ライフサイエンスコーパス: lateral septum

1 A), bed nucleus of the stria terminalis, and lateral septum.

2 the bed nucleus of the stria terminalis and lateral septum.

3 edial and central amygdaloid nuclei, and the lateral septum.

4 ay be that C3 increases NGF synthesis in the lateral septum.

5 la, bed nucleus of the stria terminalis, and lateral septum.

6 it projects to the medial CGRP layer of the lateral septum.

7 us chemoarchitectonic zones of the mammalian lateral septum.

8 of vasopressin-immunoreactive fibers in the lateral septum.

9 ffect on extracellular levels of 5-HT in the lateral septum.

10 piriform cortex, cortical amygdala, and the lateral septum.

11 gnanolone in the hippocampus, but not in the lateral septum.

12 olone injection in the dorsal hippocampus or lateral septum.

13 l and lateral hypothalamus as well as in the lateral septum.

14 roperties of the dopamine innervation of the lateral septum.

15 dial prefrontal cortex, medial amygdala, and lateral septum.

16 thalamus, medial nucleus of the amygdala and lateral septum.

17 nterior olfactory nucleus, taenia tecta, and lateral septum.

18 eurons in the ventral hippocampus and dorsal lateral septum.

19 halamic KP-producing (KP(LS)) neurons of the lateral septum.

20 s: the dorsal and intermediate region of the lateral septum.

21 serotonin removal with maximal rates in the lateral septum.

22 ppocampus, amygdala, striatum, cingulate and lateral septum.

23 cal interconnections between the rdAcbSh and lateral septum.

24 st and overlap extensively with those of the lateral septum.

25 the highest expression level limited to the lateral septum.

26 significantly more V1aR and less OTR in the lateral septum.

27 t both rostral and caudal levels, and in the lateral septum.

28 she saw her preferred male lose a fight, the lateral septum, a nucleus associated with anxiety, was a

29 idence that the firing phase of cells in the lateral septum, a region that links the two areas, may c

30 haracteristic morphology, and project to the lateral septum, a series of medial hypothalamic areas ex

31 an oxytocin (OT) receptor antagonist in the lateral septum also blocked pair bond formation induced

32 edial nucleus of the amygdala and the dorsal lateral septum also distinguished 2DG-induced torpor fro

33 munoreactive (ER-ir) cells were found in the lateral septum, amygdala pars lateralis, pallium, preopt

34 y bulb; temporal cortex; caudal hippocampus; lateral septum; amygdala; nucleus accumbens; ventral pal

35 se of oxytocin receptor (OTR) binding in the lateral septum and amygdala.

36 nown to depress cortical function, including lateral septum and anterior hypothalamus.

37 dendrites as well as MEF2A-ir nuclei in the lateral septum and bed nucleus of the stria terminalis n

38 Inputs to the LH orexin cell field from lateral septum and bed nucleus of the stria terminalis w

39 arly enriched in processes of neurons in the lateral septum and bed nucleus of the stria terminalis,

40 ns implicated in flank marking behavior (the lateral septum and central grey).

41 in the medial amygdala, ventral part of the lateral septum and cingulate cortex expression was signi

42 us, and areas outside the hippocampus (e.g., lateral septum and entorhinal cortex) were evaluated usi

43 tion in both areas and density except in the lateral septum and external subnucleus of the lateral pa

44 higher levels of OTR binding throughout the lateral septum and hippocampus.

45 ions suggest that cholinergic neurons of the lateral septum and lateral parabrachial nucleus regulate

46 us (SCN) and limbic sites, specifically, the lateral septum and medial amygdaloid nucleus, indicate g

47 unrestrained WT mice in 9 regions, including lateral septum and periaqueductal gray.

48 as associated with increased activity in the lateral septum and preoptic area, demonstrating recruitm

49 te that the proposed transition zone between lateral septum and rdAcbSh would be but one of many in t

50 e decrease in extracellular 5-HT in both the lateral septum and striatum.

51 Furthermore, neuronal cell death in the lateral septum and the cornu ammonis 1 region of hippoca

52 DRN reduced extracellular 5-HT levels in the lateral septum and the striatum.

53 hway connecting the ventral hippocampus, the lateral septum and the ventral tegmental area helps to r

54 entified in the present study, including the lateral septum and the ventromedial hypothalamus, are kn

55 nucleus and CRF(2A) receptor binding in the lateral septum and ventromedial hypothalamus were increa

56 imulated binding strongly in hippocampus and lateral septum and weakly in substantia nigra.

57 HR rats, bLRs expressed greater c-fos in the lateral septum and within multiple hypothalamic nuclei,

58 m the limbic forebrain (cingulate cortex and lateral septum) and both the medial and lateral hypothal

59 areas: (1) extended amygdaloid complex, (2) lateral septum, and (3) infralimbic, insular, and ventro

60 ng predominantly from the prefrontal cortex, lateral septum, and amygdala.

61 c area, nucleus accumbens, central amygdala, lateral septum, and cortex.

62 ns to the accumbens nucleus, basal amygdala, lateral septum, and hypothalamus.

63 bed nucleus of the stria terminalis (BNST), lateral septum, and nucleus accumbens shell in mice lack

64 id induced Fos in the amygdala, hippocampus, lateral septum, and nucleus accumbens.

65 cular nucleus, the medial preoptic area, the lateral septum, and nucleus of the solitary tract.

66 , lateral hypothalamus, thalamus, medial and lateral septum, and periaqueductal gray area.

67 th nonapeptide receptor distributions in the lateral septum, and sociality in female zebra finches wa

68 e amygdala, bed nucleus of stria terminalis, lateral septum, and spinal cord).

69 its major subcortical projection target, the lateral septum, and that expression of a truncated Eph r

70 in the ventral midbrain that project to the lateral septum, and we reveal essential roles for Neurod

71 fic nuclei of the hypothalamus and amygdala, lateral septum, and widespread regions of the cerebral c

72 he caudate-putamen; the globus pallidus; the lateral septum; and the islands of Calleja).

73 tudies have revealed that the rat medial and lateral septum are targeted by ascending projections fro

74 xpression in the ventral pallidum (VPall) or lateral septum, areas causally related to pairbond forma

75 clinical study identified vasopressin in the lateral septum as a key factor in the pathophysiology of

76 ceptor (Oxtr) gene (Oxtr), we identified the lateral septum as the brain region mediating fear-enhanc

77 tor-mRNA in the preoptic area, amygdala, and lateral septum, as compared with progesterone-insensitiv

78 hypophyseal tract, a plexus of fibers in the lateral septum, as observed in the rat brain, was not de

79 However, similar inhibition in the lateral septum attenuates active avoidance of anxiogenic

80 ced the highest number of FLI neurons in the lateral septum, bed nucleus of the stria terminalis, amy

81 were abundant in the allocortex, claustrum, lateral septum, bed nucleus of the stria terminalis, and

82 tivity, specifically in three brain regions: lateral septum, bed nucleus of the stria terminalis, and

83 aventricular nucleus (PVN), arcuate nucleus, lateral septum, bed nucleus of the stria terminalis, cen

84 of brain areas, including cingulate cortex, lateral septum, bed nucleus of the stria terminalis, med

85 cortex, medial nucleus of the amygdala, and lateral septum being significantly affected by air-puff.

86 ion of an AVP V1a receptor antagonist in the lateral septum blocked mating-induced pair bonding, wher

87 ic lesions of the medial septum, but not the lateral septum, blocked CRH-enhanced startle.

88 In the lateral septum, both species had low levels of AVP recep

89 pallidum, elements of extended amygdala, and lateral septum (but not prefrontal cortex) were activate

90 aser cells were predominantly located in the lateral septum, but also the hippocampus, anteroventral

91 ation of the two receptors in neurons of the lateral septum, but not in the median eminence or in the

92 specific antagonist, we demonstrate that the lateral septum, but not the medial amygdala, is critical

93 The reduction of extracellular 5-HT in the lateral septum by CRF (0.3 microg, i.c.v.) was blocked b

94 for these receptors were knocked out in the lateral septum by infusion of recombinant adeno-associat

95 eral hypothalamus from somatostatin-positive lateral septum cells evokes food approach without affect

96 gdala/bed nucleus of the stria terminalis to lateral septum circuit.

97 of numerous immunoreactive substances in the lateral septum closely match those of mammals (i.e., dis

98 al hippocampus, paraventricular thalamus and lateral septum correlated with genotype-related differen

99 of the basal forebrain, including medial and lateral septum, diagnoal band nuclei, ventral pallidum,

100 teral parabrachial nucleus, locus coeruleus, lateral septum, diagonal band, stratum lacunosum-molecul

101 injection of cocaine into the neostriatum or lateral septum did not.

102 Here, we describe how the dorsal lateral septum (dLS), a forebrain limbic nucleus, facili

103 mine modulates aggression through the dorsal lateral septum (dLS), a region known for aggression cont

104 at a multinodal circuitry between the dorsal lateral septum (dLS), lateral hypothalamic area (LHA), a

105 nia tecta, inner layers of cingulate cortex, lateral septum, dorsal endopiriform nucleus, fundus stri

106 For others, such as the ventral lateral septum, dorsal premammillary nucleus, and princi

107 hippocampus, dorsal tenia tecta, claustrum, lateral septum, dorsal striatum, nucleus accumbens (core

108 creased the density of BDNF-ir fibers in the lateral septum, dorsolateral area of the bed nucleus of

109 Inhibitory inputs from the lateral septum enable separate signalling by lateral hyp

110 terminalis, taenia tecta, nucleus accumbens, lateral septum, endopiriform nucleus, dorsal BST, substa

111 cal regions, the anterior olfactory nucleus, lateral septum, endopiriform nucleus, ventral forebrain,

112 s issue of Neuron, Chen et al.(1) found that lateral septum Esr1-expressing cells respond to both non

113 ntrast, in each of three subdivisions of the lateral septum, females had greater CRF2 binding than ma

114 perifornical area of the hypothalamus to the lateral septum, from the posterior thalamus to the cauda

115 The lateral septum has strong efferent projections to hypoth

116 es in the olfactory bulb, nucleus accumbens, lateral septum, hippocampus, laterodorsal thalamus, cing

117 In the lateral septum, however, marked variability was observed

118 ey brain regions and circuits, including the lateral septum, hypothalamus, amygdala, bed nucleus of t

119 ed OXT activity, whereas inactivation of the lateral septum-hypothalamus path attenuated this effect.

120 ter injection into the dorsal hippocampus or lateral septum in adult male rats.

121 of the caudal periaqueductal gray and in the lateral septum in aggressive lactating mice.

122 the ventral telencephalon), a homolog of the lateral septum in mammals.

123 eously recorded from rat CA1 and caudodorsal lateral septum in rat during a rewarded navigation task

124 logical probes to estimate the volume of the lateral septum in the BXD line of recombinant inbred mic

125 ria terminalis, and intermediate zone of the lateral septum, in which CRF1, V1aR, and OTR receptors,

126 rate species, in which VP innervation of the lateral septum is consistently greater in males than in

127 that either or both the anterior BNST or the lateral septum is ideally situated to trigger HPA axis a

128 The authors report that AVP in the lateral septum is important for pair bond formation.

129 n of the forebrain, particularly that of the lateral septum, is associated with social behaviors such

130 or colliculi, islands of Calleja, subiculum, lateral septum, lateral and dorsomedial hypothalamic nuc

131 The effects of hippocampal and lateral septum lesions were compared in rats tested in a

132 tin (0, 50, 125, 250 ng/0.5 microl) into the lateral septum (LS) and immediately afterward were rated

133 of MT and CRH immunoreactivity in the dorsal lateral septum (LS) and medial amygdala of field sparrow

134 ctional glutamatergic synaptic inputs to the lateral septum (LS) and optogenetic activation of vHPC p

135 d an increased number of Fos-ir cells in the lateral septum (LS) and the bed nucleus of the stria ter

136 Here, we show that the lateral septum (LS) and the central nucleus of the amygd

137 responding effects on neural activity in the lateral septum (LS) are both necessary and sufficient to

138 us to ventral tegmental area (VTA) that uses lateral septum (LS) as a relay.

139 ic acid-releasing (GABAergic) neurons in the lateral septum (LS) as the key player in chronic itch-in

140 A) D1 receptor antagonist SCH-23390 into the lateral septum (LS) blocks ethanol-induced suppression o

141 entify an anterior cingulate cortex (ACC) to lateral septum (LS) circuit that is more responsive to l

142 and we recently found indirect evidence that lateral septum (LS) could be a key site where benzodiaze

143 ther possible changes in NE signaling in the lateral septum (LS) could facilitate expression of mater

144 Lateral septum (LS) gates reactivity to stressors, conta

145 The lateral septum (LS) has been implicated in anxiety and f

146 The lateral septum (LS) has been implicated in the regulatio

147 Lateral septum (LS) has re-emerged as an important struc

148 AVP) V1a receptor (V1aR) antagonist into the lateral septum (LS) increased social play behavior in ma

149 The lateral septum (LS) is a basal forebrain GABAergic regio

150 Lateral septum (LS) is a brain region critically involve

151 e current study was to determine whether the lateral septum (LS) is a component of the putative neura

152 The lateral septum (LS) is a forebrain structure that is imp

153 The lateral septum (LS) is anatomically positioned to play a

154 butyric acid (GABA) neurotransmission in the lateral septum (LS) is implicated in modulating various

155 Lesioning the lateral septum (LS) is known to cause "septal rage," a p

156 nergic neurons selectively projecting to the lateral septum (LS) is sufficient for promoting aggressi

157 The lateral septum (LS) is thought to suppress fear and anxi

158 Since the lateral septum (LS) may play an important role in the in

159 mmunoreactivity in the dorsal portion of the lateral septum (LS) of both strains of mice, and strain-

160 ed the glutamate/GABA-glutamine cycle in the lateral septum (LS) of postpartum female mice.

161 The lateral septum (LS) plays an important role in regulatin

162 hypothalamus (LH) orexin cell field from the lateral septum (LS) using tract-tracing and Fos immunohi

163 ) subregion of rat vmPFC that project to the lateral septum (LS) were recruited by exposure to the sh

164 e examined the role of DH projections to the lateral septum (LS), a brain region implicated in cocain

165 er, whether GABA signaling may change in the lateral septum (LS), a core brain region for regulating

166 N unit activity and serotonin release in the lateral septum (LS), a limbic target of the DRN.

167 ticular interest are vHPC projections to the lateral septum (LS), a region that has been implicated i

168 ignaling were investigated converging on the lateral septum (LS), a region which receives dense hypot

169 ng of subcortical brain regions, such as the lateral septum (LS), a structure that plays important ro

170 vestigation through their projections to the lateral septum (LS), an area with the highest density of

171 oxytocin receptor (OXTR) system, through the lateral septum (LS), contributes to social behavior, whi

172 males had greater OT receptor binding in the lateral septum (LS), lateral amygdala (LatAmyg), and cen

173 perienced, males had less AVP binding in the lateral septum (LS), more AVP binding in the anterior ol

174 grade tracer into the medial amygdala (MeA), lateral septum (LS), or bed nucleus of the stria termina

175 In lateral septum (LS), relaxin-3 fibers were concentrated

176 terminals were observed predominately in the lateral septum (LS), whereas only a few double-labeled f

177 t; 0, 30, 100, and 300 ng) infusion into the lateral septum (LS), which abundantly expresses CRH2 but

178 The lateral septum (LS), which is innervated by the hippocam

179 s of the stria terminalis dorsal (BNSTd) and lateral septum (LS).

180 r brain region involved in aggression is the lateral septum (LS).

181 eurons of the intermediate subnucleus of the lateral septum (LSI) were examined using intracellular r

182 entricular hypothalamus (PVH) to the ventral lateral septum (LSv) that shows a scalable regulation on

183 The septal nuclei, including the medial and lateral septum, make up a basal forebrain region that sh

184 imbic cortex and limbic regions, such as the lateral septum, medial nucleus of the amygdala, subiculu

185 brain GABAergic stress pathways, such as the lateral septum, medial preoptic area or dorsomedial hypo

186 regulation of excitatory transmission in the lateral septum mediolateral nucleus (LSMLN) after chroni

187 entral nucleus of the amygdala (CeA) and the lateral septum mediolateral nucleus (LSMLN).

188 ptum (the ventral and dorsal portions of the lateral septum), midbrain (the periaqueductal gray and t

189 ding the medial part of the caudate nucleus, lateral septum, midline and mediodorsal thalamic nuclei,

190 Low OTR binding in the lateral septum might also be a permissive factor for gro

191 Here, we describe a novel population of lateral septum neurons expressing neurotensin (LS(Nts))

192 ied a population of stress/threat-responsive lateral septum neurotensin (NT(LS)) neurons that are act

193 in the NR1 +/+ and NR1 -/- mice include the lateral septum, nucleus of the solitary tract, and media

194 R-alpha-labeled cells were also found in the lateral septum, nucleus of the stria terminals, subforni

195 tor agonist urocortin 2 was infused into the lateral septum of mice under low- or high-stress (30 min

196 Reexpressing V1aR in the lateral septum of V1aR knockout mice (V1aRKO) using a vi

197 rthermore, overexpression of the V1aR in the lateral septum of wild-type (wt) mice resulted in a pote

198 inally, microinjection of glutamate into the lateral septum or the lateral parabrachial nucleus stimu

199 e sense that it is invaded by neurons of the lateral septum, or possibly transitional neuronal forms

200 ntricular zone, peri-suprachiasmatic region, lateral septum, or ventral tuberal area, the majority of

201 the PE group (1907.32+/-136.3 dpm/mg) in the lateral septum (p<0.05).

202 mmunoreactivity in the LH, as well as in the lateral septum, paraventricular hypothalamic nucleus, ve

203 ese results demonstrate that the V1aR in the lateral septum plays a critical role in the neural proce

204 s were found in the intermediate part of the lateral septum, posterior division of the bed nucleus st

205 h some of the heaviest input coming from the lateral septum, preoptic area, and posterior hypothalamu

206 hus, GluR1 subunit mRNA was prominent in the lateral septum, preoptic area, mediobasal hypothalamus,

207 uronal relays in the ventral hippocampus and lateral septum presents a new foundation for understandi

208 ecifically required for the survival of this lateral-septum projecting neuronal subset during develop

209 provide evidence suggesting that AVP in the lateral septum regulates pair bond formation in male pra

210 for example, the subparaventricular zone and lateral septum, respectively.

211 project to the dorsal region of the rostral lateral septum (rLS).

212 observed scattered rostrocaudally along the lateral septum, rostral to the medial septum.

213 Competitive binding assays in the lateral septum showed that both ligands were effectively

214 Medial and lateral septum (SM, SL), medial preoptic area (POM), and

215 he islands of Calleja, endopiriform nucleus, lateral septum, subfields of the cholinergic basal foreb

216 ulum of hippocampus; claustrum, tania tecta, lateral septum, substantia innominata, and medial and la

217 n associated with behaviors modulated by the lateral septum, such as spatial learning, anxiety, and r

218 g localization of these receptors within the lateral septum, suggesting that not only different neuro

219 n the olfactory bulb, all pallial divisions, lateral septum, suprachiasmatic nucleus, prethalamic and

220 ic pathway, namely, the ventral hippocampus, lateral septum, thalamus, amygdala, and basal forebrain.

221 e caudomedial ventral tegmental area and the lateral septum than females that did not sing.

222 eveals spatial gradients in the striatum and lateral septum that regulate complex social behavior, an

223 These include the lateral septum, the bed nucleus of the stria terminalis,

224 r- and calbindin-expressing cells within the lateral septum, the brain region in which GLP-1R is most

225 ors in the nucleus accumbens, diagonal band, lateral septum, the BST, SCN, PVN, amygdala, anterodorsa

226 nversely, MOR-1C-LI exceeded MOR-1-LI in the lateral septum, the deep laminae of the spinal cord, and

227 the ligand, ephrin-B3, is transcribed in the lateral septum, the major subcortical target of hippocam

228 cuous in the anterior olfactory nucleus, the lateral septum, the medial preoptic area, the periventri

229 areas, including the infralimbic cortex, the lateral septum, the medial preoptic area, the subfornica

230 he accumbens nucleus, the medial septum, the lateral septum, the ventromedial hypothalamic nucleus, t

231 he nucleus accumbens; the dorsal part of the lateral septum; the periventricular region of the ventra

232 ections provide gamma-rhythmic inputs to the lateral septum; these inputs are causally associated wit

233 la to the anterior hypothalamus and then the lateral septum to modulate aggression associated with ma

234 h is demonstrated for CA3 projections to the lateral septum using retrograde labeling.

235 vior had preferential neural activity in the lateral septum ventral and several medial and periventri

236 e neocortex endopiriform nucleus, claustrum, lateral septum, ventral forebrain, hypothalamus, mammill

237 cal regions, the anterior olfactory nucleus, lateral septum, ventral forebrain, several hypothalamic

238 matched that of T. granulosa, except in the lateral septum, ventral hypothalamus, and inferior colli

239 s activation in the medial amygdala, ventral lateral septum, ventromedial hypothalamus, and hypothala

240 n the rat, with notable exceptions including lateral septum, ventromedial nucleus of the hypothalamus

241 Lateral septum volume is a highly variable trait, with a

242 additively with the Chr 1 locus to increase lateral septum volume.

243 osities within the anterior hypothalamus and lateral septum was 20% higher in subjugated animals than

244 otential mediated release of dopamine in the lateral septum was established.

245 f vasopressin neurons and projections in the lateral septum were inappropriate for performing a socia

246 s receives strong descending inputs from the lateral septum, which is connected, in turn, with cortic

247 rmacogenetically suppressing activity of the lateral septum, which is the major conduit between the h

248 deactivation of somatostatin neurons in the lateral septum, which predicted social discrimination de

249 measured vasopressin immunoreactivity in the lateral septum, which was higher in gonadal males than f