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1 ted gustatory neurons in the rostral nucleus tractus solitarius.
2 ubnuclei of the trigeminal nerve and nucleus tractus solitarius.
3 ynapse of lung afferent neurons, the nucleus tractus solitarius.
4 by an NK-1 receptor mechanism in the nucleus tractus solitarius.
5 the NK-1 receptor antagonist in the nucleus tractus solitarius.
6 ive constant-latency synaptic input from the tractus solitarius.
7 d in the subnucleus centralis of the nucleus tractus solitarius.
8 cuneate nucleus, area postrema, and nucleus tractus solitarius.
9 , infected neurons were found in the nucleus tractus solitarius.
10 of premotor neurons localized in the nucleus tractus solitarius.
11 orsomedial subnucleus of the rostral nucleus tractus solitarius.
12 termediate and rostral levels of the nucleus tractus solitarius.
13 , medial and dorsal subnuclei of the nucleus tractus solitarius.
14 parabrachial nuclei, and commissural nucleus tractus solitarius.
15 or (BDNF) cells in the medial nucleus of the tractus solitarius.
16 ctivity in the trigeminal nuclei and nucleus tractus solitarius.
17 aventricular nucleus, but not in the nucleus tractus solitarius.
18 rainstem, with high abundance in the nucleus tractus solitarius.
22 upraoptic nucleus, central amygdala, nucleus tractus solitarius and area postrema compared with vehic
24 ial nucleus, intermediate and caudal nucleus tractus solitarius and area postrema), reward (the shell
25 uclei with known inputs to the RVLM (nucleus tractus solitarius and caudal VLM) unmasked tonic glycin
26 the synaptic connections between the nucleus tractus solitarius and dorsal motor nucleus of the vagus
28 the airway sensory receptors to the nucleus tractus solitarius and from this site to airway-related
29 re observed in the gustatory rostral nucleus tractus solitarius and in areas involved in vestibulo-oc
30 al and intermediate subnuclei of the nucleus tractus solitarius and in other medullary, pontine, midb
31 tocellular reticular nucleus, nucleus of the tractus solitarius and locus coeruleus also exhibited al
32 of the ITR have connections with the nucleus tractus solitarius and projections to the ventrolateral
33 ression; and oxidative stress in the nucleus tractus solitarius and rostral ventrolateral medulla as
34 on neurons whose connections to the nucleus tractus solitarius and rostral ventrolateral medulla res
35 eathing control circuitry within the nucleus tractus solitarius and the caudal part of ventral respir
36 l and medial subnuclei of the caudal nucleus tractus solitarius and the dorsolateral, dorsomedial and
37 ferent VNS induced activation in the nucleus tractus solitarius and the rostral ventrolateral medulla
38 DMH increased Fos expression in the nucleus tractus solitarius and the ventrolateral medulla bilater
39 ently evoked upon stimulation of the nucleus tractus solitarius and these responses were also blocked
40 t c-Fos expression in neurons of the nucleus tractus solitarius and ventromedial (VMH) and arcuate nu
42 tract, a caudolateral region of the nucleus tractus solitarius, and a lateral band of the principal
43 rsal horn (laminae I and II) and the nucleus tractus solitarius, and both PB subnuclei send projectio
44 X was also found in the medial portion of n. tractus solitarius, and both the rostral and caudal vent
45 and hippocampus, habenula, amygdala, nucleus tractus solitarius, and circumventricular organs such as
46 erve plexi, the medial subnucleus of nucleus tractus solitarius, and the dorsal motor nucleus of the
48 whether the infected neurons in the nucleus tractus solitarius are part of sympathetic or parasympat
49 and project centrally to the nucleus of the tractus solitarius, area postrema, and dorsal motor nucl
50 arabrachial nucleus, and commissural nucleus tractus solitarius, as previously observed in chronic mo
51 implanted bilaterally in the medial nucleus tractus solitarius at a site that produced apnea in resp
52 restoration of DBH expression in the nucleus tractus solitarius, but not in the locus coeruleus, rest
53 after electrical stimulation of the nucleus tractus solitarius, but the effect was slower than for t
54 glucagon (PPG) neurons in the medial nucleus tractus solitarius by fluorescent in situ hybridization,
55 or and increased Fos labeling in the nucleus tractus solitarius caudal region, which receives vagal c
57 The dorsolateral subnucleus of the nucleus tractus solitarius (dlNTS) was processed for the histoch
59 lpha in glutamatergic neurons of the nucleus tractus solitarius during CH significantly decreased ven
63 control distribution of cells in the nucleus tractus solitarius expressing c-fos in response to physi
65 ed an increase in trigeminal but not nucleus tractus solitarius Fos labeling, and no behavioral avoid
66 the caudal ventrolateral medulla and nucleus tractus solitarius, Fos-positive neurons projected to th
68 GABA(A) receptors on neurons in the nucleus tractus solitarius, hypoglossal nucleus, and dorsal moto
69 iety - one region which includes the nucleus tractus solitarius in the hindbrain, and another more di
71 rrents (eEPSCs) evoked by stimulation of the tractus solitarius, in a concentration-dependent manner.
72 t NTS neurones, including neurones receiving tractus solitarius input (i.e. viscerosensory) and those
75 ata suggest that NE signaling by the nucleus tractus solitarius is necessary for morphine reward.
76 ed c-Fos-ir expression mainly in the nucleus tractus solitarius, lateral reticular nucleus, lateral t
77 lateral subnucleus), area postrema, nucleus tractus solitarius, locus coeruleus, paraventricular nuc
78 long-term synaptic plasticity in the nucleus tractus solitarius may play a role in the homeostatic re
79 jun and c-fos mRNA expression in the nucleus tractus solitarius (middle, mNTS, and rostral, rNTS) and
80 kade of GABA receptors in the medial nucleus tractus solitarius (mNTS) also attenuated the PVN-induce
81 nts on neurones in the medial nucleus of the tractus solitarius (mNTS) and in the dorsal motor nucleu
82 ne-containing portions of the medial nucleus tractus solitarius (mNTS) at both intermediate (NTSi) an
83 nd contralateral sides of the medial nucleus tractus solitarius (mNTS) in rats receiving EA ST 36 com
84 hormone leptin signals in the medial nucleus tractus solitarius (mNTS) to suppress food intake, in pa
85 lateral parabrachial nucleus (LPB), nucleus tractus solitarius (NST), frontal cerebral cortex and th
86 stressors activate catecholaminergic nucleus tractus solitarius (NTS(TH)) projections in the paravent
87 ssion was similarly increased in the nucleus tractus solitarius (NTS) A2 region in virgin and pregnan
88 icant increase in AEA content in the nucleus tractus solitarius (NTS) after an increase in blood pres
89 revealed axonal degeneration of the nucleus tractus solitarius (NTS) and area postrema (AP) of the m
90 ow that glutamatergic neurons in the nucleus tractus solitarius (NTS) and caudal serotonergic neurons
91 ptic transmission between the nucleus of the tractus solitarius (NTS) and dorsal motor nucleus of the
95 i of the dorsal motor nucleus (DMN), nucleus tractus solitarius (NTS) and nucleus ambiguus (NA) with
96 signals that are transmitted to the nucleus tractus solitarius (NTS) and parabrachial nucleus (PB).
97 gions involved in autonomic control: nucleus tractus solitarius (NTS) and rostral ventrolateral medul
98 pression in two brainstem areas, the nucleus tractus solitarius (NTS) and the rostral ventrolateral m
99 cteristics of the NPY neurons in the nucleus tractus solitarius (NTS) and their interactions with SST
100 s from the area postrema (AP) to the nucleus tractus solitarius (NTS) and to examine the synaptic int
101 lateral hypothalamic area (LHA), and nucleus tractus solitarius (NTS) are co-linked to these two site
103 ical studies highlight the hindbrain nucleus tractus solitarius (NTS) as a brain region important for
104 2 enzyme) containing neurons of the nucleus tractus solitarius (NTS) become activated during low-sod
106 changes in synaptic transmission in nucleus tractus solitarius (NTS) contribute to these responses i
107 NE to the limbic system, such as the nucleus tractus solitarius (NTS) contribute to this process.
108 he dorsal vagal complex (DVC; nucleus of the tractus solitarius (NTS) dorsal motor nucleus of the vag
109 t premotor, GABAergic neurons in the nucleus tractus solitarius (NTS) form a hindbrain micro-circuit
110 e P (SP) is released from the feline nucleus tractus solitarius (NTS) in response to activation of sk
111 to quantify NO concentration in the nucleus tractus solitarius (NTS) in vitro in brain slices and in
112 lpha1-noradrenergic receptors in the nucleus tractus solitarius (NTS) influences neural processes tha
116 tween baroreceptor afferents and the nucleus tractus solitarius (NTS) is essential for reflex regulat
117 Here, we show that the hindbrain nucleus tractus solitarius (NTS) is essential for vocalization i
119 excitatory amino acid (EAA) induced nucleus tractus solitarius (NTS) neuronal activity were investig
120 e CCL8-CCR5 axis, which triggers the nucleus tractus solitarius (NTS) neuronal damage and neuronal di
122 changes in synaptic transmission in nucleus tractus solitarius (NTS) neurons of C57Bl/6J mice to the
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
126 ssions in the area postrema (AP) and nucleus tractus solitarius (NTS) of brainstem including the NTS
129 ic acid-A (GABA(A)) receptors in the nucleus tractus solitarius (NTS) participate in autonomic regula
133 in baroreceptor transmission in the nucleus tractus solitarius (NTS) remains an area of active resea
135 d rat, electrical stimulation of the nucleus tractus solitarius (NTS) synchronizes the EEG by increas
136 h concentration may have reached the nucleus tractus solitarius (nTS) to elicit depressor and bradyca
137 cond-order neurons within the caudal nucleus tractus solitarius (NTS) to initiate autonomic reflexes.
138 esponses of gustatory neurons in the nucleus tractus solitarius (NTS) to tastant stimuli were recorde
139 ectively, while Fos labelling in the nucleus tractus solitarius (NTS) was increased by 5-fold compare
140 llary depressor area (CVLM), and the nucleus tractus solitarius (nTS) were also included for comparis
141 put originating from neurones in the nucleus tractus solitarius (NTS) were determined by evoking acti
142 brain segments containing primarily nucleus tractus solitarius (NTS) were employed for slice superfu
143 within astrocytes and neurons in the nucleus tractus solitarius (NTS), a hindbrain nucleus critical f
144 ates GLP-1-expressing neurons in the nucleus tractus solitarius (NTS), a hindbrain nucleus that proje
145 POMC neurons are also found in the nucleus tractus solitarius (NTS), a region regulating satiety.
146 racteristics of CCK receptors in the nucleus tractus solitarius (NTS), a region that contains central
147 dissociated neurons of the brainstem nucleus tractus solitarius (nTS), a region that receives massive
148 undance in the caudal portion of the nucleus tractus solitarius (NTS), an area which together with th
150 fferent vagal fibers, neurons of the nucleus tractus solitarius (NTS), and the efferent fibers origin
151 r nucleus of the hypothalamus (PVN), nucleus tractus solitarius (NTS), and the parasympathetic nucleu
153 echolamine (CA) neurons found in the nucleus tractus solitarius (NTS), dorsal motor nucleus of the va
155 1beta, TNFalpha and IL6 mRNAs in the nucleus tractus solitarius (NTS), hypothalamus, hippocampus and
156 involve vagal afferent input to the nucleus tractus solitarius (NTS), including cardiopulmonary resp
158 neurons are found bilaterally within nucleus tractus solitarius (nTS), lateral to the commissural sub
160 estradiol increased Fos abundance in nucleus tractus solitarius (NTS), rostral ventrolateral medulla
161 lots of protein equivalents from the nucleus tractus solitarius (NTS), the first central relay for pe
162 l neuroanatomical hub connecting the nucleus tractus solitarius (NTS), the major central source of GL
163 a neuroanatomical hub connecting the nucleus tractus solitarius (NTS), the primary source of central
164 d synaptic function in the brainstem nucleus tractus solitarius (nTS), the principal site for integra
165 r, TrkB, are highly expressed in the nucleus tractus solitarius (nTS), the principal target of cardio
166 a region in the medial subnucleus of nucleus tractus solitarius (nTS), the reticular formation just v
167 ticity in this reflex pathway in the nucleus tractus solitarius (NTS), the site of termination of the
168 ral spinal trigeminal nucleus (VSP), nucleus tractus solitarius (NTS), ventrolateral medulla (VLM) an
169 ations functionally expressed in the nucleus tractus solitarius (NTS), we conducted several physiolog
170 nvolve glutamatergic synapses in the nucleus tractus solitarius (NTS), where afferent endings from ar
171 paraventricular nucleus (PVN) to the nucleus tractus solitarius (NTS), where cells that respond to pe
173 food has been strongly implicated in nucleus tractus solitarius (NTS)-mediated satiation, but the exa
192 ial chemoreceptors and the CNS [e.g. nucleus tractus solitarius (NTS)], although the signals for this
193 or (Calcr)-expressing neurons of the nucleus tractus solitarius (NTS; Calcr(NTS) cells) contribute to
194 rsal vagal complex (DVC, i.e. nucleus of the tractus solitarius, NTS, and dorsal motor nucleus of the
195 n the nucleus of the solitary tract (nucleus tractus solitarius; NTS) suppress food intake, including
196 t the level of the solitary nucleus (nucleus tractus solitarius; NTS), their involvement in the trans
197 ventricular nuclei in the forebrain, and the tractus solitarius nuclei, lateral parabrachial nuclei i
200 st, SR 140333, was injected into the nucleus tractus solitarius of the conscious guinea pigs who were
201 vagal afferent fibers synapse in the nucleus tractus solitarius of the medulla and then descend to ex
205 sural and medial subdivisions of the nucleus tractus solitarius of wild-type F344.Cck1r(+/+) rats, wh
206 o aversive stimuli, including the nucleus of tractus solitarius, parabrachial nucleus and central amy
207 diagonal band of Broca, hippocampus, nucleus tractus solitarius, parabrachial nucleus, paraventricula
208 urons receive GLP-1 innervation from nucleus tractus solitarius preproglucagon neurons that were acti
209 that GLP-1-producing neurons in the nucleus tractus solitarius project monosynaptically to the lPBN,
210 pathways from the spinal trigeminal, nucleus tractus solitarius, raphe magnus, raphe pallidus, and th
213 ion (5 Hz) of primary afferent fibers in the tractus solitarius resulted in a phasic depression (acco
214 he rostral, gustatory portion of the nucleus tractus solitarius (rNTS) in awake, freely licking rats
215 egmental area, parabrachial nucleus, nucleus tractus solitarius, rostral/caudal ventrolateral medulla
216 e number of CFLI cells in the caudal Nucleus Tractus Solitarius significantly more than preloads of m
217 -ir expression in the area postrema, nucleus tractus solitarius, solitary tract, and spinal trigemina
218 on caused c-Fos-ir expression in the nucleus tractus solitarius, spinal trigeminal tract, solitary tr
219 micked by endogenous release of glutamate by tractus solitarius stimulation, and was prevented by a g
220 on of GLP-1-producing neurons in the nucleus tractus solitarius that project to the ventral tegmental
221 n of sympathetic activity, including nucleus tractus solitarius, the lateral tegmental field rostral
222 se CRCs are the medullary raphe, the nucleus tractus solitarius, the ventrolateral medulla, the fasti
223 othalamus, dorsomedial hypothalamus, nucleus tractus solitarius), there appeared to be no significant
224 sensory afferents terminating in the nucleus tractus solitarius, these terminals were identified by t
225 nch of the glossopharyngeal nerve to nucleus tractus solitarius; this precipitates an impressive arra
226 ones were predominantly located close to the tractus solitarius (TS) and could be GABAergic or glutam
227 on of primary sensory afferent fibres in the tractus solitarius (ts) and currents postsynaptically ev
228 2 s, 25 Hz trains of stimuli applied to the tractus solitarius (TS), induced a small (10%) but signi
229 r cardiovascular afferent signaling (nucleus tractus solitarius, ventrolateral medulla) in both cell
230 , substantia nigra, locus coeruleus, nucleus tractus solitarius, ventrolateral medulla, pontine nucle
231 urons of the ventrolateral subnucleus of the tractus solitarius (vlNTS) act as an inspiratory off-swi
233 ely, GK message was not found in the nucleus tractus solitarius, which contains glucosensing neurons,