ライフサイエンスコーパス: intrahippocampal

1 4-6 of training, rats received posttraining intrahippocampal (1 microgram/0.5 microliter) or intraca

2 Intrahippocampal (10 micrograms), but not intra-dorsal s

3 ntra-dorsal striatal (2 micrograms), but not intrahippocampal (2, 5, or 10 micrograms) injection of A

4 either physostigmine (systemic=0.075 mg/kg; intrahippocampal=20, 40 ng/muL) or saline.

5 d P33 (Experiment 1), or following bilateral intrahippocampal administration of 2.5 or 5.0 microg per

6 In addition, intrahippocampal administration of anisomycin (100 mug/m

7 Further, intrahippocampal administration of biotin-labeled CAA mu

8 In contrast, intrahippocampal administration of BN 50730 had no effec

9 We show here that intrahippocampal administration of SP triggers self-sust

10 Here we show that direct intrahippocampal administration of the adeno-associated

11 er experiments using the plus-maze, in which intrahippocampal administrations of pharmacological agen

12 Hippocampal CA1 pyramidal neurons receive intrahippocampal and extrahipppocampal inputs during the

13 ng-term behavioral consequences of systemic, intrahippocampal and intra-medial prefrontal cortex admi

14 Here, we evaluated the influence of intrahippocampal ANI infusions on allocentric spatial na

15 Sensitivity to intrahippocampal anisomycin was observed only in the pro

16 g to birds, and birds expanded the system of intrahippocampal axon collaterals, relative to turtles a

17 All patients with intrahippocampal calcification and the control cohort de

18 The prevalence of intrahippocampal calcification appears to increase with

19 Eleven (23.4%) of 47 patients with intrahippocampal calcification had calcification within

20 The presence of intrahippocampal calcification was assessed by four read

21 Intrahippocampal calcification was demonstrated in 47 (1

22 The anatomic distribution of intrahippocampal calcification was similar to that descr

23 cations and a matched control cohort without intrahippocampal calcification.

24 Differences in proportion of patients with intrahippocampal calcifications across different age gro

25 stories were reviewed in those patients with intrahippocampal calcifications and a matched control co

26 ity was observed in epileptic mice receiving intrahippocampal CGE progenitors.

27 e histological changes occurred with altered intrahippocampal connectivity and abnormal behavior; inc

28 ovariance patterns to characterize efficient intrahippocampal connectivity.

29 manipulated hippocampal IL1 signaling using intrahippocampal delivery of IL1 receptor antagonist (IL

30 bserved in HDAC3-FLOX mice were abolished by intrahippocampal delivery of Nr4a2 small interfering RNA

31 Intrahippocampal delivery of plasminogen to plg(-/-) mic

32 histochemistry showed that focal deletion or intrahippocampal delivery of RGFP136 resulted in increas

33 M40 alone, either icv or intrahippocampal, did not affect choice accuracy in eith

34 by hippocampal volumetrics, analysis of the intrahippocampal distribution of T2 signal, and apparent

35 demonstrated that intracerebroventricular or intrahippocampal E(2) infusion immediately after object

36 Systemic (Experiment 1) and intrahippocampal (Experiment 2) injections of the acetyl

37 an Alzheimer's disease, we initiated chronic intrahippocampal expression of IFNgamma through delivery

38 An intrahippocampal gamma generator has been identified in

39 Intrahippocampal gamma oscillation emerges in the CA3 re

40 p is sufficient to explain the generation of intrahippocampal gamma-frequency oscillations.

41 nhancing effects of posttraining systemic or intrahippocampal glucocorticoid administration on memory

42 e memory enhancement induced by intra-BLA or intrahippocampal glucocorticoid receptor agonist adminis

43 Intrahippocampal IL1ra prevented synaptic dysfunction, p

44 istered intraperitoneally (0.2 mg/kg) or via intrahippocampal infusion (5.0 microg/side) immediately

45 We show that pre-training intrahippocampal infusion of a COX-2 specific inhibitor

46 We demonstrate that intrahippocampal infusion of an EphA antagonist immunoad

47 s subsequently received an intra-amygdala or intrahippocampal infusion of either 20% DMSO or the MAPK

48 Intrahippocampal infusion of leptin produced a similar a

49 In contrast, intrahippocampal infusion of SB203580, a specific inhibi

50 Thus, intrahippocampal infusion of the CB1R antagonist SR14171

51 Experiment 1 established that intrahippocampal infusion of the D(1)/D(5) dopaminergic

52 blocked by the postextinction or postnovelty intrahippocampal infusion of the NMDA receptor antagonis

53 assessed network activity after a unilateral intrahippocampal infusion of ZIP in anesthetized rats.

54 urrents were not affected by Zn(2+) Finally, intrahippocampal infusion of Zn(2+) elicited rapid epile

55 Intrahippocampal infusion studies with the AMPA-specific

56 DHT, or 3alpha-diol via Silastic capsules or intrahippocampal infusions had greater analgesia (tail f

57 In addition, although intrahippocampal infusions of 40 ng of physostigmine inc

58 We examined the capacity of intrahippocampal infusions of an alpha5 subunit-selectiv

59 , in addition to blocking protein synthesis, intrahippocampal infusions of ANI cause the suppression

60 Control studies confirmed that intrahippocampal infusions of anisomycin inhibited prote

61 We used intrahippocampal infusions of antisense oligodeoxynucleo

62 sent experiments examined whether unilateral intrahippocampal infusions of glucose would enhance spon

63 d the memory retrieval impairment induced by intrahippocampal infusions of RU 28362 given 60 min befo

64 y retrieval impairment induced by concurrent intrahippocampal infusions of RU 28362.

65 to the novelty, animals were given bilateral intrahippocampal infusions of vehicle (VEH), of the prot

66 Further, intrahippocampal inhibition of ERK activation or DNA met

67 fter infusion, an effect that was blocked by intrahippocampal inhibition of ERK or PI3K activation.

68 cement in middle-aged females was blocked by intrahippocampal inhibition of ERK or PI3K activation.

69 er memory training and that acute, selective intrahippocampal inhibition of GluT4-mediated glucose tr

70 Here we report that acute intrahippocampal inhibition of PKMzeta disrupts place ce

71 VGF by intrahippocampal injection also had novel activity in an

72 Intrahippocampal injection of 2.5 micrograms of the 3 be

73 Finally, we show that a single intrahippocampal injection of a specific oligomeric anti

74 Here we show that intrahippocampal injection of ASC specks resulted in spr

75 nduction of alphaS aggregation following the intrahippocampal injection of E46K alphaS fibrils in M20

76 task, followed by a unilateral posttraining intrahippocampal injection of either estradiol (1.0 micr

77 a Morris water maze after a single bilateral intrahippocampal injection of either saline or the selec

78 Experiment 2, the memory enhancing effect of intrahippocampal injection of estradiol was blocked by p

79 Conversely, intrahippocampal injection of JNKs inhibitors sp600125 (

80 ating limbic areas in rats made epileptic by intrahippocampal injection of kainic acid, and in patien

81 n and reactive gliosis, which was induced by intrahippocampal injection of kainic acid.

82 We also show that the intrahippocampal injection of naturally secreted Abeta i

83 The intrahippocampal injection of p17 in mice reduces their

84 Finally, induction of status epilepticus by intrahippocampal injection of pilocarpine induced biphas

85 The model is induced by unilateral intrahippocampal injection of tetanus toxin.

86 The intrahippocampal injection of the selective A2A receptor

87 Rats receiving intrahippocampal injections of 192 IgG-saporin (SAP-HPC)

88 Intrahippocampal injections of adeno-associated virus ve

89 Similarly, intrahippocampal injections of an anti-Abeta antibody re

90 Intrahippocampal injections of BN 52021 decreased the la

91 Intrahippocampal injections of estradiol delayed 2 hr po

92 Intrahippocampal injections of estradiol enhance memory

93 etention test escape latencies of rats given intrahippocampal injections of estradiol were lower than

94 Rats receiving intrahippocampal injections of glutamate predominantly d

95 We evaluated the impact of intrahippocampal injections of NMDA on CCR5 expression i

96 In Experiment 2, intrahippocampal injections of physostigmine significant

97 Furthermore, intrahippocampal injections of RhoA antisense oligodeoxy

98 g from systemic, intracerebroventricular and intrahippocampal injections of the protein synthesis inh

99 ed in two rat models of SE-induced epilepsy: intrahippocampal kainate and systemic administration of

100 ion in the absence of injury, and unilateral intrahippocampal kainate injections into the transgenic

101 trophy (granule cell dispersion) produced by intrahippocampal kainate.

102 l cell death, accompany CAST depletion after intrahippocampal kainic acid administration to mice, and

103 are consistent with previous studies in the intrahippocampal kainic acid rat model of chronic epilep

104 range of 250-600 Hz [fast ripples (FRs)] in intrahippocampal kainic acid-treated rats with spontaneo

105 within the infrahippocampal cleft as well as intrahippocampal location of graft-derived cells express

106 Intrahippocampal microdialysis was performed in freely b

107 ular concentration profile of ethanol during intrahippocampal microdialysis with 1 M ethanol was esti

108 The predominant effect of the first intrahippocampal microdialysis with ethanol was a decrea

109 w that encoding of novel PAs is sensitive to intrahippocampal microinfusion of the NMDA antagonist d-

110 Here, we report that intrahippocampal microinfusions of anisomycin in urethan

111 Whereas intrahippocampal microinjection of a conjugate of native

112 Intrahippocampal modulation of the EtOH-maintained respo

113 In experiment 3, intrahippocampal muscimol infusions did not disrupt the

114 In the current studies, we used intrahippocampal muscimol microinfusions to transiently

115 To understand how intrahippocampal networks interact during REM sleep, we

116 ished by LTP-like synaptic plasticity within intrahippocampal networks.

117 excitotoxic brain injury; in neonatal rats, intrahippocampal NMDA injection stimulates expression of

118 Field patterns, recorded from various intrahippocampal or entorhinal cortex sites, were used t

119 Intrahippocampal or intracerebroventricular E(2) infusio

120 kt phosphorylation was increased 5 min after intrahippocampal or intracerebroventricular E(2) infusio

121 latency to burying behavior was increased by intrahippocampal or intraseptal injection of 2.5 and 5 m

122 The anxiolytic effects of intrahippocampal or intraseptal injection of pregnanolon

123 Most excitatory intrahippocampal pathways are characterized by significa

124 trast, the lack of behavioral improvement by intrahippocampal physostigmine infusion in the PF rats,

125 after 15 min, and this effect was blocked by intrahippocampal PI3K, but not ERK, inhibition.

126 tated the extinction, which was inhibited by intrahippocampal protein synthesis inhibitor anisomysin,

127 This observation (systemic vs intrahippocampal) provides further support for the desig

128 Electrocorticographic or intrahippocampal recordings of epileptogenesis (from the

129 The present study utilises the intrahippocampal route to further investigate CGS 21680-

130 Parallel studies have found that intrahippocampal scopolamine (Scop) blocks contextual fe

131 cover the synaptic mechanisms underlying the intrahippocampal spread of gamma oscillations, we record

132 F levels that is dependent on the pattern of intrahippocampal stimulation.

133 ariate profile of age-related differences in intrahippocampal structures and show that HC maturity as

134 acterized by the differential development of intrahippocampal subfields and associated networks.

135 d reversible morphological reorganization of intrahippocampal subregions involved in information proc

136 hibitory theta signaling also contributes to intrahippocampal synchrony.

137 NSC) grafting in the irradiated brain, where intrahippocampal transplantation of hNSC ameliorated rad

138 Intrahippocampal transplantation of human neural stem ce

139 g athymic nude rats followed 2 days later by intrahippocampal transplantation with human neural stem