ライフサイエンスコーパス: lateral septum

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

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

3 us chemoarchitectonic zones of the mammalian lateral septum.

4 serotonin removal with maximal rates in the lateral septum.

5 of vasopressin-immunoreactive fibers in the lateral septum.

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

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

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

9 olone injection in the dorsal hippocampus or lateral septum.

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

11 roperties of the dopamine innervation of the lateral septum.

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

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

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

15 cal interconnections between the rdAcbSh and lateral septum.

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

17 the highest expression level limited to the lateral septum.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

100 The lateral septum has strong efferent projections to hypoth

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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