ライフサイエンスコーパス: radiatum

1 have a more proximal location in the stratum radiatum.

2 ns potentiation following pairing in stratum radiatum.

3 F, but slightly more numerous in CA1 stratum radiatum.

4 the volume of CA1 stratum oriens and stratum radiatum.

5 of stratum lacunosum-moleculare and stratum radiatum.

6 tern, with zeta prominent in the CA1 stratum radiatum.

7 enters into individual spines in the stratum radiatum.

8 a but not in interneurons located in stratum radiatum.

9 immunoreactivity was enhanced in CA1 stratum radiatum.

10 in hippocampal astrocytes located in stratum radiatum.

11 of stimulation electrode position in stratum radiatum.

12 d excitatory field potentials in CA1 stratum radiatum.

13 ay-associated inhibitory synapses in stratum radiatum.

14 vesicular glutamate transporter 1 in stratum radiatum.

15 MMP-3 expression and activity in CA1 stratum radiatum.

16 rs GLAST and GFAP in rat hippocampal stratum radiatum.

17 ntrol of mTOR, increased in area CA1 stratum radiatum.

18 .87%), stratum pyramidale (40%), and stratum radiatum (56.6%).

19 A1 field potentials in strata pyramidale and radiatum and assessed neuroplasticity by inducing long-t

20 gyrus inner molecular layer and CA1 stratum radiatum and in (ii) postsynaptic densities and microtub

21 d from GABAergic interneurons in CA1 stratum radiatum and induced membrane depolarization suggesting

22 reactivity in interneurons located in strata radiatum and L-M of area CA3.

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

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

25 observed only when stimulating in the strata radiatum and pyramidale but not in the stratum oriens.

26 stratum radiatum of CA1, the strata oriens, radiatum and pyramidale of CA3, the dentate molecular la

27 sharp electrodes were carried out in stratum radiatum and pyramidale.

28 CA1 pyramidal neurons predominate in stratum radiatum and receive approximately 80% of the synaptic i

29 sed by stimulating either the alveus or str. radiatum and recording the extracellular response from s

30 were concentrated at the border between str. radiatum and str. lacunosum-moleculare.

31 )S]TBPS binding, particularly between strata radiatum and strata oriens, suggesting a functional hete

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

33 entorhinal cortex (ERC) and then CA1 stratum radiatum and stratum lacunosum-moleculare (CA1-SRLM)--tw

34 heterotopic and displaced into both stratum radiatum and stratum lacunosum-moleculare.

35 opulation of immunopositive cells in stratum radiatum and stratum oriens in area CA1 during the first

36 ncated trkB.T1 mRNA receptors in the stratum radiatum and stratum oriens of the CA3 subfield.

37 eloped cytoarchitecture, such as the stratum radiatum and stratum oriens of the hippocampus, the mole

38 ransporter) in interneurons from the stratum radiatum and stratum oriens, and in CA1 pyramidal neuron

39 dence that NOS is involved in LTP in stratum radiatum and suggest that the neuronal and endothelial f

40 NOS-independent component of LTP in stratum radiatum and that LTP in stratum oriens is largely NOS i

41 rimarily with preexisting boutons in stratum radiatum and that these boutons enlarge and change shape

42 coherence between signals derived from str. radiatum and the dentate molecular layer.

43 f the CA1 region and (2) between CA1 stratum radiatum and the dentate molecular layer.

44 -immunoreactive spine numbers in CA1 stratum radiatum and the inner and outer molecular layers of den

45 re seen at the border between the CA1 strata radiatum and the lacunosum moleculare of CA1 subfield.

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

47 Surprisingly, paired radiatum and unpaired oriens pathway potentiated, unless

48 interneurons (n = 10) stratifying in stratum radiatum and, to a lesser extent, stratum oriens; (3) pe

49 cillatory potentials reversed in the stratum radiatum and/or in the stratum oriens.

50 CA3 pyramidal cell apical dendrites (stratum radiatum) and an increase in the number of thorny excres

51 out neuronal cell bodies, dendrites (stratum radiatum), and axons (fimbria), but not astrocytes.

52 , though still apparent, staining of stratum radiatum, and (c) a decrease in amplitude and slope of f

53 n, especially in the hippocampal CA1 stratum radiatum, and also diminishes GABA-mediated synaptic tra

54 An epitype is designed for S. radiatum, and its sequences have been deposited in GenBa

55 bution of alpha2A-AR-I in the strata oriens, radiatum, and lacunosum-moleculare of hippocampal CA1 an

56 1: the proximal and distal thirds of stratum radiatum, and the stratum lacunosum-moleculare.

57 sal synaptic transmission in the CA1 stratum radiatum appeared unaffected, whereas spontaneous neuron

58 We found that the spine density in stratum radiatum ( approximately 1.1 per micrometer) remained st

59 oking Ca2+ increases in the adjacent stratum radiatum astrocytes by uncaging IP3.

60 read Ca(2+) elevations in 80%-90% of stratum radiatum astrocytes do not increase neuronal Ca(2+), pro

61 nterneurons from stratum lucidum and stratum radiatum, but not in interneurons from stratum lacunosum

62 ectivity was highest in the proximal stratum radiatum, but only for those MSBs composed of nonperfora

63 nent in the extracellularly recorded stratum radiatum CA(1) field potential under low stimulation con

64 detected in neurons and astrocytes in CA1 s. radiatum, CA2 and CA3 s. pyramidale, and molecular layer

65 hippocampal formation including CA2 stratum radiatum, CA3 stratum radiatum, hilus dentate gyrus and

66 In stratum radiatum, cell loss is particularly dramatic.

67 clinical isolates were in the Schizophyllum radiatum clade with high support values and 1 isolate wa

68 responses induced by stimulation in stratum radiatum consisted of a single population spike in PrP g

69 hat numerous dendritic spines in the stratum radiatum contained the NR2 subunit of the NMDA receptor

70 t the shafts and in select spines of stratum radiatum dendrites.

71 GABAergic LTP, while interneurons of stratum radiatum, despite receiving this dual signaling, do not

72 llateral/commissural synapses in the stratum radiatum differ from those at mossy fibers but are simil

73 In the stratum radiatum, estradiol, DPN, and PPT increased PSD-95 and A

74 Because str. radiatum-evoked PPI was selectively impaired, PILO appea

75 tors contribute to hippocampal CA(1) stratum radiatum excitatory postsynaptic potentials (EPSP) is a

76 Areas such as the dentate and stratum radiatum exhibited higher CL signals than other areas wi

77 (fEPSPs) were recorded from the CA1 stratum radiatum following stimulation of the Schaffer collatera

78 nosum-moleculare and the superficial stratum radiatum, GIRK1-IR was often present immediately adjacen

79 lices where the dendrites located in stratum radiatum have been isolated from their cell bodies by a

80 including CA2 stratum radiatum, CA3 stratum radiatum, hilus dentate gyrus and presubiculum, and in t

81 itive to stimulation position in the stratum radiatum; i.e., distal stimulation elicited maximum, neg

82 ected in both stratum pyramidale and stratum radiatum in area CA1.

83 c shafts and spines) profiles in the stratum radiatum in the hippocampal CA1 region.

84 sal activities or stimulation of the stratum radiatum increases the efficacy of GABAergic synapses by

85 increased GR signal was seen in the stratum radiatum, indicating redistribution of GR to the cytosol

86 Hippocampal stratum radiatum inhibitory interneurons receive glutamatergic e

87 ynapses onto CA1 pyramidal cells and stratum radiatum interneurones are due to a higher initial relea

88 aining nAChRs in rat hippocampal CA1 stratum radiatum interneurones in slices, we describe a novel tr

89 lateral excitatory synapses onto CA1 stratum radiatum interneurones versus pyramidal cells in acute h

90 the membrane of rat hippocampal CA1 stratum radiatum interneurons and pyramidal cells in acute slice

91 ilitate excitatory transmission onto stratum radiatum interneurons but not onto CA1 pyramidal neurons

92 h [125I]-alphaBgTx demonstrated that stratum radiatum interneurons express alpha7-containing nAChRs,

93 ated in outside-out patches from CA1 stratum radiatum interneurons from thin slices of rat hippocampu

94 pathway-specific LTP in half of rat stratum radiatum interneurons if cytoplasmic integrity is preser

95 ABAergic activity in hippocampal CA1 stratum radiatum interneurons in acute rat brain slices.

96 ata suggest that rat hippocampal CA1 stratum radiatum interneurons in the slice possess at least two

97 distinct classes of cells were observed: st. radiatum interneurons that showed neither direct nor pro

98 enous application of agonists to CA1 stratum radiatum interneurons was approximately 65% higher in mK

99 e axon arborization (P-LM cells) and stratum radiatum interneurons with lacunosum-moleculare axon arb

100 tum lucidum interneurons, but not of stratum radiatum interneurons, displayed a Hebbian form of LTP t

101 tiated MF glutamatergic responses of stratum radiatum interneurons, whereas in stratum lucidum intern

102 lpha4, alpha5, alpha7 and beta2-4 in stratum radiatum interneurons; alpha2, alpha3, alpha4, alpha7, b

103 ) and CA1 apical neuropil layer [CA1-stratum radiatum lacunosum moleculare (SRLM)] thickness, and (ii

104 as predominantly detected in CA1/CA3 stratum radiatum/lacunosum moleculare and the dentate gyrus.

105 Interneurons in stratum radiatum/lacunosum-moleculare express KARs both with and

106 came significantly diminished in the stratum radiatum lamina of the GAD67-GFP (Deltaneo) mouse compar

107 rs from the hilar border, in the lucidum and radiatum layers.

108 -43 destaining from terminals in CA1 stratum radiatum, mostly representing excitatory terminals of Sc

109 llular localization of CaMKII in CA1 stratum radiatum of adult rat hippocampus, by using immuno-elect

110 s in serial sections through the CA1 stratum radiatum of adult rats.

111 ease induced by focal stimulation in stratum radiatum of area CA1 in mouse hippocampal slices.

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

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

114 highly significant in the strata oriens and radiatum of both CA1 and CA3 subfields and in the dentat

115 crease in dendritic spine density in stratum radiatum of CA1 and in the dentate gyrus.

116 indicate that synaptic plasticity in stratum radiatum of CA1 can be homeostatically regulated by the

117 By LM, the density of pAkt-I in stratum radiatum of CA1 was significantly higher in proestrus ra

118 endothelial NOS (eNOS-), but LTP in stratum radiatum of CA1 was significantly reduced in doubly muta

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

120 excitatory synapse densities in the stratum radiatum of CA1, as determined by morphology, apposition

121 e were significantly depleted in the stratum radiatum of CA1, the strata oriens, radiatum and pyramid

122 symmetric axospinous synapses in the stratum radiatum of CA1, whereas sGCbeta concentrates just insid

123 ayer, and increases in the strata oriens and radiatum of CA1-3.

124 educed Kv1.1 immunoreactivity in the stratum radiatum of CA1-CA3, indicating that Kv1.1 immunoreactiv

125 n a subpopulation of synapses in the stratum radiatum of CA1.

126 eous SP innervation was found in the stratum radiatum of CA1.

127 ]i) in the astrocytes located in the stratum radiatum of CA1.

128 ence, innervating stratum oriens and stratum radiatum of CA2 and CA1 but stopping abruptly at the CA2

129 e seen in the dentate hilar area and stratum radiatum of CA2 and CA3, and even fewer were seen at the

130 The level of pDOR-ir in stratum radiatum of CA2/CA3a was increased in control estrus (el

131 ased PSD95-IR in strata oriens, lucidum, and radiatum of CA3 in ovariectomized mice 6 h after adminis

132 eased significantly in the strata oriens and radiatum of CA3, in the dentate granule cell and molecul

133 s between astrocytes and synapses in stratum radiatum of hippocampal area CA1 in the mature rat in vi

134 We tested this hypothesis in the CA1 stratum radiatum of hippocampal slices from juvenile rats, using

135 potentials (fEPSPs) were recorded in stratum radiatum of hippocampal subfield CA1 in response to elec

136 s of the total number of MSBs in the stratum radiatum of hippocampal subfield CA1.

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

138 The CA1 striatum radiatum of rat hippocampal slices was monitored by conf

139 ects of tetanic burst stimulation in stratum radiatum of region CA1 in awake behaving animals, delive

140 lustered gephyrin is detected in CA1 stratum radiatum of rTMS-treated anaesthetized mice.

141 tracellularly at CA3-CA1 synapses in stratum radiatum of slices from adult (6-9 months) and aged (20-

142 s detected in the stratum oriens and stratum radiatum of the CA1 and CA2 subfields, in the stratum or

143 identified an ENK-expressing cell in stratum radiatum of the CA1 area by its complete axodendritic ar

144 on of the surviving afferents in the stratum radiatum of the CA1 area in kainic acid-lesioned hippoca

145 y postsynaptic potentials (pEPSP) in stratum radiatum of the CA1 area were compared.

146 ry postsynaptic potential throughout stratum radiatum of the CA1 field (sharp wave).

147 ssium, caesium or rubidium ions into stratum radiatum of the CA1 or CA3 regions of the hippocampal sl

148 timing properties were identified in stratum radiatum of the CA1 rat hippocampus.

149 e cells of the dentate gyrus and the stratum radiatum of the CA1 region and were dependent on UCP2 ex

150 e hilus of the dentate gyrus and the stratum radiatum of the CA1 region, (3) the density of ER-ir cel

151 ll changes in synapse density in the stratum radiatum of the CA1 subfield.

152 ted C57BL mice, predominantly in the stratum radiatum of the CA1, CA2 and CA3 areas of the hippocampu

153 napses was observed in the strata oriens and radiatum of the CA3a and CA2 regions, and a few were fou

154 fibers in the strata oriens, pyramidale, and radiatum of the CA3a and CA2 subfields.

155 red the structure of synapses in the stratum radiatum of the hippocampus.

156 ptors in interneurons located in the stratum radiatum of the hippocampus.

157 vitro by tetanic stimulation of the stratum radiatum or oriens were analysed using intracellular and

158 l types was primarily restricted to striatum radiatum or to striatum lacunosum-moleculare in the case

159 lacunosum moleculare (P < 0.01), the stratum radiatum (P < 0.005), and the stratum oriens (P < 0.05)

160 o 5 ms, which selectively potentiated paired radiatum pathway, since unpaired oriens pathway decrease

161 ampal inhibitory neurones located in stratum radiatum possess multiple calcium channel subtypes, incl

162 collaterals), which terminate in the strata radiatum, pyramidale, and oriens, are present throughout

163 rticular, interneurons with somata in strata radiatum (R) and lacunosum-moleculare (L-M) receive conv

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

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

166 interneurons in stratum lucidum and stratum radiatum receive both signals, while those in stratum la

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

168 recorded from stratum pyramidale and stratum radiatum respectively.

169 d 77.53% reduction in the stratum oriens and radiatum, respectively, when compared with controls.

170 e soma of inhibitory interneurons in stratum radiatum resulted in depolarization and rapid firing of

171 ellular field EPSP recordings in the stratum radiatum showed a gradual increase in the effective stim

172 In general, the strains of S. radiatum showed higher MICs than S. commune.

173 preceding presynaptic stimulation in stratum radiatum specifically led to LTP of the paired pathway i

174 ynaptogenesis in the hippocampal CA1 stratum radiatum (sr) and enhances memory in young and some aged

175 petitive synaptic stimulation in the stratum radiatum (SR) evokes large amplitude Ca2+ waves in the t

176 Schaffer collateral synapses in the stratum radiatum (SR) in CA1.

177 In contrast, in the stratum radiatum (SR) of CA1, Nav 1.1, Nav 1.2, and Nav 1.6 were

178 rcentage of GluR1 positively labeled stratum radiatum (SR) synapses was significantly increased in FZ

179 distal regions: proximal and distal stratum radiatum (SR), and stratum lacunosum-moleculare (SLM).

180 g throughout stratum oriens (SO) and stratum radiatum (SR).

181 two layers, stratum oriens (SO) and stratum radiatum (SR).

182 itation evoked by stimulation of the stratum radiatum (SR, which contains the SC) using voltage-sensi

183 interpulse intervals occurred following str. radiatum stimulation in the presence of PILO and 5 mM [K

184 long lasting loss of PPI that followed str. radiatum stimulation.

185 ed from the CA1 hippocampus following CA1 s. radiatum stimulation.

186 DG uptake in the dentate gyrus, CA-3 stratum radiatum, stratum lacunosum moleculare, and presubiculum

187 ocampal non-principal neurons at the stratum radiatum-stratum lacunosum-moleculare border (R-LM inter

188 nd GluN2B subunits was sought at CA1 stratum radiatum synapses in proximal dendrites using postembedd

189 icits an alkaline pH(e) transient in stratum radiatum that is limited by extracellular carbonic anhyd

190 elin in the sensorimotor cortex, the stratum radiatum, the corpus callosum, and the anterior commissu

191 In the hippocampal CA1 stratum radiatum, the values of the CB1 receptor-immunopositive

192 d serial electron micrographs of CA1 stratum radiatum to determine the: (1) frequency of multiple (MS

193 15, many cells seem to migrate from stratum radiatum to its border with stratum lacunosum-moleculare

194 In st. radiatum, two distinct classes of cells were observed: s

195 Axospinous synapses from the CA1 stratum radiatum were analyzed using systematic random sampling

196 Axons in CA1 stratum radiatum were evaluated with 3D reconstructions from ser

197 t protoplasmic astrocytes in the CA1 stratum radiatum were injected with fluorescent intracellular tr

198 ial pTrkB-ir and pTrkB-ir in the CA1 stratum radiatum were more abundant in high-estradiol states (pr

199 deed, these changes were seen in the stratum radiatum where synaptic pathology is readily detected, i

200 e astrocytes were predominantly found in CA3 radiatum, whereas most CA1 astrocytes were Cs+-insensiti

201 th pyramidal morphology found in the stratum radiatum, which we termed the 'pyramidal-like principal'

202 ative going potentials in the distal stratum radiatum while proximal stimulation recordings were maxi

203 neurons, in that synaptic volleys in stratum radiatum would lead to their activation, which in turn w