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1 ding from the PBel into the lateral crescent subnucleus.
2 umber/area of subdivision) within the medial subnucleus.
3 n the adjacent lateral crescent parabrachial subnucleus.
4 e dendrites extend into the lateral crescent subnucleus.
5 leus (rostral portion), and superior lateral subnucleus.
6 tinguish pvLNTB cells from cells of the main subnucleus.
7 ucleus (rostral portion), and dorsal lateral subnucleus.
8 ng was particularly high in the intermediate subnucleus.
9 vity were preferentially located in the main subnucleus.
10 but in a manner that depended on age and BLA subnucleus.
11 he trapezoid body, called the posteroventral subnucleus.
12 n that in the ventral or the interfascicular subnucleus.
13 zed animals after AMPA injection into either subnucleus.
14 binding was observed in the external lateral subnucleus.
15 o the ipsilateral dorsomedial portion of the subnucleus.
16 rbor shape that was attributed to the target subnucleus.
17 culary the rostral half of the parvocellular subnucleus.
18 oration of neuropil only in the left lateral subnucleus.
19 inputs from the ipsilateral rostrolateral IP subnucleus.
20 litarii (NTS), mainly within the commissural subnucleus.
21 only from the internal lateral parabrachial subnucleus.
22 he medial, and the other in the interstitial subnucleus.
23 projection site (a region of the commissural subnucleus, 0.1-0.5 mm caudal to the CS, 0-0.5 mm latera
25 l region, project to the superior lateral PB subnucleus, a presumed nociceptive relay site that recei
26 ns were most numerous in the rostral central subnucleus after either stimulus but had a medial bias a
28 mia was predominantly located in the lateral subnucleus, although Fos-stained medial sub-nucleus neur
29 ostrocaudal extent of the nucleus, a central subnucleus and a dorsal subnucleus, the latter two locat
32 urons were localized in the superior-lateral subnucleus, and 40% of them expressed the mRNA encoding
33 e located in the ventral parvocellular (PaV) subnucleus, and showed an oblique orientation with respe
34 ocated in the posterior parvocellular (PaPo) subnucleus, and were oriented perpendicularly with respe
35 clei; less dense in the rostral lateral (RL) subnucleus; and sparse in the ventral (V), ventral later
36 te that pacemakers in the region of the CaBP subnucleus are necessary and sufficient for the control
37 art), parabrachial nucleus (external lateral subnucleus), area postrema, nucleus tractus solitarius,
38 f the commissural NTS (NTScom) to the dorsal subnucleus at the level of the area postrema (NTSap).
39 DPAT binding were found in the ventrolateral subnucleus at the level of the caudal extent of the troc
41 portion of the ipsilateral spinal trigeminal subnucleus caudalis (SVc) and interpolaris (SVi), and th
43 DPHd neurons were found predominantly in Vsp subnucleus caudalis (Vc) and in dorsomedial subnucleus o
44 inae of the dorsomedial aspect of trigeminal subnucleus caudalis (Vc) evoked by lingual application o
45 nvestigated the potential role of sGC in the subnucleus caudalis (Vc) in mediating masseter hypersens
47 eral medulla, and lamina V of the trigeminal subnucleus caudalis (Vc), exhibited FluoroGold/Fos doubl
50 These data demonstrate that in trigeminal subnucleus caudalis activation of either NK1 or NMDA rec
51 in trigeminal ganglia and associated spinal subnucleus caudalis and C1/C2 cervical dorsal spinal cor
52 n second-order neurons in the dorsal horn of subnucleus caudalis and cervical C1/C2 spinal cord (Vc/C
53 Fos expression can be induced in trigeminal subnucleus caudalis by NMDA or neurokinin-1 receptor act
54 e immunoreactivity (SP-LI) were evaluated in subnucleus caudalis following induction of sinusitis.
56 t that neurons in superficial laminae of the subnucleus caudalis may be important for the reflex init
57 rve branches located in the main sensory and subnucleus caudalis of the brainstem and joints, respect
60 al to the obex (22% in C2, 22% in C1, 23% in subnucleus caudalis, and 18% in the transition zone betw
61 in other species, into cervical dorsal horn, subnucleus caudalis, subnucleus interpolaris, subnucleus
62 audalis (Vi/Vc) transition or the trigeminal subnucleus caudalis-cervical cord (Vc/C1) junction regio
70 ent areas (which flank the dorsal lateral PB subnucleus), central lateral subnucleus (rostral portion
71 1b immunostaining was also pronounced in the subnucleus centralis of the nucleus tractus solitarius.
72 oreactive fibers in the medial parvocellular subnucleus, dorsal division (PVNmpd) and posterior magno
74 rate decreases considerably when the short (subnucleus) fibrils lose monomers much more frequently t
75 and extends dorsally beyond, the central SCN subnucleus identified by calbindin-immunoreactive neuron
77 s to five lateral PB sites: external lateral subnucleus (inner subdivision), medial and lateral cresc
78 d septa separating darkly stained patches in subnucleus interpolaris (juvenile tissue) and subnucleus
79 e input to V nucleus principalis (PrV) and V subnucleus interpolaris (SpI) in the vinblastine-treated
82 mean areas of multiunit receptive fields in subnucleus interpolaris and caudalis were larger than pr
83 ch ray's representation differed between the subnucleus interpolaris and the principal sensory nucleu
84 polaris), and 14% rostral to the obex (6% in subnucleus interpolaris, 4% in subnucleus oralis, and 4%
86 functional anomalies in trigeminal brainstem subnucleus interpolaris, including changes in normal rec
87 were distributed throughout the ipsilateral subnucleus interpolaris, principal trigeminal nucleus, a
88 o cervical dorsal horn, subnucleus caudalis, subnucleus interpolaris, subnucleus oralis, and nucleus
89 ne whether neurons at the ventral trigeminal subnucleus interpolaris- caudalis (Vi/Vc) transition or
91 ion of substrate is such that the pyrimidine subnucleus is oriented opposite to that seen with the sl
92 ivision (PVNmpd) and posterior magnocellular subnucleus, lateral division (PVNpml) was performed in a
93 the regional volume of the MeA posterodorsal subnucleus (MeApd) is approximately 50% larger in males
94 ect to five lateral PB sites: dorsal lateral subnucleus, medial and lateral crescent areas (which fla
96 receptors, and the NTSce is the primary NTS subnucleus mediating reflexes from the muscular slowly a
97 he brain than on the right, while the medial subnucleus (MsDh) is larger on the right compared to the
102 as elicited, occupied a region in the medial subnucleus of nucleus tractus solitarius (nTS), the reti
103 ssion in the enteric nerve plexi, the medial subnucleus of nucleus tractus solitarius, and the dorsal
104 guus, hypoglossal nucleus, and ventrolateral subnucleus of solitary tract nucleus), and a non-respira
105 ntral nucleus of the amygdala (CEA) and oval subnucleus of the BST (BSTov), amphetamine administratio
106 he superficial granular layer of the lateral subnucleus of the commissural nucleus of Cajal, which is
107 rs the caudolateral part of the interpolaris subnucleus of the descending trigeminal tract, a caudola
109 gle-cell activity was recorded in the dorsal subnucleus of the lateral amygdala (LAd) of freely behav
110 ty except in the lateral septum and external subnucleus of the lateral parabrachial nucleus which con
111 he anterior preglomerular nucleus and caudal subnucleus of the lateral preglomerular nucleus receive
113 nephrine (NE) on neurons of the intermediate subnucleus of the lateral septum (LSI) were examined usi
115 erior nucleus, the dorsal part of the dorsal subnucleus of the medial geniculate complex, and the per
116 we examined inputs to neurons in the medial subnucleus of the medial geniculate nucleus (mMG) for ch
117 sibility that neurons in the central lateral subnucleus of the middle and rostral LPBN are integrally
118 ogenous mu-receptor agonist) into the medial subnucleus of the NTS (mNTS) elicit depressor and bradyc
119 as heavy in an area that included the medial subnucleus of the NTS and the DMV over their full rostra
122 the ventral optic tectum, and in the lateral subnucleus of the nuc. preglomerulosus of the thalamus.
123 of an electrolytic lesion of the commissural subnucleus of the nucleus of the solitary tract (commNTS
124 subnucleus reticularis dorsalis, commissural subnucleus of the nucleus tractus solitarii, lateral med
127 of cells expressing c-fos in the dorsomedial subnucleus of the rostral nucleus tractus solitarius.
129 rs and on second-order neurons in the medial subnucleus of the solitary tract (NTS), the area postrem
130 other respiratory nucleus, the ventrolateral subnucleus of the solitary tract nucleus (NTS(VL)), and
131 vagal afferent nerve terminals in the medial subnucleus of the tractus solitarious (mNTS) and alpha4b
133 uggest that the neurons of the ventrolateral subnucleus of the tractus solitarius (vlNTS) act as an i
136 e obex (6% in subnucleus interpolaris, 4% in subnucleus oralis, and 4% in subnucleus principalis).
140 e show that the central lateral parabrachial subnucleus (PBcl) provides Dyn inputs to the VLPO, where
141 (CTb) into the external lateral parabrachial subnucleus (PBel) produced both retrograde cell body lab
142 ing was in the external lateral parabrachial subnucleus (PBel), including dendrites extending from th
144 gressive social encounters in a hypothalamic subnucleus previously known as a locus for aggression, a
149 dy was designed to investigate a role of the subnucleus reticularis dorsalis (SRD) in the analgesia p
150 that the CPA projects preferentially to the subnucleus reticularis dorsalis, commissural nucleus tra
151 fibers with varicosities in the ipsilateral subnucleus reticularis dorsalis, commissural subnucleus
152 ntine reticular formation nuclei such as the subnucleus reticularis dorsalis, gigantocellular, dorsal
153 and lateral crescent areas, central lateral subnucleus (rostral portion), and dorsal lateral subnucl
154 rsal lateral PB subnucleus), central lateral subnucleus (rostral portion), and superior lateral subnu
155 in the secondary gustatory nucleus: a medial subnucleus spanning most of the rostrocaudal extent of t
156 eminal nuclear complex (TNC) and result from subnucleus specific inputs via certain cells of origin,
159 e nucleus, a central subnucleus and a dorsal subnucleus, the latter two located in the rostrolateral
160 er baroreceptor terminal sites, e.g., medial subnucleus, the medial commissural field, the intermedia
161 like immunoreactivity in the rostral central subnucleus, the region of the rostral solitary nucleus t
164 whereas the adjoining ventroposterior medial subnucleus, VPM, representing the head, was unlabeled.
165 DPAT binding (fmol/mg protein) in the dorsal subnucleus was lower than that in the ventral or the int
166 ng was particularly high in the interstitial subnucleus, whereas GluR2/3 immunolabeling was particula
167 lmost exclusively to the superior lateral PB subnucleus, whereas the lateral and ventrolateral PAG co
168 ected primarily to the contralateral lateral subnucleus, which innervated the perioral musculature.
169 with catecholamines in neurons in the dorsal subnucleus, which likely mediate, in part, the cardiovas
170 ions originate almost entirely in the apical subnucleus, which may be more appropriately described as
173 ctively increased FLI in the central lateral subnucleus while electrical stimulation increased FLI in
174 calized primarily to the rostral dorsomedial subnucleus, while those of smaller A- and C-fiber barore
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