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1 ty at all; half of these were in the stratum oriens.
2 n the stratum radiatum and/or in the stratum oriens.
3 y of the recording electrodes in the stratum oriens.
4 X neurons were most prevalent in CA1 stratum oriens.
5 rneurons with cell bodies in the CA1 stratum oriens.
6 diatum and pyramidale but not in the stratum oriens.
7 tate supragranular layer and the CA3 stratum oriens.
8 -moleculare and decreased numbers in stratum oriens.
9 s/alveus and innervated stratum radiatum and oriens.
11 um radiatum and, to a lesser extent, stratum oriens; (3) perforant pathway-associated interneurons (n
12 f NAAG-immunoreactive neurons in CA3 stratum oriens (35.8%) and CA1 stratum oriens (78.87%), stratum
13 n CA3 stratum oriens (35.8%) and CA1 stratum oriens (78.87%), stratum pyramidale (40%), and stratum r
14 ive labeling of SOM-expressing neurons in s. oriens, a Cre recombinase-dependent construct for channe
15 s extending into all CA subfields in stratum oriens, adapting firing patterns and a pronounced "sag"
16 rm potentiation (LTP) in hippocampal stratum oriens-alveus (O/A) interneurons requires co-activation
17 ry synapses onto hippocampal interneurons in oriens-alveus (OA-INs) which is induced by activation of
18 nd dendrites, which were confined to stratum oriens-alveus and their axons which projected to stratum
20 ls in CA1 and interneurones near the stratum oriens-alveus border revealed excitatory connections tha
21 a of CA1 pyramidal neurons and stratum (st.) oriens-alveus inhibitory interneurons in rat hippocampal
22 interneurones were classified as horizontal oriens-alveus interneurones by the pronounced 'sag' in r
23 cemaking activity in rat hippocampal stratum oriens-alveus interneurones was studied using whole-cell
25 on basilar dendrites extend into the stratum oriens-alveus while the apical dendrites project deep in
28 citatory synapses between principal cell and oriens/alveus (O/A) interneurons, a particular form of N
29 erneurons within the hippocampal CA1 stratum oriens/alveus (O/A), with preferential innervation of or
30 had horizontal dendrites restricted to str. oriens/alveus and innervated stratum radiatum and oriens
31 of distal dendritic branches within stratum oriens/alveus elicited fast Ca2+ transients, which showe
32 matostatin (SOM) interneurons in CA1 stratum oriens/alveus fire during hippocampal theta and investig
33 neurons were comprised almost exclusively of oriens/alveus interneurons with lacunosum-moleculare axo
34 somatostatin interneurons in the CA1 stratum oriens and dentate hilus (which themselves do not expres
36 in-expressing cells predominantly in stratum oriens and parvalbumin-expressing cells mostly in stratu
37 ese structures were also observed in stratum oriens and piriform cortex, and in cerebellar Purkinje c
38 showed significant reductions in the strata oriens and pyramidale of CA1, the stratum pyramidale of
39 ns and were highly significant in the strata oriens and radiatum of both CA1 and CA3 subfields and in
41 s were decreased significantly in the strata oriens and radiatum of CA3, in the dentate granule cell
42 ymmetric synapses was observed in the strata oriens and radiatum of the CA3a and CA2 regions, and a f
43 y 71.82% and 77.53% reduction in the stratum oriens and radiatum, respectively, when compared with co
44 siological properties of hippocampal stratum oriens and stratum pyramidale inhibitory interneurones,
45 ing subfield preference, innervating stratum oriens and stratum radiatum of CA2 and CA1 but stopping
46 ensin II binding was detected in the stratum oriens and stratum radiatum of the CA1 and CA2 subfields
49 rane polarization of deep (closer to stratum oriens) and superficial (closer to stratum radiatum) rat
50 co-expression was located in CA1/CA3 stratum oriens, and GAD67/alpha5 co-expression was predominantly
51 nses, was localized primarily to the stratum oriens, and had axonal projections to the stratum lacuno
52 in calbindin-positive neurons in the stratum oriens, and in a small number of interneurons that did n
54 nate in the strata radiatum, pyramidale, and oriens, are present throughout the entire transverse ext
55 C), axo-axonic (AAC), bistratified (BiC) and oriens-bistratified (O-BiC) cells, were distinguished by
56 corded from the hippocampal fissure and str. oriens but not the coherence between signals derived fro
58 us, delivered extracellularly in the stratum oriens, caused a reduction in spike frequency adaptation
60 roglia in the denervated hippocampal stratum oriens did not migrate extensively, whereas human immuno
62 king interneurons in the hippocampal stratum oriens exhibit a form of long-term potentiation of excit
63 cells in the stratum pyramidale; in stratum oriens, HC PV cells were electrophysiologically distinct
64 iological properties differentiating stratum oriens horizontal interneurons from pyramidal neurons of
69 he resting membrane potential of CA1 stratum oriens interneurones persistently increased following ex
70 rinic receptor (mAChR) activation on stratum oriens interneurones using whole-cell patch clamp record
71 s of gamma activity, two distinct classes of oriens interneurones, oriens lacunosum-moleculare (O-LM)
72 h and Girk in the same population of stratum oriens interneurons and that the modulation of these ion
73 ency spiking activity in a subset of stratum oriens interneurons controlling electrogenesis in pyrami
74 emporally correlated with spiking in stratum oriens interneurons demonstrating intrinsic theta-freque
76 caine) was detected in 30-50% of CA1 stratum oriens interneurons of various morphological classes.
77 red recordings between pyramidal neurons and oriens interneurons were obtained to determine whether L
79 alpha7, beta2 and beta3 subunits in stratum oriens interneurons; and beta2-4 in pyramidal neurons.
83 wo distinct classes of oriens interneurones, oriens lacunosum-moleculare (O-LM) and trilaminar cells,
85 l-Retzius cells receive GABAergic input from oriens lacunosum-moleculare cells and that this input ha
90 pses, we recorded mGluR1-mediated EPSCs from oriens-lacunosum moleculare (O-LM) interneurons in acute
91 CP) AMPA receptors has been characterized in oriens-lacunosum moleculare (O-LM) interneurons, which e
92 rt a surprising divergence among hippocampal oriens-lacunosum moleculare (O-LM) projecting interneuro
93 ypes of visualised presynaptic interneurone, oriens-lacunosum moleculare (O-LMC), basket (BC), axo-ax
94 icompartment neurons [pyramidal, basket, and oriens-lacunosum moleculare (OLM) cells] generated theta
95 al pyramids and facilitating inputs onto 7/7 oriens-lacunosum moleculare and 5/5 burst firing, sparse
96 veus (O/A), with preferential innervation of oriens-lacunosum moleculare cells (OLMs) through dendrit
97 essing basket, axo-axonic, bistratified, and oriens-lacunosum moleculare cells, innervating different
98 tro to study activity of pyramidal cells and oriens-lacunosum-moleculare (O-LM) interneurons during r
100 ct interneuron types--basket, axo-axonic and oriens-lacunosum-moleculare cells--visualized and define
102 r of the oscillatory activity in the stratum oriens lamina of CA3, but for the kainate-induced oscill
103 l cortex layers V and VI, the subiculum, the oriens layer of CA1, the medial septum, the diagonal ban
104 We also found massive cell death in the oriens layer of the hippocampus on P1 and in regions sur
106 agonist G1: G1 increased PSD95-IR in strata oriens, lucidum, and radiatum of CA3 in ovariectomized m
108 tively) on GABAergic interneurons in stratum oriens of area CA1 of the hippocampus were examined by u
109 labeled neurons were also detected in the s. oriens of CA1 (52%), CA2 (27%) and CA3 (36%) subfields.
110 ron microscopy (cortex, CPN, and the stratum oriens of CA1), PROT labeling was observed primarily wit
112 though significant, increases in the stratum oriens of CA3 (30%), the subiculum (20-30%) and the pres
113 eposits were found in the subiculum, stratum oriens of hippocampal field CA1, and the hilus of the de
114 ons possessing somata located within stratum oriens of hippocampal slices were classified according t
116 ive neurons could be observed in the stratum oriens of the Ammon's horn and subiculum, fewer were see
118 m the hippocampal fissure and stratum (str.) oriens of the CA1 region and (2) between CA1 stratum rad
119 7-immunopositive interneurons in the stratum oriens of the CA1 region of the hippocampus, accompanied
121 of the CA1 and CA2 subfields, in the stratum oriens of the CA3 subfield, and in the molecular layer o
125 c profiles were most concentrated in stratum oriens of the hippocampal CA1 region and dentate inner m
126 (1A)-AR EGFP-expressing cells in the stratum oriens of the hippocampal CA1 region confirmed that thes
127 n in the mossy fiber pathway and CA3 stratum oriens of the hippocampus during limbic epileptogenesis.
128 tin (SOM)-expressing neurons in stratum (s.) oriens of the hippocampus exhibit axonal sprouting beyon
130 re, such as the stratum radiatum and stratum oriens of the hippocampus, the molecular and granular la
133 Surprisingly, paired radiatum and unpaired oriens pathway potentiated, unless the pre-post delay wa
134 sely, the exact same 5 ms pairing in stratum oriens potentiated both pathways, as did AP-bursts alone
135 sine receptors counteracted unpaired stratum oriens potentiation following pairing in stratum radiatu
136 in a marked loss of SP fibers in the strata oriens, pyramidale, and radiatum of the CA3a and CA2 sub
137 lation of GABAergic terminals at the stratum oriens-pyramidale (SO-SP) or stratum lacunosum-molecular
139 d in the stratum radiatum of CA1, the strata oriens, radiatum and pyramidale of CA3, the dentate mole
140 e distribution of alpha2A-AR-I in the strata oriens, radiatum, and lacunosum-moleculare of hippocampa
142 Horizontal interneurones in the stratum oriens showed firing preference to inputs at theta frequ
146 we investigated I(M) in hippocampal stratum oriens (SO) interneurons, both from wild-type and transg
147 a down-regulation of GAD(67) in the stratum oriens (SO) of CA2/3 in both groups; CA1 only showed cha
149 ticularly between strata radiatum and strata oriens, suggesting a functional heterogeneity among hipp
150 racted DNA from laser-microdissected stratum oriens tissue of cornu ammonis 2/3 (CA2/3) and CA1 postm
152 tanic stimulation of the stratum radiatum or oriens were analysed using intracellular and multichanne
153 ified interneurones (n = 43) located in str. oriens were recorded in order to compare their functiona
154 volved in mediating synaptic potentiation in oriens, whereas NMDA and adenosine receptors counteracte
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