ライフサイエンスコーパス: myenteric plexus

1 ting an inhibitory neural pathway within the myenteric plexus.

2 expression and nNOS synthesis in the gastric myenteric plexus.

3 suggesting mediation by NO released from the myenteric plexus.

4 ve neuronal fibers were found in the colonic myenteric plexus.

5 lex following vagotomy occurs in the gastric myenteric plexus.

6 ide synthase (NOS) expression in the gastric myenteric plexus.

7 ly by impaired NOS expression in the gastric myenteric plexus.

8 n of the stimulated formation of cAMP in the myenteric plexus.

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

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

11 gic and nitrergic neurochemical codes in the myenteric plexus.

12 trergic neuronal immunochemical codes in the myenteric plexus.

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

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

15 tivate stretch-sensitive interneurons in the myenteric plexus.

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

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

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

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

20 the CM layer when it was separated from the myenteric plexus.

21 duced Fos expression in the small intestinal myenteric plexus.

22 enzymes were localized in the neurons of the myenteric plexus.

23 o detected on neurons in both submucosal and myenteric plexuses.

24 e majority of neurons in both submucosal and myenteric plexuses.

25 cts on enteric neurons in the submucosal and myenteric plexuses.

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

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

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

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

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

31 The PS contains ICC within the myenteric plexus and c-Kit immunopositive cells along th

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

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

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

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

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

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

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

39 was found in IC networks associated with the myenteric plexus and the deep muscular plexus.

40 r of NOS-immunoreactive cells in the gastric myenteric plexus and the NOS activity were significantly

41 CC that are distributed in the region of the myenteric plexus and throughout the circular muscle laye

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

43 ties were present in both the submucosal and myenteric plexuses, and the OCTs were also located in th

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

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

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

47 Within the myenteric plexus are neurons that contain neuronal nitri

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

49 ochemical changes in CGRP-li or SP-li in the myenteric plexus at any time.

50 oreactive for trk could be visualized in the myenteric plexus at ED 16.

51 responsive neurons were distinguished in the myenteric plexus because of the hyperpolarization and de

52 r messenger RNA was expressed in the colonic myenteric plexus but not in the smooth muscle cells, sug

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

54 nfirmed expression of PAR-1 and PAR-2 in the myenteric plexus by RT-PCR using primers based on sequen

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

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

57 Moreover, the longitudinal muscle myenteric plexus content of PKC alpha and PKC beta is su

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

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

60 NO released from the myenteric plexus enhances colonic transit and facilitate

61 ical, or electrical stimuli to the mucosa of myenteric plexus-free preparations (+/- extrinsic denerv

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

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

64 he mediation of NOS synthesis in the gastric myenteric plexus in rats.

65 thick bundles of fibers in proximity to the myenteric plexus in the longitudinal muscle and in assoc

66 d NOS messenger RNA (mRNA) expression of the myenteric plexus in the proximal and the distal colon in

67 ricose efferent axons throughout the gastric myenteric plexus (including that of the fundus).

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

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

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

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

72 he enteric nervous system, including reduced myenteric plexus innervation density and reduced gastroi

73 also seen in thin processes running from the myenteric plexus into the circular muscle, and in fibers

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

75 s suggest that NOS expression in the gastric myenteric plexus is controlled by the vagal nerve and ni

76 oncluded that neuronal NOS expression in the myenteric plexus is independent of vagus nerve and is ne

77 y whether the total number of neurons of the myenteric plexus is reduced with aging.

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

79 P-IR, but not VIP-IR, projects mainly to the myenteric plexus itself and the external muscle layers,

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

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

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

83 signaling in guinea pig longitudinal muscle/myenteric plexus (LMMP) preparations after chronic in vi

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

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

86 xide dismutase (MnSOD) is rapidly induced in myenteric plexus neurons (MPNs) in acute colitis and may

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

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

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

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

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

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

93 Defects in myenteric plexus neurotransmission occur both in mice wi

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

95 AR-1 and PAR-2 in > 60 % of neurons from the myenteric plexus of guinea-pig small intestine in primar

96 NOS messenger RNA expression in the gastric myenteric plexus of spontaneously diabetic biobreeding/W

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

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

99 The myenteric plexus of the enteric nervous system controls

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

101 raganglionic laminar endings (IGLEs), in the myenteric plexus of the esophagus, and 70-90% in the sto

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

103 nd nodose ganglia, as well as ganglia in the myenteric plexus of the intestine.

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

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

106 ns and the NOS activity are increased in the myenteric plexus of the proximal colon compared with the

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

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

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

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

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

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

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

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

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

116 sion in both the brains and small intestinal myenteric plexuses of control rats.

117 lyses of the small intestinal submucosal and myenteric plexuses of rats at various times after intest

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

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

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

121 The majority of ganglia in the myenteric plexus possess both HO2 and neuronal NO syntha

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

123 y) was observed in ileum longitudinal muscle myenteric plexus preparations obtained from chronic morp

124 Longitudinal muscle-myenteric plexus preparations of guinea pig intestines a

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

126 ptide immunoreactive (GRP-IR) neurons in the myenteric plexus, received vagal contacts.

127 for longitudinal muscle cells and ICs of the myenteric plexus region (IC-MY).

128 h multiple processes formed a network in the myenteric plexus region from corpus to pylorus.

129 Development and organization of ICCs of the myenteric plexus region into networks precedes the devel

130 ession of nitric oxide synthase (NOS) in the myenteric plexus remains unknown.

131 enzyme responsible for NO production in the myenteric plexus, remains unknown.

132 eganglionic fibers in the duodenal and cecal myenteric plexuses resembled the organization in the sto

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

134 ighly excitable, tonic S neurones within the myenteric plexus, since, in contrast to other S neurones

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

136 ddition, to study age-related changes in the myenteric plexus, the stomachs, small intestines, and la

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

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

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

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

141 In the developing myenteric plexus, trk immunoreactivity was present at em

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

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

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

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

146 he number of NOS-immunopositive cells in the myenteric plexus was significantly increased in tissues

147 tive cells and nNOS synthesis in the colonic myenteric plexus were significantly reduced in aged rats

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

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