ライフサイエンスコーパス: stratum radiatum

1 tum oriens potentiation following pairing in 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 ophysin immunoreactivity was enhanced in CA1 stratum radiatum.

9 urrents in hippocampal astrocytes located in stratum radiatum.

10 pendent of stimulation electrode position in stratum radiatum.

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

12 al pathway-associated inhibitory synapses in stratum radiatum.

13 protein vesicular glutamate transporter 1 in stratum radiatum.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

53 In stratum radiatum, cell loss is particularly dramatic.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

71 Hippocampal stratum radiatum inhibitory interneurons receive glutama

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

130 2A-infected C57BL mice, predominantly in the stratum radiatum of the CA1, CA2 and CA3 areas of the hi

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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