ライフサイエンスコーパス: myenteric

1 oot, which contains PPN axons, also produced myenteric activation and contractions that were comparab

2 more neurons than capsaicin, did not produce myenteric activation or contractions unless the spinal c

3 mucosal 5-HT, or the enhanced fast EPSPs in myenteric AH and S neurones.

4 pig is associated with hyperexcitability of myenteric AH neurones, enhanced synaptic activity in the

5 o normal levels the electrical properties of myenteric AH neurones, the proportion of S neurones exhi

6 g inhibitory nerve pathways was initiated by myenteric AH-neurons, or slow synaptic transmission.

7 of Cajal (ICC) networks at the level of the myenteric and deep muscular plexuses.

8 They also suggest differential mediation of myenteric and DVC responses to CCK.

9 d was differentially distributed between the myenteric and submucosal divisions of the ENS.

10 ide increased Fos-LI dose-dependently in the myenteric and submucosal neurons of the duodenum, but no

11 observed within the soma of the majority of myenteric and submucosal neurons, although faint immunor

12 n the number of Fos-immunoreactive nuclei of myenteric and submucosal neurons, following CCK injectio

13 ssociated with elevated excitability in both myenteric and submucosal neurons.

14 L-PGDS was expressed in the neurons of human myenteric and submucosal plexi.

15 mount preparations of adult (8-12-week old) myenteric and submucosal plexus stained with NADPH diaph

16 vo formed neuroglial structures similar to a myenteric and submucosal plexus, had functional intersti

17 Most of the CRF-IR fibers persisted in the myenteric and submucosal plexuses after 7 days in organo

18 The myenteric and submucosal plexuses and DVC were processed

19 , the nodose ganglia, and the ganglia of the myenteric and submucosal plexuses of the duodenum follow

20 Myenteric and submucosal plexuses were isolated from all

21 d activates the enteric nervous system (ENS; myenteric and submucosal plexuses) of the gastrointestin

22 CRF-IR nerve fibers were present in the myenteric and submucosal plexuses, in the circular muscl

23 prominently localized in nerve fibers of the myenteric and submucosal plexuses, muscularis externa an

24 of CRF1 receptor mRNA, but not CRF2, in both myenteric and submucosal plexuses.

25 CRF-IR was expressed in both the myenteric and the submucosal plexuses of all regions of

26 ivity is restricted to neurons (submucosal > myenteric) and is not seen in glia, interstitial cells o

27 tions in Ca(2+) were observed in ICCs at the myenteric border (ICC-MY).

28 mooth muscle originate at the submucosal and myenteric borders, respectively.

29 Guanethidine pretreatment attenuated myenteric but not DVC Fos-LI induced by CCK-8.

30 Mice lacking TLR4 did not exhibit WD-induced myenteric cell loss and dysmotility.

31 These disorders precede the nitrergic myenteric cell loss observed in the proximal colon.

32 receptor 4 (TLR4)(-/-) mice did not exhibit myenteric cell loss or dysmotility.

33 At birth, myenteric cholinergic neurons comprised less than half o

34 d changes on large-scale network activity in myenteric circuits has not been determined.

35 ERT-immunoreactive terminal axons surrounded myenteric dopaminergic neurons and SERT knock-out increa

36 bmucosal neuron density, and increased colon myenteric fibers per neuron when compared to the wild ty

37 In conclusion, SD rats may express more myenteric Fos-LI in response to CCK due to increased num

38 athetic neurons play a role in mediating the myenteric Fos-LI response to CCK.

39 stem in the pathway by which CCK-8 increases myenteric Fos-LI.

40 attenuate dorsal vagal complex (DVC) but not myenteric Fos-like immunoreactivity (Fos-LI) induced by

41 Human myenteric ganglia and adjacent smooth muscle were isolat

42 ding precursor cells that are located within myenteric ganglia and express both Nestin and p75NTR, bu

43 at ramified extensively through many rows of myenteric ganglia and formed nerve endings in discrete a

44 combined transcriptional profiling of human myenteric ganglia and mouse EN provides a rich foundatio

45 of their varicose branches per target) both myenteric ganglia and smooth muscle.

46 macaques showed progressive infiltration of myenteric ganglia by CD3+ T cells and IBA1+ macrophages

47 espite an abundance of inflammatory cells in myenteric ganglia during acute infection, the ENS was no

48 luo-4) used to study activity in EGCs within myenteric ganglia during CMMCs, followed by post hoc S10

49 s of neural progenitor cells, using isolated myenteric ganglia from postnatal rat ileum.

50 a majority of patients in a HSCR cohort, the myenteric ganglia from the ganglionated region are also

51 Myenteric ganglia occupied 34% +/- 4% of myenteric plexu

52 well as substance P and S100beta density in myenteric ganglia of HFD mice were increased at week 8,

53 71 +/- 0.8% of VAChT-IR varicosities in myenteric ganglia of human colon were alpha-synuclein-IR

54 Mir375 expression was increased in myenteric ganglia of mice fed HFD and associated with de

55 uronal cell loss because of apoptosis in the myenteric ganglia of the adult small intestine, total my

56 varicose endings (IGVEs) were identified in myenteric ganglia of the stomach and varicose simple-typ

57 3% of biotinamide-labeled extrinsic axons in myenteric ganglia were labeled by antisera to one of the

58 Myenteric ganglia were separated from the gut wall, disp

59 ied rostrally or caudally along many rows of myenteric ganglia with little circumferential displaceme

60 In guinea pig rectal myenteric ganglia, alpha-synuclein- and VAChT-immunoreac

61 ssued specialized polymorphic collaterals to myenteric ganglia, and a subset (41%) of antral longitud

62 ptidergic neurons innervated mucosal crypts, myenteric ganglia, and submucosa.

63 s that had nerve endings in circular muscle, myenteric ganglia, and submucosa.

64 Most of our images were of myenteric ganglia, captured using a 20x objective lens.

65 e (VIP)-IR varicosities in guinea pig rectal myenteric ganglia.

66 ve processes than in muscles also containing myenteric ganglia.

67 ber of neurons at sites normally occupied by myenteric ganglia.

68 umbar 2-3 dorsal root ganglia and in colonic myenteric ganglia.

69 the esophagus, only IGVEs were identified in myenteric ganglia.

70 7) of biotinamide-labeled extrinsic axons in myenteric ganglia.

71 ximum of 14% of biotinamide-labeled axons in myenteric ganglia.

72 d complex arbors of varicose neurites within myenteric ganglia/primary plexus and, concomitantly, lon

73 ubmucosal ganglion neurons and in almost all myenteric ganglion neurons.

74 Single myenteric ganglion volume averaged 3,527,678 +/- 573,832

75 image analysis revealed that the severity of myenteric ganglionitis increased with time after SIV inf

76 Our aims were to determine whether myenteric ICC (ICC-MY) in human jejunum are pacemaker ce

77 intain coordinated Ca(2+) transients between myenteric ICC (ICC-MY) of small intestine.

78 Internalization of NK1R was not observed in myenteric ICC or smooth muscle cells in response to nerv

79 incident in subsets of neurons (submucosal > myenteric) in guinea pig and mouse intestines in situ an

80 The high-fat diet induces changes in the myenteric innervation of the small intestine, intestinal

81 imultaneously, by synchronous firing in many myenteric interneurones.

82 rojections of circular muscle motor neurons, myenteric interneurons, and putative sensory neurons.

83 tter utilized by a system of long descending myenteric interneurons.

84 of myenteric neurons, as well as in numerous myenteric internodal fibers; immunoreactivity was rarely

85 sity clusters (CGRP+ baskets) that enveloped myenteric nerve cell bodies.

86 P(+/-));Foxf2(-/-) mice had expansion of the myenteric nerve plexus and increased proliferation of sm

87 ear inclusions), loss of nerve fibers in the myenteric nerve plexus, and delayed gastrointestinal tra

88 Slow waves originate from a myenteric network of interstitial cells of Cajal (ICC-MY

89 of a high-fat diet (HFD) is associated with myenteric neurodegeneration, which in turn is associated

90 In mice, ExPANs regulate myenteric neuron activity and smooth muscle contraction

91 Here we have developed a Swiss-Webster mouse myenteric neuron culture and examined their electrophysi

92 Het)R3(Het)) mutant mice had a reduced colon myenteric neuron density, reduced colon myenteric neuron

93 ompared with those in control animals, while myenteric neuron number was normal.

94 , in addition to colonic and ileal nitrergic myenteric neuron quantifications and motility.

95 labeling with antibody markers that identify myenteric neuron subtypes to determine when neuron subty

96 ed a computational model of a Dogiel type II myenteric neuron that successfully reproduces all experi

97 olon myenteric neuron density, reduced colon myenteric neuron to glia ratio, reduced colon submucosal

98 induced diabetic mice, there was evidence of myenteric neuronal apoptosis and reduced Akt phosphoryla

99 Deletion of TPH2, but not TPH1, decreased myenteric neuronal density and proportions of dopaminerg

100 el to compare dorsal vagal complex (DVC) and myenteric neuronal Fos-Like immunoreactivity (Fos-LI), i

101 ganglia of the adult small intestine, total myenteric neuronal numbers remain constant.

102 usively with vagal-afferent endings and some myenteric neurones in mouse and human stomach, respectiv

103 The electrical and synaptic properties of myenteric neurones in normal and inflamed guinea-pig dis

104 ECE-1 mRNA and protein were expressed by myenteric neurones of rat and mouse intestine.

105 urokinin 1 receptor (NK(1)R) in endosomes of myenteric neurones.

106 (519 cells counted, 100% were positive) and myenteric neurones.

107 Most of the CRF-IR myenteric neurons (95%) had uniaxonal morphology; the re

108 Most myenteric neurons also appeared normal in size, but NO-p

109 eous intracellular recordings were made from myenteric neurons and circular muscle (CM) cells in isol

110 monstrate the feasibility of isolating mouse myenteric neurons and establish sodium channel inhibitio

111 We evaluated SSTR2A trafficking in murine myenteric neurons and neuroendocrine AtT-20 cells by mic

112 ysiologic, and pharmacologic techniques, the myenteric neurons and neurotransmitters involved in the

113 n, a TRPV1 agonist, can initiate activity in myenteric neurons and produce muscle contraction.

114 on produced phased-locked calcium signals in myenteric neurons and produced colon contractions.

115 rom rat small intestine or to co-cultures of myenteric neurons and rat peritoneal mast cells.

116 oxypyruvate altered excitatory properties of myenteric neurons and reduced islet insulin content but

117 ocal microscopy provides detailed imaging of myenteric neurons and smooth muscle cells in the muscula

118 o expression was detected in gastric glands, myenteric neurons and smooth muscle cells.

119 nvestigated communication between ExPANs and myenteric neurons and the circuits by which ExPANs modul

120 F(2) activation inhibits CRF(1) signaling in myenteric neurons and the stress-induced colonic motor r

121 vestigate the morpho-quantitative aspects of myenteric neurons and the wall of the small intestine in

122 is an autoimmune disease in which esophageal myenteric neurons are attacked in a cell-mediated and an

123 has been demonstrated that subpopulations of myenteric neurons are differentially susceptible to the

124 well as significantly fewer nerve fibers and myenteric neurons as assessed by PGP9.5 staining.

125 ors were detected in smooth-muscle cells and myenteric neurons but not in ICC.

126 citatory postsynaptic potentials (fEPSPs) in myenteric neurons but the subunit composition of enteric

127 tion revealed that subsets of submucosal and myenteric neurons contained mRNA encoding D2 or D3.

128 d GLP2 elicit neuroprotective effects on rat myenteric neurons cultured with or without mast cells.

129 so appeared normal in size, but NO-producing myenteric neurons developed very large nuclei as a resul

130 r GCaMP, we visualized levels of activity in myenteric neurons during smooth muscle contractions indu

131 o determine the role of different classes of myenteric neurons during the CMMC.

132 We found that mouse myenteric neurons exhibit two types of tetrodotoxin-resi

133 Conversely, only 22% of gastric myenteric neurons express nitric oxide synthase (NOS) co

134 The neuronal tissue constituted of isolated myenteric neurons from four to 12 days old Wistar rats,

135 re, we used in situ patch-clamp recording of myenteric neurons from mice to define functionally the N

136 GLP1, GLP2 and VIP were added to cultured myenteric neurons from rat small intestine or to co-cult

137 The vast majority of myenteric neurons had exited the cell cycle by P10.

138 lia cells (EGCs) form a dense network around myenteric neurons in a ganglia and are likely to have no

139 to determine whether 1) different classes of myenteric neurons in the guinea pig ileum contain muOR i

140 ere made from circular muscle (CM) cells and myenteric neurons in the isolated guinea pig distal colo

141 inducing constipation and loss of nitrergic myenteric neurons in the proximal colon.

142 We did not observe any EdU+/NOS1+ myenteric neurons in the small intestine of adult mice f

143 cetylcholine neurons make up the majority of myenteric neurons in the stomach (70%), they are a minor

144 naptic and drug-induced responses from ileal myenteric neurons in vitro.

145 ord synaptic and drug-induced responses from myenteric neurons in vitro.

146 Numbers of colonic myenteric neurons increased after mice were switched fro

147 ExPANs mediate visceral pain, and myenteric neurons mediate colon motility, so we investig

148 DOReGFP was present mostly in nitrergic myenteric neurons of colon.

149 os-LI was then quantified in the DVC and the myenteric neurons of the duodenum and jejunum using a di

150 response to CCK due to increased numbers of myenteric neurons or more intestinal CCK(1) receptors th

151 tonin gene-related peptide (CGRP)-expressing myenteric neurons produce MET, the receptor for hepatocy

152 el Type II/AH sensory neurons and most other myenteric neurons responded to oral elongation with redu

153 analysis revealed that approximately 56% of myenteric neurons stained with neuronal nitric oxide syn

154 pressed more Fos-LI in the area postrema and myenteric neurons than SLE and LETO rats.

155 hat SD rats have significantly more duodenal myenteric neurons than the other strains.

156 te-mapping revealed a small subpopulation of myenteric neurons that appears to express NOS1 only tran

157 essed by neurochemically distinct classes of myenteric neurons that are likely to differ functionally

158 polysaccharide lead to apoptosis in cultured myenteric neurons that express Toll-like receptor 4 (TLR

159 s significant coexpression of NOS and VIP in myenteric neurons that is more prominent in the proximal

160 d of prolonged increases in activity in many myenteric neurons that was correlated to Ca(2+) transien

161 al development of specific nAChR subtypes in myenteric neurons using Wnt1-Cre;R26R-GCaMP3 mice, where

162 Between CMMCs, myenteric neurons usually displayed ongoing but uncoordi

163 Subsets of submucosal and myenteric neurons were also D1, D2, or D3 immunoreactive

164 Myenteric neurons were counterstained with Cuprolinic Bl

165 Unique functional classes of myenteric neurons were identified based on morphology, n

166 Nuclei from mouse myenteric neurons were isolated and subjected to single-

167 The numbers of both submucous and myenteric neurons were reduced by 27%-61% in ileum and c

168 The numbers of nitrergic myenteric neurons were reduced in the proximal colon aft

169 t proportions in the small intestine (25% of myenteric neurons were YFP+ at P0 compared to 62% in adu

170 undergoes ligand-induced internalization in myenteric neurons, and (2) the effect of long-term incre

171 ronal cell bodies, to quantify the number of myenteric neurons, and a reverse transcriptase chain pol

172 ndrites, soma, and axons in a small group of myenteric neurons, as well as in numerous myenteric inte

173 resses colon motility by acting on intrinsic myenteric neurons, but the extent of sympathetic-induced

174 was expressed in only a small population of myenteric neurons, but was abundantly expressed in the s

175 ic mice had loss of NADPH diaphorase-stained myenteric neurons, delayed gastric emptying, and increas

176 tivity was found only in approximately 1% of myenteric neurons, extensive OT-immunoreactive varicosit

177 We examined the interactions between myenteric neurons, interstitial cells of Cajal in the my

178 nal subpopulations, particularly cholinergic myenteric neurons, may be more vulnerable than others to

179 INaT was encountered in all myenteric neurons, whereas INaP was preferentially found

180 Also, myenteric neurons, which are innervated by IGLEs, were s

181 DOR localizes specifically to submucosal and myenteric neurons, which might account for the ability o

182 red in all enteric glia and most small bowel myenteric neurons, yet phenotypic effects of Rb1 loss we

183 for action potential initiation in isolated myenteric neurons.

184 with increased apoptosis and loss of colonic myenteric neurons.

185 alos, respectively, around some neighbouring myenteric neurons.

186 d 4-hydroxynonenal, increased [Ca(2+)](i) in myenteric neurons.

187 rdings from the muscle and Ca(2+) imaging of myenteric neurons.

188 yptophan hydroxylase-expressing, small bowel myenteric neurons.

189 h-muscle cells and SCF expression but not of myenteric neurons.

190 lts in increased 5-HT(3)R internalization in myenteric neurons.

191 IL-13alpha1 in smooth muscle, epithelia, and myenteric neurons.

192 ved in the initial axonal segment of colonic myenteric neurons.

193 ns throughout the ganglion, did not activate myenteric neurons.

194 xus of TRPV1-positive fibers is found around myenteric neurons.

195 nction and induces Fos expression in colonic myenteric neurons.

196 circuit was necessary for ExPANs to regulate myenteric neurons.

197 efore form motility-regulating synapses onto myenteric neurons.

198 munohistochemistry was performed to evaluate myenteric neurons.

199 responsible for the electrical signature of myenteric neurons.

200 pression of the hTDP-43 transgene in colonic myenteric plexes resulted in progressive neurodegenerati

201 reactive oxygen species (ROS) in the jejunal myenteric plexi and phosphorylation (p) of mitogen-activ

202 of neurons projected predominantly to either myenteric plexus ( approximately 13%) or smooth muscle (

203 ely 100% of an arbor's varicose branches) to myenteric plexus ( approximately 2%) or smooth muscle (

204 ICC within the plane of the myenteric plexus (ICC-MY) arise from KIT-positive progen

205 longitudinal muscle layers with the adherent myenteric plexus (LM-MP).

206 ctivation of the colonic longitudinal muscle myenteric plexus (LMMP) neurons and localization of CRF(

207 Longitudinal muscle myenteric plexus (LMMP) tissues were collected, analyzed

208 mice without colitis, NO was produced in the myenteric plexus almost completely via NOS1.

209 There are considerable differences in the myenteric plexus along different segments of the monkey

210 lexus and 50% of CSE positive neurons in the myenteric plexus also contained nNOS.

211 COX-2 expression is enhanced in the myenteric plexus and cells within the smooth muscle laye

212 large, intensely immunofluorescent axons in myenteric plexus and circular muscle, and thinner varico

213 onged satiety action than CCK-8; and (3) the myenteric plexus and DVC may play roles in these differe

214 R), which binds laminin-beta1, in human HSCR myenteric plexus and EdnrB(NCC-/-) NCC.

215 The presence of clock genes in the myenteric plexus and epithelial cells suggests a role fo

216 Clock immunoreactivity was observed in the myenteric plexus and epithelial crypt cells.

217 ing neural network, exemplified by lack of a myenteric plexus and extensive overgrowth of fibers.

218 nes in the same plexus, from neurones in the myenteric plexus and from sympathetic postganglionic neu

219 nd all layers of the retina) and peripheral (myenteric plexus and innervating nerves) nervous system

220 a series of plexuses throughout the gut: the myenteric plexus and submucosal plexus.

221 ther, these data extend our understanding of myenteric plexus architecture in maturing zebrafish, the

222 lopment, however knowledge of its developing myenteric plexus architecture was unknown.

223 sensitive, whereas those located within the myenteric plexus are also thought to respond to changes

224 Within the myenteric plexus are neurons that contain neuronal nitri

225 dense neuronal networks at the level of the myenteric plexus by embryonic week (EW) 12, with express

226 Dissected muscle and myenteric plexus contained transcripts encoding D1-D3 an

227 s from the muscularis propria containing the myenteric plexus from adult rats.

228 Quantitative analyses demonstrated myenteric plexus in 24.5% +/- 2.4% of flattened colon Z-

229 The proportions of CRF-IR cell bodies in the myenteric plexus increased progressively from the stomac

230 By late larval stages, complexity of the myenteric plexus increases such that a layer of axons is

231 e that synaptic facilitation in the inflamed myenteric plexus involves a presynaptic increase in PKA

232 was expressed by enteric glial cells in the myenteric plexus layer, and cultured primary enteric gli

233 (fl/fl); Wnt1Cre+) caused a dramatic loss of myenteric plexus MET-IR neurites and 1-1'-dioctodecyl-3,

234 de synthase (NOS)- and calretinin-containing myenteric plexus neurons and non-cholinergic secretomoto

235 A subpopulation of myenteric plexus neurons expressed VGLUT2 protein and mR

236 vating colorectum; and 3) a subpopulation of myenteric plexus neurons expressing VGLUT(2).

237 nin gene-related peptide-immunoreactive (IR) myenteric plexus neurons thought to be intrinsic primary

238 CD8 T cells homed to submucosal and myenteric plexus neurons, 60% of which were lost, clinic

239 ndritic surfaces of neurochemically distinct myenteric plexus neurons, while being on axonal compartm

240 r the alpha4-5 subunits was only detected in myenteric plexus neurons.

241 mistry indicated that LAMB4 localizes to the myenteric plexus of colonic tissue and patients harborin

242 opulation of mechanosensory S-neurons in the myenteric plexus of the distal colon which appear to be

243 (2) Possible roles for the myenteric plexus of the duodenum and the dorsal vagal co

244 The myenteric plexus of the enteric nervous system controls

245 CRF-IR cell bodies in the myenteric plexus of the ileum expressed IR for choline a

246 Here, we examine myenteric plexus of the maturing zebrafish larval fish h

247 vity was confined to enteric glia within the myenteric plexus of the mouse colon; the Cx43 inhibitors

248 Intestinal epithelial cells and the myenteric plexus of the mouse gastrointestinal tract con

249 HO2- and nNOS-containing neurons within the myenteric plexus of the rat ileum.

250 n dorsal root ganglia neurons but not in the myenteric plexus of the small and large intestine.

251 In the myenteric plexus of the small intestine, DOReGFP was pre

252 lly terminated in the hepatic artery and the myenteric plexus of the stomach and duodenum.

253 CRF1 receptor was distributed widely in the myenteric plexus of the stomach and small and large inte

254 ons of the large and small intestine and the myenteric plexus of the stomach.

255 t contribute to synaptic facilitation in the myenteric plexus of the trinitrobenzene sulphonic acid-i

256 es for HO-2, nNOS, and VIP were found in the myenteric plexus of WT IAS.

257 t and Sema3d affecting survival, presence of myenteric plexus or intestine transcriptome.

258 d microelectrode recordings from whole mount myenteric plexus preparations in guinea pigs.

259 ssed survival by counting various genotypes, myenteric plexus presence by acetylcholinesterase staini

260 reatment of opioid naive longitudinal muscle myenteric plexus tissue attenuates PLCbeta3 phosphorylat

261 lation in the guinea pig longitudinal muscle myenteric plexus tissue revealed substantial alterations

262 smural electrical stimuli confirmed that the myenteric plexus was always present and intact in these

263 not express opioids; opioid synthesis in the myenteric plexus was not altered on induction of inflamm

264 Loss of myenteric plexus was observed only in all Ret null homoz

265 that the connectivity between the LM and the myenteric plexus was required for mechanotransduction.

266 removed from progressively longer lengths of myenteric plexus, a graded reduction in the correlation

267 in the postnatal rat gut are located in the myenteric plexus, and shows that these cells can be expa

268 riginates in pacemaker cells surrounding the myenteric plexus, called interstitial cells of Cajal (IC

269 neurones, enhanced synaptic activity in the myenteric plexus, increased serotonin (5-HT) availabilit

270 ooth muscle, while simultaneously contacting myenteric plexus, is consistent with the view that these

271 the enteric nervous system, specifically the myenteric plexus, of the rhesus monkey (Macaca mulatta)

272 e majority of CM was sharp dissected off the myenteric plexus, ongoing neural activity was absent, or

273 early within the gastrointestinal mucosa and myenteric plexus, respectively.

274 When the LM was sharp dissected off the myenteric plexus, the synchronized discharge of ascendin

275 r Hu was 100% in the P3 and 71% in the adult myenteric plexus, when submucosal neurons were also OTR-

276 ration of a robust expression of DPPX in the myenteric plexus, which strongly reacted with patients'

277 the electrically stimulated guinea pig ileum myenteric plexus-longitudinal muscle preparation.

278 d expression of IL-1R1 in the ganglia of the myenteric plexus.

279 nsity of the cytotoxic T-cell assault on the myenteric plexus.

280 gic and nitrergic neurochemical codes in the myenteric plexus.

281 Myenteric ganglia occupied 34% +/- 4% of myenteric plexus.

282 trergic neuronal immunochemical codes in the myenteric plexus.

283 in the gut wall and in ganglion cells of the myenteric plexus.

284 A was expressed in the villus epithelium and myenteric plexus.

285 tion to the gastric mucosa originates in the myenteric plexus.

286 tivate stretch-sensitive interneurons in the myenteric plexus.

287 e submucosal plexus (29.9-38.0%) than in the myenteric plexus.

288 peptide Y, serotonin, or somatostatin in the myenteric plexus.

289 pithelium, smooth muscle, and the submucosal myenteric plexus.

290 ne acetyltransferase, and substance P in the myenteric plexus.

291 mically in neuronal perikarya (submucosal >> myenteric plexus; small intestine > stomach or colon).

292 n, both slow (slow waves, 2-8/min) and fast (myenteric potential oscillations [MPOs]; 16-20/min) elec

293 Feeding of LGG to mice stimulated myenteric production of ROS, increased levels of phospho

294 terstitial cells of Cajal distributed in the myenteric region (ICC-MY) and fibroblast-like cells (FLC

295 neurons, interstitial cells of Cajal in the myenteric region (ICC-MY) and smooth muscle cells during

296 In the small intestine, ICC in the myenteric region (ICC-MY), between the circular and long

297 citatory postsynaptic potentials (fEPSPs) in myenteric S neurons were evaluated, and the density of s

298 ly identified a population of mechanosensory myenteric S-interneurons in the distal colon of guinea-p

299 In contrast, when recordings were made from myenteric S-neurons, two distinct electrical patterns of

300 canine colon were pinned with submucosal or myenteric surface uppermost or cut in cross section.