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1 refrontal cortex, hippocampus, amygdala, and bed nucleus of the stria terminalis).
2 hypothalamus, the central amygdala, and the bed nucleus of the stria terminalis.
3 itofrontal cortex, basolateral amygdala, and bed nucleus of the stria terminalis.
4 -enhanced startle (LES), is dependent on the bed nucleus of the stria terminalis.
5 extended amygdala, and the posterior lateral bed nucleus of the stria terminalis.
6 tral striatum, the central amygdala, and the bed nucleus of the stria terminalis.
7 the amygdala and at 17 and 24 months in the bed nucleus of the stria terminalis.
8 a major downstream projection structure-the bed nucleus of the stria terminalis.
9 bercle, central nucleus of the amygdala, and bed nucleus of the stria terminalis.
10 ons that project out of the CeA and into the bed nucleus of the stria terminalis.
11 the medial amygdala, cortical amygdala, and bed nucleus of the stria terminalis.
12 /magnocellular preoptic nucleus (SI/MA), and bed nucleus of the stria terminalis.
13 sterodorsal medial amygdala, and 103% in the bed nucleus of the stria terminalis.
14 tria terminalis and scattered throughout the bed nucleus of the stria terminalis.
15 limb of the anterior commissure nucleus, and bed nucleus of the stria terminalis.
16 n releasing factor-containing neurons of the bed nucleus of the stria terminalis.
17 icate that CeA CRF1 neurons project into the bed nucleus of the stria terminalis.
18 drogen receptors (AR) in the medial anterior bed nucleus of the stria terminalis, a key brain area th
19 associated with increased metabolism in the bed nucleus of the stria terminalis, a key component of
21 f VMN(SF1) fibers projecting to the anterior bed nucleus of the stria terminalis (aBNST), but not to
22 eeding while activation of AgRP --> anterior bed nucleus of the stria terminalis (aBNST)vl projection
23 identified a discrete region of the anterior bed nucleus of the stria terminalis (aBST) as a candidat
24 s in a circumscribed portion of the anterior bed nucleus of the stria terminalis (aBST), which we pre
26 number of FLI neurons in the lateral septum, bed nucleus of the stria terminalis, amygdala, paraventr
27 ted with anxiety and stress behaviors (i.e., bed nucleus of the stria terminalis, amygdala, periaqued
28 d medial pallium, lateral and medial septum, bed nucleus of the stria terminalis, amygdala, preoptic
29 ing that P metabolites have an effect on the bed nucleus of the stria terminalis and anxiety rather t
31 erved in several other regions including the bed nucleus of the stria terminalis and central amygdala
32 paraventricular nucleus, supraoptic nucleus, bed nucleus of the stria terminalis and central nucleus
33 ding anterior and posterior subnuclei of the bed nucleus of the stria terminalis and lateral septum.
34 pressed heroin intake when injected into the bed nucleus of the stria terminalis and shell of the nuc
35 res the coordinated activation of D2R in the bed nucleus of the stria terminalis and the central amyg
36 l septum, the ventromedial hypothalamus, the bed nucleus of the stria terminalis and the medial amygd
37 nic acid lesions of the medial amygdala, the bed nucleus of the stria terminalis and the medial preop
38 from the medial nucleus of the amygdala, the bed nucleus of the stria terminalis and the medial preop
40 ng-induced c-fos expression in the principle bed nucleus of the stria terminalis and the ventrolatera
41 ly continuous with the medial aspects of the bed nucleus of the stria terminalis and the ventromedial
42 cluding the central nucleus of the amygdala, bed nucleus of the stria terminalis, and a transition ar
43 cluding the central nucleus of the amygdala, bed nucleus of the stria terminalis, and a transition ar
45 ost abundant in the medial preoptic nucleus, bed nucleus of the stria terminalis, and anterior hypoth
46 s densely expressed in the stress-responsive bed nucleus of the stria terminalis, and bilateral injec
47 nol-induced Fos-IR changes (caudate putamen, bed nucleus of the stria terminalis, and CA1 region of t
48 central nuclei of the amygdala and anterior bed nucleus of the stria terminalis, and densely to the
49 cularly in subdivisions of the amygdala, the bed nucleus of the stria terminalis, and hippocampus.
50 n the allocortex, claustrum, lateral septum, bed nucleus of the stria terminalis, and in many hypotha
51 T fibers throughout the hypothalamus, in the bed nucleus of the stria terminalis, and in the amygdala
52 ll of the nucleus accumbens (AccSh), lateral bed nucleus of the stria terminalis, and intermediate zo
53 the lateral septum, dorsolateral area of the bed nucleus of the stria terminalis, and lateral habenul
54 te nucleus, central nucleus of the amygdala, bed nucleus of the stria terminalis, and lateral septum.
55 al nuclei, amygdalostriatal transition area, bed nucleus of the stria terminalis, and medial habenula
56 ippocampus, central nucleus of the amygdala, bed nucleus of the stria terminalis, and medial parvocel
57 ased Fos protein expression in the amygdala, bed nucleus of the stria terminalis, and medial preoptic
58 ctal gray, thalamus, hypothalamus, amygdala, bed nucleus of the stria terminalis, and other central s
59 cell layer, dentate gyrus polymorphic layer, bed nucleus of the stria terminalis, and paraventricular
60 lamus, amygdala (central and corticomedial), bed nucleus of the stria terminalis, and prefrontal cort
61 that the shell of the nucleus accumbens, the bed nucleus of the stria terminalis, and the central nuc
62 reoptic area, periventricular preoptic area, bed nucleus of the stria terminalis, and the medial amyg
63 vities within the hippocampus, amygdala, the bed nucleus of the stria terminalis, and the prefrontal
64 order neurons in the amygdala, hypothalamus, bed nucleus of the stria terminalis, and to a remarkable
65 n heterogenous regions such as the amygdala, bed nucleus of the stria terminalis, and ventral forebra
66 ricular hypothalamus, premammillary nucleus, bed nucleus of the stria terminalis, and ventral posteri
67 h fewer neurons in the central amygdala, the bed nucleus of the stria terminalis, and visceral cortic
68 e medial and lateral hypothalamus, amygdala, bed nucleus of the stria terminalis, and visceral cortic
69 significant effect on Fos expression in the bed nucleus of the stria terminalis, another forebrain a
70 tion, including notable contributions of the bed nucleus of the stria terminalis, anterior insula, an
71 emonstrates that the medial amygdala and the bed nucleus of the stria terminalis are not involved in
72 the central nucleus of the amygdala and the bed nucleus of the stria terminalis as glucocorticoid-se
73 he preoptic area of the hypothalamus and the bed nucleus of the stria terminalis as well as novel dim
74 ocesses of neurons in the lateral septum and bed nucleus of the stria terminalis, as well as in sever
75 Also, infusion of antisauvagine-30 into the bed nucleus of the stria terminalis (BNST) 15 min, but n
77 also identified in hippocampus, the lateral bed nucleus of the stria terminalis (BNST) and globus pa
78 and increased CRF mRNA within the amygdala, bed nucleus of the stria terminalis (BNST) and paraventr
79 ue phase relationship between the MUA of the bed nucleus of the stria terminalis (BNST) and the SCN;
80 ects to the posteromedial subdivision of the bed nucleus of the stria terminalis (BNST) and to the me
81 females in the cingulate cortex and rostral bed nucleus of the stria terminalis (BNST) at 2 h, and i
82 ic paraventricular nucleus (PVN) or into the bed nucleus of the stria terminalis (BNST) but not into
84 uggests norepinephrine (NE) signaling in the bed nucleus of the stria terminalis (BNST) could have a
85 the medial amygdala (MeA) and reduced in the bed nucleus of the stria terminalis (BNST) during novelt
90 sing factor (CRF)-mediated mechanisms in the bed nucleus of the stria terminalis (BNST) have a pivota
91 , or of an alpha2-receptor agonist, into the bed nucleus of the stria terminalis (BNST) in rats marke
92 s, we identify a surprising new role for the bed nucleus of the stria terminalis (BNST) in the coordi
94 nvolvement of the central amygdala (CeA) and bed nucleus of the stria terminalis (BNST) in the genesi
95 ctional data support a critical role for the bed nucleus of the stria terminalis (BNST) in the intera
96 nal Fos results, we determined the effect of bed nucleus of the stria terminalis (BNST) injections of
98 he central nucleus of the amygdala (CeA) and bed nucleus of the stria terminalis (BNST) is a critical
106 ce abuse, and noradrenergic signaling in the bed nucleus of the stria terminalis (BNST) is thought to
110 se-activating peptide (PACAP) systems in the bed nucleus of the stria terminalis (BNST) mediates many
111 s investigated the effects of lesions of the bed nucleus of the stria terminalis (BNST) on conditione
113 alpha2-adrenergic receptors (AR) within the bed nucleus of the stria terminalis (BNST) reduce stress
114 Although specific neuronal groups in the bed nucleus of the stria terminalis (BNST) related to an
115 nspecific had lower levels of peptide in the bed nucleus of the stria terminalis (BNST) than isolated
116 interact in a serial manner to activate the bed nucleus of the stria terminalis (BNST) to drive stre
118 eived pretraining excitotoxic lesions of the bed nucleus of the stria terminalis (BNST) to that of sh
119 e potential role of CRF projections from the bed nucleus of the stria terminalis (BNST) to the VTA, C
120 ateral nucleus of the amygdala (BlA), or the bed nucleus of the stria terminalis (BNST) were evaluate
121 study examined the role of the amygdala and bed nucleus of the stria terminalis (BNST), 2 systems th
122 so assessed the role of CRF receptors in the bed nucleus of the stria terminalis (BNST), a brain regi
123 Both dynorphin and KOR are expressed in the bed nucleus of the stria terminalis (BNST), a brain regi
124 of these catecholamines are found within the bed nucleus of the stria terminalis (BNST), a brain rela
125 ises in extracellular dopamine levels is the bed nucleus of the stria terminalis (BNST), a CRF-rich c
126 o identify a precise neural mechanism in the bed nucleus of the stria terminalis (BNST), a limbic bra
128 lly depresses excitatory transmission in the bed nucleus of the stria terminalis (BNST), a region cri
129 rojections innervate distinct regions of the bed nucleus of the stria terminalis (BNST), a structure
130 central amygdaloid nucleus (CeA) and in the bed nucleus of the stria terminalis (BNST), although rob
131 pable of affecting 5-HT systems, such as the bed nucleus of the stria terminalis (BNST), amygdala, an
133 (LH), central nucleus of the amygdala (CeA), bed nucleus of the stria terminalis (BNST), and insular
134 ntral nucleus of the amygdala (CeA), lateral bed nucleus of the stria terminalis (BNST), and nucleus
135 PG-LTD) of glutamatergic transmission in the bed nucleus of the stria terminalis (BNST), and that ex
136 cular nucleus (PVN) of the hypothalamus, the bed nucleus of the stria terminalis (BNST), and the cent
137 uded the amygdala, periqueductal gray (PAG), bed nucleus of the stria terminalis (BNST), anterior cin
138 including the insular gustatory cortex (IC), bed nucleus of the stria terminalis (BNST), central nucl
139 n structures like the gustatory cortex (GC), bed nucleus of the stria terminalis (BNST), central nucl
141 entral nucleus of the amygdala (CeA) and the bed nucleus of the stria terminalis (BNST), each of whic
142 l stimulation of the CeA, or the neighboring bed nucleus of the stria terminalis (BNST), initiates bo
143 ease in both 2-DG and c-fos activity), e.g., bed nucleus of the stria terminalis (BNST), lateral habe
144 as greatly reduced in the dorsal and ventral bed nucleus of the stria terminalis (BNST), lateral sept
145 s-ir) in several brain regions including the bed nucleus of the stria terminalis (BNST), medial preop
147 f the accessory olfactory bulb (gr-AOB), the bed nucleus of the stria terminalis (BNST), MPOA, the me
148 striatum, various subfields of the amygdala, bed nucleus of the stria terminalis (BNST), optic tectum
149 was induced in several nuclei including the bed nucleus of the stria terminalis (BNST), paraventricu
150 ucleus accumbens (Acb), preoptic area (POA), bed nucleus of the stria terminalis (BNST), posterior do
151 t that in the dorsolateral and ventrolateral bed nucleus of the stria terminalis (BNST), recruitment
152 the central nucleus of the amygdala and the bed nucleus of the stria terminalis (BNST), respectively
153 culum, several preoptic nuclei, the anterior bed nucleus of the stria terminalis (BNST), the anterior
154 ether these effects require NA inputs to the bed nucleus of the stria terminalis (BNST), vehicle or s
156 MPOA are from the medial amygdala (MeA) and bed nucleus of the stria terminalis (BNST), which mediat
157 evidence implicates a tiny brain region-the bed nucleus of the stria terminalis (BNST)-in the body's
158 tion may specifically increase long-duration bed nucleus of the stria terminalis (BNST)-mediated aver
163 frontal cortex, nucleus accumbens (NAc), and bed nucleus of the stria terminalis (BNST)], whereas pro
164 iasmatic [SCN]) and extended amygdala (i.e., bed nucleus of the stria terminalis [BNST] and medial am
167 of the amygdala (CeAL) and the dorsolateral bed nucleus of the stria terminalis (BNSTDL) coordinate
168 eral nucleus of the amygdala, dorsal lateral bed nucleus of the stria terminalis (BNSTdl), anterior p
169 entral nucleus of the amygdala (CN), ventral bed nucleus of the stria terminalis (BNSTv), and nucleus
170 cocaine-induced c-fos mRNA expression in the bed nucleus of the stria terminalis (BST) and amygdala o
171 hypothalamic nucleus, medial preoptic area, bed nucleus of the stria terminalis (BST) and hippocampu
172 ed mole-rats had very few VP-ir cells in the bed nucleus of the stria terminalis (BST) and none in th
174 ciated with prosocial behavior including the bed nucleus of the stria terminalis (BST) and the medial
175 nucleus of the amygdala (Ce) and the lateral bed nucleus of the stria terminalis (BST) are highly sim
176 n the medial preoptic area and posteromedial bed nucleus of the stria terminalis (BST) in aged rats r
177 hypermetabolism in a cluster comprising the bed nucleus of the stria terminalis (BST) in rats expres
178 Numerous lines of evidence suggest that the bed nucleus of the stria terminalis (BST) is well positi
179 elevant peptide vasopressin (AVP) within the bed nucleus of the stria terminalis (BST) of adult brain
180 H), central nucleus of the amygdala (Ce) and bed nucleus of the stria terminalis (BST) than in hamste
182 ease food intake by acting on neurons of the bed nucleus of the stria terminalis (BST), a component o
183 on in the forebrain of amniotes has been the bed nucleus of the stria terminalis (BST), but numerous
184 central nucleus of the amygdala (Ce) and the bed nucleus of the stria terminalis (BST), the two major
187 ge that project to the principal part of the bed nucleus of the stria terminalis (BST; 43%), and the
188 stria terminalis (BSTv), whereas the dorsal bed nucleus of the stria terminalis (BSTd) and the media
190 ilitation of the HPA response in the lateral bed nucleus of the stria terminalis (BSTL), compared to
193 ng cells in the dorsolateral division of the bed nucleus of the stria terminalis (BSTld), part of the
194 ell, central amygdala (ceA) and laterodorsal bed nucleus of the stria terminalis (BSTLD), the bluntin
196 -opioid receptor labeling in the POM, medial bed nucleus of the stria terminalis (BSTm), and periaque
197 amygdala (CEAl) and the oval nucleus of the bed nucleus of the stria terminalis (BSTov) have been li
198 e amygdala (CEAl/c) and oval division of the bed nucleus of the stria terminalis (BSTov), which form
200 to express T-induced Fos: the posteromedial bed nucleus of the stria terminalis (BSTPM), posteromedi
202 unilaterally into the ventral portion of the bed nucleus of the stria terminalis (BSTV) to destroy ne
203 easing norepinephrine release in the ventral bed nucleus of the stria terminalis (BSTv) with the alph
204 e medial preoptic area (MPO) and the ventral bed nucleus of the stria terminalis (BSTv), whereas the
206 neurons project mainly to the ventrolateral bed nucleus of the stria terminalis (BSTvl), the pre-loc
207 the gustatory region of the thalamus and the bed nucleus of the stria terminalis but not in the insul
208 particular reduced amygdala AT1 receptor and bed nucleus of the stria terminalis c-Fos messenger RNA
209 RF-ir neurons were visualized in the cortex, bed nucleus of the stria terminalis, central amygdala, h
210 ent in the infralimbic and insular cortices, bed nucleus of the stria terminalis, central nucleus of
211 water and electrolyte balance including the bed nucleus of the stria terminalis, central nucleus of
212 leus (PVN), arcuate nucleus, lateral septum, bed nucleus of the stria terminalis, central, medial and
213 g in the anterior olfactory nucleus, LS, and bed nucleus of the stria terminalis, compared with naive
214 Two exceptions were the posterointermediate bed nucleus of the stria terminalis, containing more neu
215 lability in the amygdalohippocampal area and bed nucleus of the stria terminalis correlated positivel
216 tropin-releasing factor (CRF) neurons in the bed nucleus of the stria terminalis (CRF(BNST)) in mice.
219 ral dose) administered into the dorsolateral bed nucleus of the stria terminalis (dlBNST) immediately
221 ly gene mapping highlighted the dorsolateral bed nucleus of the stria terminalis (dlBST) as a structu
222 tively; however, both triggered increases in bed nucleus of the stria terminalis dorsal (BNSTd) and l
223 rved deep brain structures such as amygdala, bed nucleus of the stria terminalis, dorsal raphe, and l
225 triple labeled neurons were observed in the bed nucleus of the stria terminalis following WGA-Au-HRP
226 d behavioral responses: the amygdala and the bed nucleus of the stria terminalis for sustaining adapt
228 Lesions of either the medial amygdala or the bed nucleus of the stria terminalis have no effect on th
229 tion were apparent in the nucleus accumbens, bed nucleus of the stria terminalis, hippocampus, and co
230 ptic area (LPOA) and ventral division of the bed nucleus of the stria terminalis; however, lesions of
231 e present in the suprachiasmatic nucleus and bed nucleus of the stria terminalis; however, there are
232 RT-immunoreactive cells were observed in the bed nucleus of the stria terminalis, hypothalamic parave
233 abeled cells in several areas, including the bed nucleus of the stria terminalis, hypothalamic region
234 , anteroventral periventricular nucleus, and bed nucleus of the stria terminalis in a distribution co
235 FR(2) binding was higher in the encapsulated bed nucleus of the stria terminalis in males than female
236 work implicating PACAP signaling within the bed nucleus of the stria terminalis in mediating the con
237 ifferentiation: the principal nucleus of the bed nucleus of the stria terminalis, in which males have
238 as such as the septum, the amygdala, and the bed nucleus of the stria terminalis; in areas involved i
240 n the central nucleus of the amygdala (CeA), bed nucleus of the stria terminalis (lateral-dorsal divi
241 cleus (AON), and more OT binding in the AON, bed nucleus of the stria terminalis, LS, and lateral amy
243 al and posteroventral medial amygdala (MeA), bed nucleus of the stria terminalis, medial preoptic nuc
244 on increased significantly in the claustrum, bed nucleus of the stria terminalis, medial preoptic nuc
245 reactive cells were seen unilaterally in the bed nucleus of the stria terminalis, medial ventral pall
246 and moderate projections from the posterior bed nucleus of the stria terminalis, mesocortical struct
247 ntly in the preoptic area, amygdala, septum, bed nucleus of the stria terminalis, midline thalamus, a
248 c area (POA) and medial preoptic area/medial bed nucleus of the stria terminalis (mPOA/BSTm), and the
250 ction and OT/c-fos cells in the medioventral bed nucleus of the stria terminalis of female mice but n
251 binding in the medial preoptic area and the bed nucleus of the stria terminalis of non-responsive mi
252 ry synaptic transmission was enhanced in the bed nucleus of the stria terminalis of rats that perform
254 801 did not increase FLI in caudate-putamen, bed nucleus of the stria terminalis, or ventral pallidum
255 table staining in the septum, diagonal band, bed nucleus of the stria terminalis, organum vasculosum,
256 labeling from the nPGi was prominent in the bed nucleus of the stria terminalis, paraventricular nuc
257 the hypothalamus and a larger volume of the bed nucleus of the stria terminalis, paraventricular nuc
258 sion within nucleus accumbens shell, lateral bed nucleus of the stria terminalis, paraventricular nuc
259 ypothalamus, arcuate nucleus, preoptic area, bed nucleus of the stria terminalis, paraventricular tha
260 through its interactions with the amygdala, bed nucleus of the stria terminalis, periaqueductal gray
261 tioned autonomic effector regions, including bed nucleus of the stria terminalis, perifornical and an
262 s; ventral pallium; nucleus basalis Meynert; bed nucleus of the stria terminalis; preoptic area; para
263 eral injections of RXFP3 antagonist into the bed nucleus of the stria terminalis significantly decrea
264 ubfields of the cholinergic basal forebrain, bed nucleus of the stria terminalis, striohypothalamic r
265 of terminals were encountered in the septum, bed nucleus of the stria terminalis, substantia innomina
266 testing also failed a-Helical CRF9-41 in the bed nucleus of the stria terminalis suggested that this
267 continuum with the substantia innominata and bed nucleus of the stria terminalis, supporting the conc
268 rebral cortex, medial septum, preoptic area, bed nucleus of the stria terminalis, supraoptic nucleus,
269 prefrontal cortex (dmPFC), anterior insula, bed nucleus of the stria terminalis, thalamus, and midbr
270 tion of GABAA-IPSCs (D1-LTPGABA) in the oval bed nucleus of the stria terminalis that was positively
271 at control descending output (via the CNA or bed nucleus of the stria terminalis) that in turn regula
272 MEA), the central tegmental field (CTF), the bed nucleus of the stria terminalis, the anterior hypoth
273 nucleus, anteromedial and oval nuclei of the bed nucleus of the stria terminalis, the central nucleus
274 nto the central EA structures of the lateral bed nucleus of the stria terminalis, the central sublent
275 e Purkinje cell layer of the cerebellum, the bed nucleus of the stria terminalis, the claustrum (alph
276 al cortices, the lateral septal nucleus, the bed nucleus of the stria terminalis, the fundus striati,
277 l nucleus of the amygdala and to the lateral bed nucleus of the stria terminalis, the latter region r
278 including the lateral and medial septum, the bed nucleus of the stria terminalis, the medial and cent
279 ers were also seen in the septal nuclei, the bed nucleus of the stria terminalis, the paraventricular
280 , hippocampus and septum, the basal ganglia, bed nucleus of the stria terminalis, the thalamus includ
281 found in other aggression areas, such as the bed nucleus of the stria terminalis, the ventrolateral h
282 dorsal premammillary nucleus, and principal bed nucleus of the stria terminalis, this is the first i
283 were mainly observed in the medial amygdala/bed nucleus of the stria terminalis to lateral septum ci
285 exigenic cytokine, can act on neurons of the bed nucleus of the stria terminalis to reduce food intak
287 ventrolateral (subcommissural) aspect of the bed nucleus of the stria terminalis (vBNST) in motivatio
291 d FLI in caudate-putamen, nucleus accumbens, bed nucleus of the stria terminalis, ventral pallidum, c
292 reased after castration in the interstitial (bed) nucleus of the stria terminalis, ventral aspect (IN
293 the olfactory bulb, lateral septal nucleus, bed nucleus of the stria terminalis, ventromedial hypoth
297 LH orexin cell field from lateral septum and bed nucleus of the stria terminalis were Fos-activated d
298 eurons participate in specific nuclei of the bed nucleus of the stria terminalis, which plays essenti
299 us of the amygdala and then to the principal bed nucleus of the stria terminalis, which suppresses te
300 lso report a sex difference in ERbeta in the bed nucleus of the stria terminalis, with males showing
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