ライフサイエンスコーパス: nodose

1 ne also failed to activate stretch-sensitive nodose A-fibres in the lungs.

2 ischarge in nociceptive C-fibers (41/44) and nodose Adelta fibres (29/30) that are rapidly adapting l

3 innervate the intestines, and that the left nodose afferents innervate predominantly the duodenum.

4 aspects of visceral pain) are the domain of nodose afferents.

5 In addition, CARTp-IR neurons in the nodose also were stained positively for NADPH-diaphorase

6 Na(v) 1.8-Cre-tdTomato mice label 80% of nodose and dorsal root ganglia neurons.

7 eurons, as well as of sensory neurons of the nodose and dorsal root ganglia.

8 ies demonstrated the presence of PACAP-IR in nodose and dorsal root ganglion cells, but not in neuron

9 Airway-specific nodose and jugular C-fibre neurons express mRNA coding f

10 The nerve terminals within the lungs of both nodose and jugular C-fibres responded with action potent

11 After 7 d, the nodose and jugular ganglia were removed, sectioned, and

12 autonomic afferent fibre cell bodies in the nodose and jugular ganglia.

13 ely labeled nerve cell bodies located in the nodose and jugular ganglia.

14 th intact afferent vagal pathways, including nodose and jugular ganglia.

15 in the vagal sensory ganglia referred to as nodose and jugular ganglia.

16 patch clamp recording of capsaicin-sensitive nodose and jugular ganglion neurones retrogradely labell

17 Both the nodose and jugular vagal ganglia provide sensory innerva

18 The nodose and jugular vagal ganglia supply sensory innervat

19 ferent neurons whose somata reside in vagal (nodose and jugular) ganglia.

20 dies reside within two distinct ganglia, the nodose and jugular, and whose properties allow for diffe

21 nt input from BDNF-containing neurons in the nodose and petrosal cranial sensory ganglia.

22 Mature nodose and petrosal ganglia neurons (placodally derived

23 e issues we defined survival requirements of nodose and petrosal neurons for GDNF in vitro and in bdn

24 lation of ganglion cells in the dorsal root, nodose and trigeminal ganglia exhibited moderate-to-stro

25 rdings were made from dissociated guinea-pig nodose and trigeminal ganglion neurons in culture to stu

26 g cardiac ganglia, and sections of stellate, nodose, and dorsal root ganglia (DRG, thoracic levels 1-

27 neuronal populations including sympathetic, nodose, and dorsal root ganglion sensory neurons.

28 Nodose axons also grew selectively toward cocultured net

29 accompanied by action potential discharge in nodose, but not in jugular C-fibres.

30 H 58261 (0.1 microm) partially inhibited the nodose C-fibre activation by adenosine, and the combinat

31 sts, blocked the bronchoconstriction-induced nodose C-fibre discharge.

32 hat, like the nerve terminals, lung specific nodose C-fibre neurones express functional P2X receptors

33 cin and bradykinin application, but only the nodose C-fibre population responded with action potentia

34 that adenosine selectively depolarizes vagal nodose C-fibre terminals in the lungs to action potentia

35 P was not able to activate any of the airway nodose C-fibres analysed.

36 S1P activation of nodose C-fibres does not occur in S1PR3 knockout mice.

37 paration to study the electrical activity of nodose C-fibres in response to bronchoconstriction.

38 S1P activation of nodose C-fibres is inhibited by a S1PR3 antagonist.

39 The nodose C-fibres responded strongly to serotonin and this

40 Action potential generation by S1P in nodose C-fibres was effectively inhibited by the S1PR3 a

41 nosine-induced action potential discharge in nodose C-fibres was mimicked by either the selective A1

42 ction potential discharge in jugular but not nodose C-fibres.

43 pivotal role in the mechanical activation of nodose C-fibres.

44 In patch-clamp studies, nodose, coeliac and superior cervical ganglia (SCG) neur

45 We found that, although the left nodose contained significantly more neurons (7,603), tha

46 articularly significant in the brainstem and nodose cranial sensory ganglia (NGs), structures critica

47 the neurons of the geniculate, petrosal, and nodose cranial sensory ganglia.

48 ly the morphologically distinct, myelinated, nodose-derived mechanoreceptors described in animals are

49 geminal) ectoderm is grafted in place of the nodose (epibranchial) placode, Pax3-expressing cells for

50 S1P in the lungs strongly activated 81.5% of nodose fibres, 70% of which were also activated by capsa

51 branchial placodes (geniculate, petrosal and nodose) form visceral sensory neurons that innervate tas

52 innervated the bladder and colon in both the nodose ganglia (NG) and L6/S1 and L1/L2 dorsal root gang

53 om thoracolumbar (TL), lumbosacral (LS), and nodose ganglia (NG) in male and female mice.

54 pinal cord potassium channel) contributes to nodose ganglia (NG) malfunction, disrupting gastrointest

55 ed by allergic inflammation were examined in nodose ganglia (NG) removed from guinea pigs immunized t

56 t in a majority of vagal afferent neurons of nodose ganglia (NG), immunoreactivity for other NMDA rec

57 the 5-HT3A subunit in superior cervical and nodose ganglia (NG).

58 ly in both the dorsal root ganglia (DRG) and nodose ganglia (NG).

59 A small percentage of the nAChRs in nodose ganglia also contain alpha2 and alpha4 subunits.

60 60% of the labeled neurons were found in the nodose ganglia and 40% in the jugular ganglia.

61 ose-excited and glucose-inhibited neurons in nodose ganglia and characterize their glucose-sensing pr

62 mn (T1 to L1), ipsilateral and contralateral nodose ganglia and ipsilateral dorsal root ganglia from

63 2, Bmal1, and Nr1d1 mRNA is expressed in the nodose ganglia and levels oscillated over a 24 h period.

64 ve monosynaptic vagal sensory input from the nodose ganglia and spinal sensory input from the dorsal

65 ors are found in cranial afferent neurons in nodose ganglia and their central terminations within the

66 ound that aortic baroreceptor neurons in the nodose ganglia and their terminals express ASIC2.

67 ent neurons whose cell bodies resided in the nodose ganglia and whose receptive fields were located i

68 findings indicate that the nAChRs in SCG and nodose ganglia are heterogeneous, which suggests that di

69 vagal sensory neurons located in the jugular-nodose ganglia complex (JNC) with identified receptive f

70 that a majority of the nAChRs in the SCG and nodose ganglia contain the alpha3 and beta4 subunits, bu

71 in vagal afferent neurons isolated from rat nodose ganglia demonstrated that 31/118 (26%) neurons we

72 Cardiac afferents from the nodose ganglia differed from CDRGNs in having smaller ac

73 There were no changes in nodose ganglia excitability in TNX deficient mice, sugge

74 Most vagal afferent neurons in rat nodose ganglia express mRNA coding for the NR1 subunit o

75 Both rat and human nodose ganglia expressed OX-R1 as detected by RT-PCR, an

76 increased neural proliferation within adult nodose ganglia following capsaicin-induced neuronal deat

77 e used large scale two-photon imaging of the nodose ganglia from our ex vivo preparation isolated fro

78 ified in the visceral sensory neurons of the nodose ganglia from rats through immunocytochemical stud

79 Substance P/Neurokinin A positive neurons in nodose ganglia from virus-inoculated guinea pigs at Day

80 Neurites from explanted E14 nodose ganglia grew selectively toward cocultured E14 di

81 These results show that rat nodose ganglia have glucose-excited and glucose-inhibite

82 microinjection of AAV vectors into the vagal nodose ganglia in vivo leads to selective, effective and

83 nous GLP-1, we established a novel bilateral nodose ganglia injection technique to deliver a lentivir

84 To examine this hypothesis, rats received nodose ganglia injections of an adeno-associated virus (

85 Few neurons in nodose ganglia innervate the uterus.

86 etween CCK and serotonin at the level of the nodose ganglia may explain the robust postprandial pancr

87 Two groups of nodose ganglia neurones were identified: group A neurone

88 ly in gastric motor and sensory function and nodose ganglia neurones.

89 mp recordings were performed on isolated rat nodose ganglia neurons.

90 carbocyanine methanesulfonate (DiI) into the nodose ganglia of animals with prior supranodose de-effe

91 of Fos-immunoreactive neuronal nuclei in the nodose ganglia of LETO rats, but not in the nodose gangl

92 anscripts encoding DCC were expressed in the nodose ganglia of mice from E12 to adulthood but were de

93 nodose ganglia of LETO rats, but not in the nodose ganglia of OLETF rats.

94 ation of GLP-1R mRNA expression in the vagal nodose ganglia of OP rats.

95 m agglutinin-horseradish peroxidase into the nodose ganglia of rats that had received unilateral vent

96 urons in primary neuronal cell cultures from nodose ganglia of rats.

97 on of TRPV1-expressing pulmonary neurones in nodose ganglia of sensitized rats; this increase in TRPV

98 ceptor alpha and beta (LXRalpha/beta) in the nodose ganglia of the vagus nerve.

99 immunoreactive neurons in the trigeminal and nodose ganglia over this period of development.

100 ivo gene silencing of PI3K and Erk1/2 in the nodose ganglia prevented ghrelin inhibition of leptin- o

101 ve afferent neurones with cell bodies in the nodose ganglia projected to the rostral trachea and lary

102 t Lipofectamine transfection of cultured rat nodose ganglia to determine the effect of these molecule

103 Na(V)1.7 gene expression in nodose ganglia was effectively and selectively reduced w

104 OX-R1 and -R2 expression by rat and human nodose ganglia was examined by reverse-transcriptase pol

105 rade neuronal tracer (DiI) and dye uptake in nodose ganglia was examined.

106 Nodose ganglia were collected from 8-week-old female C57

107 The nodose ganglia were labeled starting 4 days PI, suggesti

108 Rat aortic baroreceptor neurones in the nodose ganglia were labelled in vivo by applying a fluor

109 MDA subunits expressed in the left and right nodose ganglia were not significantly different.

110 After at least 1 week, the nodose ganglia were removed and the neurons were culture

111 ely from the NA, neurons of the DmnX and the nodose ganglia were surveyed for DiI labeling.

112 mall neurons of dorsal root, trigeminal, and nodose ganglia) and localizes to their sensory terminals

113 gular ganglia) and placode-derived neurones (nodose ganglia) project C-fibres in the vagus, and that

114 CR analysis, its expression is restricted to nodose ganglia, and not present in cortex, hippocampus,

115 e dorsal vagal complex of the hindbrain, the nodose ganglia, and the ganglia of the myenteric and sub

116 observed scattered 5-HT1D-IR neurons in the nodose ganglia, and there was sparse terminal immunoreac

117 re given injections of dextran biotin in the nodose ganglia, and, after tracer transport, stomach who

118 cluding the petrosal, superior cervical, and nodose ganglia, as well as ganglia in the myenteric plex

119 e in lung C-fibre terminals arising from the nodose ganglia, but failed to evoke action potential dis

120 NOS-IR cells were also present in the nodose ganglia, but only some exhibited CGRP immunoreact

121 The fast-blue-positive neurons in the nodose ganglia, by contrast, were large in diameter (40

122 In nodose ganglia, CAP but not alphabeta-m-ATP evoked inwar

123 VANs, located in nodose ganglia, express receptors for various gut-derive

124 transcripts and protein were detected in the nodose ganglia, OT signaling might also affect extrinsic

125 superior cervical, and 12 of 36 and 1 of 36 nodose ganglia, respectively.

126 the superior cervical ganglia (SCG), sensory nodose ganglia, stellate ganglia, and pelvic ganglia.

127 The nodose ganglia, the stomach, the first 8 cm of duodenum,

128 arbocyanine perchlorate (DiI) bilaterally to nodose ganglia.

129 y, uterine nerve cell bodies were labeled in nodose ganglia.

130 ervating the duodenum were recorded from rat nodose ganglia.

131 polymodal Adelta-fibres that arise from the nodose ganglia.

132 hannels in sensory neurons isolated from rat nodose ganglia.

133 nal populations can be identified within the nodose ganglia.

134 fied as PCR products from mRNA prepared from nodose ganglia.

135 glion and Adelta-fibres from the jugular and nodose ganglia.

136 C6-IR cells were also present in sections of nodose ganglia.

137 rvating the intestine were recorded from rat nodose ganglia.

138 R cells and NOS-IR cells were present in the nodose ganglia.

139 ACAP-IR cells and fibers were present in the nodose ganglia.

140 ion may be carried by the circulation to the nodose ganglia.

141 NOS innervation is probably derived from the nodose ganglia.

142 of a putative sodium channel (NaNG) from dog nodose ganglia.

143 ncluding the petrosal, superior cervical and nodose ganglia.

144 CsA) on cardiac sensory neurons (CSN) of the nodose ganglia.

145 ic plexus were retrogradely labeled from the nodose ganglia.

146 gene expression is prevalent in human adult nodose ganglia.

147 lament-positive pulmonary sensory neurons in nodose ganglia.

148 d larger currents compared to those from the nodose ganglia.

149 ncreatic inflammation, we studied pancreatic nodose ganglion (NG) and dorsal root ganglion (DRG) sens

150 o autonomic ganglia of the neck, namely, the nodose ganglion (NG) and the superior cervical ganglion

151 d currents in dorsal root ganglion (DRG) and nodose ganglion (NG) neurons that innervate the stomach

152 e expressed in vagal afferent neurons in the nodose ganglion (NG), we also systematically compared MC

153 m currents are similarly distributed between nodose ganglion A-fibres and C-fibres innervating the lu

154 Those fibres derived from the nodose ganglion adapted rapidly, whereas those derived f

155 for recording of isometric tension while the nodose ganglion and attached vagus nerve were pulled int

156 ylrhodamine and biotin was injected into the nodose ganglion and used to label the terminal arbors of

157 injection of horseradish peroxidase into the nodose ganglion anterogradely labelled axonal boutons we

158 Neurons of the nodose ganglion are derived from the epibranchial placod

159 trast, embryonic day 15 superior cervical or nodose ganglion axons grew heavily into the same age hea

160 chnique, we identified cultured adult rabbit nodose ganglion cells with slow AHPs in current-clamp mo

161 acutely dissociated vagal afferent neurones (nodose ganglion cells) of the ferret to investigate the

162 vation of guinea pig airway-specific primary nodose ganglion cells.

163 The nodose ganglion contained the somata of mainly fast-cond

164 om these results we concluded that the vagal nodose ganglion contains neurones that may possess only

165 Dorsal root ganglion and nodose ganglion expressed all isoforms except for CA IX.

166 otinylated dextran amine (BDA) into the left nodose ganglion in rats.

167 Vagal afferents were labeled by nodose ganglion injections of wheat germ agglutinin-hors

168 Animals received nodose ganglion injections of wheat germ agglutinin-hors

169 roxidase (0.5-1.0 mul) was injected into the nodose ganglion ipsilateral to the vagotomized side.

170 Nodose ganglion neurones (NGNs) become less excitable fo

171 tch-clamp recording from acutely dissociated nodose ganglion neurones (NGNs) we have examined the ion

172 e in properties between P2X2/3 receptors and nodose ganglion neurones further supports the conclusion

173 neighbouring enterocytes through P2Y(2) and nodose ganglion neurones in co-cultures through P2X(2/3)

174 Cultured nodose ganglion neurones showed no changes in response t

175 Here we show that OEA directly excited nodose ganglion neurones, the cell bodies of vagal affer

176 ndles and patch clamp recordings of isolated nodose ganglion neurons (NGNs).

177 ganglion neurons, and that the responses of nodose ganglion neurons to ATP show altered kinetics and

178 ilar age-related changes in the responses of nodose ganglion neurons to BDNF were observed in culture

179 n a subpopulation of vagal afferent neurons (nodose ganglion neurons), the pattern of impulse activit

180 Unlike nodose ganglion neurons, both retinal ganglion cells (RG

181 which have only 45% of the normal number of nodose ganglion neurons, exhibit selective losses of the

182 Adult inferior vagal ganglion neurons (nodose ganglion neurons, NGNs) were acutely isolated 4-6

183 ion in the sustained ATP-induced currents in nodose ganglion neurons.

184 GFP expression in approximately one-third of nodose ganglion neurons.

185 root ganglion (DRG) and approximately 50% of nodose ganglion neurons] to evoke a depolarizing inward

186 g MTII injection into the NTS ipsilateral to nodose ganglion removal was significantly attenuated, wh

187 Finally, unilateral nodose ganglion removal, resulting in degeneration of va

188 ed synapsin I phosphorylation ipsilateral to nodose ganglion removal.

189 Nodose ganglion sensory neurones exert a significant ref

190 placode marker Pax2 and form neurons in the nodose ganglion that express the epibranchial neuron mar

191 etramethylrhodamine dextran (TMR-D) into the nodose ganglion to label vagal aortic afferents (at 3 an

192 tract that could be anterogradely labeled by nodose ganglion tracer injections was quantitatively ass

193 tracing of vagal afferents arising from the nodose ganglion was achieved with biotinylated dextran a

194 he retrograde transport of [125I]NT-3 to the nodose ganglion was reduced by NT-3 and by NGF, and the

195 main bronchi with the right vagus nerve and nodose ganglion were isolated from guinea-pigs passively

196 d 24 months of age were injected in the left nodose ganglion with 3 microl of either 4% wheat germ ag

197 urons, in developing petrosal ganglion (PG), nodose ganglion, and dorsal root ganglion neurons grown

198 hin-4 (NT-4) to perikarya in the ipsilateral nodose ganglion, and transganglionically transported [12

199 , no such changes were observed in the vagal nodose ganglion, demonstrating that the effect of high o

200 nating from neurogenic placodes, such as the nodose ganglion, failed to express EGFP, suggesting that

201 In the nodose ganglion, NF-immunoreactive neurones accounted fo

202 pathway (the nucleus tractus solitarii, NTS; nodose ganglion, NG).

203 nocortin-4 receptor (MC4R) expression in the nodose ganglion, where the cell bodies of vagal sensory

204 TrkA and TrkC and the absence of TrkB in the nodose ganglion, whereas the profile for NT-4 suggests a

205 ot affect the adaptation of rapidly adapting nodose ganglion-derived nerve endings in response to mec

206 The electrophysiological adaptation of nodose ganglion-derived neurones following prolonged sup

207 nucleus of the solitary tract, the target of nodose ganglion-derived visceral afferents.

208 rs are exclusively A-fibres arising from the nodose ganglion.

209 strema, nucleus tractus solitarius (NTS) and nodose ganglion.

210 strema, nucleus tractus solitarius (NTS) and nodose ganglion.

211 from the medulla oblongata, spinal cord, and nodose ganglion.

212 trols) was injected with WGA-HRP in the left nodose ganglion.

213 horseradish peroxidase (WGA-HRP) in the left nodose ganglion.

214 l after the main period of cell death in the nodose ganglion.

215 gglutinin-horseradish peroxidase in the left nodose ganglion.

216 are reproduced in mice lacking Piezo2 in the nodose ganglion.

217 denum by GFP-positive neurons located in the nodose ganglion.

218 Neither nodose ganglionectomy nor vagotomy altered the CB1 recep

219 By contrast, C-fibres from nodose (inferior) neurones innervate primarily structure

220 and excitation of laryngeal C neurons in the nodose/jugular (N/J) ganglia.

221 an extracellular electrode positioned in the nodose/jugular ganglion.

222 Also, the rapid adaptation of nodose nerve endings in the trachea observed during a me

223 We previously demonstrated that nodose nerve endings supplying the trachea are exquisite

224 roject neurites along central and peripheral nodose neurite pathways and survive until well after the

225 all, approximately 10% of the large-diameter nodose neurofilament-positive neurons projecting fibers

226 of NT4 and caused PNEC hyperinnervation and nodose neuron hyperactivity.

227 n of 5-HT evoked dose-dependent increases in nodose neuronal discharges.

228 These results suggested that the nodose neuronal responses to luminal osmolarity and to t

229 hibitor, abolished luminal factor-stimulated nodose neuronal responses.

230 nist each abolished the luminal 5-HT-induced nodose neuronal responses.

231 granisetron abolished luminal stimuli-evoked nodose neuronal responses.

232 G/PNa was not different for P2X2, P2X2/3 and nodose neurones (0.03) but was significantly higher (0.0

233 PNa was not different among P2X3, P2X2/3 and nodose neurones (1.2-1.5) but was significantly higher (

234 Nodose neurones all showed immunoreactivity for both P2X

235 iological recordings from gastric-projecting nodose neurones assessed the ability of glucose to modul

236 ce P (SP) responsiveness in acutely isolated nodose neurones from adult guinea-pigs was investigated

237 ward current in both control and HFD gastric nodose neurones in vitro, the 5-HT response and receptor

238 Nodose neurones incubated with 5-HT in the presence of n

239 We conclude that MS nodose neurones may be unimodal MS or bimodal MS/CS, and

240 Histologically, nodose neurones projecting lung C-fibres were different

241 A separate group of nodose neurones that possessed high-affinity CCK type A

242 at both the P2X2/3 heteromeric receptor and nodose neurones.

243 oth receptors (P2X2/3) and from cultured rat nodose neurones.

244 otentials (APs) in acutely dissociated adult nodose neurones.

245 ientations into the nuclei of BDNF-dependent nodose neurons and NGF-dependent trigeminal neurons at s

246 er a single action potential, the AHPslow in nodose neurons displays a slow rise time to peak (0.3-0.

247 th TRPV1-expressing and TRPV1-non-expressing nodose neurons express mRNA coding for the S1P receptor

248 Double labeling revealed that 30.2% of nodose neurons expressed immunoreactivity to both NR2B a

249 IH was found in all neonatal nodose neurons in vitro, contrary to previous reports wh

250 , we recorded Ca(2+) responses in individual nodose neurons in vivo while selectively stimulating bet

251 In sharp contrast, 80% of nodose neurons isolated 24 h after in vivo aerosolized a

252 ion of substance P (SP; 0.1 to 10 microM) to nodose neurons isolated from guinea pigs with normal uni

253 present in 56.7% of neurons; NR2C-expressing nodose neurons made up 49.4% of the total population; NR

254 Nodose neurons responded in vivo to chemogenetic stimula

255 l RT-PCR, we noted that the vast majority of nodose neurons retrogradely labelled from the lung, expr

256 2A receptor mRNA was expressed in individual nodose neurons retrogradely labelled from the lungs.

257 ed the airway-specific, capsaicin-sensitive, nodose neurons to action potential threshold.

258 otype such that large, capsaicin-insensitive nodose neurons with fast-conducting "Adelta" fibers prov

259 recording, CsCl, which inhibits only I(H) in nodose neurons, hyperpolarized the resting membrane pote

260 ta indicate that the M-current is present in nodose neurons, is activated at resting membrane potenti

261 reactivity colocalized with NR2D in 13.1% of nodose neurons.

262 NMDA NR1 subunit was present in 92.3% of all nodose neurons.

263 unoreactivities were colocalized in 11.5% of nodose neurons.

264 reactivity was observed in just 13.5% of all nodose neurons.

265 and HCN4 immunoreactivity was present in all nodose neurons.

266 n marker Phox2a on the same schedule as host nodose neurons.

267 changes in the tachykinin responsiveness of nodose neurons.

268 tes to the resting membrane potential in all nodose neurons.

269 CCK stimulated CARTp release from cultured nodose neurons.

270 ed among gastric- and portal vein-projecting nodose neurons.

271 in the rostral portion and non-neural crest (nodose) neurons in the more central and caudal portions

272 neurons in vivo, we analyzed development of nodose (NG), petrosal (PG), and vestibular (VG) ganglion

273 ied in dissociated primary culture of either nodose or dorsal root ganglia (DRG).

274 t the majority of neurones within either the nodose or jugular ganglion adapted rapidly to prolonged

275 ssed E3 ligases Rnf43/Znrf3, is expressed in nodose-petrosal and geniculate ganglion neurons.

276 se in neurons comprising the placode-derived nodose-petrosal complex occurred.

277 Dissociate cultures of nodose-petrosal ganglion cells from newborn rats were gr

278 particularly striking in the cranial sensory nodose-petrosal ganglion complex (NPG), in which loss of

279 The major visceral sensory population, the nodose-petrosal ganglion complex (NPG), requires BDNF an

280 ncreased the number of VIP-ir neurons in the nodose/petrosal ganglia cultures and did not alter the n

281 urons labeled for specific neurochemicals in nodose/petrosal ganglia cultures.

282 Addition of NGF to nodose/petrosal ganglia neuron-enriched cultures signifi

283 to dissociated, enriched, cultures of mature nodose/petrosal ganglia neurons, and the neurons process

284 l of 50% of visceral afferent neurons in the nodose/petrosal sensory ganglion complex, including arte

285 approximately 0.5 m s(-1)), 71% were of the nodose phenotype and 29% of the jugular phenotype.

286 Nodose (placode-derived) nociceptive-like fibres are exc

287 ion of carbohydrates elicited powerful vagal nodose responses.

288 GFRalpha1-deficient dopaminergic and nodose sensory ganglia neurons no longer respond to GDNF

289 e resting membrane potential of neonatal rat nodose sensory neurons were investigated using the whole

290 es of embryonic rat trigeminal, dorsal root, nodose, superior cervical ganglia or retina with a varie

291 y distinct sources: neurones situated in the nodose vagal ganglia and neurones situated in the jugula

292 dy addressed the hypothesis that jugular and nodose vagal ganglia contain the somata of functionally

293 nsory circuits in receipt of inputs from the nodose vagal ganglia.

294 recordings were made from single jugular or nodose vagal ganglion neurons that projected their senso

295 ot ganglia were more similar to jugular than nodose vagal neurons.

296 minals arising from the jugular (rather than nodose) vagal ganglia and the output of the Pa5 is predo

297 Unilateral supra-nodose vagotomy eliminated p55-ir from ipsilateral centr

298 ber of retrogradely labeled afferents in the nodose was very similar to the total number of DRG affer

299 All neurones possessing AHPslow in ferret nodose were C fibre neurones; all AHPslow neurones had c

300 xamined, including the superior cervical and nodose, which are severely affected in both Ret- and GDN