ライフサイエンスコーパス: solitary tract

1 ssing neurons resident in the nucleus of the solitary tract.

2 the first central relay, the nucleus of the solitary tract.

3 targeting projections to the nucleus of the solitary tract.

4 he prepositus nucleus and the nucleus of the solitary tract.

5 tem reticular nuclei, and the nucleus of the solitary tract.

6 area, the lateral septum, and nucleus of the solitary tract.

7 nd periolivary areas, and the nucleus of the solitary tract.

8 lus, locus coeruleus, and the nucleus of the solitary tract.

9 s and individual cells in the nucleus of the solitary tract.

10 ation from the stomach to the nucleus of the solitary tract.

11 ater numbers of GAD67-ir cells medial to the solitary tract.

12 nucleus of the amygdala, and nucleus of the solitary tract.

13 the locus coeruleus, and the nucleus of the solitary tract.

14 ala, parabrachial nucleus, or nucleus of the solitary tract.

15 ral parabrachial nucleus, and nucleus of the solitary tract.

16 mber of nuclei labeled in the nucleus of the solitary tract.

17 supramammillary nucleus, and nucleus of the solitary tract.

18 c paraventricular nucleus and nucleus of the solitary tract.

19 ferent terminal fields in the nucleus of the solitary tract.

20 body and relay neurons in the nucleus of the solitary tract.

21 in the area postrema and the nucleus of the solitary tract.

22 tency 3.95 +/- 0.3 ms) to stimulation of the solitary tract.

23 arry taste information to the nucleus of the solitary tract.

24 terminate in the commissural nucleus of the solitary tract.

25 c nucleus; area postrema; and nucleus of the solitary tract.

26 r nucleus; area postrema; and nucleus of the solitary tract.

27 was removed by inhibition of nucleus of the solitary tract.

28 ir central projections in the nucleus of the solitary tract.

29 afferent excitability in the nucleus of the solitary tract.

30 produced in the ileum and the nucleus of the solitary tract.

31 is mediated by neurons in the nucleus of the solitary tract.

32 s; 5) parahypoglossal nucleus/nucleus of the solitary tract; 6) parabrachial/Kolliker-Fuse nuclei; an

33 lowing central and localized, nucleus of the solitary tract, administration of N6-cyclohexyladenosine

34 ptors in the fidelity of transmission across solitary tract afferent-NTS neuron synapses.

35 directly into the caudomedial nucleus of the solitary tract also abolished duodenal lipid-induced act

36 percent of the neurons in the nucleus of the solitary tract and 47 % of the neurons in the dorsal mot

37 alamus and brainstem regions (nucleus of the solitary tract and A5 region) also project to both tissu

38 velopment of area postrema -> nucleus of the solitary tract and arcuate hypothalamic nucleus -> parav

39 activation of neurons in the nucleus of the solitary tract and area postrema, key hindbrain areas fo

40 atiety signals, including the nucleus of the solitary tract and area postrema.

41 a, parabrachial nucleus (PB), nucleus of the solitary tract and central amygdalar nucleus, other refe

42 of gut-related neurons in the nucleus of the solitary tract and in the dorsal motor nucleus of the va

43 rsally in the medulla, in the nucleus of the solitary tract and in the locus caeruleus at the pontome

44 i), gustatory system (rostral nucleus of the solitary tract and medial parabrachial nucleus), neuroen

45 ber of neurons project to the nucleus of the solitary tract and parabrachial nucleus.

46 ous report, medullary afferent fibers in the solitary tract and spinal trigeminal tract labelled for

47 presence of OX2R mRNA in the nucleus of the solitary tract and the lateral reticular field (LRt).

48 lements of both the gustatory nucleus of the solitary tract and the nucleus ambiguus.

49 e c-Fos positive cells in the nucleus of the solitary tract and the parabrachial, medial vestibular,

50 nd two medullary regions, the nucleus of the solitary tract and ventrolateral medulla, also showed si

51 ea, and caudal regions of the nucleus of the solitary tract and ventrolateral medulla.

52 m the carotid bodies (via the nucleus of the solitary tract) and central through the direct sensing o

53 eruleus, subcoeruleus region, nucleus of the solitary tract, and C3 cell group.

54 omedial hypothalamic nucleus, nucleus of the solitary tract, and caudal ventrolateral medulla.

55 ression in the area postrema, nucleus of the solitary tract, and dorsal motor nucleus of the vagus.

56 Neurons in the A1, nucleus of the solitary tract, and dorsomedial hypothalamus are activat

57 in the ventrolateral medulla, nucleus of the solitary tract, and locus coeruleus.

58 e include the lateral septum, nucleus of the solitary tract, and medial hypothalamic regions.

59 medial octavolateral nucleus, nucleus of the solitary tract, and the dorsal column nucleus.

60 luding the area postrema, the nucleus of the solitary tract, and the dorsal motor nucleus of the vagu

61 tory column, the caudolateral nucleus of the solitary tract, and the pontine Kolliker-Fuse, intertrig

62 cluding the parabrachial nucleus, nucleus of solitary tract, and ventrolateral medulla.

63 Neurones were recorded in the nuclei of the solitary tracts, and in the rostral and caudal ventral r

64 C1 catecholamine cell group; nucleus of the solitary tract; and dorsal motor nucleus of vagus.

65 immunopositive neurons in the nucleus of the solitary tract, area postrema, and dorsal vagal motor nu

66 a (both commissural and medial nuclei of the solitary tract, area postrema, and the dorsal motor nucl

67 (GABA-A agonist) injection in or next to the solitary tract at area postrema level desynchronized PND

68 he intermediate region of the nucleus of the solitary tract blocked the robust increase in fat intake

69 n (PPG) neurons in the caudal nucleus of the solitary tract (cNTS) that produce glucagon-like peptide

70 ic transmission in the caudal nucleus of the solitary tract (cNTS), which is critically important for

71 riaqueductal gray, and medial nucleus of the solitary tract compared to isotonic saline controls.

72 tely to medial amygdala, locus coeruleus and solitary tract, consistent with the existence of PVHCrh-

73 No caudal subnuclei medial to the solitary tract contained labeled afferent fibers.

74 the intermediate dorsomedial nucleus of the solitary tract (dmNTS) because this region receives auto

75 lateral parabrachial nucleus, nucleus of the solitary tract, dorsal motor nucleus of the vagus (DMV),

76 rabrachial nucleus and caudal nucleus of the solitary tract, dorsal motor nucleus of the vagus nerve,

77 Electrical stimulation of the solitary tract evoked EPSPs and IPSPs in DVN neurons and

78 trigeminal nucleus and in the nucleus of the solitary tract express aromatase.

79 oguvacine injections into the nucleus of the solitary tract further reduced vagal tone: remaining sou

80 The adult nucleus of the solitary tract has abundant polysialic acid (polySia) an

81 rons of the area postrema and nucleus of the solitary tract in mice and humans, and genetic deletion

82 of Olig3, determinant of the nucleus of the solitary tract in mice), reveals that the superficial po

83 expression in the ipsilateral nucleus of the solitary tract in singing birds.

84 bition of PKC activity in the nucleus of the solitary tract in situ abolished the Ang II-mediated dep

85 o transmit information to the nucleus of the solitary tract in the brainstem.

86 and the area postrema and the nucleus of the solitary tract in the hindbrain.

87 s expressing Fos included the nucleus of the solitary tract in the medulla, parabrachial, locus coeru

88 ral ventrolateral medulla and nucleus of the solitary tract), in regions associated with anxiety and

89 the gustatory portion of the nucleus of the solitary tract) includes the vagal lobe, which is a larg

90 4) The medial nucleus of the solitary tract (including A2 noradrenergic and aldostero

91 dentified in the intermediate nucleus of the solitary tract (iNTS) with little expression in other br

92 Input from the nucleus of the solitary tract is relayed to vagal efferent neurons that

93 rogenase type 2 (HSD2) in the nucleus of the solitary tract is sufficient to drive consumption of sod

94 al activation in areas of the nucleus of the solitary tract known to be targeted by GLP-1R agonism, o

95 respiratory control (lateral nucleus of the solitary tract), locomotor or exploratory behavior contr

96 into the medial or comissural nucleus of the solitary tract (mNTS and comNTS, respectively) resulted

97 he area postrema (AP), medial nucleus of the solitary tract (mNTS), dorsal motor nucleus of the vagus

98 ay, parabrachial nucleus, and nucleus of the solitary tract), neuroendocrine system (paraventricular

99 experience, especially during nucleus of the solitary tract neurogenesis, leads to a restructuring of

100 f cardiac and respiratory inputs onto single solitary tract neurons may be in part responsible for in

101 aste-activated neurons in the nucleus of the solitary tract (NST) and subjacent reticular formation (

102 t the LH projects to both the nucleus of the solitary tract (NST) and the dorsal motor nucleus of the

103 amus (LH) send projections to the nucleus of solitary tract (NST) and the parabrachial nucleus (PBN)

104 activity was measured in the nucleus of the solitary tract (NST) in anesthetized B6 and 129 mice to

105 mation from taste buds to the nucleus of the solitary tract (NST) in the medulla.

106 Taste neurons in the nucleus of the solitary tract (NST) not only send axons to the parabrac

107 The nucleus of the solitary tract (NST) processes gustatory and related som

108 The nucleus of the solitary tract (NST) processes substantial visceral affe

109 The nucleus of the solitary tract (NST), located in the dorsomedial medulla

110 ntral subdivision (RC) of the nucleus of the solitary tract (NST), the principal site where geniculat

111 e centrally within the caudal nucleus of the solitary tract (NST), with signals subsequently relayed

112 ed initially to the hindbrain nucleus of the solitary tract (NST).

113 in the rostral portion of the nucleus of the solitary tract (NST).

114 chorda tympani nerves in the nucleus of the solitary tract (NST).

115 stsynaptic neurons in the rat nucleus of the solitary tract (NST).

116 es and not the neurons in the nucleus of the solitary tract (NST; principal locus integrating viscera

117 ia vagal afferents within the nucleus of the solitary tract [NST].

118 rone-sensitive neurons in the nucleus of the solitary tract (NTS(HSD2) neurons) were shown to drive s

119 39% in the middle part of the nucleus of the solitary tract (NTS) and 33% in the caudal NTS.

120 tergic connection between the nucleus of the solitary tract (NTS) and a segment of the ventrolateral

121 DVC, specifically within the nucleus of the solitary tract (NTS) and area postrema (AP) nuclei.

122 =2-h) c-Fos expression in the nucleus of the solitary tract (NTS) and area postrema of the brainstem

123 5-HT immunoreactivity in the nucleus of the solitary tract (nTS) and dorsal motor nucleus of the vag

124 tion arrives in the brainstem nucleus of the solitary tract (NTS) and is relayed to other CNS sites f

125 (PPG) neurons located in the nucleus of the solitary tract (NTS) and projecting to numerous brain re

126 ts reduced NPY content in the nucleus of the solitary tract (NTS) and the dorsal motor nucleus of the

127 nomic functions involving the nucleus of the solitary tract (NTS) and the dorsal motor nucleus of the

128 ted were within the brainstem nucleus of the solitary tract (NTS) and the hypothalamic retrochiasmati

129 activation of neurons in the nucleus of the solitary tract (NTS) and their efferent target nuclei in

130 y nuclei of the hypothalamus, nucleus of the solitary tract (NTS) and ventrolateral medulla (VLM), an

131 e brainstem, primarily in the nucleus of the solitary tract (NTS) and ventrolateral medulla (VLM), co

132 lized with SP and CGRP in the nucleus of the solitary tract (NTS) and with SP, CGRP and MOR in the pa

133 le amount of expansion in the nucleus of the solitary tract (NTS) as a result of early dietary sodium

134 es in the rostral pole of the nucleus of the solitary tract (NTS) at adulthood.

135 The nucleus of the solitary tract (NTS) contains a subpopulation of neurons

136 The nucleus of the solitary tract (NTS) contains a unique subpopulation of

137 The nucleus of the solitary tract (NTS) contains a unique subpopulation of

138 Leptin signaling within the nucleus of the solitary tract (NTS) contributes to the control of food

139 SN), locus coeruleus (LC) and the nucleus of solitary tract (NTS) depending on dose of administration

140 d GABA is released within the nucleus of the solitary tract (NTS) during hypoxia and modulates the re

141 l as the area postrema (APOS) and nucleus of solitary tract (NTS) following AMN+LEP administration.

142 vated neurones throughout the nucleus of the solitary tract (NTS) in A-IV(+/+) mice, measured by immu

143 of neuronal activation in the nucleus of the solitary tract (NTS) in response to intragastric adminis

144 ricular (PVN) nuclei, and the nucleus of the solitary tract (NTS) in the medulla.

145 The nucleus of the solitary tract (NTS) integrates peripheral afferents wit

146 The nucleus of the solitary tract (NTS) is a critical integrative site for

147 The nucleus of the solitary tract (NTS) is a critical structure involved in

148 The nucleus of the solitary tract (NTS) is a key gateway for meal-related s

149 The nucleus of the solitary tract (NTS) is activated by vagal afferents fro

150 The nucleus of the solitary tract (NTS) is critical for the central integra

151 from the vagus nerve onto the nucleus of the solitary tract (NTS) is one mechanism by which the vagus

152 A) to identify CeA-projecting nucleus of the solitary tract (NTS) neurons for synaptic characterizati

153 m single cells in the rostral nucleus of the solitary tract (NTS) of anesthetized rats.

154 isualized concurrently in the nucleus of the solitary tract (NTS) of developmentally sodium-restricte

155 oA-IV) gene expression in the nucleus of the solitary tract (NTS) of lean ovariectomized (OVX) rodent

156 n of neurons in the hindbrain nucleus of the solitary tract (NTS) of rats that are activated during s

157 2-expressing) neurons in the nucleus of the solitary tract (NTS) of the rat are aldosterone-sensitiv

158 tly presented tastants in the nucleus of the solitary tract (NTS) of urethane-anesthetized rats.

159 lated neurocircuitry, and the nucleus of the solitary tract (NTS) plays a critical role in cardiovasc

160 The nucleus of the solitary tract (NTS) plays a pivotal role in the ventila

161 erence was used to knock down nucleus of the solitary tract (NTS) preproglucagon (PPG), and chronic i

162 melanotan-II (MTII) into the nucleus of the solitary tract (NTS) produces rapid and sustained reduct

163 Neurons within the nucleus of the solitary tract (NTS) receive vagal afferent innervations

164 The nucleus of the solitary tract (NTS) receives inputs from both arterial

165 The nucleus of the solitary tract (NTS) regulates life-sustaining functions

166 nl) delivered into the medial nucleus of the solitary tract (NTS) significantly increased 15% sucrose

167 onse patterns of cells in the nucleus of the solitary tract (NTS) to representatives of four basic ta

168 e gut activate neurons in the nucleus of the solitary tract (NTS) via the vagus nerve.

169 nformation is conveyed to the nucleus of the solitary tract (NTS) where it initiates neuroendocrine,

170 spiratory control such as the nucleus of the solitary tract (NTS), a site that receives chemosensory

171 central gustatory relay, the nucleus of the solitary tract (nTS), after transection of the CT.

172 alpha-MSH) into the overlying nucleus of the solitary tract (NTS), an important component of "vago-va

173 rabrachial nucleus (PBN), and nucleus of the solitary tract (NTS), and activation of cell bodies in t

174 c-Fos immunoreactivity in the nucleus of the solitary tract (NTS), and steady-state levels of IL-1bet

175 sal nucleus, subnuclei of the nucleus of the solitary tract (NTS), and the dorsal motor nucleus of th

176 ostral raphe pallidus (rRPa), nucleus of the solitary tract (NTS), and ventrolateral medulla (VLM).

177 were not observed within the nucleus of the solitary tract (NTS), another brainstem site critical fo

178 antly increased Fos-IR in the nucleus of the solitary tract (NTS), area postrema (AP), rostral ventro

179 ricular nucleus (PVN) and the nucleus of the solitary tract (NTS), both of which are responsive to sy

180 c responses of neurons in the nucleus of the solitary tract (NTS), but their exact role remains uncle

181 gustatory information to the nucleus of the solitary tract (NTS), displays terminal field reorganiza

182 d many neurons throughout the nucleus of the solitary tract (NTS), including A2 noradrenergic neurons

183 In the nucleus of the solitary tract (NTS), Kv3.1b-IR neurones were predominan

184 chemoreception including the nucleus of the solitary tract (NTS), medullary raphe and retrotrapezoid

185 region [pF(V) ] and pF(L) ), nucleus of the solitary tract (NTS), reticular formation (RF), pontine

186 e show that astrocytes of the nucleus of the solitary tract (NTS), the brain area that receives and i

187 In the nucleus of the solitary tract (NTS), the first relay in the central gus

188 n POMC neurons located in the nucleus of the solitary tract (NTS), the only other known population of

189 h Fos-immunoreactivity in the nucleus of the solitary tract (NTS), ventrolateral medulla (VLM), and p

190 ateral medulla (RVLM) and the nucleus of the solitary tract (NTS), where VMH efferents make close con

191 ject centrally to the rostral nucleus of the solitary tract (NTS), whereas neurons providing general

192 (ARC) and showed none in the nucleus of the solitary tract (NTS), which relays visceral feeding sign

193 entral-lateral portion of the nucleus of the solitary tract (nTS)-the same area that shows increased

194 y nucleus of the medulla, the nucleus of the solitary tract (nTS).

195 cond-order neurons within the nucleus of the solitary tract (NTS).

196 rones in the dorsal medullary nucleus of the solitary tract (NTS).

197 ry for the development of the nucleus of the solitary tract (NTS).

198 s in the brainstem in the rat nucleus of the solitary tract (NTS).

199 cting 0.5 nmol capsaicin into nucleus of the solitary tract (nTS).

200 body, petrosal ganglion, and nucleus of the solitary tract (NTS).

201 icted distribution within the nucleus of the solitary tract (NTS).

202 utonomic functions within the nucleus of the solitary tract (NTS).

203 rocessing occurs first in the nucleus of the solitary tract (NTS).

204 teral medulla (RVLM), and the nucleus of the solitary tract (NTS).

205 rgic interneurones within the nucleus of the solitary tract (NTS).

206 nt in these situations is the nucleus of the solitary tract (NTS).

207 us of the amygdala (CeA), and nucleus of the solitary tract (NTS).

208 x and the rostral part of the nucleus of the solitary tract (nTS).

209 s, prefrontal cortex, and the nucleus of the solitary tract (NTS).

210 l bodies were observed in the nucleus of the solitary tract (NTS).

211 r primary central target, the nucleus of the solitary tract (NTS).

212 nal field organization in the nucleus of the solitary tract (NTS).

213 in the following regions: the nucleus of the solitary tract (NTS, 6% of CTB-ir neurons), area postrem

214 nt inhibition in cells in the nucleus of the solitary tract (NTS, the first central relay in the gust

215 a vasopressor region) and the nucleus of the solitary tract (NTS; a vasodepressor region).

216 and olfaction interact in the nucleus of the solitary tract (NTS; the first neural relay in the centr

217 electrical stimulation of the nucleus of the solitary tract (NTS; the first synaptic relay for taste)

218 ular, brainstem nuclei (e.g., nucleus of the solitary tract; NTS) and the basolateral nucleus of the

219 rons were found in the reticular, raphe, and solitary tract nuclei, and in the interstitial nucleus o

220 cimol injection into commissural part of the solitary tract nucleus (commNTS) had no effect on PND or

221 nucleus, the ventrolateral subnucleus of the solitary tract nucleus (NTS(VL)), and in a non-respirato

222 stem A2/C2 catecholamine (CA) neurons in the solitary tract nucleus (NTS) are thought to play an impo

223 The solitary tract nucleus (NTS) conveys visceral informatio

224 cting on ANGII type 1 (AT1) receptors in the solitary tract nucleus (NTS) depresses the baroreflex.

225 ranial visceral afferent terminals in caudal solitary tract nucleus (NTS) display pronounced, activit

226 Phox2b was expressed by many solitary tract nucleus (NTS) neurons including those tha

227 ular reflexes; however, the phenotype of the solitary tract nucleus (NTS) neurons involved is not kno

228 ion and whether the input is direct from the solitary tract nucleus (NTS) or indirect via the respira

229 ns are catecholamine (CA) neurons within the solitary tract nucleus (NTS) that influence many homeost

230 al visceral afferents enter the brain at the solitary tract nucleus (NTS) to control the heart, lungs

231 BDA-ir varicosities were found in the solitary tract nucleus (NTS), all ventral respiratory co

232 rimary afferents enter the CNS at the caudal solitary tract nucleus (NTS), and activate central pathw

233 ia and their central terminations within the solitary tract nucleus (NTS), but little is known about

234 RPV1) receptors in synaptic terminals at the solitary tract nucleus (NTS).

235 eEPSCs) and/or spontaneous (sEPSCs) EPSCs at solitary tract nucleus neurons.

236 ium sources at afferent terminals within the solitary tract nucleus to independently modify release f

237 sal nucleus, and ventrolateral subnucleus of solitary tract nucleus), and a non-respiratory cuneate n

238 ps were also located in the locus coeruleus, solitary tract nucleus, and area postrema within the rho

239 , commissural and ventrolateral subnuclei of solitary tract nucleus, and retrotrapezoid nucleus/paraf

240 ls, gigantocellular nucleus, inferior olive, solitary tract nucleus, dorsal vagal motor and hypogloss

241 e octavolateral area, dorsal column nucleus, solitary tract nucleus, motoneurons, and reticular forma

242 ar nuclei, magnocellular vestibular nucleus, solitary tract nucleus, nucleus medianus magnocellularis

243 density of PYY fibers was present within the solitary tract nucleus, specifically within the dorsal a

244 ry nucleus and in cholinergic neurons of the solitary tract nucleus.

245 nstem nuclei including the area postrema and solitary tract nucleus.

246 a neuronal projection originating within the solitary tract nucleus.

247 e for their homology with the nucleus of the solitary tract of mammals and suggesting that a single a

248 ntrast, PKC inhibition in the nucleus of the solitary tract of SHR only partially reduced the effect

249 neuronal cell bodies from the nucleus of the solitary tract of the medulla oblongata.

250 ns in ascending raphe nuclei, nucleus of the solitary tract, or ventrolateral medulla are VGLUT2 posi

251 n the raphe pallidus nucleus, nucleus of the solitary tract, periaqueductal gray, hypothalamic parave

252 t not EM-2-ir neurons, in the nucleus of the solitary tract projected their axons to the RVM.

253 xcitatory transmission in the nucleus of the solitary tract, regulating sympathetic nerve activity.

254 The rostral portion of the nucleus of the solitary tract (rNST) is an obligatory relay for gustato

255 ion of neurons in the rostral nucleus of the solitary tract (rNST) that respond to gustatory input fr

256 nt of synapses in the rostral nucleus of the solitary tract (rNST) was investigated in rat to determi

257 cond order neurons in the rostral nucleus of solitary tract (rNST).

258 single neurons of the rostral nucleus of the solitary tract (rNTS), but anatomical evidence has been

259 n: the rostral portion of the nucleus of the solitary tract (rNTS), the lateral parabrachial nucleus

260 tivated, provide input to the nucleus of the solitary tract (Sol) and paratrigeminal nucleus (Pa5) in

261 of primary sensory afferents (nucleus of the solitary tract, spinal trigeminal nucleus, and dorsal ho

262 In horizontal brainstem slices, solitary tract (ST) activation evoked EPSCs.

263 Solitary tract (ST) afferents converged onto NTS-CeA sec

264 rojection neurons, we recently reported that solitary tract (ST) afferents directly contact NTS neuro

265 SST neurons (57%) received direct input from solitary tract (ST) afferents, indicating that they form

266 ess visceral afferent information carried by solitary tract (ST) afferents, we identified CA neurons

267 ilitation of glutamatergic transmission from solitary tract (ST) afferents.

268 Graded shocks to the solitary tract (ST) always (93%) triggered EPSCs at CeA

269 (but not peripheral) vagal afferents in the solitary tract (ST) and nucleus; p55-ir is also present

270 Electrical activation of the solitary tract (ST) evoked EPSCs in NTS POMC-EGFP neuron

271 t horizontal brainstem slices, activation of solitary tract (ST) primary afferents generated ST-eEPSC

272 In brainstem slices, we activated solitary tract (ST) primary afferents to release glutama

273 Primary afferent axons within the solitary tract (ST) relay homeostatic information via gl

274 Solitary tract (ST) stimulation-evoked EPSCs, first dete

275 Cranial visceral afferents travel via the solitary tract (ST) to contact neurons within the ST nuc

276 slices containing caudal NTS, shocks to the solitary tract (ST) triggered synchronous ST-EPSCs and t

277 PSCs) evoked by electrically stimulating the solitary tract (ST) under GABA(A) receptor blockade.

278 tite, are strongly and directly activated by solitary tract (ST) visceral afferents.

279 Excitatory transmission from primary solitary tract (ST)-afferents consists of multiple conta

280 type) and unmyelinated (C-type) axons in the solitary tract (ST).

281 vagal afferents, which arrive there via the solitary tract (ST).

282 voked EPSPs and the ability of low-intensity solitary tract stimulation to evoke action potentials in

283 Activation of neurons in the nucleus of the solitary tract substantially suppressed fluid intake and

284 Responses to electrical stimulation of the solitary tract suggest that PPG cells are mostly second-

285 Direct synaptic input from the solitary tract suggests that peripheral signals (includi

286 -li) in the area postrema and nucleus of the solitary tract that predominantly characterizes other 2D

287 aracterized in rodents is the nucleus of the solitary tract, the first relay for visceral sensory inp

288 ssary for proper formation of the nucleus of solitary tract, the target for visceral sensory afferent

289 and medulla as well as in the nucleus of the solitary tract, the target of nodose ganglion-derived vi

290 neurons within the brainstem nucleus of the solitary tract to acutely suppress food intake by reduci

291 ion from GLP-1 neurons in the nucleus of the solitary tract to the NAc.

292 the amplitude of miniature EPSCs as well as solitary tract (TS) evoked EPSC amplitude and action pot

293 5-HT2AR activation augmented solitary tract (TS) evoked EPSC amplitude whereas 5-HT2A

294 mygdaloid nuclei, cerebellum, nucleus of the solitary tract, ventral tegmental area, and spinal trige

295 effect on the neurons of the nucleus of the solitary tract was inhibition.

296 Electrical stimulation of the solitary tract was used to evoke EPSCs.

297 whereas those evoked via the nucleus of the solitary tract were unaltered.

298 omises the development of the nucleus of the solitary tract, which processes viscerosensory informati

299 leus (LC) stimulation via the nucleus of the solitary tract, which receives afferent vagal inputs.

300 observed with neurons of the nucleus of the solitary tract whose activation by gastrointestinal food