ライフサイエンスコーパス: preganglionic

1 t projections through the pons medial to the preganglionics.

2 ular reference to the control of sympathetic preganglionic activity and interneuronal activity in the

3 odulate the coordinated actions of autonomic preganglionic and functionally related skeletal MN activ

4 eptide immunoreactivity so far identified in preganglionic and postganglionic cells of the ciliary ga

5 e (ChAT)-expressing cells were used to label preganglionic and postganglionic cholinergic neurons and

6 ction, yet, the precise anatomical extent of preganglionic and postganglionic inputs to the inguinal

7 a impaired the survival and proliferation of preganglionic and postganglionic neurons of the sympathe

8 ges in response to electrical stimulation of preganglionic and postganglionic parasympathetic neurons

9 ly significant difference in MTR between the preganglionic and postganglionic regions in all lumbar s

10 ograde tracing from the iWAT, we defined the preganglionic and postganglionic sympathetic input to iW

11 ding inhibition from the nPGi is by means of preganglionic and somatic efferents and spinal interneur

12 lateral motor column (LMC) neurons and from preganglionic autonomic neurons of the Column of Terni (

13 It was observed that infection in preganglionic autonomic nuclei (i.e., Edinger-Westphal n

14 n cells in the rhesus monkey are most likely preganglionic axon terminals of mesencephalic parasympat

15 tion of presynaptic specializations, but not preganglionic axonal ingrowth from the spinal cord into

16 ary gland related to the identities of their preganglionic axonal innervation.

17 Thus BDNF released by preganglionic axons acts chemotactically on TrkB-positiv

18 oes not occur in the absence of contact with preganglionic axons, and this is mediated by BDNF/TrkB s

19 tes of divergence indicates that the average preganglionic B neuron forms connections with 50 ganglio

20 ns relaying parasympathetic information from preganglionic brain stem neurons to the heart.

21 rily determined by the activity of brainstem preganglionic cardioinhibitory vagal neurons (CVNs) in t

22 s and from this site to airway-related vagal preganglionic cells that regulate the tracheal circulati

23 rebrate cats, recordings were taken from the preganglionic cervical sympathetic (CSy) nerves and from

24 MICG) after transection of the predominantly preganglionic cervical sympathetic trunk (CST).

25 ainly adrenergic neurons, were surrounded by preganglionic cholinergic boutons.

26 y-dependent amplifiers of spinal output from preganglionic circuitry.

27 d to the spinal cord, in the parasympathetic preganglionic column in the lumbosacral spinal cord and

28 identified which project to both the LC and preganglionic column of the lumbosacral spinal cord.

29 d PRV-labeled neurons in the parasympathetic preganglionic column of the lumbosacral spinal cord.

30 are consistent with the hypothesis that the preganglionic controls of cardiac rate and left ventricu

31 Cervical vagus stimulation (preganglionic) demonstrated attenuated responses in the

32 Here we show that the essential preganglionic differentiation factor is an isoform of be

33 rns of cMRF input to C-group motoneurons and preganglionic Edinger-Westphal motoneurons suggest that

34 neurons (pIIIu), previously known as the non-preganglionic Edinger-Westphal nucleus (npEW).

35 -1 transcripts are expressed in the midbrain preganglionic Edinger-Westphal nucleus at developmental

36 have evolved a special relationship with the preganglionic Edinger-Westphal nucleus, suggesting these

37 d outside the nucleus, and extended into the preganglionic Edinger-Westphal nucleus.

38 In cats, these motoneurons make up the preganglionic Edinger-Westphal population, which lies ro

39 onsequently, we have adopted the identifiers preganglionic (EW(PG)) and urocortin-containing (EW(U))

40 12%, of the PNs, respectively; and (9) vagal preganglionics exhibited a degree of lateralization: Sig

41 These data suggest that the preganglionic factor required for the development of K(C

42 Preganglionic fibers originating in the brainstem projec

43 ganglion formation by the nerves that carry preganglionic fibers, a parsimonious way of wiring the p

44 entricular physiology by vagal C and vagal B preganglionic fibres is examined as well as differences

45 pothesize that in vivo PACAP released during preganglionic firing may modulate neurotransmission with

46 ent each lumbar segment (L2-L5) and regions (preganglionic, ganglionic and postganglionic).

47 fasting leads to altered transmission at the preganglionic --> chromaffin cell synapse.

48 To ensure that preganglionic input and different levels of baseline sym

49 ating that the difference was independent of preganglionic input and sympathetic activity.

50 The pterygopalatine ganglion (PPG) receives preganglionic input from the superior salivatory nucleus

51 he accessory oculomotor neurons, eliminating preganglionic inputs as another site for action of the a

52 Thus, the preganglionic motoneurons found in the cat display morph

53 ase (ChAT) in macaque monkeys, in which most preganglionic motoneurons inhabit the EW, and in cats, i

54 Preganglionic motoneurons retrogradely labeled by introd

55 Preganglionic motoneurons supplying the ciliary ganglion

56 The dendrites of preganglionic motoneurons within the anteromedian nucleu

57 e observed in close association with labeled preganglionic motoneurons, particularly in the rostral p

58 fferent classes of synaptic profiles contact preganglionic motoneurons, suggesting that their activit

59 egions (PPR) regulates vagal and sympathetic preganglionic motoneurons.

60 e, and project directly to nuclei containing preganglionic motoneurons.

61 In contrast, MC4Rs in cholinergic preganglionic motor neurons (sympathetic and parasympath

62 In both species, GBR1b was expressed in preganglionic motor neurons and, in ferrets, the recepto

63 al motor nucleus of the vagus (DMV) contains preganglionic motor neurons that control viscera along t

64 he first survival factor for parasympathetic preganglionic motor neurons through GFRalpha3/Syndecan-3

65 ion of FluoroGold, indicating that most were preganglionic motor neurons.

66 By extension, specializations of the preganglionic motor pools are more likely to result from

67 efined the light microscopic distribution of preganglionic negative inotropic neurons in the CNS whic

68 Airway preganglionic nerve activity is regulated by subsets of

69 ency stimulation (LFS, 3-5 Hz/15 min) of the preganglionic nerve produced a long-lasting (up to 3 h )

70 pophilic dye delivered by diffusion down the preganglionic nerve reveals a large membrane structure e

71 Short, high-frequency (20 Hz) preganglionic nerve stimulation evoked action potentials

72 ions, continuous low-frequency (0.05-0.5 Hz) preganglionic nerve stimulation evoked action potentials

73 a water-soluble dye by diffusion through the preganglionic nerve suggests large discontinuities in th

74 ervations suggested that PACAP released from preganglionic nerve terminals during tetanic stimulation

75 neurons requires interactions with afferent preganglionic nerve terminals.

76 In phasic neurons, stimulation of preganglionic nerves elicited one or two populations of

77 These data suggest that peptides released by preganglionic nerves modulate dendritic growth in sympat

78 ediated via thoracolumbar spinal sympathetic preganglionic neurones (AD-SPN).

79 vity of cardiac and bronchoconstrictor vagal preganglionic neurones (CVPNs and BVPNs) in the nucleus

80 zed cats to determine if these cardiac vagal preganglionic neurones (CVPNs) in the nucleus ambiguus (

81 cluding Fluoro-gold-labelled parasympathetic preganglionic neurones (PPNs), in slices of the rat medu

82 oject to spinal areas containing sympathetic preganglionic neurones (SPNs) and therefore may directly

83 Sympathetic preganglionic neurones (SPNs) convey sympathetic activit

84 al synaptic transmission between sympathetic preganglionic neurones (SPNs) in slices of rat spinal co

85 ecordings were obtained from 190 sympathetic preganglionic neurones (SPNs) in spinal cord slices of n

86 tic transmission to neonatal rat sympathetic preganglionic neurones (SPNs) was investigated utilizing

87 ophasic depolarisation in 28% of sympathetic preganglionic neurones and a biphasic effect consisting

88 co-lumbar spinal cord containing sympathetic preganglionic neurones are rich in dopamine terminals.

89 onal activity to the tail (SNAT) arises from preganglionic neurones at T11-L2.

90 Three percent of sympathetic preganglionic neurones did not respond to the applicatio

91 e from antidromically identified sympathetic preganglionic neurones in (400 micrometers) transverse n

92 s were made from a total of sixty-four vagal preganglionic neurones in the dorsal vagal motor nucleus

93 rol of LV contractility is provided by vagal preganglionic neurones located in the dorsal motor nucle

94 ntricular contractility is provided by vagal preganglionic neurones of the dorsal motor nucleus (DVMN

95 y between the afferent nociceptive input and preganglionic neurones projecting to the adrenal medulla

96 neuroanatomical mapping revealed that vagal preganglionic neurones that have an impact on left ventr

97 occurring in a sub-population of sympathetic preganglionic neurones was mimicked by quinpirole, a D2

98 asic hyperpolarisation in 46% of sympathetic preganglionic neurones, a slow monophasic depolarisation

99 ary neurones, known to innervate sympathetic preganglionic neurones, can induce sympathetic rhythmic

100 the left and right DVMN revealed that vagal preganglionic neurones, which have an impact on LV contr

101 nopositive cells in the IML were sympathetic preganglionic neurones, while those in lamina X were unl

102 DMN is not due to primary vagal afferents or preganglionic neurones.

103 DMN is not due to primary vagal afferents or preganglionic neurones.

104 risation or vice-versa in 23% of sympathetic preganglionic neurones.

105 However, whether airway-related vagal preganglionic neurons (AVPNs) produce BDNF and contain T

106 metric and asymmetric synapses onto presumed preganglionic neurons (nitric oxide synthase-ir profiles

107 pinal sites (brainstem and hypothalamus), in preganglionic neurons (PGN) and in unlabeled segmental i

108 The effects of PACAP-38 on phasic and tonic preganglionic neurons (PGN) in L6 and S1 spinal cord sli

109 ophysiological properties of parasympathetic preganglionic neurons (PGN) in L6 and S1 spinal cord sli

110 mata of 25 electrophysiologically identified preganglionic neurons (PGN) obtained from the sacral spi

111 n slices produced EPSCs in 71% of tested DMV preganglionic neurons (PGNs) but no IPSCs.

112 The axons of sacral parasympathetic preganglionic neurons (PGNs) originate on a primary dend

113 some experiments we labelled parasympathetic preganglionic neurons (PPNs) in the L6-S1 spinal cord by

114 both sympathetic (SPNs) and parasympathetic preganglionic neurons (PPNs) were aberrant in the mutant

115 up to half the synaptic input to sympathetic preganglionic neurons (SPGNs) is GABAergic or glycinergi

116 determine the chemical codes of sympathetic preganglionic neurons (SPN) activated by glucoprivation,

117 Our past study shows that sympathetic preganglionic neurons (SPN) in mice lacking the reelin g

118 udy showed that the migration of sympathetic preganglionic neurons (SPN) in the spinal cord is affect

119 ts of Reelin in the migration of sympathetic preganglionic neurons (SPN) in the spinal cord of the ch

120 also affects the positioning of sympathetic preganglionic neurons (SPN) in the spinal cord.

121 function of Reelin in control of sympathetic preganglionic neurons (SPN) migration in the spinal cord

122 ry afferents project directly to sympathetic preganglionic neurons (SPN).

123 Dab1, control the positioning of sympathetic preganglionic neurons (SPN); however, it is not known wh

124 hesized that sympathetic and parasympathetic preganglionic neurons (SPNs and PPNs) would exhibit migr

125 orase expression was observed in sympathetic preganglionic neurons (SPNs) and interneurons of the ven

126 also depletion of TH fibers and sympathetic preganglionic neurons (SPNs) in the 2 MSA cases examined

127 citatory and project directly to sympathetic preganglionic neurons (SPNs) in the thoracic spinal cord

128 n the two populations of adrenal sympathetic preganglionic neurons (SPNs) regulating the release of e

129 trophysiologically characterized sympathetic preganglionic neurons (SPNs) were recorded using the who

130 o restore supraspinal control of sympathetic preganglionic neurons (SPNs), we grafted embryonic brain

131 output cells in the spinal cord, sympathetic preganglionic neurons (SPNs).

132 containing retrogradely labeled sympathetic preganglionic neurons (SPNs).

133 by obstructing the inhibition of sympathetic preganglionic neurons (SPNs).

134 als synapse upon negative chronotropic vagal preganglionic neurons (VPNs), but not upon negative drom

135 tion of many sympathetic and parasympathetic preganglionic neurons and a subset of somatic motor neur

136 w and that their spinal targets include both preganglionic neurons and GABAergic interneurons.

137 ized projections to both adrenal sympathetic preganglionic neurons and gastrocnemius motoneurons, wer

138 ved in the UG reflex were found close to the preganglionic neurons and in the dorsal horn and interme

139 ely provide a major ENK input to sympathetic preganglionic neurons and PPE mRNA is the first identifi

140 Finally, our results show that sympathetic preganglionic neurons and somatic motor neurons in Cdk5-

141 Accordingly, sacral preganglionic neurons are considered parasympathetic, as

142 o date, only sympathetic and parasympathetic preganglionic neurons are known to migrate abnormally in

143 olateral medulla, where airway-related vagal preganglionic neurons are located, abolished the reflex

144 The projections of sympathetic preganglionic neurons are segmentally specific.

145 MC4-R mRNA in the IML and DMV were autonomic preganglionic neurons as cells in both sites coexpressed

146 increases the number of rostrally projecting preganglionic neurons at that level.

147 t provides evidence that activation of those preganglionic neurons can cause cerebral vasodilatation

148 nts were transplanted to the cervical level, preganglionic neurons did not maintain their original pr

149 iliary ganglion neurons, but the clusters on preganglionic neurons do not.

150 Preganglionic neurons do, however, stain for lipid raft

151 Sympathetic preganglionic neurons exhibit segment-specific projectio

152 eted Reelin product may normally prevent the preganglionic neurons from migrating too far medially.

153 esent study also compares the projections of preganglionic neurons from transplants of multiple neura

154 ts and total dendritic length of sympathetic preganglionic neurons in both nulliparous and multiparou

155 so discussed that, because VIP is present in preganglionic neurons in normal animals, its release dur

156 These results show that preganglionic neurons in rats that are presumed to regul

157 ing whole cell patch recordings, sympathetic preganglionic neurons in spinal cord slices of Cx36-KO m

158 ilarities between LES- and fundic-projecting preganglionic neurons in terms of their organization in

159 w that MC4R agonists inhibit parasympathetic preganglionic neurons in the brainstem.

160 nfection, nor did lesions of parasympathetic preganglionic neurons in the Edinger-Westphal nucleus.

161 roportion of parasympathetic and sympathetic preganglionic neurons in the intermediolateral cell colu

162 ion nor did it prevent infection of putative preganglionic neurons in the intermediolateral cell colu

163 dy was to investigate age-related changes in preganglionic neurons in the lumbar and sacral spinal co

164 chick ciliary ganglion, calyx terminals from preganglionic neurons in the midbrain form early in deve

165 Over 91% of vagal preganglionic neurons in the NA-VL projecting to either

166 1, and midline raphe, as well as sympathetic preganglionic neurons in the spinal cord and central tar

167 ced Fos-like immunoreactivity in sympathetic preganglionic neurons in the spinal cord as well as seve

168 wever, we show that migration of sympathetic preganglionic neurons in the spinal cord is affected by

169 ntrol, including the location of sympathetic preganglionic neurons in the spinal cord, was characteri

170 the brain, including densely to sympathetic preganglionic neurons in the spinal cord, yet their func

171 contrast, MC4R agonists activate sympathetic preganglionic neurons in the spinal cord.

172 e of C1 neurons in the region of sympathetic preganglionic neurons in the spinal cord; however, regio

173 virus (PRV) in rats, we previously localized preganglionic neurons in the superior salivatory nucleus

174 Sympathetic preganglionic neurons in the T11-L2 (mainly L1) levels o

175 Since activation of autonomic sympathetic preganglionic neurons in the thoracic spinal cord produc

176 es CART/POMC neurons innervating sympathetic preganglionic neurons in the thoracic spinal cord sugges

177 that presumptive negative dromotropic vagal preganglionic neurons in the ventrolateral nucleus ambig

178 Therefore, we determined the location of preganglionic neurons innervating the ferret LES, with s

179 The activity of the vagal preganglionic neurons is predominantly regulated by GABA

180 ascular nucleus tractus solitarii to pontine preganglionic neurons labeled retrogradely from the pter

181 Preganglionic neurons located in rostral spinal segments

182 Efferent output includes preganglionic neurons located in the lateral gray of L5-

183 nts were transplanted to the cervical level, preganglionic neurons maintained projection patterns cha

184 he Cx36 protein was confirmed in sympathetic preganglionic neurons of Cx36-knockout (KO) mice.

185 which the axons branch to drive sympathetic preganglionic neurons of more than one functional class

186 in the spinal cord, and that they may excite preganglionic neurons of more than one functional class.

187 Sympathetic preganglionic neurons of the chick are located between t

188 omatomotor neurons of the FacN and autonomic preganglionic neurons of the DMNX and AmbSC; 3) cardiova

189 de and sent a focused bundle dorsally to the preganglionic neurons of the Edinger-Westphal nucleus, w

190 between P10 and adulthood and is present in preganglionic neurons of the intermediolateral cell colu

191 GluR1 mRNA was decreased in the sympathetic preganglionic neurons of the intermediolateral horn.

192 They most likely represent the preganglionic neurons of the superior salivatory nucleus

193 substance P-containing axons and sympathetic preganglionic neurons possessing the neurokinin-1 recept

194 ered by both the elimination and addition of preganglionic neurons projecting into the sympathetic tr

195 Sympathetic preganglionic neurons receive direct, monosynaptic input

196 of the largest population of brainstem vagal preganglionic neurons residing in the brainstem's dorsal

197 he relationship between reelin and migrating preganglionic neurons suggests that reelin acts as a bar

198 do so by contacting specific populations of preganglionic neurons that are distributed across a wide

199 ource of excitatory drive to the sympathetic preganglionic neurons that control blood pressure is fro

200 laying visceral sensory input to sympathetic preganglionic neurons that elicit autonomic dysreflexia

201 in the brainstem consists primarily of vagal preganglionic neurons that innervate postganglionic neur

202 l sympathetic trunks (CSTs) contain axons of preganglionic neurons that innervate the superior cervic

203 Cholinergic parasympathetic preganglionic neurons that project to meibomian gland-in

204 s intricately connected network, composed of preganglionic neurons that reside in the spinal cord and

205 modulate much of the activity of sympathetic preganglionic neurons through an indirect non-synaptic m

206 Labeled preganglionic neurons were cholinergic and were located

207 In all, 95 sympathetic preganglionic neurons were examined and 79% of these wer

208 Motoneurons and parasympathetic preganglionic neurons were filled with both markers, but

209 Individual cell bodies of ectopic preganglionic neurons were found in the ventral spinal c

210 Preganglionic neurons were identified using antisera aga

211 Sympathetic preganglionic neurons were labelled retrogradely with Fl

212 retrograde labeling revealed that choroidal preganglionic neurons were localized to the rostral medi

213 Labeled preganglionic neurons were scanned, processed and analyz

214 noreactive axons not only made contacts with preganglionic neurons which were immunoreactive for the

215 ial baroreceptor nerves, projects to pontine preganglionic neurons whose stimulation elicits cerebral

216 mbryogenesis may involve the interactions of preganglionic neurons with those from neighboring spinal

217 Proper positioning of sympathetic preganglionic neurons(SPNs) in the spinal cord is regula

218 n cholinergic neurons (including sympathetic preganglionic neurons) restores obesity-associated hyper

219 s disinhibition of thoracolumbar sympathetic preganglionic neurons, and intraspinal sprouting of nerv

220 estinations: sympathetic and parasympathetic preganglionic neurons, as well as dorsally originating a

221 dorsal and medial borders of both groups of preganglionic neurons, but did not form a solid barrier.

222 Splenic sympathetic preganglionic neurons, identified in rats injected with

223 e it is known that the PAG projects to vagal preganglionic neurons, including possibly cardiovagal mo

224 nction and feeding, and innervates autonomic preganglionic neurons, making it a candidate to regulate

225 we propose that they project to sympathetic preganglionic neurons, most of which are in the L1-L2 sp

226 include peripheral motoneurons, presumptive preganglionic neurons, neurons adjacent to the lateral m

227 "nontraditional" neurotransmitters in vagal preganglionic neurons, nitric oxide synthase (NOS), and

228 both postganglionic nerves and terminals of preganglionic neurons, showed no such difference between

229 ct projections to spinal cardiac sympathetic preganglionic neurons, that receive a tonic, GABAergic i

230 an abnormal hyperactivity of parasympathetic preganglionic neurons, whereas the 2DG-induced activatio

231 t it is expressed in motor but not autonomic preganglionic neurons.

232 ss GHSR mRNA, including many parasympathetic preganglionic neurons.

233 n wild-type neurons bordering both groups of preganglionic neurons.

234 amine neurons providing input to sympathetic preganglionic neurons.

235 ization and neurochemistry of LES-projecting preganglionic neurons.

236 ighly expressed in identified LES-projecting preganglionic neurons.

237 e neurochemical phenotype of parasympathetic preganglionic neurons.

238 lds and large somata) are different types of preganglionic neurons.

239 ns from the medulla oblongata to sympathetic preganglionic neurons.

240 effect is specific for rostrally projecting preganglionic neurons.

241 dendritic morphology of aged parasympathetic preganglionic neurons.

242 lin-1, a differentiation factor expressed in preganglionic neurons.

243 ge groups for sympathetic or parasympathetic preganglionic neurons.

244 ections to the cerebral cortex and autonomic preganglionic neurons.

245 direct excitatory projections to sympathetic preganglionic neurons.

246 ugh direct projections to spinal sympathetic preganglionic neurons.

247 column, and in particular to the sympathetic preganglionic neurons.

248 eral input rostrally to thoracic sympathetic preganglionic neurons.

249 functionally dissimilar (lumbar and cardiac) preganglionic neurons.

250 retention of TH-LI in lumbosacral autonomic preganglionic nuclei, did not mimic the changes in the p

251 usly provide polysynaptic input to brainstem preganglionic nuclei.

252 d SCG but not denervated SCG, suggesting the preganglionic origin.

253 ions via two serially connected neurons: one preganglionic, originating in the dorsal motor nucleus o

254 w facilitation, metabotropic mechanisms, and preganglionic oscillators regulate synaptic amplificatio

255 of ARC POMC neurons innervate the liver via preganglionic parasympathetic acetylcholine (ACh) neuron

256 in guinea pig cardiac ganglia are primarily preganglionic parasympathetic axons.

257 ventral tegmental area (VTA) are sources of preganglionic parasympathetic innervation of intraocular

258 recurrent laryngeal nerves, thus leaving the preganglionic parasympathetic innervation of the trachea

259 us (NTS) form a hindbrain micro-circuit with preganglionic parasympathetic motorneurons of the dorsal

260 on, stimulation of ExPANs, or stimulation of preganglionic parasympathetic neuron (PPN) axons.

261 eral L5-S2 ventral root avulsion on efferent preganglionic parasympathetic neurons (PPNs) and pelvic

262 rential innervation of medullary and pontine preganglionic parasympathetic neurons by different regio

263 nstrate for the first time that EA activates preganglionic parasympathetic neurons in the NAmb.

264 cardiovascular nucleus tractus solitarii to preganglionic parasympathetic neurons in the pons.

265 of which contain neurons that project to the preganglionic parasympathetic neurons in the superior sa

266 ascular nucleus tractus solitarii to pontine preganglionic parasympathetic neurons that project to th

267 OS-IR fibers were not IR for ChAT (marker of preganglionic parasympathetic neurons), tyrosine hydroxy

268 cleus tractus solitarii projected to pontine preganglionic parasympathetic neurons, but more rostral

269 Although not projecting to pontine preganglionic parasympathetic neurons, regions lateral,

270 traditionally described as the source of the preganglionic parasympathetic outflow to the ciliary gan

271 eurons by EA, their relation to cholinergic (preganglionic parasympathetic) neurons and those contain

272 was to find an extraorbital approach to the preganglionic part of cranial nerve VII and to reveal it

273 lateral motor column (LMC) MNs to a thoracic preganglionic (PGC) identity, elevating Bmi1 expression

274 as the periculomotor urocortin (pIII(U)) and preganglionic (pIII(PG)) populations.

275 nal differences suggesting that this rostral preganglionic population is specialized for pupil contro

276 ulates the activities of the brainstem vagal preganglionic, presympathetic and respiratory neural net

277 the segment-specific pattern of sympathetic preganglionic projections and that this effect is mediat

278 These results indicate that the direction of preganglionic projections can be influenced by neurons f

279 g that the formation of segmentally specific preganglionic projections during embryogenesis may invol

280 ube manipulations show that the direction of preganglionic projections is altered by both the elimina

281 o determine the segment-specific identity of preganglionic projections.

282 k-quail intestinal chimeras by transplanting preganglionic quail hindguts into the coelomic cavity of

283 T and were widely distributed in PPG and its preganglionic root, the greater petrosal nerve.

284 Two weeks after preganglionic section of dorsal roots L4-L6, the peronea

285 iac-related peaks in coherence in spectra of preganglionic splanchnic and cervical sympathetic nerves

286 In tonic neurons, single preganglionic stimuli evoked two to five populations of

287 Preganglionic sympathetic and parasympathetic neurons of

288 lated neuropeptides that are released by the preganglionic sympathetic axons.

289 Because FGF2 also reduced the loss of preganglionic sympathetic motoneurons after injury, this

290 l cord where they form synaptic contact with preganglionic sympathetic motor neurons.

291 termine whether partial spectral analysis of preganglionic sympathetic nerve discharges would reveal

292 ere those afferents terminate, as well as by preganglionic sympathetic neurons and their sympathetic

293 Cbln2 is also expressed by preganglionic sympathetic neurons and their targets in t

294 These tonic inhibitory inputs are relayed to preganglionic sympathetic neurons by way of dopaminergic

295 OXT(PVH) cells project to preganglionic, sympathetic neurons in the thoracic spina

296 ity phasically alters membrane potentials of preganglionic vagal and sympathetic motoneurones and con

297 exist which would permit the parasympathetic preganglionic vagal control of left ventricular contract

298 g within the DVC to modulate the activity of preganglionic vagal motor neurones that supply the stoma

299 ally expressed among distinct populations of preganglionic vagal motor neurones, recordings were made

300 imately 70% to electrical stimulation of the preganglionic vagus nerve.