ライフサイエンスコーパス: nucleus tractus solitarius

1 d activated gustatory neurons in the rostral nucleus tractus solitarius.

2 uated by the NK-1 receptor antagonist in the nucleus tractus solitarius.

3 ronounced in the subnucleus centralis of the nucleus tractus solitarius.

4 external cuneate nucleus, area postrema, and nucleus tractus solitarius.

5 days PI, infected neurons were found in the nucleus tractus solitarius.

6 etworks of premotor neurons localized in the nucleus tractus solitarius.

7 in the dorsomedial subnucleus of the rostral nucleus tractus solitarius.

8 n the intermediate and rostral levels of the nucleus tractus solitarius.

9 missural, medial and dorsal subnuclei of the nucleus tractus solitarius.

10 medial parabrachial nuclei, and commissural nucleus tractus solitarius.

11 ase in activity in the trigeminal nuclei and nucleus tractus solitarius.

12 amic paraventricular nucleus, but not in the nucleus tractus solitarius.

13 in the brainstem, with high abundance in the nucleus tractus solitarius.

14 uclei, subnuclei of the trigeminal nerve and nucleus tractus solitarius.

15 entral synapse of lung afferent neurons, the nucleus tractus solitarius.

16 in part by an NK-1 receptor mechanism in the nucleus tractus solitarius.

17 lex (2-fold), area postrema (7-fold) and the nucleus tractus solitarius (4-fold).

18 erplasia of the noradrenergic neurons in the nucleus tractus solitarius, A5 and A7, was also observed

19 lamus, supraoptic nucleus, central amygdala, nucleus tractus solitarius and area postrema compared wi

20 Furthermore, the brainstem's nucleus tractus solitarius and area postrema showed incr

21 arabrachial nucleus, intermediate and caudal nucleus tractus solitarius and area postrema), reward (t

22 instem nuclei with known inputs to the RVLM (nucleus tractus solitarius and caudal VLM) unmasked toni

23 luRs on the synaptic connections between the nucleus tractus solitarius and dorsal motor nucleus of t

24 a region in dorsal medulla that includes the nucleus tractus solitarius and dorsal reticular nucleus.

25 uts from the airway sensory receptors to the nucleus tractus solitarius and from this site to airway-

26 urons were observed in the gustatory rostral nucleus tractus solitarius and in areas involved in vest

27 terstitial and intermediate subnuclei of the nucleus tractus solitarius and in other medullary, ponti

28 Neurons of the ITR have connections with the nucleus tractus solitarius and projections to the ventro

29 eceptors on neurons whose connections to the nucleus tractus solitarius and rostral ventrolateral med

30 se 2 expression; and oxidative stress in the nucleus tractus solitarius and rostral ventrolateral med

31 clude breathing control circuitry within the nucleus tractus solitarius and the caudal part of ventra

32 mmissural and medial subnuclei of the caudal nucleus tractus solitarius and the dorsolateral, dorsome

33 ctive afferent VNS induced activation in the nucleus tractus solitarius and the rostral ventrolateral

34 n of the DMH increased Fos expression in the nucleus tractus solitarius and the ventrolateral medulla

35 consistently evoked upon stimulation of the nucleus tractus solitarius and these responses were also

36 ed robust c-Fos expression in neurons of the nucleus tractus solitarius and ventromedial (VMH) and ar

37 Blockade of output from the nucleus tractus solitarius and/or disinhibition of the C

38 igeminal tract, a caudolateral region of the nucleus tractus solitarius, and a lateral band of the pr

39 icial dorsal horn (laminae I and II) and the nucleus tractus solitarius, and both PB subnuclei send p

40 septum and hippocampus, habenula, amygdala, nucleus tractus solitarius, and circumventricular organs

41 nteric nerve plexi, the medial subnucleus of nucleus tractus solitarius, and the dorsal motor nucleus

42 The area postrema and nucleus tractus solitarius (AP/NTS) of the hindbrain are

43 unclear whether the infected neurons in the nucleus tractus solitarius are part of sympathetic or pa

44 ateral parabrachial nucleus, and commissural nucleus tractus solitarius, as previously observed in ch

45 lae were implanted bilaterally in the medial nucleus tractus solitarius at a site that produced apnea

46 Viral restoration of DBH expression in the nucleus tractus solitarius, but not in the locus coerule

47 s evoked after electrical stimulation of the nucleus tractus solitarius, but the effect was slower th

48 g preproglucagon (PPG) neurons in the medial nucleus tractus solitarius by fluorescent in situ hybrid

49 e behavior and increased Fos labeling in the nucleus tractus solitarius caudal region, which receives

50 The dorsolateral subnucleus of the nucleus tractus solitarius (dlNTS) was processed for the

51 The dorsal medial nucleus tractus solitarius (dmNTS) has long been appreci

52 f HIF-1alpha in glutamatergic neurons of the nucleus tractus solitarius during CH significantly decre

53 A novel group of neurons in the nucleus tractus solitarius expresses the enzyme 11-beta-

54 The control distribution of cells in the nucleus tractus solitarius expressing c-fos in response

55 e compared with low-sucrose beverages in the nucleus tractus solitarius for both groups.

56 h elicited an increase in trigeminal but not nucleus tractus solitarius Fos labeling, and no behavior

57 In the caudal ventrolateral medulla and nucleus tractus solitarius, Fos-positive neurons project

58 edial hypothalamus) and two hindbrain sites (nucleus tractus solitarius, fourth ventricle).

59 r extent GABA(A) receptors on neurons in the nucleus tractus solitarius, hypoglossal nucleus, and dor

60 duce satiety - one region which includes the nucleus tractus solitarius in the hindbrain, and another

61 brainstem cardiorespiratory-related region (nucleus tractus solitarius) in vitro.

62 The contiguous nucleus tractus solitarius, involved in integrating sens

63 This neural circuitry within the nucleus tractus solitarius is consistent with a complex

64 These data suggest that NE signaling by the nucleus tractus solitarius is necessary for morphine rew

65 on induced c-Fos-ir expression mainly in the nucleus tractus solitarius, lateral reticular nucleus, l

66 external lateral subnucleus), area postrema, nucleus tractus solitarius, locus coeruleus, paraventric

67 sic and long-term synaptic plasticity in the nucleus tractus solitarius may play a role in the homeos

68 cible c-jun and c-fos mRNA expression in the nucleus tractus solitarius (middle, mNTS, and rostral, r

69 Blockade of GABA receptors in the medial nucleus tractus solitarius (mNTS) also attenuated the PV

70 echolamine-containing portions of the medial nucleus tractus solitarius (mNTS) at both intermediate (

71 ateral and contralateral sides of the medial nucleus tractus solitarius (mNTS) in rats receiving EA S

72 derived hormone leptin signals in the medial nucleus tractus solitarius (mNTS) to suppress food intak

73 n (CPu), lateral parabrachial nucleus (LPB), nucleus tractus solitarius (NST), frontal cerebral corte

74 s acute stressors activate catecholaminergic nucleus tractus solitarius (NTS(TH)) projections in the

75 os expression was similarly increased in the nucleus tractus solitarius (NTS) A2 region in virgin and

76 a significant increase in AEA content in the nucleus tractus solitarius (NTS) after an increase in bl

77 sis that revealed axonal degeneration of the nucleus tractus solitarius (NTS) and area postrema (AP)

78 re we show that glutamatergic neurons in the nucleus tractus solitarius (NTS) and caudal serotonergic

79 The nucleus tractus solitarius (NTS) and dorsal motor nucleu

80 ent in cell bodies within the area postrema, nucleus tractus solitarius (NTS) and nodose ganglion.

81 ent in cell bodies within the area postrema, nucleus tractus solitarius (NTS) and nodose ganglion.

82 ll nuclei of the dorsal motor nucleus (DMN), nucleus tractus solitarius (NTS) and nucleus ambiguus (N

83 o neural signals that are transmitted to the nucleus tractus solitarius (NTS) and parabrachial nucleu

84 rain [regions involved in autonomic control: nucleus tractus solitarius (NTS) and rostral ventrolater

85 mRNA expression in two brainstem areas, the nucleus tractus solitarius (NTS) and the rostral ventrol

86 al characteristics of the NPY neurons in the nucleus tractus solitarius (NTS) and their interactions

87 pathways from the area postrema (AP) to the nucleus tractus solitarius (NTS) and to examine the syna

88 (MPN), lateral hypothalamic area (LHA), and nucleus tractus solitarius (NTS) are co-linked to these

89 A subset of neurons in the nucleus tractus solitarius (NTS) are uniquely sensitive

90 rmacological studies highlight the hindbrain nucleus tractus solitarius (NTS) as a brain region impor

91 ase-type 2 enzyme) containing neurons of the nucleus tractus solitarius (NTS) become activated during

92 PSCs evoked by electrical stimulation of the nucleus tractus solitarius (NTS) but not evoked EPSCs.

93 to which changes in synaptic transmission in nucleus tractus solitarius (NTS) contribute to these res

94 pplying NE to the limbic system, such as the nucleus tractus solitarius (NTS) contribute to this proc

95 esis that premotor, GABAergic neurons in the nucleus tractus solitarius (NTS) form a hindbrain micro-

96 Substance P (SP) is released from the feline nucleus tractus solitarius (NTS) in response to activati

97 ere used to quantify NO concentration in the nucleus tractus solitarius (NTS) in vitro in brain slice

98 ion of alpha1-noradrenergic receptors in the nucleus tractus solitarius (NTS) influences neural proce

99 The nucleus tractus solitarius (NTS) is a key central integr

100 The nucleus tractus solitarius (NTS) is essential for orches

101 ssion between baroreceptor afferents and the nucleus tractus solitarius (NTS) is essential for reflex

102 Here, we show that the hindbrain nucleus tractus solitarius (NTS) is essential for vocali

103 ol, 100 nl; n=12) in rats with contralateral nucleus tractus solitarius (NTS) lesion.

104 eous and excitatory amino acid (EAA) induced nucleus tractus solitarius (NTS) neuronal activity were

105 n via the CCL8-CCR5 axis, which triggers the nucleus tractus solitarius (NTS) neuronal damage and neu

106 modulating vagal afferent evoked activity of nucleus tractus solitarius (NTS) neurones.

107 ution of changes in synaptic transmission in nucleus tractus solitarius (NTS) neurons of C57Bl/6J mic

108 al visceral afferents innervate second-order nucleus tractus solitarius (NTS) neurons via myelinated

109 properties and synaptic transmission in the nucleus tractus solitarius (NTS) neurons, the first syna

110 ) is produced in the small intestines and in nucleus tractus solitarius (NTS) neurons.

111 os expressions in the area postrema (AP) and nucleus tractus solitarius (NTS) of brainstem including

112 c-Fos expression in the nucleus tractus solitarius (NTS) of the rat has been fou

113 Axons of other neurons ramified within the nucleus tractus solitarius (NTS) or DMV.

114 inobutyric acid-A (GABA(A)) receptors in the nucleus tractus solitarius (NTS) participate in autonomi

115 Neurons in the rat nucleus tractus solitarius (NTS) possess morphologic cha

116 In rats, cisplatin activates nucleus tractus solitarius (NTS) projections to the late

117 The nucleus tractus solitarius (NTS) receives dense terminat

118 e P (SP) in baroreceptor transmission in the nucleus tractus solitarius (NTS) remains an area of acti

119 A subset of neurons within the nucleus tractus solitarius (NTS) shows c-Fos activation

120 pinalized rat, electrical stimulation of the nucleus tractus solitarius (NTS) synchronizes the EEG by

121 P, enough concentration may have reached the nucleus tractus solitarius (nTS) to elicit depressor and

122 onto second-order neurons within the caudal nucleus tractus solitarius (NTS) to initiate autonomic r

123 The responses of gustatory neurons in the nucleus tractus solitarius (NTS) to tastant stimuli were

124 2%, respectively, while Fos labelling in the nucleus tractus solitarius (NTS) was increased by 5-fold

125 ral medullary depressor area (CVLM), and the nucleus tractus solitarius (nTS) were also included for

126 aptic input originating from neurones in the nucleus tractus solitarius (NTS) were determined by evok

127 edullary brain segments containing primarily nucleus tractus solitarius (NTS) were employed for slice

128 calizes within astrocytes and neurons in the nucleus tractus solitarius (NTS), a hindbrain nucleus cr

129 ne activates GLP-1-expressing neurons in the nucleus tractus solitarius (NTS), a hindbrain nucleus th

130 POMC neurons are also found in the nucleus tractus solitarius (NTS), a region regulating sa

131 ding characteristics of CCK receptors in the nucleus tractus solitarius (NTS), a region that contains

132 de from dissociated neurons of the brainstem nucleus tractus solitarius (nTS), a region that receives

133 nd in abundance in the caudal portion of the nucleus tractus solitarius (NTS), an area which together

134 The locus coeruleus (LC), nucleus tractus solitarius (NTS), and retrotrapezoid nuc

135 sed of afferent vagal fibers, neurons of the nucleus tractus solitarius (NTS), and the efferent fiber

136 ntricular nucleus of the hypothalamus (PVN), nucleus tractus solitarius (NTS), and the parasympatheti

137 otor nucleus (DMN), and all subnuclei of the nucleus tractus solitarius (NTS), but one.

138 lary catecholamine (CA) neurons found in the nucleus tractus solitarius (NTS), dorsal motor nucleus o

139 The nucleus tractus solitarius (NTS), especially its ventrol

140 eased IL1beta, TNFalpha and IL6 mRNAs in the nucleus tractus solitarius (NTS), hypothalamus, hippocam

141 ons that involve vagal afferent input to the nucleus tractus solitarius (NTS), including cardiopulmon

142 trol in the brainstem, in particular, in the nucleus tractus solitarius (NTS), is well established.

143 y relay neurons are found bilaterally within nucleus tractus solitarius (nTS), lateral to the commiss

144 Its neighboring nuclei, the nucleus tractus solitarius (NTS), responds to acute gluc

145 d that oestradiol increased Fos abundance in nucleus tractus solitarius (NTS), rostral ventrolateral

146 estern blots of protein equivalents from the nucleus tractus solitarius (NTS), the first central rela

147 potential neuroanatomical hub connecting the nucleus tractus solitarius (NTS), the major central sour

148 ions as a neuroanatomical hub connecting the nucleus tractus solitarius (NTS), the primary source of

149 analyzed synaptic function in the brainstem nucleus tractus solitarius (nTS), the principal site for

150 receptor, TrkB, are highly expressed in the nucleus tractus solitarius (nTS), the principal target o

151 ccupied a region in the medial subnucleus of nucleus tractus solitarius (nTS), the reticular formatio

152 tic plasticity in this reflex pathway in the nucleus tractus solitarius (NTS), the site of terminatio

153 n bilateral spinal trigeminal nucleus (VSP), nucleus tractus solitarius (NTS), ventrolateral medulla

154 configurations functionally expressed in the nucleus tractus solitarius (NTS), we conducted several p

155 t they involve glutamatergic synapses in the nucleus tractus solitarius (NTS), where afferent endings

156 halamic paraventricular nucleus (PVN) to the nucleus tractus solitarius (NTS), where cells that respo

157 In nucleus tractus solitarius (NTS)-A2 and NTS-C2, both NPY

158 tion of food has been strongly implicated in nucleus tractus solitarius (NTS)-mediated satiation, but

159 1 opioid receptors, has been reported in the nucleus tractus solitarius (nTS).

160 shaping autonomic signal transmission in the nucleus tractus solitarius (NTS).

161 properties at this first synapse within the nucleus tractus solitarius (NTS).

162 atory effects of hypoxia at the level of the nucleus tractus solitarius (NTS).

163 lated dextran amine were made into the LC or nucleus tractus solitarius (NTS).

164 ardiac vagal neurons upon stimulation of the nucleus tractus solitarius (NTS).

165 125I]NT-4 to the central terminal field, the nucleus tractus solitarius (NTS).

166 ffer with regards to their dependence on the nucleus tractus solitarius (NTS).

167 to vagal preganglionic neurons and/or to the nucleus tractus solitarius (NTS).

168 ucagon-like peptide-1 (GLP-1) neurons in the nucleus tractus solitarius (NTS).

169 Centrally they innervated the nucleus tractus solitarius (nTS).

170 ors and central autonomic nuclei such as the nucleus tractus solitarius (NTS).

171 notably in cardiorespiratory regions of the nucleus tractus solitarius (nTS).

172 ly via centrally projecting neurons from the nucleus tractus solitarius (NTS).

173 wo specific subpopulations of neurons in the nucleus tractus solitarius (NTS).

174 rginine vasopressin (AVP) released in medial nucleus tractus solitarius (NTS).

175 in arterial chemoreceptors and the CNS [e.g. nucleus tractus solitarius (NTS)], although the signals

176 n receptor (Calcr)-expressing neurons of the nucleus tractus solitarius (NTS; Calcr(NTS) cells) contr

177 eurons in the nucleus of the solitary tract (nucleus tractus solitarius; NTS) suppress food intake, i

178 mation at the level of the solitary nucleus (nucleus tractus solitarius; NTS), their involvement in t

179 a bitterlike sensation when delivered to the nucleus tractus solitarius of behaving rats.

180 le (mNTS) and rostral (rNTS) portions of the nucleus tractus solitarius of SHRs and WKY rats.

181 antagonist, SR 140333, was injected into the nucleus tractus solitarius of the conscious guinea pigs

182 Cardiac vagal afferent fibers synapse in the nucleus tractus solitarius of the medulla and then desce

183 order synapses of the medial and commissural nucleus tractus solitarius of the medulla.

184 calized exclusively in the area postrema and nucleus tractus solitarius of the mouse brainstem.

185 , commissural and medial subdivisions of the nucleus tractus solitarius of wild-type F344.Cck1r(+/+)

186 ygdala, diagonal band of Broca, hippocampus, nucleus tractus solitarius, parabrachial nucleus, parave

187 PVT neurons receive GLP-1 innervation from nucleus tractus solitarius preproglucagon neurons that w

188 indicate that GLP-1-producing neurons in the nucleus tractus solitarius project monosynaptically to t

189 ing the pathways from the spinal trigeminal, nucleus tractus solitarius, raphe magnus, raphe pallidus

190 GK mRNA was also found in the area postrema/nucleus tractus solitarius region by RT-PCR.

191 ppocampus, cerebellum, posterior cortex, and nucleus tractus solitarius regions.

192 lls in the rostral, gustatory portion of the nucleus tractus solitarius (rNTS) in awake, freely licki

193 entral tegmental area, parabrachial nucleus, nucleus tractus solitarius, rostral/caudal ventrolateral

194 eased the number of CFLI cells in the caudal Nucleus Tractus Solitarius significantly more than prelo

195 ed c-Fos-ir expression in the area postrema, nucleus tractus solitarius, solitary tract, and spinal t

196 e infusion caused c-Fos-ir expression in the nucleus tractus solitarius, spinal trigeminal tract, sol

197 activation of GLP-1-producing neurons in the nucleus tractus solitarius that project to the ventral t

198 egulation of sympathetic activity, including nucleus tractus solitarius, the lateral tegmental field

199 s of these CRCs are the medullary raphe, the nucleus tractus solitarius, the ventrolateral medulla, t

200 rior hypothalamus, dorsomedial hypothalamus, nucleus tractus solitarius), there appeared to be no sig

201 s nerve sensory afferents terminating in the nucleus tractus solitarius, these terminals were identif

202 ia a branch of the glossopharyngeal nerve to nucleus tractus solitarius; this precipitates an impress

203 rtant for cardiovascular afferent signaling (nucleus tractus solitarius, ventrolateral medulla) in bo

204 c nuclei, substantia nigra, locus coeruleus, nucleus tractus solitarius, ventrolateral medulla, ponti

205 gic innervation to cardiac vagal neurons the nucleus tractus solitarius was electrically stimulated.

206 Conversely, GK message was not found in the nucleus tractus solitarius, which contains glucosensing