. the nucleus tractus solitarii (NTS) and the dorsal motor nucleus (DM

8 sly up to twenty-two neurones in the nucleus tractus solitarii (NTS) and ventral respiratory group (V

9 e course of adenosine release in the nucleus tractus solitarii (NTS) and ventrolateral medulla (VLM)

10 ventrolateral medulla (VLM) and the nucleus tractus solitarii (NTS) are implicated in the control of

11 AMPA-type glutamate receptors in the nucleus tractus solitarii (NTS) are necessary for the barorecept

12 O) donors exogenously applied to the nucleus tractus solitarii (NTS) depressed the baroreceptor cardi

13 of the brainstem and from within the nucleus tractus solitarii (NTS) during the defence response evok

14 tergic signalling is critical in the nucleus tractus solitarii (nTS) for cardiorespiratory homeostasi

15 he obex (caudal C1 area) or into the nucleus tractus solitarii (NTS) greatly attenuated the barorefle

16 the caudal aspect of the commissural nucleus tractus solitarii (NTS) in mediating the peripheral chem

17 urons and fibers in subnuclei of the nucleus tractus solitarii (NTS) in the squirrel monkey, Saimuri

18 ones were recorded simultaneously in nucleus tractus solitarii (NTS) including the dorsal respiratory

19 Electrical stimulation of nucleus tractus solitarii (NTS) induced excitatory postsynaptic

20 eptin to the fourth ventricle or the nucleus tractus solitarii (NTS) inhibits food intake and weight

21 The nucleus tractus solitarii (NTS) integrates inputs from cardiovas

22 The nucleus tractus solitarii (NTS) is essential for coordinating ar

23 The nucleus tractus solitarii (NTS) is the first brain site that rec

24 The nucleus tractus solitarii (NTS) is the first site of integration

25 ircuitry activated by vagal input to nucleus tractus solitarii (NTS) neurones in immature rats.

26 es the afferent neurotransmission in nucleus tractus solitarii (NTS) neurons, which affect respirator

27 Fos was induced in the nucleus tractus solitarii (NTS) of hypotensive piglets.

28 damages catecholamine neurons in the nucleus tractus solitarii (NTS) of rat, attenuates arterial baro

29 gested that nitric oxide (NO) in the nucleus tractus solitarii (NTS) participates in modulating cardi

30 n caudomedial aspects of commissural nucleus tractus solitarii (NTS) received input from cardiopulmon

31 s response, we hypothesized that the Nucleus Tractus Solitarii (NTS) region of the medulla oblongata,

32 f the inhibitory transmission in the nucleus tractus solitarii (NTS) remain unclear, even though this

33 s via a noradrenergic relay from the nucleus tractus solitarii (NTS) to corticotropin releasing hormo

34 r by way of direct pathways from the nucleus tractus solitarii (NTS) to the olfactory tubercle and th

35 ection of L-S-nitrosocysteine in the nucleus tractus solitarii (NTS) were compared and contrasted wit

36 Vestibular afferents to the nucleus tractus solitarii (NTS) were identified for the first ti

37 se (NADPHd) staining patterns in the nucleus tractus solitarii (NTS) were spatially related to termin

38 is study, we examined LTD in the rat nucleus tractus solitarii (NTS), a brainstem nucleus that relays

39 AT2) is present on astrocytes in the nucleus tractus solitarii (nTS), an important nucleus in cardior

40 anoreceptors excites neurones in the nucleus tractus solitarii (NTS), but discharge patterns evoked b

41 citatory amino acids (EAAs) into the nucleus tractus solitarii (nTS), in a region located immediately

42 ilaterally in the caudal zone of the nucleus tractus solitarii (NTS), mainly within the commissural s

43 rabrachial nucleus, cuneate nucleus, nucleus tractus solitarii (NTS), paraventricular nucleus of the

44 vagal C-fibre-activated neurones in nucleus tractus solitarii (NTS), phrenic nerve activity, trachea

45 and in the CNS, particularly in the nucleus tractus solitarii (NTS), the first central site for syna

46 age, NR1 expression increased in the nucleus tractus solitarii (nTS), whereas it decreased in the hyp

47 and gastrointestinal tissues to the nucleus tractus solitarii (NTS).

48 abinoids on neurotransmission in the nucleus tractus solitarii (nTS).

49 mission of baroreflex signals in the nucleus tractus solitarii (NTS).

50 ty in identified subdivisions of the nucleus tractus solitarii (NTS).

51 noradrenergic input arising from the nucleus tractus solitarii (NTS).

52 rgic (A2 cell group) neurones in the nucleus tractus solitarii (NTS).

53 only one exception these cells responded to tractus solitarii (TS) stimulation with a monophasic exc

54 nd glutamatergic transmission in the nucleus tractus solitarii abolished rimonabant-induced hypophagi

55 pontine region to the cardiovascular nucleus tractus solitarii and evaluated the confluence of tracin

56 alized to visceral relay nuclei: the nucleus tractus solitarii and pontine parabrachial complex, and

57 t more rostral and caudal regions of nucleus tractus solitarii did not.

58 6-hydroxydopamine or vitamin C into nucleus tractus solitarii of the rat and evaluated the cardiopul

59 terial baroreceptive neurones in the nucleus tractus solitarii of the rat.

60 The cardiovascular nucleus tractus solitarii projected to pontine preganglionic par

61 In contrast, all three regions of nucleus tractus solitarii projected to the nucleus ambiguus and

62 ostral, and caudal to cardiovascular nucleus tractus solitarii sent projections through the pons medi

63 ergic excitatory currents (eEPSCs) evoked by tractus solitarii stimulation (TS-eEPSC) of second-order

64 e of tracing from the cardiovascular nucleus tractus solitarii to pontine preganglionic neurons label

65 y from neurons in the cardiovascular nucleus tractus solitarii to pontine preganglionic parasympathet

66 rade tracing from the cardiovascular nucleus tractus solitarii to preganglionic parasympathetic neuro

67 and deep dorsal horn project to the nucleus tractus solitarii via two distinct pathways.

68 h increases its neural output to the nucleus tractus solitarii with a subsequent activation of severa

69 ventrolateral medulla (CVL) and the nucleus tractus solitarii with immunocytochemical identification

70 s in the nucleus raphe obscurus, the nucleus tractus solitarii, and the regions of the retrofacial nu

71 ceptors in the area postrema and the nucleus tractus solitarii, believed to be involved in terminal e

72 us reticularis dorsalis, commissural nucleus tractus solitarii, lateral medulla, A5 area, and interna

73 salis, commissural subnucleus of the nucleus tractus solitarii, lateral medulla, medial facial nucleu

74 the baroreflex afferent pathway (the nucleus tractus solitarii, NTS; nodose ganglion, NG).

75 ventral tegmentum/substantia nigra, nucleus tractus solitarii, nucleus accumbens, thalamus/subthalam

76 ubpostremal and central subnuclei of nucleus tractus solitarii, spinal trigeminal nucleus caudalis, a

77 e hypothesis that the cardiovascular nucleus tractus solitarii, the site of termination of arterial b

78 neurons by different regions of the nucleus tractus solitarii.

79 y in the lateral areas of the caudal nucleus tractus solitarii.

80 audal ventrolateral medulla, and the nucleus tractus solitarii.

81 ve terminals in the medial subnucleus of the tractus solitarious (mNTS) and alpha4beta2, respectively

82 that neurons of NG projecting to the nucleus tractus solitarium and those of dorsal root ganglia proj

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

109 2 enzyme) containing neurons of the nucleus tractus solitarius (NTS) become activated during low-sod

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

153 1beta, TNFalpha and IL6 mRNAs in the nucleus tractus solitarius (NTS), hypothalamus, hippocampus and

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

180 4 to the central terminal field, the nucleus tractus solitarius (NTS).

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

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

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

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

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

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

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

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

189 2 s, 25 Hz trains of stimuli applied to the tractus solitarius (TS), induced a small (10%) but signi

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

267 ubnuclei of the trigeminal nerve and nucleus tractus solitarius.

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

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

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

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

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

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

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

275 of premotor neurons localized in the nucleus tractus solitarius.

276 orsomedial subnucleus of the rostral nucleus tractus solitarius.

277 termediate and rostral levels of the nucleus tractus solitarius.

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

279 parabrachial nuclei, and commissural nucleus tractus solitarius.

280 ctivity in the trigeminal nuclei and nucleus tractus solitarius.

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

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

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

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