ライフサイエンスコーパス: medial septum

1 loss of the cholinergic projection from 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 omosomes, an unreplicated genome, and a wide medial septum.

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

6 elative number of cholinergic neurons in the medial septum.

7 he induction of ChAT immunoreactivity in the medial septum.

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

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

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

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

12 input from the anterior cingulate cortex and medial septum.

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

14 opulations of the dorsal caudate-putamen and medial septum.

15 ts, including the cholinergic input from the medial septum.

16 + interneurons or cholinergic input from the medial septum.

17 ntially affected by muscimol inactivation of medial septum.

18 er than on unidirectional regulation via the medial septum.

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

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

21 nterneurons receive GABAergic input from the medial septum.

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

23 late specifically cholinergic neurons in the medial septum.

24 lated by afferent cholinergic input from the medial septum.

25 ppocampus and cholinergic afferents from the medial septum.

26 ation by afferent cholinergic input from the medial septum.

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

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

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

30 somatosensory cortex, entorhinal cortex, and medial septum.

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

32 pikes in the presence of inhibition from the medial septum; (2) compress learned spike sequences in t

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

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

35 The medial septum, a part of the basal forebrain that innerv

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

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

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

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

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

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

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

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

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

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

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

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

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

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

50 the hippocampal subregions (CA1, CA2, CA3), medial septum and diagonal band, retrosplenial cortex, S

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

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

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

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

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

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

57 MHb and its sole identified GABA input, the medial septum and nucleus of the diagonal band (MSDB).

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

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

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

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

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

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

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

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

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

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

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

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

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

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

72 ated by subcortical structures including the medial septum, but it is unclear how spatial information

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

74 Inhibition of cholinergic neurons in the medial septum by DREADD (designer receptors exclusively

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

76 M) subtype of GABAergic neurons in the mouse medial septum complex (MS), but not parvalbumin subtype

77 3 fiber plexuses were observed in regions of medial septum containing hippocampal-projecting choline

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

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

80 hese effects were observed in BFCNs from the medial septum diagonal band and horizontal diagonal band

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

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

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

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

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

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

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

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

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

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

91 albumin-containing projection neurons of the medial-septum-diagonal band of Broca ([Formula: see text

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

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

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

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

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

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

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

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

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

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

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

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

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

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

106 e hippocampus from fibers originating in the medial septum/diagonal band of Broca (MSDB) complex, is

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

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

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

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

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

112 Models of path integration use medial septum/diagonal band of Broca (MSDB)-dependent ME

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

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

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

116 , GABAergic, or glutamatergic neurons in the medial septum/diagonal band of Broca does not affect mod

117 l formation, cholinergic modulation from the medial septum/diagonal band of Broca is known to correla

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

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

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

121 hat in adult male Wistar rats, silencing the medial septum during recall did not affect avoidance mem

122 stimulation, we report here that closed-loop medial septum electrical stimulation can quickly termina

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

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

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

126 ealed that the precisely timed activation of medial septum GABAergic neurons underlaid the effects.

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

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

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

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

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

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

133 The medial septum implements cortical theta oscillations, a

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

135 Inactivation of the neighboring medial septum in males produced no effect on avoidance,

136 iated currents in cholinergic neurons of the medial septum in mGluR5 KO mice.

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

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

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

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

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

142 In contrast, the medial septum is a promising target to govern hippocampa

143 The avian medial septum is clearly defined by peptidergic markers

144 The medial septum is hypothesized to modulate whether the hi

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

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

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

148 We have demonstrated that medial septum (MS) activation simultaneously increased V

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

150 ng SOM(+) neurons, can robustly regulate the medial septum (MS) and supramammillary nucleus (SuM)-two

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

152 Here we identify the medial septum (MS) as a dCA2 input region that is critic

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

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

155 this issue of the JCI, Sun et al. explored a medial septum (MS) circuit linking these behaviors in a

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

157 e direction and type of interaction with the medial septum (MS) in male, urethane-anesthetized rats.

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

159 The medial septum (MS) is critical in theta generation by tw

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

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

162 Medial septum (MS) lesions lead to perseverative, inflex

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

164 ver, theta-nested gamma-band activity in the medial septum (MS) suggests that the MS may control supr

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

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

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

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

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

170 ns in the SI/nBM-mPFC circuit but not in the medial septum (MS)-hippocampus pathway, and impaired tem

171 Our results suggest that medial septum (MS)-projecting, fast-firing, theta phase-

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

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

174 ized by these brain regions supported by the medial septum, nucleus reuniens, and parahippocampal reg

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

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

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

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

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

180 nfluence of neural dynamics regulated by the medial septum on the functional encoding of space and ti

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

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

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

184 100, 237.5 or 375 ng of 192-saporin into the medial septum produced dose-related deficits in a variab

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

186 ice indicate that cholinergic neurons in the medial septum represent a key cell type involved in sens

187 demonstrated that cholinergic neurons in the medial septum represent a key cell-type involved in sens

188 novel computational model that includes the medial septum, represented as a set of abstract Kuramoto

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

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

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

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

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

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

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

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

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

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

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

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

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

202 o be an excess of GABAergic innervation from medial septum to the hippocampus.

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

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

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

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

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

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

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

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

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

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

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

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