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

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

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

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

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

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

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

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

8 medial parabrachial nuclei, and commissural nucleus tractus solitarius.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

53 The contiguous nucleus tractus solitarius, involved in integrating sens

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

99 The nucleus tractus solitarius (NTS) receives dense terminat

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

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

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

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

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

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

106 2%, respectively, while Fos labelling in the nucleus tractus solitarius (NTS) was increased by 5-fold

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

144 125I]NT-4 to the central terminal field, the nucleus tractus solitarius (NTS).

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

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

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

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

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

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

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

152 1 opioid receptors, has been reported in the nucleus tractus solitarius (nTS).

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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