ライフサイエンスコーパス: medial amygdala

1 nd predominately within the hypothalamus and medial amygdala.

2 region projects to the deeper laminae of the medial amygdala.

3 mice exhibited an induction of Fos-IR in the medial amygdala.

4 rons in the paraventricular nucleus (PVN) or medial amygdala.

5 bed nucleus of the stria terminalis and the medial amygdala.

6 ventricular nucleus of the hypothalamus; and medial amygdala.

7 rt of the bed nucleus, and the posterodorsal medial amygdala.

8 stimulation of the lateral hypothalamus and medial amygdala.

9 ain regions, one of the major hubs being the medial amygdala.

10 organ, and downstream limbic neurons in the medial amygdala.

11 2) increased volume of the posterior dorsal medial amygdala.

12 n regional volume and neuronal number of the medial amygdala.

13 also receives moderate Ucn 3 input from the medial amygdala.

14 urine) increased expression only in anterior medial amygdala.

15 ugh its action on OT receptors (OTRs) in the medial amygdala.

16 ria terminalis, paraventricular nucleus, and medial amygdala.

17 ypothalamus, ventrolateral hypothalamus, and medial amygdala.

18 d with a decrease in c-fos expression in the medial amygdala.

19 aced parallel projections from the posterior medial amygdala, activated by reproductive or defensive

20 ings further suggest that stimulation of the medial amygdala activates substance P receptors in the m

21 rrelation between the left fusiform and left medial amygdala activation only in normal females, and o

22 Projections sites of the medial amygdala also failed to show a Fos-IR induction i

23 ore Fos-immunoreactive (Fos-ir) cells in the medial amygdala (AMYGme) and medial preoptic area (MPO)

24 FI-B expression in the PVN, arcuate nucleus, medial amygdala and all hippocampal subfields of virgin

25 imulating electrodes were implanted into the medial amygdala and cannula electrodes were implanted in

26 ar neurones in suprachiasmatic nuclei (SCN), medial amygdala and habenular nuclei in JP17 rats; the r

27 ally, the effects of dual stimulation of the medial amygdala and lateral hypothalamus upon response l

28 y elevated following dual stimulation of the medial amygdala and lateral hypothalamus.

29 In the medial amygdala and medial posterior BST, exposure to no

30 pulation; and (iv) ERalpha expression in the medial amygdala and medial preoptic area may fully media

31 s in Foxp2 distribution, most notably in the medial amygdala and nucleus accumbens, and in layer V co

32 n regions (for example, the locus coeruleus, medial amygdala and paraventricular nucleus), implicatin

33 of these regions, such as the posterodorsal medial amygdala and several medial hypothalamic sites, i

34 The present study demonstrates that the medial amygdala and the bed nucleus of the stria termina

35 as observed within the same subnuclei of the medial amygdala and ventromedial hypothalamus, regions i

36 othalamic nucleus, 123% in the posterodorsal medial amygdala, and 103% in the bed nucleus of the stri

37 l preoptic nucleus, paraventricular nucleus, medial amygdala, and cortical amygdala in association wi

38 bed nucleus of the stria terminalis, and the medial amygdala, and in brainstem regions including the

39 -dorsal and postero-ventral divisions of the medial amygdala, and into the postero-medial cortical am

40 ventromedial hypothalamus, and posterodorsal medial amygdala, and it was maintained in these sites by

41 affected, i.e. the medial prefrontal cortex, medial amygdala, and lateral septum.

42 ncluding the bed nucleus of stria terminalis,medial amygdala, and medial parabrachial nucleus.

43 ens, ventral pallidum, medial preoptic area, medial amygdala, and the supraoptic nucleus of the hypot

44 memory, including OTR in the hippocampus and medial amygdala, and V1aR in the anterior and laterodors

45 os-positive cells in the prelimbic mPFC, the medial amygdala, and ventral PAG.

46 and, to a lesser extent, the anterior dorsal medial amygdala; and 2) increased volume of the posterio

47 cluded hypothalamic paraventricular nucleus, medial amygdala, anterior cingulate, frontal, parietal,

48 mammals the median preoptic nucleus and the medial amygdala are located.

49 ) of the medial preoptic area (MPOA) and the medial amygdala are two brain regions in which male rat

50 he medial preoptic nucleus and posterodorsal medial amygdala at PND 20 and 25, respectively.

51 in the bed nucleus of the stria terminalis, medial amygdala, basal septal region, magnocellular basa

52 y numbers, which were mainly observed in the medial amygdala/bed nucleus of the stria terminalis to l

53 ted dopamine in raphe, lateral amygdala, and medial amygdala but decreased dopamine in septum and loc

54 r of neuronal activation) in the central and medial amygdala but had normal c-fos responses in parave

55 n subiculum, hippocampus, nucleus accumbens, medial amygdala, but not lateral amygdala, septum, and h

56 tor (tPA) was upregulated in the central and medial amygdala by acute restraint stress, where it prom

57 n the PVN, median eminence, arcuate nucleus, medial amygdala, CA2 and CA3 subfields of the hippocampu

58 clei, hippocampal formation, basolateral and medial amygdala, central gray, pontine nuclei, interpedu

59 cells; beta5-broadly distributed, neocortex, medial amygdala, cerebellar granule and Purkinje cells,

60 e septum, preoptic region, stria terminalis, medial amygdala, claustrum, internal capsule, and globus

61 This categorization of responses in medial amygdala conforms to our previously reported find

62 The highest activity was found in the medial amygdala, cortical amygdala, and bed nucleus of t

63 ion is that targeting neuromodulation in the medial amygdala could potentially help prevent developme

64 Muscimol infusion into the medial amygdala decreased freezing to the male rat but n

65 e medial preoptic area, arcuate nucleus, and medial amygdala differentiate into either mature neurons

66 he medial preoptic nucleus (MPN), the dorsal medial amygdala (dMEA), the central tegmental field (CTF

67 ession in different sub-regions of posterior medial amygdala (dorsal and ventral, respectively).

68 Here we demonstrate that OT acts in the medial amygdala during the initial exposure to facilitat

69 In the caudal part of the posterodorsal medial amygdala, estrogen increased OFQ/N mRNA levels, a

70 eral amygdala, and are also prevalent in the medial amygdala for sensory stimuli that are emotionally

71 ctrodes were implanted into sites within the medial amygdala from which subseizure levels of stimulat

72 lei, nucleus of the lateral olfactory tract, medial amygdala, hippocampal formation, substantia nigra

73 clusion, pubertal testosterone organizes the medial amygdala in a subregion-specific manner, which ma

74 m1 neurons likely occurs in both the PVH and medial amygdala, in contrast to energy expenditure regul

75 elective BLA damage and a functional central-medial amygdala invest nearly 100% more money in unfamil

76 monstrate that OT receptor activation in the medial amygdala is both necessary and sufficient for soc

77 The medial amygdala is important in social behaviors, many o

78 The medial amygdala is known to powerfully suppress predator

79 The medial amygdala is known to powerfully suppress predator

80 nstrate that the lateral septum, but not the medial amygdala, is critical for social recognition.

81 increased IEG expression in mouse posterior medial amygdala (like conspecific stimuli).

82 e nucleus accumbens shell, and moderately to medial amygdala, locus coeruleus and solitary tract, con

83 rade labeling in two chemosensory areas: the medial amygdala (MA) and the lateral posterior hypothala

84 onasal recipient (nucleus sphericus, NS, and medial amygdala, MA), and nonchemosensory (e.g., posteri

85 s (MPN), the ventromedial nucleus (VMN), the medial amygdala (mAMY), and the cortical amygdala (CoAMY

86 subparaventricular zone of the hypothalamus, medial amygdala, margin of the lateral habenula, posteri

87 These patterns of IEG expression in medial amygdala may provide glimpses of a tertiary sorti

88 The medial amygdala (Me) has been implicated in various soci

89 ing in sexually naive VNX males and enhances medial amygdala (Me) immediate-early gene activation by

90 of the accessory olfactory tract, BAOT, and medial amygdala, ME, replicating our previous study) and

91 lutamatergic inputs to the MPOA are from the medial amygdala (MeA) and bed nucleus of the stria termi

92 C-Fos activity was elevated in the medial amygdala (MeA) and reduced in the bed nucleus of

93 ons expressing single-minded-1 (SIM1) in the medial amygdala (MeA) and that loss of ERalpha in these

94 ucleus of the stria terminalis (BST) and the medial amygdala (MeA) are anatomically connected sites n

95 h responses to predators have implicated the medial amygdala (MeA) as an important region involved in

96 (DSD) in both the central amygdala (CeA) and medial amygdala (MeA) but not in the basolateral amygdal

97 es have a larger anterior subdivision of the medial amygdala (MeA) compared to adults.

98 d that single-minded-1 (SIM1) neurons in the medial amygdala (MeA) express abundant levels of ERalpha

99 ignificantly reduced c-Fos activation in the medial amygdala (MeA) following both footshock and fear

100 eptor in aromatase-expressing neurons of the medial amygdala (MeA) fully recapitulates the eliminatio

101 While the medial amygdala (MeA) has been implicated in prototypic

102 This study examined the participation of the medial amygdala (MeA) in unconditioned fear.

103 The medial amygdala (MeA) is a central hub in the olfactory

104 The medial amygdala (MeA) is crucial in the expression of se

105 ng males as subjects have indicated that the medial amygdala (MeA) is involved in discrimination betw

106 The medial amygdala (MeA) occupies a central position in the

107 The medial amygdala (MeA) plays a critical role in processin

108 of the CRS-induced structural remodeling of medial amygdala (MeA) stellate neurons.

109 males also displayed less ERalpha-IR in the medial amygdala (MeA) than IL females.

110 unique sex difference in the developing rat medial amygdala (MeA) that is regulated by cannabinoids.

111 that regulate social behavior, including the medial amygdala (MeA), and the expression of male prosoc

112 us of the stria terminalis (BNST), MPOA, the medial amygdala (MeA), and the region corresponding to t

113 (IR) in the posterodorsal and posteroventral medial amygdala (MeA), bed nucleus of the stria terminal

114 ignificantly decreased GR-ir in the POA, mp, medial amygdala (MeA), BNST, and rostral pars distalis.

115 tely lower in the central amygdala (CeA) and medial amygdala (MeA), but not in the basolateral amygda

116 icroinjected with retrograde tracer into the medial amygdala (MeA), lateral septum (LS), or bed nucle

117 cannulated targeting central amygdala (CeA), medial amygdala (MeA), or basolateral amygdala (BLA), an

118 lfactory bulb (MOB) projects directly to the medial amygdala (MeA), traditionally considered a target

119 Both these systems innervate the medial amygdala (MeA), where activity of the neuropeptid

120 A major source of input to the MPOA is the medial amygdala (MeA), which processes and relays olfact

121 ucleus of the stria terminalis (BST) and the medial amygdala (MeA).

122 jor source of innervation to the MPOA is the medial amygdala (MeA).

123 nals from the PV MOB to the anterior part of medial amygdala (MeA).

124 riment 1), the basolateral amygdala (BLA) or medial amygdala (MeA; Experiment 2) influence the neopho

125 d nucleus of the stria terminalis [BNST] and medial amygdala [MeA]), and these groups of neurons have

126 N) and the lateral part of the posterodorsal medial amygdala (MeApd) express Fos with ejaculation in

127 The posterodorsal subnucleus of the medial amygdala (MeApd) is particularly sensitive to gon

128 MDA receptor activation in the posterodorsal medial amygdala (MEApd) is required at the time of matin

129 PdPN), the lateral part of the posterodorsal medial amygdala (MeApd), the medial cell group of the se

130 The posterodorsal medial amygdala (MeApd), the posterodorsal preoptic nucl

131 one in the lateral part of the posterodorsal medial amygdala (MeApd)-are activated at ejaculation in

132 leus of the BST (pBST) and the posterodorsal medial amygdala (MeAPd).

133 Fos protein expression in the anteroventral medial amygdala (MeAv) with MOB stimulation, but no effe

134 dorsal and posterior ventral regions of the medial amygdala (MePD and MePV, respectively), and parav

135 trocytes in the posterodorsal portion of the medial amygdala (MePD) are sexually dimorphic in adult r

136 The posterodorsal medial amygdala (MePD) exhibits numerous sex differences

137 The posterodorsal nucleus of the medial amygdala (MePD) has a greater volume in male rats

138 The posterodorsal aspect of the medial amygdala (MePD) in rats is sexually dimorphic, be

139 The posterodorsal medial amygdala (MePD) in rodents integrates olfactory a

140 The posterodorsal medial amygdala (MePD) is a sex-steroid-sensitive area t

141 The adult rat posterodorsal medial amygdala (MePD) is sexually dimorphic in regional

142 The posterodorsal aspect of the medial amygdala (MePD) is sexually dimorphic in regional

143 The posterodorsal portion of the medial amygdala (MePD) is sexually dimorphic in several

144 model, we have identified the posteriodorsal medial amygdala (MePD) via excitotoxic lesion studies as

145 emale estrous cycle in the rat posterodorsal medial amygdala (MePD), a relevant area for the modulati

146 fect of stimulation or GnRH in posterodorsal medial amygdala (MePd).

147 eurons in the posteroventral division of the medial amygdala (MePV) using the GAD67-GFP mouse.

148 nd that CIC activity in the hypothalamus and medial amygdala modulates social interactions.

149 rm an intrinsic network (referred to as the "medial amygdala network") that supports social functioni

150 d stronger intrinsic connectivity within the medial amygdala network.

151 about how olfactory inputs are processed by medial amygdala neurons.

152 unique subclass of inhibitory neurons in the medial amygdala nucleus.

153 Injections into the medial amygdala, nucleus accumbens, posterior hypothalam

154 biculum, hippocampus, nucleus accumbens, and medial amygdala of animals in which the eyespots were ma

155 tic pattern of IEG expression appears in the medial amygdala of each species in response to conspecif

156 polymeric microparticles to deliver, in the medial amygdala of female mice, "locked nucleic acid" an

157 tivity in the dorsal lateral septum (LS) and medial amygdala of field sparrows but not song sparrows.

158 in the caudal preoptic area, caudal BST, and medial amygdala of male gerbils is also described.

159 G) expression in both anterior and posterior medial amygdala of male mice, whereas most heterospecifi

160 on olfactory input in MePd than elsewhere in medial amygdala of VNX males.

161 at and had decreased c-fos expression in the medial amygdala on day 14 and in the medial and lateral

162 e number of neurons in the posterior ventral medial amygdala only in males that did not experience en

163 Lesions of either the medial amygdala or the bed nucleus of the stria terminal

164 Other areas of the forebrain, including medial amygdala, piriform cortex, and ventrolateral sept

165 The medial amygdala plays a key role in regulating adult soc

166 antified in the posterodorsal portion of the medial amygdala posterodorsal (MePD), lateral (PLCo), an

167 the presence of deramified microglia in the medial amygdala, prefrontal cortex, and hippocampus.

168 In male hamsters, the medial amygdala responded in a categorically different w

169 nections between the BST and the central and medial amygdala, septal territories, medial pallium, pre

170 ects on volume of specific subregions of the medial amygdala such that the presence of pubertal testo

171 eased neuronal number in the anterior dorsal medial amygdala, suggesting a possible mechanism by whic

172 the effects of ibotenic acid lesions of the medial amygdala, the bed nucleus of the stria terminalis

173 In the medial amygdala, the number of cells expressing AVP mRNA

174 hypothalamus; the basolateral, central, and medial amygdala; the lateral and principal nuclei of the

175 ing suppression of predatory attack from the medial amygdala to the lateral hypothalamus projects to

176 pport for the view that the pathway from the medial amygdala to the lateral hypothalamus underlying s

177 onal arc: the first neuron projects from the medial amygdala to the medial hypothalamus and its funct

178 is mediated, in part, by a pathway from the medial amygdala to the medial hypothalamus which utilize

179 vior includes a substance P pathway from the medial amygdala to the medial hypothalamus.

180 abeled for substance P that project from the medial amygdala to the ventromedial hypothalamus as demo

181 d in late pregnant animals; and (iii) in the medial amygdala, ventral part of the lateral septum and

182 paraventricular thalamic nucleus, habenula, medial amygdala, ventrolateral septum (LSV), most subfie

183 ese studies, in several groups Fos-Li in the medial amygdala was positively correlated with the post-

184 area of the posterodorsal subdivision of the medial amygdala was significantly smaller in prepubertal

185 The derived model indicated that medial amygdala was the source of key efferent and affer

186 Posterodorsal (MePD) and posteroventral medial amygdala were examined for the first time in asso

187 wn to be prolactin-sensitive, notably in the medial amygdala, were identified.

188 ience showed increased Fos expression in the medial amygdala when pheromone exposure and GnRH injecti

189 rumental behaviors and regulates the central-medial amygdala, which subserves impulsive behaviors.

190 hways, but also enhanced the hippocampus and medial amygdala within a day, whereas partial transectio