ライフサイエンスコーパス: medial septum

1 f GCs with activity patterns governed by the medial septum.

2 reased cholinergic neuron size by 34% in the medial septum.

3 s and projects to the neurotrophin-sensitive medial septum.

4 ntially affected by muscimol inactivation of medial septum.

5 omosomes, an unreplicated genome, and a wide medial septum.

6 limb of the diagonal band of Broca, and the medial septum.

7 elative number of cholinergic neurons in the medial septum.

8 he induction of ChAT immunoreactivity in the medial septum.

9 ctrodes in medial temporal cortex as well as medial septum.

10 l and central nuclei of the amygdala and the medial septum.

11 ippocampus: the locus coeruleus (LC) and the medial septum.

12 er than on unidirectional regulation via the medial septum.

13 d are strongly influenced by inputs from the medial septum.

14 limbic system depend on the integrity of the medial septum.

15 nterneurons receive GABAergic input from the medial septum.

16 lly along the lateral septum, rostral to the medial septum.

17 GABAergic cells in the DG and project to the medial septum.

18 lated by afferent cholinergic input from the medial septum.

19 ppocampus and cholinergic afferents from the medial septum.

20 ation by afferent cholinergic input from the medial septum.

21 brain neuron cultures from the region of the medial septum.

22 cending rhythmic input, most likely from the medial septum.

23 F-receptor-IR axonal varicosities in the rat medial septum.

24 somatosensory cortex, entorhinal cortex, and medial septum.

25 us infusion of 192IgG-saporin toxin into the medial septum.

26 loss of the cholinergic projection from the medial septum.

27 The largest increases were detected in the medial septum (47.8%) and the horizontal limb of the dia

28 c acid decarboxylase mRNA disappeared in the medial septum 7 days after the neurotoxin administration

29 location-specific firing, we inactivated the medial septum, a treatment that compromises hippocampus-

30 logical modulation of relaxin-3 receptors in medial septum alters hippocampal theta rhythm and spatia

31 -immunoreactive (ChAT-IR) cell counts in the medial septum and AChE-positive fiber counts in the hipp

32 Other causes included a medial septum and an accessory fissure other than the in

33 that in young animals was diminished in the medial septum and diagonal band but was unchanged in the

34 gest that the GABAergic innervation from the medial septum and diagonal band complex contributes to t

35 GABAergic projections from the medial septum and diagonal band complex exclusively inne

36 The medial septum and diagonal band of Broca (MS-DBB) has an

37 gic input to the hippocampus arises from the medial septum and diagonal band of Broca (MS-DBB), and w

38 The medial septum and diagonal band of Broca (MSDB) are majo

39 vity and extracellular units recorded in the medial septum and diagonal band of Broca (MSDB) in freel

40 ions of noradrenaline (NA) on neurons of the medial septum and diagonal band of Broca (MSDB) were exa

41 within the PFP originate from neurons in the medial septum and diagonal band of Broca complex.

42 at a population of neurons in the medial BF (medial septum and diagonal band of Broca) of macaque mon

43 nucleus (SCN) that paralleled changes in the medial septum and hippocampus, but not in other neural s

44 transferase (ChAT) was increased in both the medial septum and hippocampus.

45 ively more dense ascending NI projections to medial septum and hippocampus.

46 Intact cholinergic innervation from the medial septum and noradrenergic innervation from the loc

47 does not protect cholinergic neurons in the medial septum and nucleus basalis from the effects of ex

48 Cholinergic neurons in the medial septum and nucleus basalis were detected and quan

49 jor input from the rostral BF, including the medial septum and the vertical and horizontal limbs of t

50 that includes condensed chromosomes, a wide medial septum, and a fragmented nuclear envelope.

51 re we recorded theta cells from hippocampus, medial septum, and anterior thalamus of freely behaving

52 d PIN was found in the medial preoptic area, medial septum, and cortex, and less in the paraventricul

53 dial preoptic area, paraventricular nucleus, medial septum, and cortex, but not in the supraoptic nuc

54 ergic agonist carbachol was infused into the medial septum, and hippocampal CA1 place cells were reco

55 vertical limbs of the diagonal band nuclei, medial septum, and hippocampal formation.

56 l or rare cell clusters within the amygdala, medial septum, and inferior raphe.

57 ikarya were found in the olfactory bulb, the medial septum, and the diagonal band.

58 uced Fos-IR in the nucleus accumbens (core), medial septum, and the hippocampus (dentate and CA3).

59 ects of selective cholinergic lesions of the medial septum area (MS) or nucleus basalis magnocellular

60 is, and in the ipsilateral and contralateral medial septum, at 2 weeks following a unilateral injecti

61 hese include: prefrontal cortex, lateral and medial septum, basolateral amygdala, paraventricular and

62 g the dorsal and medial pallium, lateral and medial septum, bed nucleus of the stria terminalis, amyg

63 t was found that electrolytic lesions of the medial septum, but not the lateral septum, blocked CRH-e

64 suggesting that electrolytic lesions to the medial septum can enhance LI in a CTA paradigm.

65 3 fiber plexuses were observed in regions of medial septum containing hippocampal-projecting choline

66 praoptic nucleus, septohypothalamic nucleus, medial septum, cortex, and in some of the nNOS staining

67 the firing characteristics of neurons in the medial septum/diagnol band of Broca complex (MS/DB) foll

68 tory effect of electrical stimulation in the medial septum diagonal band of broca (MSDB) on neuronal

69 t lateral ventricle and sections through the medial septum, diagonal band of Broca, nucleus basalis m

70 olfactory bulb, cerebral cortex, lateral and medial septum, diagonal band of Broca, nucleus basalis o

71 ergic neurons) across its different regions (medial septum, diagonal band, magnocellular preoptic are

72 ction velocities of antidromically activated medial septum-diagonal band (MS-DB) neurons were examine

73 into the cholinergic cell body region of the medial septum-diagonal band (MS-DBB) inhibited acetylcho

74 The medial septum-diagonal band (MSDB) complex, via the sept

75 oth GABAergic and cholinergic neurons in the medial septum-diagonal band of Broca (MSDB) have been as

76 orexins, provide a dense innervation to the medial septum-diagonal band of Broca (MSDB), a sleep-ass

77 s kainate-2 subunit mRNA was abundant in the medial septum-diagonal band, median and anteroventral pr

78 cholinergic neurons freshly dissociated from medial septum/diagonal band (MS/DB) exhibit relatively s

79 rrents (mPSCs) was substantially blunted for medial septum/diagonal band (MS/DB) neurons in brain sli

80 l patch-clamp recordings in acutely isolated medial septum/diagonal band (MS/DB) neurons were used to

81 n of GABAA receptors (GABAARs) in developing medial septum/diagonal band (MS/DB) neurons, suggesting

82 ung mice, the properties of I(h) currents in medial septum/diagonal band (MS/DB) neurons.

83 studied in acutely isolated neurons from the medial septum/diagonal band (MS/DB) of adult rats using

84 In the medial septum/diagonal band (MS/DB), no effect of treatm

85 tive cell bodies at three levels through the medial septum/diagonal band (MS/DBv) of these rats revea

86 The medial septum/diagonal band (MSDB), which gives rise to

87 saporin (SAP) or artificial CSF (C) into the medial septum/diagonal band complex (MSDB).

88 all fields of basal forebrain, including the medial septum/diagonal band complex and striatum.

89 tide that coexists with acetylcholine in the medial septum/diagonal band in the rat and impairs choic

90 f acute NGF exposure on neurons in the mouse medial septum/diagonal band of Broca (MS/DB), focusing o

91 that ramify densely and abut neurons in the medial septum/diagonal band of Broca (MS/DB).

92 es suggest that muscarinic mechanisms in the medial septum/diagonal band of Broca (MSDB) may contribu

93 , it could be an indirect action through the medial septum/diagonal band of Broca (MSDB) pacemaker ce

94 the cholinergic and GABAergic nucleus of the medial septum/diagonal band of Broca (MSDB) which projec

95 mic area, provide a dense innervation to the medial septum/diagonal band of Broca (MSDB), a sleep-ass

96 l studies in rats have demonstrated that the medial septum/diagonal band of Broca (MSDB), which sends

97 atory optogenetic protein oChIEF-tdTomato in medial septum/diagonal band of Broca cholinergic neurons

98 The medial septum/diagonal band of Broca complex (MSDB) is a

99 otransmitter acetylcholine, derived from the medial septum/diagonal band of Broca complex, has been a

100 The medial septum/diagonal band region (MSDB), which provide

101 receives a major cholinergic input from the medial septum/diagonal band, is important in memory and

102 wever, fiber-sparing chemical lesions of the medial septum did not block CRH-enhanced startle, sugges

103 Critically, at P12, inactivation of the medial septum eliminates theta in both structures.

104 rimary cholinergic efferent pathway from the medial septum exhibited reduced vesicular ACh transporte

105 rease in ChAT-positive cells detected in the medial septum following unilateral transection of the fi

106 ing that parvalbumin-containing cells in the medial septum generate theta.

107 in which BFCNs and some GABA neurons in the medial septum had been destroyed by mu P75-saporin, huma

108 holine uptake) in the terminal fields of the medial septum (hippocampus, cingulate, entorhinal cortex

109 ons containing estrogen receptors within the medial septum, horizontal limb of the diagonal band of B

110 Lidocaine-induced inactivation of the medial septum immediately after training or prior to tes

111 Morphine injected into the medial septum impaired memory both for avoidance trainin

112 , debate continues regarding the role of the medial septum in behavior (MS).

113 ergic projection from the hippocampus to the medial septum in rats, and thereby simulate hippocampal

114 ined gene expression of whole septum (LS and medial septum) in selectively bred maternal mice.

115 first demonstration that HCN channels in the medial septum influence memory.

116 isecond-long timescale, and was dependent on medial septum inputs.

117 rated by intrinsic hippocampal circuits; (3) medial-septum inputs pace and augment oscillations; (4)

118 The avian medial septum is clearly defined by peptidergic markers

119 The medial septum is hypothesized to modulate whether the hi

120 A major fiber bundle passing through the medial septum is the fornix, the primary efferent pathwa

121 nd that when this toxin is injected into the medial septum, it lesions the parvalbumin and cholinergi

122 cts of microinfusion of scopolamine into the medial septum (MS Scp) on hippocampal neurophysiology an

123 In the medial septum (MS) and striatum, the highest levels of C

124 NA revealed high levels of expression in the medial septum (MS) and the diagonal band of Broca (DBB),

125 entify GABAergic projection neurons from the medial septum (MS) as the major afferents to dentate PV

126 dependent loss of cholinergic neurons in the medial septum (MS) but no marked loss of cholinergic neu

127 osum of the lamina terminalis (DBB/OVLT) and medial septum (MS) in adults as compared to juvenile mal

128 network theta rhythm oscillations caused by medial septum (MS) inactivation with muscimol.

129 The medial septum (MS) is required for theta rhythmic oscill

130 The medial septum (MS) is strongly linked to locomotor behav

131 nzodiazepine (BDZ) receptor ligands into the medial septum (MS) produces a bidirectional modulation o

132 uctuations in the levels of trkA mRNA in the medial septum (MS), and BDNF mRNA in regions CA1 and CA3

133 relative number of type 1 neurons within the medial septum (MS), horizontal limb of the diagonal band

134 C received auditory input primarily from the medial septum (MS), rather than AC.

135 nd the number of immunoreactive cells in the medial septum (MS), the horizontal limb of the diagonal

136 in early pregnant and diestrous rats in the medial septum (MS), vertical and horizontal diagonal ban

137 eased in rostral LS, but not in caudal LS or medial septum (MS).

138 al limb of the diagonal band, but not in the medial septum, nucleus basalis, or striatum of females v

139 studied in acutely isolated neurons from the medial septum/nucleus diagonal band (MS/nDB) of adult ra

140 The effect of injection into the medial septum of a toxin selective for cholinergic neuro

141 us that is histochemically comparable to the medial septum of mammals.

142 tribution of synaptic circuits involving the medial septum of mice, we have identified postsynaptic c

143 utyric acid (GABA) agonist muscimol into the medial septum on memory for inhibitory avoidance learnin

144 Urocortin 2 infusion into the medial septum or lateral ventricle did not affect anxiet

145 Injection of anterograde tracers into medial septum, or triangular septal and septofimbrial nu

146 uclei, laminae IV-VI of the cerebral cortex, medial septum, preoptic area, bed nucleus of the stria t

147 100, 237.5 or 375 ng of 192-saporin into the medial septum produced dose-related deficits in a variab

148 Muscimol infusion into medial septum reduced the probability of TGC and success

149 monstrates that the selective removal of the medial septum retards delay eyeblink conditioning in a m

150 However, the precise contributions of the medial septum's cholinergic neurones to these functions

151 on reported that electrolytic lesions of the medial septum significantly retard eyeblink conditioning

152 somatic GABAergic input originating from the medial septum that preferentially targets AACs.

153 median raphe drives GABA interneurons in the medial septum that synapse on cholinergic neurons projec

154 In the basal forebrain medial septum, the application of beta (25-35) resulted

155 the same regions, including the lateral and medial septum, the bed nucleus of the stria terminalis,

156 the subiculum, the oriens layer of CA1, the medial septum, the diagonal band complex, the substantia

157 y bulb, the dentate gyrus and subiculum, the medial septum, the diagonal band of Broca, the ventral p

158 of aFGF and ChAT mRNAs were observed in the medial septum, the diagonal bands of Broca, the magnocel

159 caudate putamen, the accumbens nucleus, the medial septum, the lateral septum, the ventromedial hypo

160 nce of cholinergic projection neurons in the medial septum, the magnocellular preoptic area, and the

161 In rat medial septum, tkP3BzPB produced a greater inhibition of

162 ed 192-IgG saporin (SAP) or vehicle into the medial septum-vertical limb of the diagonal band (MS-vDB

163 uction in ChAT-IR cell profile counts in the medial septum/vertical diagonal band (MS/vDB).

164 lective immunotoxin 192 IgG-saporin into the medial septum/vertical limb of the diagonal band (MS/VDB

165 holinergic input to the hippocampus from the medial septum/vertical limb of the diagonal band (MS/VDB

166 gion of the basal forebrain encompassing the medial septum/vertical limb of the diagonal band of Broc

167 erents could influence ECoG and HEEG are the medial septum/vertical limb of the diagonal band of Broc

168 campal cholinergic projection neurons in the medial septum/vertical limb of the diagonal band of Broc

169 eduction of enzyme expressions in the LC and medial septum was less from these substituted peptides t

170 In the present study, the medial septum was selectively lesioned with ibotenic aci

171 In the medial septum, we observed relaxin-3-immunoreactive cont

172 ampus and immunohistochemistry of the LC and medial septum were examined 1 week following the second

173 we focus on one hypocretin target site, the medial septum, where there is a dense collection of hypo