コーパス検索結果 (１語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
1 atory neurons in the rostral nucleus tractus solitarius.
2 of the trigeminal nerve and nucleus tractus solitarius.
3 f lung afferent neurons, the nucleus tractus solitarius.
4 -1 receptor mechanism in the nucleus tractus solitarius.
5 1 receptor antagonist in the nucleus tractus solitarius.
6 tant-latency synaptic input from the tractus solitarius.
7 subnucleus centralis of the nucleus tractus solitarius.
8 nucleus, area postrema, and nucleus tractus solitarius.
9 bers were found in the region of the nucleus solitarius.
10 ed neurons were found in the nucleus tractus solitarius.
11 tor neurons localized in the nucleus tractus solitarius.
12 al subnucleus of the rostral nucleus tractus solitarius.
13 te and rostral levels of the nucleus tractus solitarius.
14 and dorsal subnuclei of the nucleus tractus solitarius.
15 hial nuclei, and commissural nucleus tractus solitarius.
16 ) cells in the medial nucleus of the tractus solitarius.
17 in the trigeminal nuclei and nucleus tractus solitarius.
18 ular nucleus, but not in the nucleus tractus solitarius.
19 , with high abundance in the nucleus tractus solitarius.
23 c nucleus, central amygdala, nucleus tractus solitarius and area postrema compared with vehicle injec
24 Furthermore, the brainstem's nucleus tractus solitarius and area postrema showed increased expression
25 eus, intermediate and caudal nucleus tractus solitarius and area postrema), reward (the shell of the
26 ABAergic neurons, bordering both the nucleus solitarius and caudal vestibular complex, emphasizes the
27 th known inputs to the RVLM (nucleus tractus solitarius and caudal VLM) unmasked tonic glycinergic in
30 way sensory receptors to the nucleus tractus solitarius and from this site to airway-related vagal pr
31 ved in the gustatory rostral nucleus tractus solitarius and in areas involved in vestibulo-ocular pro
32 ntermediate subnuclei of the nucleus tractus solitarius and in other medullary, pontine, midbrain, an
33 ar reticular nucleus, nucleus of the tractus solitarius and locus coeruleus also exhibited altered pa
34 TR have connections with the nucleus tractus solitarius and projections to the ventrolateral medulla.
35 and oxidative stress in the nucleus tractus solitarius and rostral ventrolateral medulla as well as
36 ons whose connections to the nucleus tractus solitarius and rostral ventrolateral medulla result in s
37 control circuitry within the nucleus tractus solitarius and the caudal part of ventral respiratory co
38 dial subnuclei of the caudal nucleus tractus solitarius and the dorsolateral, dorsomedial and medial
41 reased Fos expression in the nucleus tractus solitarius and the ventrolateral medulla bilaterally wit
42 oked upon stimulation of the nucleus tractus solitarius and these responses were also blocked by bicu
43 expression in neurons of the nucleus tractus solitarius and ventromedial (VMH) and arcuate nuclei of
44 Blockade of output from the nucleus tractus solitarius and/or disinhibition of the CVLM unmasked ton
45 a caudolateral region of the nucleus tractus solitarius, and a lateral band of the principal sensory
46 n (laminae I and II) and the nucleus tractus solitarius, and both PB subnuclei send projections to li
47 so found in the medial portion of n. tractus solitarius, and both the rostral and caudal ventrolatera
48 ocampus, habenula, amygdala, nucleus tractus solitarius, and circumventricular organs such as subforn
49 xi, the medial subnucleus of nucleus tractus solitarius, and the dorsal motor nucleus of the vagus, b
51 the infected neurons in the nucleus tractus solitarius are part of sympathetic or parasympathetic af
53 ject centrally to the nucleus of the tractus solitarius, area postrema, and dorsal motor nucleus of t
54 ial nucleus, and commissural nucleus tractus solitarius, as previously observed in chronic morphine-t
55 ed bilaterally in the medial nucleus tractus solitarius at a site that produced apnea in response to
56 ion of DBH expression in the nucleus tractus solitarius, but not in the locus coeruleus, restored CPP
57 lectrical stimulation of the nucleus tractus solitarius, but the effect was slower than for the enhan
58 (PPG) neurons in the medial nucleus tractus solitarius by fluorescent in situ hybridization, suggest
59 ncreased Fos labeling in the nucleus tractus solitarius caudal region, which receives vagal chemosens
61 rsolateral subnucleus of the nucleus tractus solitarius (dlNTS) was processed for the histochemical v
63 glutamatergic neurons of the nucleus tractus solitarius during CH significantly decreased ventilation
66 ovel group of neurons in the nucleus tractus solitarius expresses the enzyme 11-beta-hydroxysteroid d
67 distribution of cells in the nucleus tractus solitarius expressing c-fos in response to physiological
69 crease in trigeminal but not nucleus tractus solitarius Fos labeling, and no behavioral avoidance.
70 al ventrolateral medulla and nucleus tractus solitarius, Fos-positive neurons projected to the Sm, PB
72 receptors on neurons in the nucleus tractus solitarius, hypoglossal nucleus, and dorsal motor nucleu
73 ne region which includes the nucleus tractus solitarius in the hindbrain, and another more distribute
76 urones, including neurones receiving tractus solitarius input (i.e. viscerosensory) and those involve
78 neural circuitry within the nucleus tractus solitarius is consistent with a complex central control
80 SA, the endemic 'Io, or Hawaiian Hawk (Buteo solitarius), is a species of conservation concern that l
81 -ir expression mainly in the nucleus tractus solitarius, lateral reticular nucleus, lateral tegmental
82 subnucleus), area postrema, nucleus tractus solitarius, locus coeruleus, paraventricular nucleus of
83 m synaptic plasticity in the nucleus tractus solitarius may play a role in the homeostatic regulation
84 c-fos mRNA expression in the nucleus tractus solitarius (middle, mNTS, and rostral, rNTS) and the ros
85 GABA receptors in the medial nucleus tractus solitarius (mNTS) also attenuated the PVN-induced tachyc
86 eurones in the medial nucleus of the tractus solitarius (mNTS) and in the dorsal motor nucleus of the
87 ining portions of the medial nucleus tractus solitarius (mNTS) at both intermediate (NTSi) and caudal
88 alateral sides of the medial nucleus tractus solitarius (mNTS) in rats receiving EA ST 36 compared wi
89 leptin signals in the medial nucleus tractus solitarius (mNTS) to suppress food intake, in part, by a
90 parabrachial nucleus (LPB), nucleus tractus solitarius (NST), frontal cerebral cortex and the parvoc
91 s activate catecholaminergic nucleus tractus solitarius (NTS(TH)) projections in the paraventricular
92 s similarly increased in the nucleus tractus solitarius (NTS) A2 region in virgin and pregnant rats 9
93 crease in AEA content in the nucleus tractus solitarius (NTS) after an increase in blood pressure (BP
94 d axonal degeneration of the nucleus tractus solitarius (NTS) and area postrema (AP) of the medulla.
95 glutamatergic neurons in the nucleus tractus solitarius (NTS) and caudal serotonergic neurons control
96 nsmission between the nucleus of the tractus solitarius (NTS) and dorsal motor nucleus of the vagus (
100 dorsal motor nucleus (DMN), nucleus tractus solitarius (NTS) and nucleus ambiguus (NA) with a sham c
102 volved in autonomic control: nucleus tractus solitarius (NTS) and rostral ventrolateral medulla (RVLM
103 in two brainstem areas, the nucleus tractus solitarius (NTS) and the rostral ventrolateral medulla (
104 cs of the NPY neurons in the nucleus tractus solitarius (NTS) and their interactions with SST neurons
105 he area postrema (AP) to the nucleus tractus solitarius (NTS) and to examine the synaptic interaction
107 A subset of neurons in the nucleus tractus solitarius (NTS) are uniquely sensitive to the adrenal s
108 dies highlight the hindbrain nucleus tractus solitarius (NTS) as a brain region important for GLP-1R-
109 e) containing neurons of the nucleus tractus solitarius (NTS) become activated during low-sodium and
111 in synaptic transmission in nucleus tractus solitarius (NTS) contribute to these responses is unclea
113 l vagal complex (DVC; nucleus of the tractus solitarius (NTS) dorsal motor nucleus of the vagus (DMV)
114 or, GABAergic neurons in the nucleus tractus solitarius (NTS) form a hindbrain micro-circuit with pre
115 is released from the feline nucleus tractus solitarius (NTS) in response to activation of skeletal m
116 tify NO concentration in the nucleus tractus solitarius (NTS) in vitro in brain slices and in vivo in
117 radrenergic receptors in the nucleus tractus solitarius (NTS) influences neural processes that are in
121 roreceptor afferents and the nucleus tractus solitarius (NTS) is essential for reflex regulation of b
122 , we show that the hindbrain nucleus tractus solitarius (NTS) is essential for vocalization in mice.
124 ory amino acid (EAA) induced nucleus tractus solitarius (NTS) neuronal activity were investigated by
125 CR5 axis, which triggers the nucleus tractus solitarius (NTS) neuronal damage and neuronal disconnect
127 in synaptic transmission in nucleus tractus solitarius (NTS) neurons of C57Bl/6J mice to their respo
128 rents innervate second-order nucleus tractus solitarius (NTS) neurons via myelinated (A-type) and unm
129 synaptic transmission in the nucleus tractus solitarius (NTS) neurons, the first synaptic station of
131 n the area postrema (AP) and nucleus tractus solitarius (NTS) of brainstem including the NTS neurons
132 c-Fos expression in the nucleus tractus solitarius (NTS) of the rat has been found to follow adm
134 A (GABA(A)) receptors in the nucleus tractus solitarius (NTS) participate in autonomic regulation of
136 In rats, cisplatin activates nucleus tractus solitarius (NTS) projections to the lateral parabrachial
138 receptor transmission in the nucleus tractus solitarius (NTS) remains an area of active research.
139 subset of neurons within the nucleus tractus solitarius (NTS) shows c-Fos activation during prolonged
140 lectrical stimulation of the nucleus tractus solitarius (NTS) synchronizes the EEG by increasing the
141 tration may have reached the nucleus tractus solitarius (nTS) to elicit depressor and bradycardic res
143 of gustatory neurons in the nucleus tractus solitarius (NTS) to tastant stimuli were recorded before
144 , while Fos labelling in the nucleus tractus solitarius (NTS) was increased by 5-fold compared with v
145 pressor area (CVLM), and the nucleus tractus solitarius (nTS) were also included for comparison of di
146 inating from neurones in the nucleus tractus solitarius (NTS) were determined by evoking activity in
147 egments containing primarily nucleus tractus solitarius (NTS) were employed for slice superfusion stu
148 strocytes and neurons in the nucleus tractus solitarius (NTS), a hindbrain nucleus critical for energ
149 -1-expressing neurons in the nucleus tractus solitarius (NTS), a hindbrain nucleus that projects mono
151 tics of CCK receptors in the nucleus tractus solitarius (NTS), a region that contains central termina
152 ted neurons of the brainstem nucleus tractus solitarius (nTS), a region that receives massive primary
153 in the caudal portion of the nucleus tractus solitarius (NTS), an area which together with the dorsal
154 The locus coeruleus (LC), nucleus tractus solitarius (NTS), and retrotrapezoid nucleus (RTN) are c
155 vagal fibers, neurons of the nucleus tractus solitarius (NTS), and the efferent fibers originating in
156 s of the hypothalamus (PVN), nucleus tractus solitarius (NTS), and the parasympathetic nucleus of the
158 ne (CA) neurons found in the nucleus tractus solitarius (NTS), dorsal motor nucleus of the vagus (DMV
160 NFalpha and IL6 mRNAs in the nucleus tractus solitarius (NTS), hypothalamus, hippocampus and somatose
161 vagal afferent input to the nucleus tractus solitarius (NTS), including cardiopulmonary responses, g
163 are found bilaterally within nucleus tractus solitarius (nTS), lateral to the commissural subnucleus
164 Its neighboring nuclei, the nucleus tractus solitarius (NTS), responds to acute glucose infusion by
165 l increased Fos abundance in nucleus tractus solitarius (NTS), rostral ventrolateral medulla (RVLM),
166 protein equivalents from the nucleus tractus solitarius (NTS), the first central relay for peripheral
167 natomical hub connecting the nucleus tractus solitarius (NTS), the major central source of GLP-1, wit
168 natomical hub connecting the nucleus tractus solitarius (NTS), the primary source of central GLP-1, w
169 ic function in the brainstem nucleus tractus solitarius (nTS), the principal site for integration of
170 are highly expressed in the nucleus tractus solitarius (nTS), the principal target of cardiovascular
171 in the medial subnucleus of nucleus tractus solitarius (nTS), the reticular formation just ventral t
172 n this reflex pathway in the nucleus tractus solitarius (NTS), the site of termination of the chemose
173 al trigeminal nucleus (VSP), nucleus tractus solitarius (NTS), ventrolateral medulla (VLM) and inferi
174 unctionally expressed in the nucleus tractus solitarius (NTS), we conducted several physiological and
175 lutamatergic synapses in the nucleus tractus solitarius (NTS), where afferent endings from arterial c
176 ricular nucleus (PVN) to the nucleus tractus solitarius (NTS), where cells that respond to peripheral
178 been strongly implicated in nucleus tractus solitarius (NTS)-mediated satiation, but the exact cellu
197 oreceptors and the CNS [e.g. nucleus tractus solitarius (NTS)], although the signals for this plastic
198 r)-expressing neurons of the nucleus tractus solitarius (NTS; Calcr(NTS) cells) contribute to the lon
199 al complex (DVC, i.e. nucleus of the tractus solitarius, NTS, and dorsal motor nucleus of the vagus,
200 cleus of the solitary tract (nucleus tractus solitarius; NTS) suppress food intake, including avoidan
201 vel of the solitary nucleus (nucleus tractus solitarius; NTS), their involvement in the transmission
202 lar nuclei in the forebrain, and the tractus solitarius nuclei, lateral parabrachial nuclei in the hi
206 40333, was injected into the nucleus tractus solitarius of the conscious guinea pigs who were then ex
207 ferent fibers synapse in the nucleus tractus solitarius of the medulla and then descend to excite upp
211 d medial subdivisions of the nucleus tractus solitarius of wild-type F344.Cck1r(+/+) rats, whereas CC
212 ve stimuli, including the nucleus of tractus solitarius, parabrachial nucleus and central amygdala.
213 band of Broca, hippocampus, nucleus tractus solitarius, parabrachial nucleus, paraventricular nucleu
214 tions: descending trigeminal, retroambiguus, solitarius, posterior octaval, descending octaval, magno
215 ceive GLP-1 innervation from nucleus tractus solitarius preproglucagon neurons that were activated by
216 P-1-producing neurons in the nucleus tractus solitarius project monosynaptically to the lPBN, providi
217 from the spinal trigeminal, nucleus tractus solitarius, raphe magnus, raphe pallidus, and the rostra
220 z) of primary afferent fibers in the tractus solitarius resulted in a phasic depression (accommodatio
221 al, gustatory portion of the nucleus tractus solitarius (rNTS) in awake, freely licking rats show lic
222 area, parabrachial nucleus, nucleus tractus solitarius, rostral/caudal ventrolateral medulla, or tho
223 of CFLI cells in the caudal Nucleus Tractus Solitarius significantly more than preloads of mineral o
224 ession in the area postrema, nucleus tractus solitarius, solitary tract, and spinal trigeminal tract.
225 d c-Fos-ir expression in the nucleus tractus solitarius, spinal trigeminal tract, solitary tract, and
226 y endogenous release of glutamate by tractus solitarius stimulation, and was prevented by a group II
227 P-1-producing neurons in the nucleus tractus solitarius that project to the ventral tegmental area (V
228 pathetic activity, including nucleus tractus solitarius, the lateral tegmental field rostral to the o
229 are the medullary raphe, the nucleus tractus solitarius, the ventrolateral medulla, the fastigial nuc
230 s, dorsomedial hypothalamus, nucleus tractus solitarius), there appeared to be no significant differe
231 afferents terminating in the nucleus tractus solitarius, these terminals were identified by the anter
232 he glossopharyngeal nerve to nucleus tractus solitarius; this precipitates an impressive array of car
233 e predominantly located close to the tractus solitarius (TS) and could be GABAergic or glutamatergic.
234 imary sensory afferent fibres in the tractus solitarius (ts) and currents postsynaptically evoked by
235 Hz trains of stimuli applied to the tractus solitarius (TS), induced a small (10%) but significant r
236 vascular afferent signaling (nucleus tractus solitarius, ventrolateral medulla) in both cell bodies a
237 ntia nigra, locus coeruleus, nucleus tractus solitarius, ventrolateral medulla, pontine nuclei, and i
238 the ventrolateral subnucleus of the tractus solitarius (vlNTS) act as an inspiratory off-switch and
240 message was not found in the nucleus tractus solitarius, which contains glucosensing neurons, or in e