ライフサイエンスコーパス: subnucleus

1 inputs from the ipsilateral rostrolateral IP subnucleus.

2 only from the internal lateral parabrachial subnucleus.

3 he medial, and the other in the interstitial subnucleus.

4 ding from the PBel into the lateral crescent subnucleus.

5 umber/area of subdivision) within the medial subnucleus.

6 n the adjacent lateral crescent parabrachial subnucleus.

7 e dendrites extend into the lateral crescent subnucleus.

8 leus (rostral portion), and superior lateral subnucleus.

9 tinguish pvLNTB cells from cells of the main subnucleus.

10 ucleus (rostral portion), and dorsal lateral subnucleus.

11 ng was particularly high in the intermediate subnucleus.

12 vity were preferentially located in the main subnucleus.

13 he trapezoid body, called the posteroventral subnucleus.

14 n that in the ventral or the interfascicular subnucleus.

15 zed animals after AMPA injection into either subnucleus.

16 binding was observed in the external lateral subnucleus.

17 o the ipsilateral dorsomedial portion of the subnucleus.

18 rbor shape that was attributed to the target subnucleus.

19 the CEAl were located in the DsRed-negative subnucleus.

20 but in a manner that depended on age and BLA subnucleus.

21 culary the rostral half of the parvocellular subnucleus.

22 oration of neuropil only in the left lateral subnucleus.

23 litarii (NTS), mainly within the commissural subnucleus.

24 projection site (a region of the commissural subnucleus, 0.1-0.5 mm caudal to the CS, 0-0.5 mm latera

25 Within the interfascicular subnucleus, [3H]8-OH-DPAT binding decreased progressivel

26 l region, project to the superior lateral PB subnucleus, a presumed nociceptive relay site that recei

27 ns were most numerous in the rostral central subnucleus after either stimulus but had a medial bias a

28 However, this subnucleus also projected to all the other intralaminar

29 mia was predominantly located in the lateral subnucleus, although Fos-stained medial sub-nucleus neur

30 ostrocaudal extent of the nucleus, a central subnucleus and a dorsal subnucleus, the latter two locat

31 e medial commissural field, the intermediate subnucleus and a ventral A2 noradrenergic area.

32 for white matter tracts originating in each subnucleus and examined longitudinal change in PD-halluc

33 osensors in the nostrils through the muralis subnucleus and onto both the preBotzinger and facial mot

34 solitarius (nTS), lateral to the commissural subnucleus and perhaps in the medial subnuclei.

35 urons were localized in the superior-lateral subnucleus, and 40% of them expressed the mRNA encoding

36 e located in the ventral parvocellular (PaV) subnucleus, and showed an oblique orientation with respe

37 ocated in the posterior parvocellular (PaPo) subnucleus, and were oriented perpendicularly with respe

38 clei; less dense in the rostral lateral (RL) subnucleus; and sparse in the ventral (V), ventral later

39 te that pacemakers in the region of the CaBP subnucleus are necessary and sufficient for the control

40 art), parabrachial nucleus (external lateral subnucleus), area postrema, nucleus tractus solitarius,

41 f the commissural NTS (NTScom) to the dorsal subnucleus at the level of the area postrema (NTSap).

42 DPAT binding were found in the ventrolateral subnucleus at the level of the caudal extent of the troc

43 ease from MHb terminals depending on the IPN subnucleus, but the role of KCTDs is unknown.

44 ubnucleus interpolaris (juvenile tissue) and subnucleus caudalis (juvenile and adult tissue).

45 portion of the ipsilateral spinal trigeminal subnucleus caudalis (SVc) and interpolaris (SVi), and th

46 in the nociceptive lamina of the trigeminal subnucleus caudalis (TSNC) in the brainstem.

47 DPHd neurons were found predominantly in Vsp subnucleus caudalis (Vc) and in dorsomedial subnucleus o

48 inae of the dorsomedial aspect of trigeminal subnucleus caudalis (Vc) evoked by lingual application o

49 nvestigated the potential role of sGC in the subnucleus caudalis (Vc) in mediating masseter hypersens

50 of chemonociceptive responses of trigeminal subnucleus caudalis (Vc) neurons in rats.

51 eral medulla, and lamina V of the trigeminal subnucleus caudalis (Vc), exhibited FluoroGold/Fos doubl

52 omatosensory region of the spinal trigeminal subnucleus caudalis (Vc), which projects to the PbN.

53 ciceptive properties similar to those in the subnucleus caudalis (Vc).

54 corneal surface of the eye to the trigeminal subnucleus caudalis (Vc).

55 These data demonstrate that in trigeminal subnucleus caudalis activation of either NK1 or NMDA rec

56 in trigeminal ganglia and associated spinal subnucleus caudalis and C1/C2 cervical dorsal spinal cor

57 n second-order neurons in the dorsal horn of subnucleus caudalis and cervical C1/C2 spinal cord (Vc/C

58 Fos expression can be induced in trigeminal subnucleus caudalis by NMDA or neurokinin-1 receptor act

59 e immunoreactivity (SP-LI) were evaluated in subnucleus caudalis following induction of sinusitis.

60 PrV, SpI, or the magnocellular portion of V subnucleus caudalis in these animals.

61 t that neurons in superficial laminae of the subnucleus caudalis may be important for the reflex init

62 rve branches located in the main sensory and subnucleus caudalis of the brainstem and joints, respect

63 Subnucleus caudalis represented the face in a three-dime

64 y and spinal dorsal horn from the trigeminal subnucleus caudalis to C2.

65 al to the obex (22% in C2, 22% in C1, 23% in subnucleus caudalis, and 18% in the transition zone betw

66 in other species, into cervical dorsal horn, subnucleus caudalis, subnucleus interpolaris, subnucleus

67 audalis (Vi/Vc) transition or the trigeminal subnucleus caudalis-cervical cord (Vc/C1) junction regio

68 re localized to lamina II of the ipsilateral subnucleus caudalis.

69 r CGRP-LI and SP-LI increased in ipsilateral subnucleus caudalis.

70 rimary afferent profiles in lamina II of rat subnucleus caudalis.

71 tic axonal terminals within lamina II of the subnucleus caudalis.

72 inal trigeminal subnucleus interpolaris, and subnucleus caudalis.

73 ositive cells were counted in the trigeminal subnucleus caudalis.

74 the observed antinociception occurred at the subnucleus caudalis.

75 ent areas (which flank the dorsal lateral PB subnucleus), central lateral subnucleus (rostral portion

76 1b immunostaining was also pronounced in the subnucleus centralis of the nucleus tractus solitarius.

77 oreactive fibers in the medial parvocellular subnucleus, dorsal division (PVNmpd) and posterior magno

78 (2) are located in the external lateral (el) subnucleus, express calcitonin gene-related peptide (CGR

79 taining SCN tissue but lacking cells of this subnucleus fail to restore rhythmicity.

80 rate decreases considerably when the short (subnucleus) fibrils lose monomers much more frequently t

81 and extends dorsally beyond, the central SCN subnucleus identified by calbindin-immunoreactive neuron

82 le vagal nerve terminals in the central (Ce) subnucleus in the intermediate/caudal NST.

83 s to five lateral PB sites: external lateral subnucleus (inner subdivision), medial and lateral cresc

84 Neurons in a third, intermediate VPM subnucleus innervate through branched axons both S1 and

85 Neurons from the rostral VPM subnucleus innervate trigeminal S1 in point-to-point fas

86 In contrast, a caudal VPM subnucleus innervates heavily and topographically second

87 d septa separating darkly stained patches in subnucleus interpolaris (juvenile tissue) and subnucleus

88 e input to V nucleus principalis (PrV) and V subnucleus interpolaris (SpI) in the vinblastine-treated

89 ll loss in the V ganglion, PrV, and spinal V subnucleus interpolaris (SpVi).

90 The subnucleus interpolaris (Vi) has been identified as a ma

91 mean areas of multiunit receptive fields in subnucleus interpolaris and caudalis were larger than pr

92 ch ray's representation differed between the subnucleus interpolaris and the principal sensory nucleu

93 polaris), and 14% rostral to the obex (6% in subnucleus interpolaris, 4% in subnucleus oralis, and 4%

94 principal sensory nucleus, spinal trigeminal subnucleus interpolaris, and subnucleus caudalis.

95 functional anomalies in trigeminal brainstem subnucleus interpolaris, including changes in normal rec

96 were distributed throughout the ipsilateral subnucleus interpolaris, principal trigeminal nucleus, a

97 o cervical dorsal horn, subnucleus caudalis, subnucleus interpolaris, subnucleus oralis, and nucleus

98 ne whether neurons at the ventral trigeminal subnucleus interpolaris- caudalis (Vi/Vc) transition or

99 At the level of the trigeminal subnucleus interpolaris/caudalis (Vi/Vc) transition zone

100 ion of substrate is such that the pyrimidine subnucleus is oriented opposite to that seen with the sl

101 ivision (PVNmpd) and posterior magnocellular subnucleus, lateral division (PVNpml) was performed in a

102 the regional volume of the MeA posterodorsal subnucleus (MeApd) is approximately 50% larger in males

103 ect to five lateral PB sites: dorsal lateral subnucleus, medial and lateral crescent areas (which fla

104 The NTScd is the primary NTS subnucleus mediating reflexes from the mucosal rapidly a

105 receptors, and the NTSce is the primary NTS subnucleus mediating reflexes from the muscular slowly a

106 he brain than on the right, while the medial subnucleus (MsDh) is larger on the right compared to the

107 f olfactory pathways.(9) We investigated how subnucleus muralis cells mediate apnea in rat.

108 A midline area in the commissural subnucleus (nCom) of nTS is the site of peripheral chemo

109 Within the rostral central subnucleus, neurons that exhibited Fos-like immunoreacti

110 In the commissural subnucleus of nTS, the responses comparable to those eli

111 elicited occupied the margins of the medial subnucleus of nTS.

112 as elicited, occupied a region in the medial subnucleus of nucleus tractus solitarius (nTS), the reti

113 ssion in the enteric nerve plexi, the medial subnucleus of nucleus tractus solitarius, and the dorsal

114 guus, hypoglossal nucleus, and ventrolateral subnucleus of solitary tract nucleus), and a non-respira

115 ntral nucleus of the amygdala (CEA) and oval subnucleus of the BST (BSTov), amphetamine administratio

116 he superficial granular layer of the lateral subnucleus of the commissural nucleus of Cajal, which is

117 rs the caudolateral part of the interpolaris subnucleus of the descending trigeminal tract, a caudola

118 Notably, the lateral subnucleus of the Dh (LsDh) is larger on the left side o

119 ptophan-hydroxylase-2 (TPH2), in the ventral subnucleus of the dorsal raphe nucleus (DRv).

120 gle-cell activity was recorded in the dorsal subnucleus of the lateral amygdala (LAd) of freely behav

121 ty except in the lateral septum and external subnucleus of the lateral parabrachial nucleus which con

122 he anterior preglomerular nucleus and caudal subnucleus of the lateral preglomerular nucleus receive

123 The rostral subnucleus of the lateral preglomerular nucleus receives

124 nephrine (NE) on neurons of the intermediate subnucleus of the lateral septum (LSI) were examined usi

125 The posterodorsal subnucleus of the medial amygdala (MeApd) is particularl

126 erior nucleus, the dorsal part of the dorsal subnucleus of the medial geniculate complex, and the per

127 we examined inputs to neurons in the medial subnucleus of the medial geniculate nucleus (mMG) for ch

128 sibility that neurons in the central lateral subnucleus of the middle and rostral LPBN are integrally

129 ogenous mu-receptor agonist) into the medial subnucleus of the NTS (mNTS) elicit depressor and bradyc

130 as heavy in an area that included the medial subnucleus of the NTS and the DMV over their full rostra

131 yrosine hydroxylase in neurons in the dorsal subnucleus of the NTS.

132 se to significant projections to the central subnucleus of the NTS.

133 the ventral optic tectum, and in the lateral subnucleus of the nuc. preglomerulosus of the thalamus.

134 of an electrolytic lesion of the commissural subnucleus of the nucleus of the solitary tract (commNTS

135 subnucleus reticularis dorsalis, commissural subnucleus of the nucleus tractus solitarii, lateral med

136 The dorsolateral subnucleus of the nucleus tractus solitarius (dlNTS) was

137 ral vestibular nucleus, and internal lateral subnucleus of the parabrachial complex.

138 of cells expressing c-fos in the dorsomedial subnucleus of the rostral nucleus tractus solitarius.

139 rder ventromedially to encompass the central subnucleus of the SCN (SCNce).

140 rs and on second-order neurons in the medial subnucleus of the solitary tract (NTS), the area postrem

141 other respiratory nucleus, the ventrolateral subnucleus of the solitary tract nucleus (NTS(VL)), and

142 the nasal cavity that project to the muralis subnucleus of the spinal trigeminal complex.(7)(,)(8) No

143 vagal afferent nerve terminals in the medial subnucleus of the tractus solitarious (mNTS) and alpha4b

144 inputs terminate principally in the central subnucleus of the tractus solitarius (cNTS).

145 uggest that the neurons of the ventrolateral subnucleus of the tractus solitarius (vlNTS) act as an i

146 ther VPM, representing the face, or the hand subnucleus of VPL.

147 Subnucleus oralis contained a small number of induced ne

148 e obex (6% in subnucleus interpolaris, 4% in subnucleus oralis, and 4% in subnucleus principalis).

149 ubnucleus caudalis, subnucleus interpolaris, subnucleus oralis, and nucleus principalis.

150 subnucleus caudalis (Vc) and in dorsomedial subnucleus oralis.

151 spinal trigeminal nucleus, specifically the subnucleus oralis.

152 e show that the central lateral parabrachial subnucleus (PBcl) provides Dyn inputs to the VLPO, where

153 (CTb) into the external lateral parabrachial subnucleus (PBel) produced both retrograde cell body lab

154 ing was in the external lateral parabrachial subnucleus (PBel), including dendrites extending from th

155 between adjacent subnuclei are critical for subnucleus position.

156 discrete subregion resembling the calbindin subnucleus previously described.

157 gressive social encounters in a hypothalamic subnucleus previously known as a locus for aggression, a

158 rpolaris, 4% in subnucleus oralis, and 4% in subnucleus principalis).

159 h four of the six cells filled in the medial subnucleus projected only to nucleus centralis.

160 The external lateral parabrachial subnucleus projected to the lateral parafascicular, reun

161 Cells forming the posteroventral subnucleus (pvLNTB), when investigated by light microsco

162 dy was designed to investigate a role of the subnucleus reticularis dorsalis (SRD) in the analgesia p

163 that the CPA projects preferentially to the subnucleus reticularis dorsalis, commissural nucleus tra

164 fibers with varicosities in the ipsilateral subnucleus reticularis dorsalis, commissural subnucleus

165 ntine reticular formation nuclei such as the subnucleus reticularis dorsalis, gigantocellular, dorsal

166 and lateral crescent areas, central lateral subnucleus (rostral portion), and dorsal lateral subnucl

167 rsal lateral PB subnucleus), central lateral subnucleus (rostral portion), and superior lateral subnu

168 with stronger nAChR function in the rostral subnucleus [rostral IPN (IPR)].

169 A small anterodorsal subnucleus selectively innervates dysgranular S1.

170 The parvicellular VPM subnucleus selectively targets the insular cortex and ad

171 in the secondary gustatory nucleus: a medial subnucleus spanning most of the rostrocaudal extent of t

172 eminal nuclear complex (TNC) and result from subnucleus specific inputs via certain cells of origin,

173 lcholine receptor (nAChR) subtypes, leads to subnucleus-specific alterations in BFCN excitability and

174 lcholine receptor (nAChR) subtypes, leads to subnucleus-specific alterations in BFCN excitability and

175 These results demonstrate discrete, subnucleus-specific effects of social deprivation on the

176 The only apparent subnucleus-specific projection pattern involved cells at

177 ple cortical cell-type-specific and thalamic subnucleus-specific recurrent loops, with both CT and PT

178 ecific projection motifs reveal a caudal MPu subnucleus that innervates inferior and ventral temporal

179 and ventral temporal areas and a rostral MPu subnucleus that innervates temporal, ventral prefrontal,

180 e nucleus, a central subnucleus and a dorsal subnucleus, the latter two located in the rostrolateral

181 er baroreceptor terminal sites, e.g., medial subnucleus, the medial commissural field, the intermedia

182 like immunoreactivity in the rostral central subnucleus, the region of the rostral solitary nucleus t

183 clei by 41%, and the ventroposterior lateral subnucleus (VPL) of the thalamus by 20%.

184 The ventroposterior medial subnucleus (VPM) for touch was identified as separate fr

185 whereas the adjoining ventroposterior medial subnucleus, VPM, representing the head, was unlabeled.

186 DPAT binding (fmol/mg protein) in the dorsal subnucleus was lower than that in the ventral or the int

187 ng was particularly high in the interstitial subnucleus, whereas GluR2/3 immunolabeling was particula

188 lmost exclusively to the superior lateral PB subnucleus, whereas the lateral and ventrolateral PAG co

189 la (CEAl) - were found in the DsRed-positive subnucleus, whereas those projecting to the CEAl were lo

190 ected primarily to the contralateral lateral subnucleus, which innervated the perioral musculature.

191 with catecholamines in neurons in the dorsal subnucleus, which likely mediate, in part, the cardiovas

192 ions originate almost entirely in the apical subnucleus, which may be more appropriately described as

193 The internal lateral PB subnucleus, which projects exclusively to the intralamin

194 M2 projected bilaterally to the medial subnucleus, which supplied the auricular musculature.

195 ctively increased FLI in the central lateral subnucleus while electrical stimulation increased FLI in

196 calized primarily to the rostral dorsomedial subnucleus, while those of smaller A- and C-fiber barore