ライフサイエンスコーパス: stratum radiatum

1 and post-synapse, and synapse density in CA1 stratum radiatum.

2 ut the HF, but slightly more numerous in CA1 stratum radiatum.

3 ons, in the volume of CA1 stratum oriens and stratum radiatum.

4 e border of stratum lacunosum-moleculare and stratum radiatum.

5 stic pattern, with zeta prominent in the CA1 stratum radiatum.

6 calcium enters into individual spines in the stratum radiatum.

7 cell soma but not in interneurons located in stratum radiatum.

8 tum oriens potentiation following pairing in stratum radiatum.

9 ophysin immunoreactivity was enhanced in CA1 stratum radiatum.

10 urrents in hippocampal astrocytes located in stratum radiatum.

11 pendent of stimulation electrode position in stratum radiatum.

12 as sharp waves, occur simultaneously in the stratum radiatum.

13 l-induced excitatory field potentials in CA1 stratum radiatum.

14 al pathway-associated inhibitory synapses in stratum radiatum.

15 protein vesicular glutamate transporter 1 in stratum radiatum.

16 ic markers GLAST and GFAP in rat hippocampal stratum radiatum.

17 ease in MMP-3 expression and activity in CA1 stratum radiatum.

18 r the control of mTOR, increased in area CA1 stratum radiatum.

19 ynapses have a more proximal location in the stratum radiatum.

20 iens (78.87%), stratum pyramidale (40%), and stratum radiatum (56.6%).

21 dentate gyrus inner molecular layer and CA1 stratum radiatum and in (ii) postsynaptic densities and

22 recorded from GABAergic interneurons in CA1 stratum radiatum and induced membrane depolarization sug

23 Interneurons in CA1/CA3 stratum radiatum and moleculare, and in the hilus region

24 tricted to str. oriens/alveus and innervated stratum radiatum and oriens.

25 s using sharp electrodes were carried out in stratum radiatum and pyramidale.

26 ites of CA1 pyramidal neurons predominate in stratum radiatum and receive approximately 80% of the sy

27 in all layers of CA1 but more frequently in stratum radiatum and stratum lacunosum moleculare.

28 ith the entorhinal cortex (ERC) and then CA1 stratum radiatum and stratum lacunosum-moleculare (CA1-S

29 ons were heterotopic and displaced into both stratum radiatum and stratum lacunosum-moleculare.

30 dense population of immunopositive cells in stratum radiatum and stratum oriens in area CA1 during t

31 effect of dopamine on synaptic plasticity in stratum radiatum and stratum oriens layers of both ventr

32 n of truncated trkB.T1 mRNA receptors in the stratum radiatum and stratum oriens of the CA3 subfield.

33 well-developed cytoarchitecture, such as the stratum radiatum and stratum oriens of the hippocampus,

34 r GABA transporter) in interneurons from the stratum radiatum and stratum oriens, and in CA1 pyramida

35 etic evidence that NOS is involved in LTP in stratum radiatum and suggest that the neuronal and endot

36 s also a NOS-independent component of LTP in stratum radiatum and that LTP in stratum oriens is large

37 napses primarily with preexisting boutons in stratum radiatum and that these boutons enlarge and chan

38 oriens of the CA1 region and (2) between CA1 stratum radiatum and the dentate molecular layer.

39 nophilin-immunoreactive spine numbers in CA1 stratum radiatum and the inner and outer molecular layer

40 hat the late potential is minimal in the mid-stratum radiatum and thus suggest that this site is most

41 ociated interneurons (n = 10) stratifying in stratum radiatum and, to a lesser extent, stratum oriens

42 slow oscillatory potentials reversed in the stratum radiatum and/or in the stratum oriens.

43 sity on CA3 pyramidal cell apical dendrites (stratum radiatum) and an increase in the number of thorn

44 throughout neuronal cell bodies, dendrites (stratum radiatum), and axons (fimbria), but not astrocyt

45 h lesser, though still apparent, staining of stratum radiatum, and (c) a decrease in amplitude and sl

46 anization, especially in the hippocampal CA1 stratum radiatum, and also diminishes GABA-mediated syna

47 two less-defined hippocampal subregions, CA1 stratum radiatum, and oriens.

48 ential recorded from the stratum pyramidale, stratum radiatum, and stratum lacunosum moleculare of th

49 area CA1: the proximal and distal thirds of stratum radiatum, and the stratum lacunosum-moleculare.

50 ll as basal synaptic transmission in the CA1 stratum radiatum appeared unaffected, whereas spontaneou

51 We found that the spine density in stratum radiatum ( approximately 1.1 per micrometer) rem

52 while evoking Ca2+ increases in the adjacent stratum radiatum astrocytes by uncaging IP3.

53 t widespread Ca(2+) elevations in 80%-90% of stratum radiatum astrocytes do not increase neuronal Ca(

54 ion in interneurons from stratum lucidum and stratum radiatum, but not in interneurons from stratum l

55 MSB connectivity was highest in the proximal stratum radiatum, but only for those MSBs composed of no

56 nt component in the extracellularly recorded stratum radiatum CA(1) field potential under low stimula

57 r in the hippocampal formation including CA2 stratum radiatum, CA3 stratum radiatum, hilus dentate gy

58 In stratum radiatum, cell loss is particularly dramatic.

59 ause (i) responses induced by stimulation in stratum radiatum consisted of a single population spike

60 vealed that numerous dendritic spines in the stratum radiatum contained the NR2 subunit of the NMDA r

61 hroughout the shafts and in select spines of stratum radiatum dendrites.

62 form of GABAergic LTP, while interneurons of stratum radiatum, despite receiving this dual signaling,

63 affer collateral/commissural synapses in the stratum radiatum differ from those at mossy fibers but a

64 In the stratum radiatum, estradiol, DPN, and PPT increased PSD-

65 DA receptors contribute to hippocampal CA(1) stratum radiatum excitatory postsynaptic potentials (EPS

66 Areas such as the dentate and stratum radiatum exhibited higher CL signals than other

67 tentials (fEPSPs) were recorded from the CA1 stratum radiatum following stimulation of the Schaffer c

68 tum lacunosum-moleculare and the superficial stratum radiatum, GIRK1-IR was often present immediately

69 that dendrite-targeting interneurons in the stratum radiatum had an elevated resting membrane potent

70 campal slices where the dendrites located in stratum radiatum have been isolated from their cell bodi

71 ormation including CA2 stratum radiatum, CA3 stratum radiatum, hilus dentate gyrus and presubiculum,

72 charge transfer onto postnatal day 11-15 CA1 stratum radiatum hippocampal interneurons but is without

73 was sensitive to stimulation position in the stratum radiatum; i.e., distal stimulation elicited maxi

74 d be detected in both stratum pyramidale and stratum radiatum in area CA1.

75 dendritic shafts and spines) profiles in the stratum radiatum in the hippocampal CA1 region.

76 ed by basal activities or stimulation of the stratum radiatum increases the efficacy of GABAergic syn

77 however, increased GR signal was seen in the stratum radiatum, indicating redistribution of GR to the

78 Hippocampal stratum radiatum inhibitory interneurons receive glutama

79 etween synapses onto CA1 pyramidal cells and stratum radiatum interneurones are due to a higher initi

80 ha7-containing nAChRs in rat hippocampal CA1 stratum radiatum interneurones in slices, we describe a

81 ffer collateral excitatory synapses onto CA1 stratum radiatum interneurones versus pyramidal cells in

82 ptors on the membrane of rat hippocampal CA1 stratum radiatum interneurons and pyramidal cells in acu

83 nels facilitate excitatory transmission onto stratum radiatum interneurons but not onto CA1 pyramidal

84 ents with [125I]-alphaBgTx demonstrated that stratum radiatum interneurons express alpha7-containing

85 investigated in outside-out patches from CA1 stratum radiatum interneurons from thin slices of rat hi

86 y evokes pathway-specific LTP in half of rat stratum radiatum interneurons if cytoplasmic integrity i

87 hR, on GABAergic activity in hippocampal CA1 stratum radiatum interneurons in acute rat brain slices.

88 this PAM on both CA1 pyramidal cells and CA1 stratum radiatum interneurons in immature hippocampus.

89 These data suggest that rat hippocampal CA1 stratum radiatum interneurons in the slice possess at le

90 by exogenous application of agonists to CA1 stratum radiatum interneurons was approximately 65% high

91 oleculare axon arborization (P-LM cells) and stratum radiatum interneurons with lacunosum-moleculare

92 of stratum lucidum interneurons, but not of stratum radiatum interneurons, displayed a Hebbian form

93 on potentiated MF glutamatergic responses of stratum radiatum interneurons, whereas in stratum lucidu

94 d were alpha4, alpha5, alpha7 and beta2-4 in stratum radiatum interneurons; alpha2, alpha3, alpha4, a

95 tex (ERC) and CA1 apical neuropil layer [CA1-stratum radiatum lacunosum moleculare (SRLM)] thickness,

96 ession was predominantly detected in CA1/CA3 stratum radiatum/lacunosum moleculare and the dentate gy

97 Interneurons in stratum radiatum/lacunosum-moleculare express KARs both

98 er 5 pyramidal neurons of the RSG to the CA1 stratum radiatum/lacunosum-moleculare of the dorsal hipp

99 power became significantly diminished in the stratum radiatum lamina of the GAD67-GFP (Deltaneo) mous

100 s of FM1-43 destaining from terminals in CA1 stratum radiatum, mostly representing excitatory termina

101 he subcellular localization of CaMKII in CA1 stratum radiatum of adult rat hippocampus, by using immu

102 or NMDARs in serial sections through the CA1 stratum radiatum of adult rats.

103 sine release induced by focal stimulation in stratum radiatum of area CA1 in mouse hippocampal slices

104 cordings from visualized interneurons in the stratum radiatum of area CA1 in rat hippocampal slices.

105 pulation of CA3-->CA1 axons in the middle of stratum radiatum of area CA1.

106 icant increase in dendritic spine density in stratum radiatum of CA1 and in the dentate gyrus.

107 results indicate that synaptic plasticity in stratum radiatum of CA1 can be homeostatically regulated

108 By LM, the density of pAkt-I in stratum radiatum of CA1 was significantly higher in proe

109 ation in endothelial NOS (eNOS-), but LTP in stratum radiatum of CA1 was significantly reduced in dou

110 citatory postsynaptic potentials (pEPSPs) in stratum radiatum of CA1 were eliminated 10-15 min after

111 pine and excitatory synapse densities in the stratum radiatum of CA1, as determined by morphology, ap

112 rboxylase were significantly depleted in the stratum radiatum of CA1, the strata oriens, radiatum and

113 ane of asymmetric axospinous synapses in the stratum radiatum of CA1, whereas sGCbeta concentrates ju

114 ically reduced Kv1.1 immunoreactivity in the stratum radiatum of CA1-CA3, indicating that Kv1.1 immun

115 homogeneous SP innervation was found in the stratum radiatum of CA1.

116 m ([Ca2+]i) in the astrocytes located in the stratum radiatum of CA1.

117 ticity in a subpopulation of synapses in the stratum radiatum of CA1.

118 d preference, innervating stratum oriens and stratum radiatum of CA2 and CA1 but stopping abruptly at

119 ewer were seen in the dentate hilar area and stratum radiatum of CA2 and CA3, and even fewer were see

120 The level of pDOR-ir in stratum radiatum of CA2/CA3a was increased in control es

121 tionships between astrocytes and synapses in stratum radiatum of hippocampal area CA1 in the mature r

122 tratum oriens inhibits subsequent LTP in the stratum radiatum of hippocampal area CA1, potentially by

123 We tested this hypothesis in the CA1 stratum radiatum of hippocampal slices from juvenile rat

124 ynaptic potentials (fEPSPs) were recorded in stratum radiatum of hippocampal subfield CA1 in response

125 estimates of the total number of MSBs in the stratum radiatum of hippocampal subfield CA1.

126 Synapses were examined in the stratum radiatum of hippocampal subfield CA1.

127 the effects of tetanic burst stimulation in stratum radiatum of region CA1 in awake behaving animals

128 ion in clustered gephyrin is detected in CA1 stratum radiatum of rTMS-treated anaesthetized mice.

129 mined extracellularly at CA3-CA1 synapses in stratum radiatum of slices from adult (6-9 months) and a

130 nding was detected in the stratum oriens and stratum radiatum of the CA1 and CA2 subfields, in the st

131 ivo, we identified an ENK-expressing cell in stratum radiatum of the CA1 area by its complete axodend

132 timulation of the surviving afferents in the stratum radiatum of the CA1 area in kainic acid-lesioned

133 xcitatory postsynaptic potentials (pEPSP) in stratum radiatum of the CA1 area were compared.

134 excitatory postsynaptic potential throughout stratum radiatum of the CA1 field (sharp wave).

135 ing potassium, caesium or rubidium ions into stratum radiatum of the CA1 or CA3 regions of the hippoc

136 t spike-timing properties were identified in stratum radiatum of the CA1 rat hippocampus.

137 n granule cells of the dentate gyrus and the stratum radiatum of the CA1 region and were dependent on

138 on in the hilus of the dentate gyrus and the stratum radiatum of the CA1 region, (3) the density of E

139 nd overall changes in synapse density in the stratum radiatum of the CA1 subfield.

140 2A-infected C57BL mice, predominantly in the stratum radiatum of the CA1, CA2 and CA3 areas of the hi

141 and altered the structure of synapses in the stratum radiatum of the hippocampus.

142 Ch) receptors in interneurons located in the stratum radiatum of the hippocampus.

143 n CA1 in vitro by tetanic stimulation of the stratum radiatum or oriens were analysed using intracell

144 stratum lacunosum moleculare (P < 0.01), the stratum radiatum (P < 0.005), and the stratum oriens (P

145 t hippocampal inhibitory neurones located in stratum radiatum possess multiple calcium channel subtyp

146 tum pyramidale that feature current sinks in stratum radiatum (Rad(sink)) versus stratum lacunosum-mo

147 itatory synapses on pyramidal neurons in the stratum radiatum rarely occurs in hippocampal area CA2.

148 o stratum oriens) and superficial (closer to stratum radiatum) rat CA1 PCs during sharp-wave ripples.

149 Many interneurons in stratum lucidum and stratum radiatum receive both signals, while those in st

150 rvation of GluN1/GluN2A receptors in the CA1 stratum radiatum region during BZ withdrawal.

151 of EPSP recorded from stratum pyramidale and stratum radiatum respectively.

152 h) to the soma of inhibitory interneurons in stratum radiatum resulted in depolarization and rapid fi

153 Extracellular field EPSP recordings in the stratum radiatum showed a gradual increase in the effect

154 ed with preceding presynaptic stimulation in stratum radiatum specifically led to LTP of the paired p

155 reased synaptogenesis in the hippocampal CA1 stratum radiatum (sr) and enhances memory in young and s

156 Repetitive synaptic stimulation in the stratum radiatum (SR) evokes large amplitude Ca2+ waves

157 cally at Schaffer collateral synapses in the stratum radiatum (SR) in CA1.

158 In contrast, in the stratum radiatum (SR) of CA1, Nav 1.1, Nav 1.2, and Nav

159 The percentage of GluR1 positively labeled stratum radiatum (SR) synapses was significantly increas

160 essively distal regions: proximal and distal stratum radiatum (SR), and stratum lacunosum-moleculare

161 urons in two layers, stratum oriens (SO) and stratum radiatum (SR).

162 ulare (SLM) of the dCA1 area, but not in the stratum radiatum (SR).

163 ramifying throughout stratum oriens (SO) and stratum radiatum (SR).

164 d on excitation evoked by stimulation of the stratum radiatum (SR, which contains the SC) using volta

165 es in 2-DG uptake in the dentate gyrus, CA-3 stratum radiatum, stratum lacunosum moleculare, and pres

166 Hippocampal non-principal neurons at the stratum radiatum-stratum lacunosum-moleculare border (R-

167 luN2A, and GluN2B subunits was sought at CA1 stratum radiatum synapses in proximal dendrites using po

168 erals elicits an alkaline pH(e) transient in stratum radiatum that is limited by extracellular carbon

169 ) and myelin in the sensorimotor cortex, the stratum radiatum, the corpus callosum, and the anterior

170 In the hippocampal CA1 stratum radiatum, the values of the CB1 receptor-immunop

171 ugh coded serial electron micrographs of CA1 stratum radiatum to determine the: (1) frequency of mult

172 ys 5 and 15, many cells seem to migrate from stratum radiatum to its border with stratum lacunosum-mo

173 Axospinous synapses from the CA1 stratum radiatum were analyzed using systematic random s

174 Axons in CA1 stratum radiatum were evaluated with 3D reconstructions

175 adjacent protoplasmic astrocytes in the CA1 stratum radiatum were injected with fluorescent intracel

176 l and glial pTrkB-ir and pTrkB-ir in the CA1 stratum radiatum were more abundant in high-estradiol st

177 Indeed, these changes were seen in the stratum radiatum where synaptic pathology is readily det

178 urons with pyramidal morphology found in the stratum radiatum, which we termed the 'pyramidal-like pr

179 mum, negative going potentials in the distal stratum radiatum while proximal stimulation recordings w

180 iasing" neurons, in that synaptic volleys in stratum radiatum would lead to their activation, which i