ライフサイエンスコーパス: myenteric

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

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

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

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

5 dense mitochondrial network particularly in myenteric AH/Type-II neurons, supporting the importance

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

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

8 plexus is an example of differences between myenteric and submucosal components of the enteric nervo

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

10 t staining with NADPH-diaphorase showed that myenteric and submucosal ganglia formed interconnecting

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

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

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

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

15 dized-ATP suppressed these responses in both myenteric and submucosal neurons.

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

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

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

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

20 The myenteric and submucosal plexuses and DVC were processed

21 in to colonise the hindgut in large numbers, myenteric and submucosal plexuses in the hindgut almost

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

23 in morphologically identified neurons in the myenteric and submucosal plexuses of the guinea pig ente

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

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

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

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

28 NF145 was expressed in nerve fibers in both myenteric and submucosal plexuses.

29 rface of enterochromaffin-like cells, and of myenteric and submucous neurons, and to fibers distribut

30 ies and associated with nerve fibers in both myenteric and submucous plexuses.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

47 munoreactivity was observed on nerves within myenteric ganglia and interganglionic fiber tracts throu

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

49 -dependent myenteric neurons innervate other myenteric ganglia and/or the longitudinal muscle.

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

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

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

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

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

55 71 +/- 0.8% of VAChT-IR varicosities in myenteric ganglia of human colon were alpha-synuclein-IR

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

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

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

59 3% of biotinamide-labeled extrinsic axons in myenteric ganglia were labeled by antisera to one of the

60 Myenteric ganglia were separated from the gut wall, disp

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

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

63 teric plexus; injections of (125)I-NT-3 into myenteric ganglia, the tertiary plexus, and muscle, labe

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

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

66 sensory, interneuronal, and motor neurons in myenteric ganglia.

67 neurons in underlying submucosal and distant myenteric ganglia.

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

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

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

71 ve processes than in muscles also containing myenteric ganglia.

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

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

74 NF145-IR was not found in myenteric ganglion cells with Dogiel type II morphology.

75 The myenteric ganglion cells with NF145-IR had electrophysio

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

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

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

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

80 Myenteric ICC networks were reduced in W/W(V) mice, part

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

82 e slow-wave activity or an intact network of myenteric ICC.

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

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

85 imultaneously, by synchronous firing in many myenteric interneurones.

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

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

88 at NF145 is localized to distinct subsets of myenteric motor neurons and interneurons.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

107 (519 cells counted, 100% were positive) and myenteric neurones.

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

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

110 In the ileum, 81.6% of GAL-R1 myenteric neurons and 70.7% of GAL-R1 submucosal neurons

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

112 A1R is expressed in jejunal myenteric neurons and colonic submucosal neurons.

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

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

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

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

117 ris macrophages, a discrete subpopulation of myenteric neurons and recruited monocytes.

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

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

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

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

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

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

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

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

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

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

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

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

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

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 all choline acetyltransferase-immunoreactive myenteric neurons expressed CB(1) receptors in ganglia f

135 rkers were used to identify and characterise myenteric neurons expressing cannabinoid receptors.

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

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

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

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

140 evidence for presynaptic CB(1) receptors on myenteric neurons has been found in vitro.

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

142 acellular Ca2+ ([Ca2+]i) and excitability of myenteric neurons in guinea pig ileum, using microelectr

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

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

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

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

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

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

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

150 and/or secretomotor, whereas NT-3-dependent myenteric neurons innervate other myenteric ganglia and/

151 This study identified the effects on myenteric neurons of activating PARs and investigated un

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

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

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

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

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

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

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

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

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

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

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

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

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

165 Between CMMCs, myenteric neurons usually displayed ongoing but uncoordi

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

167 Myenteric neurons were counterstained with Cuprolinic Bl

168 Approximately 46% of muOR myenteric neurons were immunoreactive for vasoactive int

169 In the ileum, where 8% of the myenteric neurons were OFQ-IR, all OFQ-IR neurons expres

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

187 yptophan hydroxylase-expressing, small bowel myenteric neurons.

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

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

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

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

192 nction and induces Fos expression in colonic myenteric neurons.

193 igomycin (10 microm) had variable effects on myenteric neurons.

194 GAL-R1 submucosal neurons, but not in GAL-R1 myenteric neurons.

195 ctances, thus regulating the excitability of myenteric neurons.

196 ate (BzBzATP) activated an inward current in myenteric neurons.

197 munohistochemistry was performed to evaluate myenteric neurons.

198 responsible for the electrical signature of myenteric neurons.

199 for action potential initiation in isolated myenteric neurons.

200 with increased apoptosis and loss of colonic myenteric neurons.

201 alos, respectively, around some neighbouring myenteric neurons.

202 d-type (WT) and W/W(V) mice, which have only myenteric (pacemaker) ICC in the stomach.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

220 Within the myenteric plexus are neurons that contain neuronal nitri

221 g fast and slow synaptic transmission in the myenteric plexus are organized in a polarity- (ascending

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

223 Normally, a dominant pacemaker near the myenteric plexus drives slow waves that actively propaga

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

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

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

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

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

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

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

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

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

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

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

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

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

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

238 The myenteric plexus of the enteric nervous system controls

239 of Kit-positive cells is evident within the myenteric plexus of the entire GI tract.

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

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

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

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

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

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

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

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

248 n cells with Dogiel type I morphology in the myenteric plexus of the stomach and small and large inte

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

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

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

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

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

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

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

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

257 beta), in the guinea pig longitudinal muscle myenteric plexus tissue.

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

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

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

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

262 In the myenteric plexus, 50% of muOR-immunoreactive neurons con

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

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

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

266 rebral cortex, pituitary, spinal cord, colon myenteric plexus, dorsal root ganglion, and prenatal cor

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

268 ng and projection patterns in the guinea pig myenteric plexus, indicate that OFQ-IR is expressed pref

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

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

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

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

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

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

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

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

277 gic and nitrergic neurochemical codes in the myenteric plexus.

278 trergic neuronal immunochemical codes in the myenteric plexus.

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

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

281 tivate stretch-sensitive interneurons in the myenteric plexus.

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

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

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

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

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

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

288 neurons in ganglia of the submucosal but not myenteric plexus; injections of (125)I-NT-3 into myenter

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

290 in cholinergic neurons in the submucosal and myenteric plexuses, but not in enterocytes.

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

292 Whole mounts of rat and guinea pig myenteric preparations were dually labelled with antibod

293 nicotinic synaptic potentials evoked by the myenteric projections and with noradrenergic IPSPs evoke

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.