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1 edial preoptic area, the lateral septum, and nucleus of the solitary tract.
2 subcoeruleus and periolivary areas, and the nucleus of the solitary tract.
3 uperior colliculus, locus coeruleus, and the nucleus of the solitary tract.
4 by neuron types and individual cells in the nucleus of the solitary tract.
5 sensory information from the stomach to the nucleus of the solitary tract.
6 e nerves that carry taste information to the nucleus of the solitary tract.
7 ucleus, central nucleus of the amygdala, and nucleus of the solitary tract.
8 achial nucleus, the locus coeruleus, and the nucleus of the solitary tract.
9 sterior thalamic nucleus; area postrema; and nucleus of the solitary tract.
10 solateral amygdala, parabrachial nucleus, or nucleus of the solitary tract.
11 c nucleus, lateral parabrachial nucleus, and nucleus of the solitary tract.
12 the relative number of nuclei labeled in the nucleus of the solitary tract.
13 entral amygdalar nucleus; area postrema; and nucleus of the solitary tract.
14 gdalar nucleus, supramammillary nucleus, and nucleus of the solitary tract.
15 the hypothalamic paraventricular nucleus and nucleus of the solitary tract.
16 in the carotid body and relay neurons in the nucleus of the solitary tract.
17 eactivity (FLI) in the area postrema and the nucleus of the solitary tract.
18 levels of the ventrolateral medulla, and the nucleus of the solitary tract.
19 re of taste-sensitive neurons in the rostral nucleus of the solitary tract.
20 al area, substantia nigra pars compacta, and nucleus of the solitary tract.
21 remaining tone was removed by inhibition of nucleus of the solitary tract.
22 l thalamus, dorsal hypothalamic nucleus, and nucleus of the solitary tract.
23 e gigantocellular reticular nucleus, and the nucleus of the solitary tract.
24 such as the lateral parabrachial nucleus and nucleus of the solitary tract.
25 , the medullary reticular formation, and the nucleus of the solitary tract.
26 lighter labeling in the globus pallidus and nucleus of the solitary tract.
27 e periaqueductal gray and medial part of the nucleus of the solitary tract.
28 into the rostral (gustatory) portion of the nucleus of the solitary tract.
29 density of their central projections in the nucleus of the solitary tract.
30 y control vagal afferent excitability in the nucleus of the solitary tract.
31 e-1 (GLP-1) is produced in the ileum and the nucleus of the solitary tract.
32 mogenesis that is mediated by neurons in the nucleus of the solitary tract.
33 re gustatory afferent terminal fields in the nucleus of the solitary tract.
34 1 peptide-expressing neurons resident in the nucleus of the solitary tract.
35 minal fields in the first central relay, the nucleus of the solitary tract.
36 medial medulla, targeting projections to the nucleus of the solitary tract.
37 asymmetry in the prepositus nucleus and the nucleus of the solitary tract.
38 several brainstem reticular nuclei, and the nucleus of the solitary tract.
39 rapezoid nucleus; 5) parahypoglossal nucleus/nucleus of the solitary tract; 6) parabrachial/Kolliker-
40 e induction of c-Fos-immunoreactivity in the nucleus of the solitary tract, a cellular correlate of t
41 nerve, situated subjacent to the commissural nucleus of the solitary tract, a site of pro-opiomelanoc
42 etized rats following central and localized, nucleus of the solitary tract, administration of N6-cycl
43 blocker MK-801 directly into the caudomedial nucleus of the solitary tract also abolished duodenal li
44 Eighty-one percent of the neurons in the nucleus of the solitary tract and 47 % of the neurons in
45 s of the hypothalamus and brainstem regions (nucleus of the solitary tract and A5 region) also projec
46 t of CCK on the activation of neurons in the nucleus of the solitary tract and area postrema, key hin
49 ypothalamic area, parabrachial nucleus (PB), nucleus of the solitary tract and central amygdalar nucl
50 rates of 65 % of gut-related neurons in the nucleus of the solitary tract and in the dorsal motor nu
51 i, and, more dorsally in the medulla, in the nucleus of the solitary tract and in the locus caeruleus
52 alivatory nuclei), gustatory system (rostral nucleus of the solitary tract and medial parabrachial nu
53 hemorrhage, nuclear Fos-IR increased in the nucleus of the solitary tract and other brainstem region
54 nly limited number of neurons project to the nucleus of the solitary tract and parabrachial nucleus.
55 first time, the presence of OX2R mRNA in the nucleus of the solitary tract and the lateral reticular
56 ure combining elements of both the gustatory nucleus of the solitary tract and the nucleus ambiguus.
57 gnificantly more c-Fos positive cells in the nucleus of the solitary tract and the parabrachial, medi
58 ts, increased c-fos labeling was seen in the nucleus of the solitary tract and ventrolateral medulla
59 us coeruleus, and two medullary regions, the nucleus of the solitary tract and ventrolateral medulla,
60 ericoeruleus area, and caudal regions of the nucleus of the solitary tract and ventrolateral medulla.
61 ar nucleus, central nucleus of the amygdala, nucleus of the solitary tract, and area postrema, a patt
63 of cells: dorsomedial hypothalamic nucleus, nucleus of the solitary tract, and caudal ventrolateral
64 marked Fos expression in the area postrema, nucleus of the solitary tract, and dorsal motor nucleus
67 and NR1 -/- mice include the lateral septum, nucleus of the solitary tract, and medial hypothalamic r
68 onstitutive expression of CRF-R2 mRNA in the nucleus of the solitary tract, and stress-inducible expr
69 eus, the nucleus subcoeruleus ventralis, the nucleus of the solitary tract, and the caudolateral medu
70 al complex, including the area postrema, the nucleus of the solitary tract, and the dorsal motor nucl
71 em regions, including the area postrema, the nucleus of the solitary tract, and the lateral parabrach
72 ventral respiratory column, the caudolateral nucleus of the solitary tract, and the pontine Kolliker-
74 , including the C1 catecholamine cell group; nucleus of the solitary tract; and dorsal motor nucleus
75 tered on the area postrema (AP) and adjacent nucleus of the solitary tract (AP/mNTS-lesions) are repo
76 mined whether the area postrema and adjacent nucleus of the solitary tract (AP/NTS) is necessary for
77 ggest that the efferent connections from the nucleus of the solitary tract are more widespread than p
78 number of Fos-immunopositive neurons in the nucleus of the solitary tract, area postrema, and dorsal
79 mg/kg, p.o.), induced Fos expression in the nucleus of the solitary tract, area postrema, lateral pa
80 nuclei; parabrachial nuclei; locus ceruleus, nucleus of the solitary tract; area postrema; dorsal nuc
81 ntal area, or the intermediate region of the nucleus of the solitary tract blocked the robust increas
82 e Schreiner organs may be represented in the nucleus of the solitary tract, but this structure is cer
83 entiate GABAergic transmission in the caudal nucleus of the solitary tract (cNTS), which is criticall
84 lesion of the commissural subnucleus of the nucleus of the solitary tract (commNTS) on body weight,
85 tic nucleus, periaqueductal gray, and medial nucleus of the solitary tract compared to isotonic salin
86 dies focused on the intermediate dorsomedial nucleus of the solitary tract (dmNTS) because this regio
87 ray, lateral parabrachial nucleus and caudal nucleus of the solitary tract, dorsal motor nucleus of t
88 ueductal gray, lateral parabrachial nucleus, nucleus of the solitary tract, dorsal motor nucleus of t
90 nt bilateral isoguvacine injections into the nucleus of the solitary tract further reduced vagal tone
92 Q(1-13)NH(2) induces c-Fos expression in the nucleus of the solitary tract, hypothalamic paraventricu
93 xpressed in neurons of the area postrema and nucleus of the solitary tract in mice and humans, and ge
94 g4 (a homologue of Olig3, determinant of the nucleus of the solitary tract in mice), reveals that the
96 parations, inhibition of PKC activity in the nucleus of the solitary tract in situ abolished the Ang
99 Brainstem sites expressing Fos included the nucleus of the solitary tract in the medulla, parabrachi
100 r nucleus, rostral ventrolateral medulla and nucleus of the solitary tract), in regions associated wi
101 (equivalent to the gustatory portion of the nucleus of the solitary tract) includes the vagal lobe,
103 (c-FLI) in the intermediate division of the nucleus of the solitary tract (iNTS) has been shown to b
104 e immunoreactivity (FLI) in the intermediate nucleus of the solitary tract (iNTS) have been seen cons
106 FLI has been identified in the intermediate nucleus of the solitary tract (iNTS) with little express
108 xysteroid dehydrogenase type 2 (HSD2) in the nucleus of the solitary tract is sufficient to drive con
109 to trigger neural activation in areas of the nucleus of the solitary tract known to be targeted by GL
110 cular nucleus), respiratory control (lateral nucleus of the solitary tract), locomotor or exploratory
111 s to autonomic effector regions, such as the nucleus of the solitary tract, magnocellular neurosecret
112 ection of PrRP into the medial or comissural nucleus of the solitary tract (mNTS and comNTS, respecti
113 s detected in the area postrema (AP), medial nucleus of the solitary tract (mNTS), dorsal motor nucle
115 riaqueductal gray, parabrachial nucleus, and nucleus of the solitary tract), neuroendocrine system (p
116 ods of altered experience, especially during nucleus of the solitary tract neurogenesis, leads to a r
117 examined the distribution of neurons in the nucleus of the solitary tract (NST) activated by the int
118 nctions via oxytocinergic projections to the nucleus of the solitary tract (NST) and dorsal motor nuc
119 elements and taste-activated neurons in the nucleus of the solitary tract (NST) and subjacent reticu
120 emonstrated that the LH projects to both the nucleus of the solitary tract (NST) and the dorsal motor
121 it taste-evoked activity was measured in the nucleus of the solitary tract (NST) in anesthetized B6 a
122 rry taste information from taste buds to the nucleus of the solitary tract (NST) in the medulla.
130 the rostral central subdivision (RC) of the nucleus of the solitary tract (NST), the principal site
131 s that terminate centrally within the caudal nucleus of the solitary tract (NST), with signals subseq
137 to the astrocytes and not the neurons in the nucleus of the solitary tract (NST; principal locus inte
139 FO) and aldosterone-sensitive neurons in the nucleus of the solitary tract (NTS(HSD2) neurons) were s
140 t and CD rats showed increased Fos-li in the nucleus of the solitary tract (NTS) after injection of 2
141 8% in the VLM, 39% in the middle part of the nucleus of the solitary tract (NTS) and 33% in the cauda
142 clude a glutamatergic connection between the nucleus of the solitary tract (NTS) and a segment of the
143 stension in the DVC, specifically within the nucleus of the solitary tract (NTS) and area postrema (A
144 of the c-fos protooncogene product, FOS, in nucleus of the solitary tract (NTS) and area postrema (A
145 ed a rapid (<or=2-h) c-Fos expression in the nucleus of the solitary tract (NTS) and area postrema of
146 s and decreased 5-HT immunoreactivity in the nucleus of the solitary tract (nTS) and dorsal motor nuc
147 ats had more Fos-positive cell nuclei in the nucleus of the solitary tract (NTS) and in the dorsal ho
148 fferent information arrives in the brainstem nucleus of the solitary tract (NTS) and is relayed to ot
149 ) immunoreactivity (IR) were examined in the nucleus of the solitary tract (NTS) and parabrachial nuc
150 preproglucagon (PPG) neurons located in the nucleus of the solitary tract (NTS) and projecting to nu
151 ulators of autonomic functions involving the nucleus of the solitary tract (NTS) and the dorsal motor
152 on in intact rats reduced NPY content in the nucleus of the solitary tract (NTS) and the dorsal motor
153 ation was detected were within the brainstem nucleus of the solitary tract (NTS) and the hypothalamic
154 neously in pairs of single cells: one in the nucleus of the solitary tract (NTS) and the other in the
155 We studied the activation of neurons in the nucleus of the solitary tract (NTS) and their efferent t
156 y neurosecretory nuclei of the hypothalamus, nucleus of the solitary tract (NTS) and ventrolateral me
157 e neurons in the brainstem, primarily in the nucleus of the solitary tract (NTS) and ventrolateral me
158 EM2 was colocalized with SP and CGRP in the nucleus of the solitary tract (NTS) and with SP, CGRP an
159 entral nucleus of the amygdala (CNA) and the nucleus of the solitary tract (NTS) are important in the
160 show a remarkable amount of expansion in the nucleus of the solitary tract (NTS) as a result of early
165 itory amino acid GABA is released within the nucleus of the solitary tract (NTS) during hypoxia and m
166 f c-Fos-like immunoreactivity (c-FLI) in the nucleus of the solitary tract (NTS) has been shown to be
167 caine (2%) was infused (0.5 microl) into the nucleus of the solitary tract (NTS) immediately before i
168 awake mice activated neurones throughout the nucleus of the solitary tract (NTS) in A-IV(+/+) mice, m
169 d as a measure of neuronal activation in the nucleus of the solitary tract (NTS) in response to intra
170 c) and paraventricular (PVN) nuclei, and the nucleus of the solitary tract (NTS) in the medulla.
175 tamate release from the vagus nerve onto the nucleus of the solitary tract (NTS) is one mechanism by
176 he amygdala (CeA) to identify CeA-projecting nucleus of the solitary tract (NTS) neurons for synaptic
177 re recorded from single cells in the rostral nucleus of the solitary tract (NTS) of anesthetized rats
178 ) nerves were visualized concurrently in the nucleus of the solitary tract (NTS) of developmentally s
179 rotein A-IV (apoA-IV) gene expression in the nucleus of the solitary tract (NTS) of lean ovariectomiz
180 of a population of neurons in the hindbrain nucleus of the solitary tract (NTS) of rats that are act
181 ydrogenase type 2-expressing) neurons in the nucleus of the solitary tract (NTS) of the rat are aldos
182 es to subsequently presented tastants in the nucleus of the solitary tract (NTS) of urethane-anesthet
183 croinjecting angiotensin II (ANGII) into the nucleus of the solitary tract (NTS) on both baroreceptor
184 rt of stress-related neurocircuitry, and the nucleus of the solitary tract (NTS) plays a critical rol
186 n of RNA interference was used to knock down nucleus of the solitary tract (NTS) preproglucagon (PPG)
187 eceptor agonist melanotan-II (MTII) into the nucleus of the solitary tract (NTS) produces rapid and s
188 iously shown that neurons originating in the nucleus of the solitary tract (NTS) project to a region
191 techniques, the discharge of neurones in the nucleus of the solitary tract (NTS) receiving aortic dep
192 2.0 microg/100 nl) delivered into the medial nucleus of the solitary tract (NTS) significantly increa
193 corded the response patterns of cells in the nucleus of the solitary tract (NTS) to representatives o
194 and protein expression that conformed in the nucleus of the solitary tract (NTS) to the termination p
195 signals from the gut activate neurons in the nucleus of the solitary tract (NTS) via the vagus nerve.
196 , the region of the parabrachial nucleus and nucleus of the solitary tract (NTS) were most conspicuou
197 actions of angiotensin II (ANGII) within the nucleus of the solitary tract (NTS) were studied using r
198 or immunoreactivity is present in the caudal nucleus of the solitary tract (NTS) where vagal sensory
199 phenylephrine (PE) activates neurons in the nucleus of the solitary tract (NTS) whose distribution c
200 olved in the respiratory control such as the nucleus of the solitary tract (NTS), a site that receive
201 es in the first central gustatory relay, the nucleus of the solitary tract (nTS), after transection o
202 sts (MT-II and alpha-MSH) into the overlying nucleus of the solitary tract (NTS), an important compon
203 lular region of the paraventricular nucleus, nucleus of the solitary tract (NTS), and caudal thoracic
204 ha (TNFalpha), c-Fos immunoreactivity in the nucleus of the solitary tract (NTS), and steady-state le
205 ucleus (PVN), suprachiasmatic nucleus (SCN), nucleus of the solitary tract (NTS), and the dorsal and
206 ng the hypoglossal nucleus, subnuclei of the nucleus of the solitary tract (NTS), and the dorsal moto
207 eruleus (LC), rostral raphe pallidus (rRPa), nucleus of the solitary tract (NTS), and ventrolateral m
208 NPY projections were not observed within the nucleus of the solitary tract (NTS), another brainstem s
209 Isop significantly increased Fos-IR in the nucleus of the solitary tract (NTS), area postrema (AP),
210 arily in hindbrain structures, including the nucleus of the solitary tract (NTS), area postrema (AP),
211 alamic paraventricular nucleus (PVN) and the nucleus of the solitary tract (NTS), both of which are r
212 to the synaptic responses of neurons in the nucleus of the solitary tract (NTS), but their exact rol
213 lar formation and commissural nucleus of the nucleus of the solitary tract (NTS), corresponding to th
214 ves that convey gustatory information to the nucleus of the solitary tract (NTS), displays terminal f
215 intake activated many neurons throughout the nucleus of the solitary tract (NTS), including A2 noradr
217 ortant sites of chemoreception including the nucleus of the solitary tract (NTS), medullary raphe and
218 sal raphe and interpeduncular nuclei and the nucleus of the solitary tract (NTS), most prominent seat
219 n neurons of the medial, and/or dorsolateral nucleus of the solitary tract (NTS), rostral to obex, an
220 xonal boutons were visualized throughout the nucleus of the solitary tract (nTS), the dorsal motonucl
222 tin signaling in POMC neurons located in the nucleus of the solitary tract (NTS), the only other know
223 (PVH), although Fos-immunoreactivity in the nucleus of the solitary tract (NTS), ventrolateral medul
224 rostral ventrolateral medulla (RVLM) and the nucleus of the solitary tract (NTS), where VMH efferents
225 te buds and project centrally to the rostral nucleus of the solitary tract (NTS), whereas neurons pro
226 arcuate nucleus (ARC) and showed none in the nucleus of the solitary tract (NTS), which relays viscer
227 ticular formation immediately ventral to the nucleus of the solitary tract (NTS), which we term the d
228 a restricted central-lateral portion of the nucleus of the solitary tract (nTS)-the same area that s
255 d the numbers of Fos-positive neurons in the nucleus of the solitary tract (NTS)/area postrema (AP),
256 CTB-ir neurons in the following regions: the nucleus of the solitary tract (NTS, 6% of CTB-ir neurons
257 nitiate recurrent inhibition in cells in the nucleus of the solitary tract (NTS, the first central re
258 medulla (RVLM; a vasopressor region) and the nucleus of the solitary tract (NTS; a vasodepressor regi
259 sis that taste and olfaction interact in the nucleus of the solitary tract (NTS; the first neural rel
260 ick-contingent electrical stimulation of the nucleus of the solitary tract (NTS; the first synaptic r
263 lecular evidence for their homology with the nucleus of the solitary tract of mammals and suggesting
265 from GLP-1-IR neuronal cell bodies from the nucleus of the solitary tract of the medulla oblongata.
266 rojecting neurons in ascending raphe nuclei, nucleus of the solitary tract, or ventrolateral medulla
267 equence of OFQ injection was observed in the nucleus of the solitary tract, paraventricular nucleus o
268 revious anatomical studies indicate that the nucleus of the solitary tract, pars centralis (NSTc) con
269 est densities in the raphe pallidus nucleus, nucleus of the solitary tract, periaqueductal gray, hypo
270 -ir neurons, but not EM-2-ir neurons, in the nucleus of the solitary tract projected their axons to t
271 behavior and excitatory transmission in the nucleus of the solitary tract, regulating sympathetic ne
272 rebellar nuclei, vestibular nuclear complex, nucleus of the solitary tract, reticular formation, dors
274 The distribution of neurons in the rostral nucleus of the solitary tract (rNST) that respond to gus
275 ted from second order neurons in the rostral nucleus of the solitary tract (rNST) to the parabrachial
276 yonic development of synapses in the rostral nucleus of the solitary tract (rNST) was investigated in
278 ent axons onto single neurons of the rostral nucleus of the solitary tract (rNTS), but anatomical evi
279 um gratification: the rostral portion of the nucleus of the solitary tract (rNTS), the lateral parabr
280 ative brainstem structures (locus coeruleus, nucleus of the solitary tract, rostral ventrolateral med
281 li and, when activated, provide input to the nucleus of the solitary tract (Sol) and paratrigeminal n
282 oxious visceral sensory information from the nucleus of the solitary tract, spinal cord, and spinal t
284 gray, parabrachial nucleus, locus ceruleus, nucleus of the solitary tract, spinal trigeminal nucleus
286 thin the locus coeruleus, cerebellar cortex, nucleus of the solitary tract, thalamus, and striatum an
287 ons of the spinal trigeminal nucleus and the nucleus of the solitary tract that have been associated
288 reactivity (Fos-li) in the area postrema and nucleus of the solitary tract that predominantly charact
289 aventricular nucleus of the hypothalamus and nucleus of the solitary tract) the blood-brain barrier.
290 t structures characterized in rodents is the nucleus of the solitary tract, the first relay for visce
291 he spinal cord and medulla as well as in the nucleus of the solitary tract, the target of nodose gang
293 pothalamus, and neurons within the brainstem nucleus of the solitary tract to acutely suppress food i
296 and cortical amygdaloid nuclei, cerebellum, nucleus of the solitary tract, ventral tegmental area, a
298 ields of the chorda tympani nerve within the nucleus of the solitary tract were investigated via ante
299 of Ptf1a compromises the development of the nucleus of the solitary tract, which processes viscerose
300 were frequently observed with neurons of the nucleus of the solitary tract whose activation by gastro
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