ライフサイエンスコーパス: solitarius

1 1 receptor antagonist in the nucleus tractus solitarius.

2 tant-latency synaptic input from the tractus solitarius.

3 subnucleus centralis of the nucleus tractus solitarius.

4 nucleus, area postrema, and nucleus tractus solitarius.

5 bers were found in the region of the nucleus solitarius.

6 ed neurons were found in the nucleus tractus solitarius.

7 tor neurons localized in the nucleus tractus solitarius.

8 al subnucleus of the rostral nucleus tractus solitarius.

9 te and rostral levels of the nucleus tractus solitarius.

10 and dorsal subnuclei of the nucleus tractus solitarius.

11 hial nuclei, and commissural nucleus tractus solitarius.

12 in the trigeminal nuclei and nucleus tractus solitarius.

13 ular nucleus, but not in the nucleus tractus solitarius.

14 , with high abundance in the nucleus tractus solitarius.

15 of the trigeminal nerve and nucleus tractus solitarius.

16 f lung afferent neurons, the nucleus tractus solitarius.

17 -1 receptor mechanism in the nucleus tractus solitarius.

18 ea postrema (7-fold) and the nucleus tractus solitarius (4-fold).

19 noradrenergic neurons in the nucleus tractus solitarius, A5 and A7, was also observed.

20 eceptor center of the nucleus of the tractus solitarius accounts for these actions.

21 c nucleus, central amygdala, nucleus tractus solitarius and area postrema compared with vehicle injec

22 eus, intermediate and caudal nucleus tractus solitarius and area postrema), reward (the shell of the

23 ABAergic neurons, bordering both the nucleus solitarius and caudal vestibular complex, emphasizes the

24 ptic connections between the nucleus tractus solitarius and dorsal motor nucleus of the vagus.

25 al medulla that includes the nucleus tractus solitarius and dorsal reticular nucleus.

26 way sensory receptors to the nucleus tractus solitarius and from this site to airway-related vagal pr

27 ved in the gustatory rostral nucleus tractus solitarius and in areas involved in vestibulo-ocular pro

28 ntermediate subnuclei of the nucleus tractus solitarius and in other medullary, pontine, midbrain, an

29 ar reticular nucleus, nucleus of the tractus solitarius and locus coeruleus also exhibited altered pa

30 TR have connections with the nucleus tractus solitarius and projections to the ventrolateral medulla.

31 and oxidative stress in the nucleus tractus solitarius and rostral ventrolateral medulla as well as

32 ons whose connections to the nucleus tractus solitarius and rostral ventrolateral medulla result in s

33 control circuitry within the nucleus tractus solitarius and the caudal part of ventral respiratory co

34 dial subnuclei of the caudal nucleus tractus solitarius and the dorsolateral, dorsomedial and medial

35 neurons were additionally present in nucleus solitarius and the gracile and cuneate nuclei.

36 reased Fos expression in the nucleus tractus solitarius and the ventrolateral medulla bilaterally wit

37 oked upon stimulation of the nucleus tractus solitarius and these responses were also blocked by bicu

38 a caudolateral region of the nucleus tractus solitarius, and a lateral band of the principal sensory

39 n (laminae I and II) and the nucleus tractus solitarius, and both PB subnuclei send projections to li

40 so found in the medial portion of n. tractus solitarius, and both the rostral and caudal ventrolatera

41 ocampus, habenula, amygdala, nucleus tractus solitarius, and circumventricular organs such as subforn

42 xi, the medial subnucleus of nucleus tractus solitarius, and the dorsal motor nucleus of the vagus, b

43 the infected neurons in the nucleus tractus solitarius are part of sympathetic or parasympathetic af

44 ii, E. avium, E. durans, E. columbae, and E. solitarius are presented herein.

45 ial nucleus, and commissural nucleus tractus solitarius, as previously observed in chronic morphine-t

46 ed bilaterally in the medial nucleus tractus solitarius at a site that produced apnea in response to

47 ion of DBH expression in the nucleus tractus solitarius, but not in the locus coeruleus, restored CPP

48 lectrical stimulation of the nucleus tractus solitarius, but the effect was slower than for the enhan

49 ncreased Fos labeling in the nucleus tractus solitarius caudal region, which receives vagal chemosens

50 lly in the central subnucleus of the tractus solitarius (cNTS).

51 rsolateral subnucleus of the nucleus tractus solitarius (dlNTS) was processed for the histochemical v

52 The dorsal medial nucleus tractus solitarius (dmNTS) has long been appreciated as a primar

53 al stimulation of the nucleus of the tractus solitarius evoked EPSCs and IPSCs.

54 Constant latency tractus solitarius-evoked EPSCs were decreased in amplitude by l

55 ovel group of neurons in the nucleus tractus solitarius expresses the enzyme 11-beta-hydroxysteroid d

56 distribution of cells in the nucleus tractus solitarius expressing c-fos in response to physiological

57 low-sucrose beverages in the nucleus tractus solitarius for both groups.

58 crease in trigeminal but not nucleus tractus solitarius Fos labeling, and no behavioral avoidance.

59 al ventrolateral medulla and nucleus tractus solitarius, Fos-positive neurons projected to the Sm, PB

60 us) and two hindbrain sites (nucleus tractus solitarius, fourth ventricle).

61 receptors on neurons in the nucleus tractus solitarius, hypoglossal nucleus, and dorsal motor nucleu

62 ne region which includes the nucleus tractus solitarius in the hindbrain, and another more distribute

63 orespiratory-related region (nucleus tractus solitarius) in vitro.

64 eEPSCs) evoked by stimulation of the tractus solitarius, in a concentration-dependent manner.

65 urones, including neurones receiving tractus solitarius input (i.e. viscerosensory) and those involve

66 The contiguous nucleus tractus solitarius, involved in integrating sensory input to mai

67 neural circuitry within the nucleus tractus solitarius is consistent with a complex central control

68 est that NE signaling by the nucleus tractus solitarius is necessary for morphine reward.

69 -ir expression mainly in the nucleus tractus solitarius, lateral reticular nucleus, lateral tegmental

70 subnucleus), area postrema, nucleus tractus solitarius, locus coeruleus, paraventricular nucleus of

71 m synaptic plasticity in the nucleus tractus solitarius may play a role in the homeostatic regulation

72 c-fos mRNA expression in the nucleus tractus solitarius (middle, mNTS, and rostral, rNTS) and the ros

73 GABA receptors in the medial nucleus tractus solitarius (mNTS) also attenuated the PVN-induced tachyc

74 eurones in the medial nucleus of the tractus solitarius (mNTS) and in the dorsal motor nucleus of the

75 ining portions of the medial nucleus tractus solitarius (mNTS) at both intermediate (NTSi) and caudal

76 alateral sides of the medial nucleus tractus solitarius (mNTS) in rats receiving EA ST 36 compared wi

77 leptin signals in the medial nucleus tractus solitarius (mNTS) to suppress food intake, in part, by a

78 parabrachial nucleus (LPB), nucleus tractus solitarius (NST), frontal cerebral cortex and the parvoc

79 s similarly increased in the nucleus tractus solitarius (NTS) A2 region in virgin and pregnant rats 9

80 crease in AEA content in the nucleus tractus solitarius (NTS) after an increase in blood pressure (BP

81 d axonal degeneration of the nucleus tractus solitarius (NTS) and area postrema (AP) of the medulla.

82 glutamatergic neurons in the nucleus tractus solitarius (NTS) and caudal serotonergic neurons control

83 nsmission between the nucleus of the tractus solitarius (NTS) and dorsal motor nucleus of the vagus (

84 The nucleus tractus solitarius (NTS) and dorsal motor nucleus of the vagus n

85 es within the area postrema, nucleus tractus solitarius (NTS) and nodose ganglion.

86 es within the area postrema, nucleus tractus solitarius (NTS) and nodose ganglion.

87 dorsal motor nucleus (DMN), nucleus tractus solitarius (NTS) and nucleus ambiguus (NA) with a sham c

88 that are transmitted to the nucleus tractus solitarius (NTS) and parabrachial nucleus (PB).

89 in two brainstem areas, the nucleus tractus solitarius (NTS) and the rostral ventrolateral medulla (

90 he area postrema (AP) to the nucleus tractus solitarius (NTS) and to examine the synaptic interaction

91 hypothalamic area (LHA), and nucleus tractus solitarius (NTS) are co-linked to these two sites.

92 A subset of neurons in the nucleus tractus solitarius (NTS) are uniquely sensitive to the adrenal s

93 dies highlight the hindbrain nucleus tractus solitarius (NTS) as a brain region important for GLP-1R-

94 e) containing neurons of the nucleus tractus solitarius (NTS) become activated during low-sodium and

95 lectrical stimulation of the nucleus tractus solitarius (NTS) but not evoked EPSCs.

96 e limbic system, such as the nucleus tractus solitarius (NTS) contribute to this process.

97 l vagal complex (DVC; nucleus of the tractus solitarius (NTS) dorsal motor nucleus of the vagus (DMV)

98 is released from the feline nucleus tractus solitarius (NTS) in response to activation of skeletal m

99 tify NO concentration in the nucleus tractus solitarius (NTS) in vitro in brain slices and in vivo in

100 radrenergic receptors in the nucleus tractus solitarius (NTS) influences neural processes that are in

101 The nucleus of the tractus solitarius (NTS) is a primary termination zone for laryn

102 The nucleus tractus solitarius (NTS) is essential for orchestrating barorefl

103 roreceptor afferents and the nucleus tractus solitarius (NTS) is essential for reflex regulation of b

104 , we show that the hindbrain nucleus tractus solitarius (NTS) is essential for vocalization in mice.

105 ) in rats with contralateral nucleus tractus solitarius (NTS) lesion.

106 ory amino acid (EAA) induced nucleus tractus solitarius (NTS) neuronal activity were investigated by

107 afferent evoked activity of nucleus tractus solitarius (NTS) neurones.

108 rents innervate second-order nucleus tractus solitarius (NTS) neurons via myelinated (A-type) and unm

109 synaptic transmission in the nucleus tractus solitarius (NTS) neurons, the first synaptic station of

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

111 c-Fos expression in the nucleus tractus solitarius (NTS) of the rat has been found to follow adm

112 neurons ramified within the nucleus tractus solitarius (NTS) or DMV.

113 A (GABA(A)) receptors in the nucleus tractus solitarius (NTS) participate in autonomic regulation of

114 Neurons in the rat nucleus tractus solitarius (NTS) possess morphologic characteristics tha

115 In rats, cisplatin activates nucleus tractus solitarius (NTS) projections to the lateral parabrachial

116 The nucleus tractus solitarius (NTS) receives dense terminations from crania

117 receptor transmission in the nucleus tractus solitarius (NTS) remains an area of active research.

118 subset of neurons within the nucleus tractus solitarius (NTS) shows c-Fos activation during prolonged

119 lectrical stimulation of the nucleus tractus solitarius (NTS) synchronizes the EEG by increasing the

120 tration may have reached the nucleus tractus solitarius (nTS) to elicit depressor and bradycardic res

121 er neurons within the caudal nucleus tractus solitarius (NTS) to initiate autonomic reflexes.

122 of gustatory neurons in the nucleus tractus solitarius (NTS) to tastant stimuli were recorded before

123 , while Fos labelling in the nucleus tractus solitarius (NTS) was increased by 5-fold compared with v

124 pressor area (CVLM), and the nucleus tractus solitarius (nTS) were also included for comparison of di

125 inating from neurones in the nucleus tractus solitarius (NTS) were determined by evoking activity in

126 egments containing primarily nucleus tractus solitarius (NTS) were employed for slice superfusion stu

127 strocytes and neurons in the nucleus tractus solitarius (NTS), a hindbrain nucleus critical for energ

128 -1-expressing neurons in the nucleus tractus solitarius (NTS), a hindbrain nucleus that projects mono

129 eurons are also found in the nucleus tractus solitarius (NTS), a region regulating satiety.

130 tics of CCK receptors in the nucleus tractus solitarius (NTS), a region that contains central termina

131 ted neurons of the brainstem nucleus tractus solitarius (nTS), a region that receives massive primary

132 in the caudal portion of the nucleus tractus solitarius (NTS), an area which together with the dorsal

133 vagal fibers, neurons of the nucleus tractus solitarius (NTS), and the efferent fibers originating in

134 s of the hypothalamus (PVN), nucleus tractus solitarius (NTS), and the parasympathetic nucleus of the

135 N), and all subnuclei of the nucleus tractus solitarius (NTS), but one.

136 ne (CA) neurons found in the nucleus tractus solitarius (NTS), dorsal motor nucleus of the vagus (DMV

137 The nucleus tractus solitarius (NTS), especially its ventrolateral, dorsolat

138 NFalpha and IL6 mRNAs in the nucleus tractus solitarius (NTS), hypothalamus, hippocampus and somatose

139 vagal afferent input to the nucleus tractus solitarius (NTS), including cardiopulmonary responses, g

140 nstem, in particular, in the nucleus tractus solitarius (NTS), is well established.

141 are found bilaterally within nucleus tractus solitarius (nTS), lateral to the commissural subnucleus

142 l increased Fos abundance in nucleus tractus solitarius (NTS), rostral ventrolateral medulla (RVLM),

143 protein equivalents from the nucleus tractus solitarius (NTS), the first central relay for peripheral

144 natomical hub connecting the nucleus tractus solitarius (NTS), the major central source of GLP-1, wit

145 ic function in the brainstem nucleus tractus solitarius (nTS), the principal site for integration of

146 are highly expressed in the nucleus tractus solitarius (nTS), the principal target of cardiovascular

147 in the medial subnucleus of nucleus tractus solitarius (nTS), the reticular formation just ventral t

148 n this reflex pathway in the nucleus tractus solitarius (NTS), the site of termination of the chemose

149 al trigeminal nucleus (VSP), nucleus tractus solitarius (NTS), ventrolateral medulla (VLM) and inferi

150 unctionally expressed in the nucleus tractus solitarius (NTS), we conducted several physiological and

151 lutamatergic synapses in the nucleus tractus solitarius (NTS), where afferent endings from arterial c

152 ricular nucleus (PVN) to the nucleus tractus solitarius (NTS), where cells that respond to peripheral

153 In nucleus tractus solitarius (NTS)-A2 and NTS-C2, both NPY+ and TH+ neuron

154 been strongly implicated in nucleus tractus solitarius (NTS)-mediated satiation, but the exact cellu

155 autonomic nuclei such as the nucleus tractus solitarius (NTS).

156 rs, has been reported in the nucleus tractus solitarius (nTS).

157 c signal transmission in the nucleus tractus solitarius (NTS).

158 his first synapse within the nucleus tractus solitarius (NTS).

159 by stimulation of the nucleus of the tractus solitarius (NTS).

160 hypoxia at the level of the nucleus tractus solitarius (NTS).

161 he amygdala (CeA) and nucleus of the tractus solitarius (NTS).

162 ine were made into the LC or nucleus tractus solitarius (NTS).

163 rons upon stimulation of the nucleus tractus solitarius (NTS).

164 central terminal field, the nucleus tractus solitarius (NTS).

165 s to their dependence on the nucleus tractus solitarius (NTS).

166 lionic neurons and/or to the nucleus tractus solitarius (NTS).

167 iorespiratory regions of the nucleus tractus solitarius (nTS).

168 projecting neurons from the nucleus tractus solitarius (NTS).

169 opulations of neurons in the nucleus tractus solitarius (NTS).

170 sin (AVP) released in medial nucleus tractus solitarius (NTS).

171 ide-1 (GLP-1) neurons in the nucleus tractus solitarius (NTS).

172 al complex (DVC, i.e. nucleus of the tractus solitarius, NTS, and dorsal motor nucleus of the vagus,

173 vel of the solitary nucleus (nucleus tractus solitarius; NTS), their involvement in the transmission

174 lar nuclei in the forebrain, and the tractus solitarius nuclei, lateral parabrachial nuclei in the hi

175 sation when delivered to the nucleus tractus solitarius of behaving rats.

176 stral (rNTS) portions of the nucleus tractus solitarius of SHRs and WKY rats.

177 cleus of the hypothalamus and nucleus tactus solitarius of the brainstem.

178 40333, was injected into the nucleus tractus solitarius of the conscious guinea pigs who were then ex

179 ferent fibers synapse in the nucleus tractus solitarius of the medulla and then descend to excite upp

180 f the medial and commissural nucleus tractus solitarius of the medulla.

181 ely in the area postrema and nucleus tractus solitarius of the mouse brainstem.

182 d medial subdivisions of the nucleus tractus solitarius of wild-type F344.Cck1r(+/+) rats, whereas CC

183 band of Broca, hippocampus, nucleus tractus solitarius, parabrachial nucleus, paraventricular nucleu

184 tions: descending trigeminal, retroambiguus, solitarius, posterior octaval, descending octaval, magno

185 ceive GLP-1 innervation from nucleus tractus solitarius preproglucagon neurons that were activated by

186 P-1-producing neurons in the nucleus tractus solitarius project monosynaptically to the lPBN, providi

187 from the spinal trigeminal, nucleus tractus solitarius, raphe magnus, raphe pallidus, and the rostra

188 o found in the area postrema/nucleus tractus solitarius region by RT-PCR.

189 ellum, posterior cortex, and nucleus tractus solitarius regions.

190 z) of primary afferent fibers in the tractus solitarius resulted in a phasic depression (accommodatio

191 area, parabrachial nucleus, nucleus tractus solitarius, rostral/caudal ventrolateral medulla, or tho

192 of CFLI cells in the caudal Nucleus Tractus Solitarius significantly more than preloads of mineral o

193 ession in the area postrema, nucleus tractus solitarius, solitary tract, and spinal trigeminal tract.

194 d c-Fos-ir expression in the nucleus tractus solitarius, spinal trigeminal tract, solitary tract, and

195 y endogenous release of glutamate by tractus solitarius stimulation, and was prevented by a group II

196 pathetic activity, including nucleus tractus solitarius, the lateral tegmental field rostral to the o

197 are the medullary raphe, the nucleus tractus solitarius, the ventrolateral medulla, the fastigial nuc

198 s, dorsomedial hypothalamus, nucleus tractus solitarius), there appeared to be no significant differe

199 afferents terminating in the nucleus tractus solitarius, these terminals were identified by the anter

200 he glossopharyngeal nerve to nucleus tractus solitarius; this precipitates an impressive array of car

201 e predominantly located close to the tractus solitarius (TS) and could be GABAergic or glutamatergic.

202 imary sensory afferent fibres in the tractus solitarius (ts) and currents postsynaptically evoked by

203 Hz trains of stimuli applied to the tractus solitarius (TS), induced a small (10%) but significant r

204 vascular afferent signaling (nucleus tractus solitarius, ventrolateral medulla) in both cell bodies a

205 ntia nigra, locus coeruleus, nucleus tractus solitarius, ventrolateral medulla, pontine nuclei, and i

206 the ventrolateral subnucleus of the tractus solitarius (vlNTS) act as an inspiratory off-switch and

207 to cardiac vagal neurons the nucleus tractus solitarius was electrically stimulated.

208 message was not found in the nucleus tractus solitarius, which contains glucosensing neurons, or in e