ライフサイエンスコーパス: solitary tract

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

2 targeting projections to the nucleus of the solitary tract.

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

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

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

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

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

8 arry taste information to 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 c nucleus; area postrema; and nucleus of the solitary tract.

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

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

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

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

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

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

19 supramammillary nucleus, and nucleus of the solitary tract.

20 c paraventricular nucleus and nucleus of the solitary tract.

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

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

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

24 entrolateral medulla, and the nucleus of the solitary tract.

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

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

27 afferent excitability in the nucleus of the solitary tract.

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

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

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

31 the first central relay, 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 ry dendrites, and branches often entered the solitary tract and also extended across the ipsilateral

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 clear Fos-IR increased in the nucleus of the solitary tract and other brainstem regions known to regu

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

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

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

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

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

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

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

53 tral nucleus of the amygdala, nucleus of the solitary tract, and area postrema, a pattern of neuronal

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

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

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

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

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

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

60 ression of CRF-R2 mRNA in the nucleus of the solitary tract, and stress-inducible expression of CRF-R

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

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

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

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

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

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

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

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

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

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 led somata were dorsomedial or medial to the solitary tract from -0.3 mm to +1.5 mm with regard to ob

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

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

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

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

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

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

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

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

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

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

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

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

92 ity (FLI) in the intermediate nucleus of the solitary tract (iNTS) have been seen consistently as a c

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

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

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

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

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

98 effector regions, such as the nucleus of the solitary tract, magnocellular neurosecretory cell groups

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

122 39% in the middle part of the nucleus of the solitary tract (NTS) and 33% in the caudal NTS.

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

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

125 =2-h) c-Fos expression in the nucleus of the solitary tract (NTS) and area postrema of the brainstem

126 5-HT immunoreactivity in the nucleus of the solitary tract (nTS) and dorsal motor nucleus of the vag

127 s-positive cell nuclei in the nucleus of the solitary tract (NTS) and in the dorsal horn of the spina

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

158 2-expressing) neurons in the nucleus of the solitary tract (NTS) of the rat are aldosterone-sensitiv

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

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

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

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

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

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

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

166 discharge of neurones in the nucleus of the solitary tract (NTS) receiving aortic depressor nerve (A

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

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

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

170 (PE) activates neurons in the nucleus of the solitary tract (NTS) whose distribution conforms to thos

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

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

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

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

175 uprachiasmatic nucleus (SCN), nucleus of the solitary tract (NTS), and the dorsal and median raphe nu

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

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

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

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

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

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

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

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

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

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

186 rder neurons in the medial subnucleus of the solitary tract (NTS), the area postrema (AP), and the do

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

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

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

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

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

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

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

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

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

203 utonomic functions within 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 rachial nucleus (Pb), and the nucleus of the solitary tract (NTS).

209 n of response profiles in the nucleus of the solitary tract (NTS).

210 supragenual nucleus, and the nucleus of the solitary tract (NTS).

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

226 The solitary tract nucleus (NTS) conveys visceral informatio

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

248 a neuronal projection originating within the solitary tract nucleus.

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

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

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

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

253 injection was observed in the nucleus of the solitary tract, paraventricular nucleus of the hypothala

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

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

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

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

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

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

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

261 n the rostral division of the nucleus of the solitary tract (rNST).

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

288 cleus of the hypothalamus and nucleus of the solitary tract) the blood-brain barrier.

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

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

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

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

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

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

295 5-HT2AR activation augmented solitary tract (TS) evoked EPSC amplitude whereas 5-HT2A

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

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

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

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

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