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1 tract (NTS) and with SP, CGRP and MOR in the parabrachial nucleus.
2 the innermost region of the external lateral parabrachial nucleus.
3 antial projection may be relayed through the parabrachial nucleus.
4 teral medulla, A5 area, and internal lateral parabrachial nucleus.
5 ay matter, dorsal raphe nucleus, and lateral parabrachial nucleus.
6 ssing neurons in the CeA that project to the parabrachial nucleus.
7 y VR1-positive fibers project to the lateral parabrachial nucleus.
8 re expressed at higher levels in the lateral parabrachial nucleus.
9 dbrain raphe nuclei, periaqueductal gray and parabrachial nucleus.
10 dalar nucleus, retrorubral area, and lateral parabrachial nucleus.
11 pothalamus, periaqueductal gray, and lateral parabrachial nucleus.
12 cleus of the solitary tract, and the lateral parabrachial nucleus.
13 ration provide an input to the region of the parabrachial nucleus.
14 aterodorsal tegmental nucleus (LDT), and the parabrachial nucleus.
15 r neurons and is relayed through the lateral parabrachial nucleus.
16 -characterised pathway via the exterolateral parabrachial nucleus.
17 nical feeding regions of arcuate nucleus and parabrachial nucleus.
18 n structures such as the locus coeruleus and parabrachial nucleus.
19 er-Fuse, intertrigeminal region, and lateral parabrachial nucleus.
20 ect to the nucleus of the solitary tract and parabrachial nucleus.
21 stria terminalis,medial amygdala, and medial parabrachial nucleus.
22 d subparafascicular nucleus, and the lateral parabrachial nucleus.
23 sensory trigeminal nucleus, and the lateral parabrachial nucleus.
24 targets the viscerosensory subregions of the parabrachial nucleus.
25 us nucleus and reversed the asymmetry in the parabrachial nucleus.
26 ad axons that projected to the contralateral parabrachial nucleus.
27 ne (PZ)-project to the wake-promoting medial parabrachial nucleus; (2) PZ neurons express c-Fos after
28 tral amygdala neurotensin neurons was to the parabrachial nucleus, a brain region known to be importa
29 o play a role in appetite suppression is the parabrachial nucleus, a heterogeneous population of neur
30 oreover, we show that CCK VN inputs onto the parabrachial nucleus activate Calca-expressing neurons a
32 tial input from glutamatergic neurons in the parabrachial nucleus and adjacent precoeruleus area.
34 tomic assay, and applied it to map the mouse parabrachial nucleus and analyze changes in neuropathic
35 , ventrolateral periaqueductal gray, lateral parabrachial nucleus and caudal nucleus of the solitary
36 al organ and increased Fos-ir in the lateral parabrachial nucleus and caudal ventrolateral medulla.
37 e activation of neurons localized within the parabrachial nucleus and central amygdala, which constit
39 on in the rostral pons, at the border of the parabrachial nucleus and locus coeruleus, produced a 20-
40 ways associated with affective pain, such as parabrachial nucleus and medial thalamic nucleus, as wel
41 seen throughout the brain, the region of the parabrachial nucleus and nucleus of the solitary tract (
42 a, and brainstem regions such as the lateral parabrachial nucleus and nucleus of the solitary tract.
43 cal arousal, whereas the projection from the parabrachial nucleus and precoeruleus region, relayed by
44 gustatory thalamus, receives input from the parabrachial nucleus and relays taste sensation to the g
45 nnervation of BNST originates in the pontine parabrachial nucleus and targets its anterolateral secto
46 , the A5 area, the ventrolateral part of the parabrachial nucleus and the Kolliker-Fuse nucleus were
47 ke-immunoreactive fibers was detected in the parabrachial nucleus and the NTS, with notable staining
48 y rely on reciprocal connections between the parabrachial nucleus and the nucleus ambiguus, are conse
49 s, and reduced spinofugal innervation of the parabrachial nucleus and the periaqueductal gray, import
50 al tegmental nucleus, nucleus pontis oralis, parabrachial nucleus and the white matter in between the
51 ent projections-to the lateral hypothalamus, parabrachial nucleus and ventral tegmental area-each imp
52 us (mPVN), 4.1-times in the external lateral parabrachial nucleus, and 2.6-times in both the inferior
53 eriaqueductal gray, locus coeruleus, lateral parabrachial nucleus, and commissural nucleus tractus so
55 mentum, medial vestibular nuclei and lateral parabrachial nucleus, and in brainstem regions associate
56 regions including the infralimbic cortex and parabrachial nucleus, and limbic regions including the l
58 mic area, ventrolateral periaqueductal gray, parabrachial nucleus, and nucleus of the solitary tract)
59 s, dorsomedial hypothalamic nucleus, lateral parabrachial nucleus, and nucleus of the solitary tract.
60 in pons, midbrain (mesencephalic tegmentum, parabrachial nucleus, and periaqueductal gray), hypothal
61 l- and external-lateral subnuclei of lateral parabrachial nucleus, and present intracellularly in the
62 y sensation, receives primary input from the parabrachial nucleus, and projects to the insular cortex
63 ates the activity of pain-related neurons in parabrachial nucleus, and that, in chronic pain, this in
66 in, including the ventrolateral medulla, the parabrachial nucleus, and the medial geniculate body.
67 alcitonin gene-related peptide (CGRP) in the parabrachial nucleus are critical for relaying pain sign
68 trate that parallel outputs from the lateral parabrachial nucleus arise from specific cell types with
69 ateral and Kolliker-Fuse subdivisions of the parabrachial nucleus at 6 and 24 hours postinjection and
70 primary thermoceptive neurons in the pontine parabrachial nucleus becoming well characterized(1).
71 ocebo responses differentially activated the parabrachial nucleus but overlapped in engagement of the
72 somatic afferents to the VRG via the lateral parabrachial nucleus causes resetting of respiratory rhy
73 f the solitary tract, area postrema, lateral parabrachial nucleus, central lateral nucleus of the amy
75 eas many NPS-positive neurons in the lateral parabrachial nucleus coexpress corticotropin-releasing f
76 up, ventrolateral medulla, central amygdala, parabrachial nucleus, cuneate nucleus, nucleus tractus s
77 lamic nucleus, lateral hypothalamus, lateral parabrachial nucleus, dorsal raphe nucleus, and nucleus
78 retroambiguus, but not those innervating the parabrachial nucleus, elicited USVs in both male and fem
81 tral nucleus of the amygdala (lateral part), parabrachial nucleus (external lateral subnucleus), area
82 tions in the lateral and medial parts of the parabrachial nucleus; far fewer were seen after injectio
83 ed with regard to the forebrain influence on parabrachial nucleus function during CTA acquisition.
85 tegmental field rostral to the obex, and the parabrachial nucleus, had no appreciable effect on the a
87 dial hypothalamus, lateral hypothalamus, and parabrachial nucleus, identifying these brain regions as
88 euron synapses and excitatory neurons in the parabrachial nucleus impaired both oil droplet- and C-LT
94 lei, locus coeruleus, raphe complex, lateral parabrachial nucleus, inferior olivary complex, vestibul
95 t thermosensing glutamatergic neurons of the parabrachial nucleus innervate tanycytes either directly
96 th aversion learning (the lateral and medial parabrachial nucleus, intermediate and caudal nucleus tr
97 nuclei, but some were also found in lateral parabrachial nucleus, intertrigeminal nucleus, principal
98 lpha-hCRH was microinjected into the lateral parabrachial nucleus ipsilateral to the LC recording sit
100 e data suggest that taste information in the parabrachial nucleus is conveyed by multiple populations
101 ion of projections from these neurons to the parabrachial nucleus is reinforcing, and increases ethan
103 detected in: paratrigeminal nucleus, lateral parabrachial nucleus, Kolliker-Fuse nucleus, ventrolater
104 nuclei, nucleus of the posterior commissure, parabrachial nucleus, laterodorsal and pedunculopontine
105 area, lateral habenula, periaqueductal gray, parabrachial nucleus, locus ceruleus, nucleus of the sol
106 h neuropil also, particularly in the lateral parabrachial nucleus, locus coeruleus, lateral septum, d
107 , periaqueductal gray, raphe nuclei, lateral parabrachial nucleus, locus coeruleus, spinal trigeminal
109 us of the solitary tract (rNTS), the lateral parabrachial nucleus (LPB), and the central amygdala (Ce
110 rolateral periaqueductal gray (PAG), lateral parabrachial nucleus (LPB), caudal pressor area, and lam
111 inalis (BST), caudate-putamen (CPu), lateral parabrachial nucleus (LPB), nucleus tractus solitarius (
112 at neurons in the dorsal part of the lateral parabrachial nucleus (LPBd) glutamatergically transmit c
113 or (Htr2c)-expressing neurons in the lateral parabrachial nucleus (LPBN(Htr2c) neurons) inhibit sodiu
114 solitarius (NTS) projections to the lateral parabrachial nucleus (lPBN) and calcitonin-gene related
115 NMDA) glutamatergic receptors in the lateral parabrachial nucleus (LPBN) are involved in the control
116 y was to investigate the role of the lateral parabrachial nucleus (LPBN) in mediating dorsal PAG modu
117 ergide injected bilaterally into the lateral parabrachial nucleus (LPBN) increases NaCl intake in sev
119 re designed to determine whether the lateral parabrachial nucleus (lPBN) mediates acquisition of cond
122 V-GFP-Cre once into the ARC, PVN, or lateral parabrachial nucleus (LPBN) to obtain Nmnat2 (ARC-/-) ,
123 We also report that neurons in the lateral parabrachial nucleus (LPBN), a brain area that is also i
124 CeA(CAM) neurons) and project to the lateral parabrachial nucleus (LPBN), a brainstem region known fo
125 ight the dorsal vagal complex (DVC), lateral parabrachial nucleus (lPBN), and central nucleus of the
130 al ventrolateral medulla (RVLM), and lateral parabrachial nucleus (lPBN); however, EB significantly a
131 somatic afferents, (2) establish whether the parabrachial nucleus mediates entrainment, (3) examine r
132 er photometry-based calcium responses in the parabrachial nucleus, mitigated aversive behavioral resp
134 s of the solitary tract (rNST) to the medial parabrachial nucleus (mPBN) in male Wistar rats using Di
136 ral nucleus of the solitary tract and medial parabrachial nucleus), neuroendocrine system (periventri
139 rvate autonomic control sites, including the parabrachial nucleus, nucleus of solitary tract, and ven
140 tices, paraventricular hypothalamic nucleus, parabrachial nucleus, nucleus of the solitary tract, and
141 f the amygdala, periaqueductal gray, lateral parabrachial nucleus, nucleus of the solitary tract, dor
142 gray, dorsal raphe, ventral tegmental area, parabrachial nucleus, nucleus tractus solitarius, rostra
143 tatory nucleus of catfish, like those of the parabrachial nucleus of birds and mammals, do not posses
144 oxytocin-receptor-expressing neurons in the parabrachial nucleus of mice (Oxtr(PBN) neurons) are key
145 he solitary tract (NTS) and the other in the parabrachial nucleus of the pons (PbN), respectively the
146 1) opioid receptor subtype is present in the parabrachial nucleus of the pons and that these receptor
148 ne-related peptide (CGRP) signaling from the parabrachial nucleus on this diametrically opposed later
150 lar cortex, but not in basolateral amygdala, parabrachial nucleus, or nucleus of the solitary tract.
152 ca, hippocampus, nucleus tractus solitarius, parabrachial nucleus, paraventricular nucleus of the hyp
153 s is caused by the increased inputs from the parabrachial nucleus (PB) driven by the injured peripher
160 the periaqueductal gray matter (PAG) to the parabrachial nucleus (PB) were studied in the rat follow
161 ea (LHA), the periaqueductal gray (PAG), the parabrachial nucleus (Pb), and the nucleus of the solita
162 the nucleus submedius of the thalamus (Sm), parabrachial nucleus (PB), lateral hypothalamus (LH), or
163 othalamic nuclei, lateral hypothalamic area, parabrachial nucleus (PB), nucleus of the solitary tract
164 These NST neurons project extensively to the parabrachial nucleus (PB), where LPS-activated neurons a
165 ratory chemosensory pathways converge on the parabrachial nucleus (PB), which sends glutamatergic pro
167 lutamatergic neurons in the external lateral parabrachial nucleus (PBel) containing calcitonin gene r
168 lutamatergic neurons in the external lateral parabrachial nucleus (PBel) play a critical role in arou
170 receptor)-expressing neurons in the lateral parabrachial nucleus (PBL) are crucial for coordinating
171 receptor)-expressing neurons in the lateral parabrachial nucleus (PBL) are crucial for coordinating
173 hypothalamus (PVN), and the pontine lateral parabrachial nucleus (PBL; an important component of asc
174 Rs specifically reduce excitatory drive from parabrachial nucleus (PBN) afferents onto CRF neurons.
175 the nucleus of the solitary tract (NTS) and parabrachial nucleus (PBN) after peripheral cholecystoki
176 tergic input to the BNST originates from the parabrachial nucleus (PBN) and consists of asymmetric ax
177 rain areas have been shown to project to the parabrachial nucleus (PBN) and exert inhibitory and exci
178 rvation is due to aberrant activation of the parabrachial nucleus (PBN) and it could be prevented by
179 rior vestibular nucleus (IVN) project to the parabrachial nucleus (PBN) and Kolliker-Fuse (KF) nucleu
180 two major extranuclear targets of rNST, the parabrachial nucleus (PBN) and medullary reticular forma
182 ve (CT) afferents, those connecting with the parabrachial nucleus (PBN) and reticular formation (RF),
183 optic area of the hypothalamus (POA) and the parabrachial nucleus (PBN) as nodes in the thermosensory
185 eviously reported that lesions of the medial parabrachial nucleus (PBN) enhanced d-fenfluramine (DFEN
186 entered in the gustatory zone of the pontine parabrachial nucleus (PBN) failed to acquire a condition
189 e "waist" area and external subnuclei of the parabrachial nucleus (PBN) have been implicated in the p
190 es for cannabinoid mechanisms of the pontine parabrachial nucleus (PBN) in modulating intake of presu
191 receives ascending gustatory inputs from the parabrachial nucleus (PbN) in the brainstem and sends pr
193 esions of the gustatory (medial) zone of the parabrachial nucleus (PBN) in the pons eliminate the sal
195 recordings were made from neurons in the rat parabrachial nucleus (PBN) in three rostro-caudal brain
200 ctivity (FLI) in several subdivisions of the parabrachial nucleus (PBN) known to be responsive to gus
201 LepRb neurons, which project to and activate parabrachial nucleus (PBN) neurons that control SNS acti
202 Here, we extended these findings in the parabrachial nucleus (PBN) of male and female KO1+3 mice
205 Retrograde labeling studies in mice from the parabrachial nucleus (PBN) show that less than 20% of su
209 the nucleus of solitary tract (NST) and the parabrachial nucleus (PBN) that modulate taste-elicited
210 n gene-related peptide (CGRP) neurons in the parabrachial nucleus (PBN) that transmit anorexic signal
211 n of excitatory synaptic transmission in the parabrachial nucleus (PBN) to central amygdala (CeA) pat
212 ns in the gustatory and visceral zone of the parabrachial nucleus (PBN) to gamma-aminobutyric acid (G
213 evaluated the contributions of the hindbrain parabrachial nucleus (PBN) to systemic Ex4-induced hypop
214 ated with augmented neuronal activity in the parabrachial nucleus (PBN), a brainstem nucleus that rel
215 ions, direct delivery of bretazenil into the parabrachial nucleus (PBN), a direct target of AgRP neur
216 mpathetic afferents activates neurons in the parabrachial nucleus (PBN), a region known to play a rol
217 at assessment are strongly influenced by the parabrachial nucleus (PBN), a structure that responds to
218 bed nucleus of the stria terminalis (vBNST), parabrachial nucleus (PBN), and nucleus of the solitary
219 ectivity among the locus coeruleus (LC), the parabrachial nucleus (PBN), and the central nucleus of a
220 as seen not only in the iNTS but also in the parabrachial nucleus (PBN), and the central nucleus of t
221 oral somatosensory and taste activity in the parabrachial nucleus (PbN), implicated for roles in gust
222 area postrema (AP), vestibular nucleus (VN), parabrachial nucleus (PBN), nucleus ambiguus (NA), dorsa
223 The two major components of the pontine parabrachial nucleus (PBN), the medial (gustatory) and l
224 potential component of this circuitry is the parabrachial nucleus (PBN), which is involved in encodin
231 d Fos-li in the external lateral division of parabrachial nucleus (PBNel) in intact but not in CD rat
232 in brainstem regions, including the lateral parabrachial nucleus, periaqeductal gray, and ventrolate
233 and pontine reticular formation, cerebellum, parabrachial nucleus, periaqueductal gray, thalamus, hyp
234 d double-labeled neurons originated from the parabrachial nucleus, pericoeruleus area, and caudal reg
235 d in brainstem regions including the lateral parabrachial nucleus, peripeduncular area and ventrolate
236 ), ventrolateral periaqueductal gray, dorsal parabrachial nucleus, periventricular and rhomboid nucle
237 r, dorsal and central superior raphe nuclei, parabrachial nucleus, pre-locus coeruleus region, NTS, a
238 eurons or ablation of CGRP(+) neurons in the parabrachial nucleus prevented sleep fragmentation, wher
240 de (PACAP)-expressing neurons in the lateral parabrachial nucleus projecting to the dorsal raphe are
241 e data suggest that this central amygdala to parabrachial nucleus projection influences the expressio
242 ereas the projection of these neurons to the parabrachial nucleus promotes consumption of ethanol as
243 ic neurons of the lateral septum and lateral parabrachial nucleus regulate pancreatic secretion.
244 ral and external lateral subdivisions of the parabrachial nucleus (slPB and elPB, respectively), the
245 amate into the lateral septum or the lateral parabrachial nucleus stimulated vagal pancreatic efferen
246 Here we show that, in mice, neurons in the parabrachial nucleus that express the prodynorphin gene
247 on of neurons in the gustatory region of the parabrachial nucleus that express the transcription fact
248 ere, we show that neurons within the lateral parabrachial nucleus that express the u-opioid receptor
249 rsomedial hypothalamus from the dorsolateral parabrachial nucleus that plays a critical role in media
250 he outer external lateral subdivision of the parabrachial nucleus that project to the laterocapsular
251 However, the identities of neurons in the parabrachial nucleus that regulate feeding are unknown,
252 dings of significant c-Fos expression in the parabrachial nucleus, the central nucleus of the amygdal
253 thalamic neurons, the subiculum, the lateral parabrachial nucleus, the cuneate/gracilis nuclei, and t
255 ar hypothalamic nuclei, the external lateral parabrachial nucleus, the locus coeruleus, and the nucle
256 from the nucleus of solitary tract and then parabrachial nucleus, the MS SOM neurons receive rewardi
257 ervous system regions, including the lateral parabrachial nucleus, the periaqueductal gray, and lamin
258 cold-induced c-Fos expression in the lateral parabrachial nucleus, thus indicating a site of action w
259 y input from CeL and send projections to the parabrachial nucleus to promote appetitive behavior.
261 emonstrate that this neural circuit from the parabrachial nucleus to the central nucleus of the amygd
262 Further, cholinergic input from the lateral parabrachial nucleus to the hypothalamus plays a major r
265 tphal nucleus, locus coeruleus (LC), lateral parabrachial nucleus, ventrolateral medulla (VLM) and do
266 c area, bed nucleus of the stria terminalis, parabrachial nucleus, ventrolateral medulla, and nucleus
268 ing transcriptionally defined neurons in the parabrachial nucleus, we identify a subset of neurons th
269 for parallel processing was reflected in the parabrachial nucleus, where sweetened milk intake result
270 mitted by separate ascending pathways to the parabrachial nucleus, where they engage separate populat
271 eptum and external subnucleus of the lateral parabrachial nucleus which contained more CRF-ir neurons
272 are synaptically connected to neurons in the parabrachial nucleus, which relays visceral information
273 lateral and external medial subnuclei of the parabrachial nucleus while a significant increase in kap