ライフサイエンスコーパス: stratum oriens

1 vicinity of the recording electrodes in the stratum oriens.

2 in interneurons with cell bodies in the CA1 stratum oriens.

3 trata radiatum and pyramidale but not in the stratum oriens.

4 the dentate supragranular layer and the CA3 stratum oriens.

5 acunosum-moleculare and decreased numbers in stratum oriens.

6 c activity at all; half of these were in the stratum oriens.

7 versed in the stratum radiatum and/or in the stratum oriens.

8 alpha-BTX neurons were most prevalent in CA1 stratum oriens.

9 in stratum radiatum and, to a lesser extent, stratum oriens; (3) perforant pathway-associated interne

10 uction of NAAG-immunoreactive neurons in CA3 stratum oriens (35.8%) and CA1 stratum oriens (78.87%),

11 eurons in CA3 stratum oriens (35.8%) and CA1 stratum oriens (78.87%), stratum pyramidale (40%), and s

12 dendrites extending into all CA subfields in stratum oriens, adapting firing patterns and a pronounce

13 long-term potentiation (LTP) in hippocampal stratum oriens-alveus (O/A) interneurons requires co-act

14 somata and dendrites, which were confined to stratum oriens-alveus and their axons which projected to

15 idal cells in CA1 and interneurones near the stratum oriens-alveus border revealed excitatory connect

16 le in pacemaking activity in rat hippocampal stratum oriens-alveus interneurones was studied using wh

17 eration of spontaneous firing in hippocampal stratum oriens-alveus interneurones.

18 dal neuron basilar dendrites extend into the stratum oriens-alveus while the apical dendrites project

19 stribution of the alpha5-GABA(A)R in the CA1 stratum oriens/alveus (O/A) using a combination of immun

20 s of interneurons within the hippocampal CA1 stratum oriens/alveus (O/A), with preferential innervati

21 mulation of distal dendritic branches within stratum oriens/alveus elicited fast Ca2+ transients, whi

22 ) and somatostatin (SOM) interneurons in CA1 stratum oriens/alveus fire during hippocampal theta and

23 nearby somatostatin interneurons in the CA1 stratum oriens and dentate hilus (which themselves do no

24 ion was observed in selected interneurons in stratum oriens and in the hilus of the dentate gyrus.

25 matostatin-expressing cells predominantly in stratum oriens and parvalbumin-expressing cells mostly i

26 me of these structures were also observed in stratum oriens and piriform cortex, and in cerebellar Pu

27 erized by 71.82% and 77.53% reduction in the stratum oriens and radiatum, respectively, when compared

28 the physiological properties of hippocampal stratum oriens and stratum pyramidale inhibitory interne

29 ed striking subfield preference, innervating stratum oriens and stratum radiatum of CA2 and CA1 but s

30 Angiotensin II binding was detected in the stratum oriens and stratum radiatum of the CA1 and CA2 s

31 no seasonal variations, in the volume of CA1 stratum oriens and stratum radiatum.

32 pical dendrites and in interneurons in CA1-3 stratum oriens and the dentate hilus.

33 ite membrane polarization of deep (closer to stratum oriens) and superficial (closer to stratum radia

34 /alpha2 co-expression was located in CA1/CA3 stratum oriens, and GAD67/alpha5 co-expression was predo

35 ng responses, was localized primarily to the stratum oriens, and had axonal projections to the stratu

36 well as in calbindin-positive neurons in the stratum oriens, and in a small number of interneurons th

37 n interneurons from the stratum radiatum and stratum oriens, and in CA1 pyramidal neurons.

38 recordings, Nkx2.1-Cre+ interneurons in the stratum oriens, but not Chrna2-Cre+ or Htr3a-GFP+ cells,

39 spine density, as well as increased basilar (stratum oriens) CA3 spine density.

40 e stimulus, delivered extracellularly in the stratum oriens, caused a reduction in spike frequency ad

41 In contrast, stratum oriens cell types with axon arborization pattern

42 ated microglia in the denervated hippocampal stratum oriens did not migrate extensively, whereas huma

43 GluR5-containing KARs on interneurons in stratum oriens do not contribute substantially to the EP

44 transmission to hippocampal interneurons in stratum oriens does not require NMDA receptors and the i

45 ular-spiking interneurons in the hippocampal stratum oriens exhibit a form of long-term potentiation

46 ratified cells in the stratum pyramidale; in stratum oriens, HC PV cells were electrophysiologically

47 ctrophysiological properties differentiating stratum oriens horizontal interneurons from pyramidal ne

48 ibitory input to pyramidal cells, but not to stratum oriens horizontal interneurons.

49 In particular, stratum oriens 'horizontal' interneurones are easily rec

50 immunopositive cells in stratum radiatum and stratum oriens in area CA1 during the first postnatal we

51 strong high-frequency priming stimulation in stratum oriens inhibits subsequent LTP in the stratum ra

52 nce in the resting membrane potential of CA1 stratum oriens interneurones persistently increased foll

53 of muscarinic receptor (mAChR) activation on stratum oriens interneurones using whole-cell patch clam

54 e both Ih and Girk in the same population of stratum oriens interneurons and that the modulation of t

55 ta frequency spiking activity in a subset of stratum oriens interneurons controlling electrogenesis i

56 re all temporally correlated with spiking in stratum oriens interneurons demonstrating intrinsic thet

57 d bupivacaine) was detected in 30-50% of CA1 stratum oriens interneurons of various morphological cla

58 ibitory postsynaptic currents (IPSCs) in CA1 stratum oriens interneurons.

59 reset the phase of spontaneously firing CA1 stratum oriens interneurons.

60 alpha4, alpha7, beta2 and beta3 subunits in stratum oriens interneurons; and beta2-4 in pyramidal ne

61 t of LTP in stratum radiatum and that LTP in stratum oriens is largely NOS independent.

62 ge, sustained afterdepolarizations (ADPs) of stratum oriens-lacunosum moleculare (O-LM) interneurones

63 rea power of the oscillatory activity in the stratum oriens lamina of CA3, but for the kainate-induce

64 to depolarise GABAergic interneurons in the stratum oriens layer of the hippocampus.

65 synaptic plasticity in stratum radiatum and stratum oriens layers of both ventral and dorsal hippoca

66 on CA1 neurons in the stratum pyramidale and stratum oriens layers of KO hippocampus may contribute t

67 In CA3 pyramidal cells and stratum oriens non-fast-spiking and fast-spiking interne

68 , respectively) on GABAergic interneurons in stratum oriens of area CA1 of the hippocampus were exami

69 by electron microscopy (cortex, CPN, and the stratum oriens of CA1), PROT labeling was observed prima

70 The entire CA2 region, the stratum oriens of CA1, CA3, and the subiculum were dense

71 small, though significant, increases in the stratum oriens of CA3 (30%), the subiculum (20-30%) and

72 sitive deposits were found in the subiculum, stratum oriens of hippocampal field CA1, and the hilus o

73 nterneurons possessing somata located within stratum oriens of hippocampal slices were classified acc

74 vity in both the mossy fiber pathway and CA3 stratum oriens of hippocampus.

75 unoreactive neurons could be observed in the stratum oriens of the Ammon's horn and subiculum, fewer

76 ween SP-containing boutons and somata in the stratum oriens of the Ammon's horn.

77 ed GAD-67-immunopositive interneurons in the stratum oriens of the CA1 region of the hippocampus, acc

78 campus but were particularly concentrated in stratum oriens of the CA1 region.

79 adiatum of the CA1 and CA2 subfields, in the stratum oriens of the CA3 subfield, and in the molecular

80 1 mRNA receptors in the stratum radiatum and stratum oriens of the CA3 subfield.

81 he traced pathway and ran exclusively in the stratum oriens of the hilus and CA3.

82 pathway, the endfolial fiber pathway, in the stratum oriens of the hilus and field CA3.

83 esynaptic profiles were most concentrated in stratum oriens of the hippocampal CA1 region and dentate

84 om alpha(1A)-AR EGFP-expressing cells in the stratum oriens of the hippocampal CA1 region confirmed t

85 orylation in the mossy fiber pathway and CA3 stratum oriens of the hippocampus during limbic epilepto

86 In stratum oriens of the hippocampus, EGFP-expressing inter

87 chitecture, such as the stratum radiatum and stratum oriens of the hippocampus, the molecular and gra

88 Many interneurons located in stratum oriens of the rodent hippocampus exhibit a form

89 iring patterns, are primarily located in the stratum oriens or pyramidale, have sparsely spiny dendri

90 ), the stratum radiatum (P < 0.005), and the stratum oriens (P < 0.05) of the hippocampus.

91 Conversely, the exact same 5 ms pairing in stratum oriens potentiated both pathways, as did AP-burs

92 nd adenosine receptors counteracted unpaired stratum oriens potentiation following pairing in stratum

93 al stimulation of GABAergic terminals at the stratum oriens-pyramidale (SO-SP) or stratum lacunosum-m

94 Stimulation in stratum oriens reliably elicited a slow mGluR1-mediated

95 Horizontal interneurones in the stratum oriens showed firing preference to inputs at the

96 es and regulate synaptic transmission in the stratum oriens (SO) and lacunosum-moleculare (SLM) of th

97 tified cells with axons ramifying throughout stratum oriens (SO) and stratum radiatum (SR).

98 orm synapses with CA1 neurons in two layers, stratum oriens (SO) and stratum radiatum (SR).

99 ivation on the oscillatory properties of CA1 stratum oriens (SO) interneurones in vitro.

100 Here, we investigated I(M) in hippocampal stratum oriens (SO) interneurons, both from wild-type an

101 ange was a down-regulation of GAD(67) in the stratum oriens (SO) of CA2/3 in both groups; CA1 only sh

102 repair, is significantly up-regulated in the stratum oriens (SO) of CA3/2 and CA1 in SZs and BDs.

103 In particular, stratum oriens SST cells display severe axonal dysmyelin

104 We extracted DNA from laser-microdissected stratum oriens tissue of cornu ammonis 2/3 (CA2/3) and C

105 By contrast, LTP in stratum oriens was normal in the doubly mutant mice.

106 f CA2 axon fluorescence intensity in the CA1 stratum oriens, where CA2 axons preferentially project,