ライフサイエンスコーパス: raphe nucleus

1 etected in the basal forebrain or the dorsal raphe nucleus.

2 ca, supramammillary nuclei (SUM), and median raphe nucleus.

3 reticular formation, including the inferior raphe nucleus.

4 thin the dorsal portion of the caudal dorsal raphe nucleus.

5 l raphe nucleus (DRN) and part of the median raphe nucleus.

6 in serotonin-producing neurons of the dorsal raphe nucleus.

7 dunculopontine tegmental nucleus, and dorsal raphe nucleus.

8 haviors after microinjection into the median raphe nucleus.

9 elated to the serotonin system in the dorsal raphe nucleus.

10 ncrease in OT receptor density in the dorsal raphe nucleus.

11 l reticular nucleus, hypoglossal nucleus and raphe nucleus.

12 et of serotonergic neurons within the dorsal raphe nucleus.

13 itries, including striatum, hippocampus, and raphe nucleus.

14 5-HT transmission at the level of the dorsal raphe nucleus.

15 al area, interfascicular nucleus, and dorsal raphe nucleus.

16 hat is activated by 8-OH-DPAT, in the dorsal raphe nucleus.

17 nergic (5-HTergic) neurons within the dorsal raphe nucleus.

18 ther areas such as the cerebellum and dorsal raphe nucleus.

19 activity of serotonergic cells of the dorsal raphe nucleus.

20 urons in the rat median raphe but not dorsal raphe nucleus.

21 al nucleus of the amygdala and in the dorsal raphe nucleus.

22 e and the alpha4 nAChR subunit in the dorsal raphe nucleus.

23 located in the ventral portion of the dorsal raphe nucleus.

24 omedial subregion of the intermediate dorsal raphe nucleus.

25 dinal fasciculi and extended into the median raphe nucleus.

26 eptors can induce 5-HT release in the dorsal raphe nucleus.

27 any serotonergic group other than the dorsal raphe nucleus.

28 tine binding was also observed in the median raphe nucleus.

29 ions, but was markedly reduced in the dorsal raphe nucleus.

30 assical 5-HT neurones recorded in the dorsal raphe nucleus.

31 of the serotonergic perikarya in the dorsal raphe nucleus.

32 als in the NAcSh originating from the dorsal raphe nucleus.

33 ng in amygdala, caudate, putamen, and median raphe nucleus.

34 R translocation were performed in the dorsal raphe nucleus.

35 l nucleus of the hypothalamus and the dorsal raphe nucleus.

36 gma) of the dorsal subdivision of the dorsal raphe nucleus 2 h after drug treatment.

37 after 0.3 mg/kg of citalopram in the dorsal raphe nucleus (5%), as well as after 0.3 mg/kg of vortio

38 Here we show that 5-HT from the dorsal raphe nucleus (5-HT(DRN)) enhances fear and anxiety and

39 droxytryptamine (5-HT) neurons in the dorsal Raphe nucleus (5-HT(DRN)) regulate different types of fe

40 nculopontine tegmental nucleus (86%); dorsal raphe nucleus (53%); dorsal medial periaqueductal gray (

41 ontine tegmental nucleus (55.7%), and dorsal raphe nucleus (54.0%) but not in the nucleus locus coeru

42 he firing rate of 5-HT neurons in the dorsal raphe nucleus, a major source of serotonergic input to t

43 identified synaptic contacts, and the dorsal raphe nucleus, a somatodendritic region with rare synapt

44 he stria terminalis, amygdala, habenula, and raphe nucleus), all of which express mu opioid receptors

45 uch as the ventral tegmental area and dorsal raphe nucleus among others, that are implicated in the r

46 essed downstream neurons in the serotonergic raphe nucleus and caused behavioral passivity, whereas i

47 uit from the lateral hypothalamus and dorsal raphe nucleus and defined a discrete subset of transcrip

48 les in the pons, but not in globus palludus, Raphe nucleus and hypothalamus.

49 Here, we show that the raphe nucleus and its serotonergic projections regulate

50 The dorsal raphe nucleus and its serotonin-releasing neurons are th

51 xytryptamine (5,7-DHT) lesions of the dorsal raphe nucleus and median raphe nucleus prevents LiCl-ind

52 e on the levels of 5-HT1B mRNA in the dorsal raphe nucleus and several postsynaptic brain areas using

53 sing the nucleus accumbens shell, the dorsal raphe nucleus and the medial prefrontal cortex.

54 ojecting to the amygdala, such as the dorsal raphe nucleus and ventral tegmental area, providing evid

55 ), separated for 5-HT autoinhibition (dorsal raphe nucleus) and local inhibition (heteroreceptors in

56 gic tuberomammillary nucleus, serotoninergic raphe nucleus, and dopaminergic ventral tegmental area.

57 the nucleus accumbens (NAC) shell and dorsal raphe nucleus, and found that disruption of NF-kappaB-ex

58 ng in the periaqueductal gray matter, dorsal raphe nucleus, and lateral parabrachial nucleus.

59 s, ventromedial hypothalamic nucleus, dorsal raphe nucleus, and locus coeruleus.

60 mentation in serotonin neurons of the dorsal raphe nucleus, and long-term Ovx monkeys had fewer serot

61 alamus, lateral parabrachial nucleus, dorsal raphe nucleus, and nucleus accumbens shell), all of whic

62 e amygdala, brainstem in the vicinity of the raphe nucleus, and reticular formation, hypothalamus, an

63 d much later in basolateral amygdala, dorsal raphe nucleus, and the substantia nigra pars compacta.

64 d afferents from the locus coeruleus, dorsal raphe, nucleus annularis, central superior nucleus, pont

65 tion of responsive neurons within the dorsal raphe nucleus are consistent with the hypothesis that en

66 unknown whether BDNF and TrkB in the dorsal raphe nucleus are involved in these processes.

67 ess, we show that 5-HT neurons in the dorsal raphe nucleus are less responsive to stimulation.

68 ased by electrical stimulation of the dorsal raphe nucleus attenuated odor-evoked responses without d

69 ulo-parieto-occipital regions and the dorsal raphe nucleus, but intensified Salience Network connecti

70 effect on c-Fos expression within the median raphe nucleus, consistent with the hypothesis that Ucn 2

71 atment enhances 5-HTP accumulation in dorsal raphe nucleus, cortex and caudate nucleus, but not in me

72 Here, we demonstrate that the dorsal raphe nucleus DA neurons are critical modulators of beha

73 tonergic (5-HT(+)) neuron-enriched embryonic raphe nucleus-derived neural stem cells/progenitors (RN-

74 Consequently, grafted raphe nucleus-derived neural stem cells/progenitors acte

75 anted serotonergic neuron enriched embryonic raphe nucleus-derived neural stem cells/progenitors into

76 nography, we observed time-delineated dorsal raphe nucleus dopaminergic (DRN(DA)) activity upon expos

77 feat on slc6a4 mRNA expression in the dorsal raphe nucleus (DR) and caudal linear nucleus.

78 DCN, spinal trigeminal nucleus (Sp5), dorsal raphe nucleus (DR) and locus coeruleus (LC).

79 The rat dorsal raphe nucleus (DR) and the locus coeruleus (LC) receive

80 HT) containing neurons located in the dorsal raphe nucleus (DR) comprise the main source of forebrain

81 The dorsal raphe nucleus (DR) contains serotonergic (5-HT) neurons

82 Among the brainstem raphe nuclei, the dorsal raphe nucleus (DR) contains the greatest number of Pet1-

83 The dorsal raphe nucleus (DR) controls forebrain serotonin neurotra

84 The dorsal raphe nucleus (DR) has a topographic neuroanatomy consis

85 Serotonin released within the dorsal raphe nucleus (DR) induces feedback inhibition of seroto

86 The dorsal raphe nucleus (DR) is innervated by fibers containing th

87 The dorsal raphe nucleus (DR) is the major source of serotonin (5-h

88 CN and that serotonergic cells in the dorsal raphe nucleus (DR) project to the IGL.

89 onal neuroanatomy of the serotonergic dorsal raphe nucleus (DR) to propose such a mechanistic account

90 rotonin transporters within the human dorsal raphe nucleus (DR) were determined by quantitative autor

91 tive disorders through effects on the dorsal raphe nucleus (DR), a source of forebrain-projecting ser

92 e level of three glutamate afferents: dorsal raphe nucleus (DR), pedunculopontine nucleus (PPN), and

93 in the ventral tegmental area (VTA), dorsal raphe nucleus (DR), periaqueductal grey area (PAG) and l

94 tingly, the RMTg also projects to the dorsal raphe nucleus (DR), which also receives direct LHb proje

95 serotonergic innervation is from the dorsal raphe nucleus (DR), which contains both serotonin and GA

96 quent responses of an anxiety-related dorsal raphe nucleus (DR)-basolateral amygdala system to pharma

97 The dorsal raphe nucleus (DR)-serotonin (5-HT) system has been impl

98 ceptor on serotonergic neurons in the dorsal raphe nucleus (DR).

99 odulating serotonergic systems in the dorsal raphe nucleus (DR).

100 including the median (MnR) and caudal dorsal raphe nucleus (DRC), may contribute to the behavioral ef

101 ; 1 microgram) microinjected into the dorsal raphe nucleus (DRN) 15 min before IS.

102 proach to isolate the contribution of dorsal raphe nucleus (DRN) 5-HT neurons and 5-HT innervation of

103 We found that activating dorsal raphe nucleus (DRN) 5-HT neurons induced a strong suppre

104 that stimulation of the serotonergic dorsal raphe nucleus (DRN) afferents to the nucleus accumbens (

105 Stimulation of the dorsal raphe nucleus (DRN) alters arterial pressure, heart rate

106 eptor 1 (AdipoR1) is expressed in the dorsal raphe nucleus (DRN) and colocalized with tryptophan hydr

107 Injections of rhodamine-B into the dorsal raphe nucleus (DRN) and Fluoro-Gold into the lateral gen

108 The dorsal raphe nucleus (DRN) and its serotonergic terminal region

109 uring 5-HT neurons that will form the dorsal raphe nucleus (DRN) and part of the median raphe nucleus

110 f distribution (V(T)) for presynaptic dorsal raphe nucleus (DRN) and postsynaptic cortical regions.

111 ses through axonal collaterals to the dorsal raphe nucleus (DRN) and SC.

112 The dorsal raphe nucleus (DRN) and the median raphe nucleus (MRN) a

113 also examined two control areas, the dorsal raphe nucleus (DRN) and the periaqueductal gray (PAG), i

114 serotonin (5-HT) in 5-HT cells of the dorsal raphe nucleus (DRN) and to determine which 5-HT receptor

115 lopontine tegmentum, up to 4 h in the dorsal raphe nucleus (DRN) and up to 6 h in the locus coeruleus

116 Serotonin (5-HT) neurons in the dorsal raphe nucleus (DRN) are implicated in mediating learned

117 the periaqueductal gray (PAG) and the dorsal raphe nucleus (DRN) are involved in morphine-induced c-F

118 nd serotonergic (5-HT) neurons of the dorsal raphe nucleus (DRN) are mostly active during waking and

119 edial prefrontal cortex (mPFC) in the dorsal raphe nucleus (DRN) are of particular interest, in part,

120 (5-HT) from neurons within the caudal dorsal raphe nucleus (DRN) both at the time of IS and later beh

121 Serotonergic neurons of the dorsal raphe nucleus (DRN) cease firing during active sleep (AS

122 ased discharge of 5-HT neurons in the dorsal raphe nucleus (DRN) compared with control rats.

123 The brainstem dorsal raphe nucleus (DRN) contains an abundant distribution of

124 ow doses of CRF administered into the dorsal raphe nucleus (DRN) decrease DRN unit activity and serot

125 one (CRH) receptors within the caudal dorsal raphe nucleus (DRN) during inescapable tailshock (IS) ha

126 B), but not GABA(A), receptors in the dorsal raphe nucleus (DRN) escalated aggressive behaviors.

127 direct pathway from the retina to the dorsal raphe nucleus (DRN) has been demonstrated in both albino

128 ial projection from the retina to the dorsal raphe nucleus (DRN) has been demonstrated in the Chilean

129 y, local injection of morphine in the dorsal raphe nucleus (DRN) has been shown to increase serotonin

130 The serotonergic dorsal raphe nucleus (DRN) has previously been found to be an i

131 Retinal afferents to the dorsal raphe nucleus (DRN) have been described in a number of s

132 ion in 5-HT1A receptor domains in the dorsal raphe nucleus (DRN) in brain slices and in vivo, which i

133 IOD) measures obtained throughout the dorsal raphe nucleus (DRN) in Mongolian gerbils at selected tim

134 The dorsal raphe nucleus (DRN) in the midbrain is a key center for

135 or (CRF) inhibits 5-HT neurons in the dorsal raphe nucleus (DRN) in vivo.

136 edial prefrontal cortex (mPFC) to the dorsal raphe nucleus (DRN) induced fast anxiolytic effects.

137 5-HT(7) receptors in the dorsal raphe nucleus (DRN) influence circadian rhythms, sleep,

138 The dorsal raphe nucleus (DRN) is an important brain area for body-

139 The dorsal raphe nucleus (DRN) is an important source of neuromodul

140 The dorsal raphe nucleus (DRN) is implicated in mood regulation, co

141 The serotonergic dorsal raphe nucleus (DRN) is innervated by corticotropin-relea

142 The brainstem dorsal raphe nucleus (DRN) maintains a rough topographic cell o

143 edial prefrontal cortex (PFC) and the dorsal raphe nucleus (DRN) may be dysfunctional in major depres

144 hesized that GABAergic neurons in the dorsal raphe nucleus (DRN) may participate in socioaffective re

145 , we discovered that the serotonergic dorsal raphe nucleus (DRN) mediates short-term locomotor learni

146 lysis was used to analyze the role of dorsal raphe nucleus (DRN) neurons in regulating the sleep-waki

147 on activation of serotonergic (5-HT) dorsal raphe nucleus (DRN) neurons that project to the basolate

148 r (CRF) receptors in the serotonergic dorsal raphe nucleus (dRN) of adult rats.

149 Thus, we used microdialysis in the dorsal raphe nucleus (DRN) of freely behaving rats to study the

150 Recent studies suggest that the dorsal raphe nucleus (DRN) of the brainstem contains several su

151 Recent evidence suggests that the dorsal raphe nucleus (DRN) of the brainstem is a collection of

152 5-HT neurons in the dorsal raphe nucleus (DRN) often fire locked to sensory stimuli

153 ed that electrical stimulation of the dorsal raphe nucleus (DRN) or median raphe nucleus (MRN) in ham

154 ptors regulate serotonin release from dorsal raphe nucleus (DRN) projections throughout rat forebrain

155 e serotonin release from terminals of dorsal raphe nucleus (DRN) projections.

156 ) in the locus coeruleus (LC) and the dorsal raphe nucleus (DRN) regions of postmortem human brains.

157 ow short- and long-term activation of dorsal raphe nucleus (DRN) serotonergic neurons induces robust

158 -command Mauthner cells also activate dorsal raphe nucleus (DRN) serotonergic neurons, which project

159 s that median raphe nucleus (MRN) and dorsal raphe nucleus (DRN) serotonergic projections differentia

160 (alpha1-ARs) control the activity of dorsal raphe nucleus (DRn) serotonin (5-HT) neurons and play cr

161 The dorsal raphe nucleus (DRN) serotonin (5-HT) system has been imp

162 ions and is extensively innervated by dorsal raphe nucleus (DRN) serotonin (5-hydroxytryptamine [5-HT

163 ll patch-clamp recordings in an acute dorsal raphe nucleus (DRN) slice preparation, we report that or

164 The serotonin (5-HT) pathway from the dorsal raphe nucleus (DRN) to the medial prefrontal cortex (mPF

165 yric acid (GABA) projections from the dorsal raphe nucleus (DRN) to the NAcSh (DRN -> NAcSh) is the n

166 yric acid (GABA) projections from the dorsal raphe nucleus (DRN) to the NAcSh (DRN NAcSh) is the neur

167 ically identified 5-HT cells from the dorsal raphe nucleus (DRN) were examined with whole-cell record

168 also assayed these gene levels in the dorsal raphe nucleus (DRN) with RNAScope.

169 mbined optogenetic stimulation of the dorsal raphe nucleus (DRN) with wide-field calcium imaging, ext

170 TrkB are both highly expressed in the dorsal raphe nucleus (DRN), a brain region that has been sugges

171 erformed single-unit recording in the dorsal raphe nucleus (DRN), a major source of serotonin, and th

172 PFC cells projecting to the brainstem dorsal raphe nucleus (DRN), a serotonergic nucleus implicated i

173 the periaqueductal gray (PAG) and the dorsal raphe nucleus (DRN), adjoining mesencephalic cell groups

174 laterodorsal tegmental nucleus (LDT), dorsal raphe nucleus (DRN), and locus ceruleus (LC).

175 7, t = 2.57, df = 7, P = 0.04) in the dorsal raphe nucleus (DRN), and not different between suicides

176 of the KOR antagonist norBNI into the dorsal raphe nucleus (DRN), blocked aversive responses to the K

177 tivity of serotonergic neurons in the dorsal raphe nucleus (DRN), but the mechanisms involved have no

178 In the dorsal raphe nucleus (DRN), feedback activation by Galphai/o -c

179 ns in the dorsolateral portion of the dorsal raphe nucleus (DRN), hereafter DRN(Vgat) neurons, are ac

180 functional role for DA neurons in the dorsal raphe nucleus (DRN), in which we observe synaptic change

181 nfralimbic prefrontal cortex (PFC) or dorsal raphe nucleus (DRN), prevented disruption of DRL perform

182 locus of serotonergic neurons is the dorsal raphe nucleus (DRN), providing brain-wide serotonergic i

183 IS activates serotonin neurons in the dorsal raphe nucleus (DRN), rendering them hyperexcitable.

184 eable binding potential (BPND) in the dorsal raphe nucleus (DRN), the core area of 5-HT synthesis, an

185 The dorsal raphe nucleus (DRN), the major source of serotonergic in

186 of the three target areas as follows: dorsal raphe nucleus (DRN), ventral tegmental area (VTA), or ro

187 la receive 5-HT innervations from the dorsal raphe nucleus (DRN), we determined if PDA lesions might

188 any regions of the CNS, including the dorsal raphe nucleus (DRN), where serotonin (5-HT) neurons are

189 e ventral tegmental area (VTA) to the dorsal raphe nucleus (DRN), with differential mu-opioid recepto

190 or brain serotonin (5-HT) system, the dorsal raphe nucleus (DRN)-5-HT system as a point of convergenc

191 easing factor (CRF) in regulating the dorsal raphe nucleus (DRN)-serotonin (5-HT) system.

192 esumed serotonergic neuron of the rat dorsal raphe nucleus (DRN).

193 ceive serotonergic afferents from the dorsal raphe nucleus (DRN).

194 om the median raphe nucleus (MRN) and dorsal raphe nucleus (DRN).

195 of serotonergic (5-HT) neurons in the dorsal raphe nucleus (DRN).

196 cused on brainstem nuclei such as the dorsal raphe nucleus (DRN).

197 eral ventral tegmental area (VTA) and dorsal raphe nucleus (DRN).

198 otonin (5-HT) and GABA neurons of the dorsal raphe nucleus (DRN).

199 (5-HT) neurons in the female macaque dorsal raphe nucleus (DRN).

200 al amygdala (BA) 5-HT inputs from the dorsal raphe nucleus (DRN).

201 omedial prefrontal cortex (vmPFC) and dorsal raphe nucleus (DRN).

202 neurons send dense projections to the dorsal raphe nucleus (DRN).

203 including 5-HT2c-Rs, are found in the dorsal raphe nucleus (DRN); however, the function of 5-HT2c-Rs

204 nd the median raphe nucleus [MRN] and dorsal raphe nucleus [DRN]).

205 H2), in the ventral subnucleus of the dorsal raphe nucleus (DRv).

206 Finally, blocking OT receptors in the dorsal raphe nucleus during estrogen withdrawal prevented the h

207 hat serotonergic changes occur in the dorsal raphe nucleus during inescapable shock and that such cha

208 al tuberal nucleus, substantia nigra, dorsal raphe nucleus, Edinger-Westphal nucleus, and the locus c

209 Our data suggest that the dorsal raphe nucleus encodes participation in a behavioral task

210 (SVc) and interpolaris (SVi), and the dorsal raphe nucleus exhibited a greater number of c-Fos labele

211 Here, we show that neurons in the dorsal raphe nucleus, expressing vesicular transporters for GAB

212 lls or selectively in the area of the dorsal raphe nucleus failed to form an aversion to formalin-ind

213 periaqueductal gray, area postrema, pontine raphe nucleus, gracile nucleus, spinal trigeminal nucleu

214 ortex and caudate nucleus, but not in median raphe nucleus, hippocampus or nucleus accumbens.

215 tress increases 5-HTP accumulation in median raphe nucleus, hippocampus, cortex, and nucleus accumben

216 f previous studies of the role of the dorsal raphe nucleus in sleep, because many of those experiment

217 al gray substance of the midbrain and dorsal raphe nucleus in the midbrain; and parabrachial nucleus

218 containing neurones of the guinea pig dorsal raphe nucleus in vitro.

219 noradrenergic locus coeruleus and the dorsal raphe nucleus, in parallel with decreased DNA methylatio

220 balance of responses within the serotonergic raphe nucleus, including a coordination of corticotropin

221 vation of serotonergic neurons in the dorsal raphe nucleus increases active coping with inescapable s

222 The serotonergic cells of the dorsal raphe nucleus innervate much of the forebrain and are th

223 clei, laterodorsal tegmental nucleus, dorsal raphe nucleus, interpeduncular nucleus, medial mammillar

224 d reduction in 5-HT7 receptors in the dorsal raphe nucleus is an important neurochemical mechanism le

225 The serotonergic dorsal raphe nucleus is considered an important modulator of st

226 raffic in pathways emanating from the dorsal raphe nucleus is controlled by 5-HT(1) autoreceptors.

227 The dorsal raphe nucleus is the predominant source of central serot

228 In the dorsal raphe nucleus, it is known that serotonin release activa

229 inent ipsilateral labeling within the dorsal raphe nucleus, just ventral to the cerebral aqueduct.

230 i of pontomesencephalic central gray (dorsal raphe nucleus, laterodorsal tegmental nucleus, and Barri

231 s in the following brain-stem nuclei: dorsal raphe nucleus, locus coeruleus, lateral and medial parab

232 al nucleus, Edinger-Westphal nucleus, dorsal raphe nucleus, locus coeruleus, or hypoglossal nucleus.

233 hypothalamic area, trochlear nucleus, dorsal raphe nucleus, medial lemniscus, pontine nuclei, vagus n

234 evoked serotonin transmission in the dorsal raphe nucleus mediated by metabotropic 5-HT1A autorecept

235 tonergic neurons in the mesencephalic median raphe nucleus (MnR) also give rise to a major SCN affere

236 b), interpeduncular nucleus (IP), and median raphe nucleus (MnR).

237 Injections of muscimol into the median raphe nucleus (MR) elicit intense drinking in normally h

238 strate that serotonergic cells in the median raphe nucleus (MR) project to the SCN and that serotoner

239 the GABA-A agonist muscimol into the median raphe nucleus (MR) result in large increases in the inta

240 erotonergic fibers originating in the median raphe nucleus (MR).

241 We tested the hypothesis that median raphe nucleus (MRN) and dorsal raphe nucleus (DRN) serot

242 tion of the forebrain arises from the median raphe nucleus (MRN) and dorsal raphe nucleus (DRN).

243 he dorsal raphe nucleus (DRN) and the median raphe nucleus (MRN) are known to densely innervate the O

244 of the dorsal raphe nucleus (DRN) or median raphe nucleus (MRN) in hamsters evoked 5-HT release in t

245 llowing electrical stimulation of the median raphe nucleus (MRN) in unanesthetized prenatally malnour

246 e 5-HT1A agonist, 8-OH-DPAT, into the median raphe nucleus (MRN) of urethane-anesthetized rats.

247 The median raphe nucleus (MRN), which contains a major population o

248 eral geniculate nuclei [LGN], and the median raphe nucleus [MRN] and dorsal raphe nucleus [DRN]).

249 lamus (VMH) (bilaterally, n = 6), the dorsal raphe nucleus (n = 3), and the lateral ventricle (n = 3)

250 Deakin and Graeff argued that the median raphe nucleus normally acts to inhibit consolidation of

251 roject to the ventral tegmental area, dorsal raphe nucleus, nucleus accumbens, and spinal cord, and o

252 ion of extracellular serotonin in the dorsal raphe nucleus of freely behaving rats.

253 -B, and tryptophan hydroxylase in the dorsal raphe nucleus of highly perseverative rats.

254 Serotonin neurons located in the raphe nucleus of the hindbrain have crucial roles in reg

255 tral and dorsal tegmental nuclei, the median raphe nucleus of the pons, the ventral part of the medul

256 ced GR translocation were observed in dorsal raphe nucleus of vulnerable mice after chronic social de

257 ortex, and nucleus accumbens, but not dorsal raphe nucleus or caudate nucleus.

258 on) failed to inhibit activity in the dorsal raphe nucleus or use the ventromedial prefrontal cortex,

259 , but not in the nucleus basalis of Meynert, raphe nucleus, or other brain regions.

260 The dorsal raphe nucleus/ periaqueductal grey region of the midbrai

261 erent aspects of 5-HT function in the dorsal raphe nucleus presenting new therapeutic opportunities.

262 sions of the dorsal raphe nucleus and median raphe nucleus prevents LiCl-induced conditioned disgust

263 ude that burst-firing neurones in the dorsal raphe nucleus project to the forebrain, and each spike g

264 ct to all four PAG columns, while the dorsal raphe nucleus projects only to the ventrolateral and lat

265 ptic somatodendritic autoreceptors on dorsal raphe nucleus relative to each of the other three groups

266 in the ventral tegmental area and the dorsal raphe nucleus, respectively.

267 whether functional connectivity (FC) of the raphe nucleus (RN), the major source of most serotonergi

268 mrEn1-Pet1(7) in the mouse brainstem median raphe nucleus segregates serotonin from VGLUT3 (also kno

269 A subgroup of approximately 25% of dorsal raphe nucleus serotonergic neurons in cat was strongly a

270 Here, we show in the mouse that raphe nucleus serotonin neurons activate ventral tegment

271 -releasing factor (CRF) regulates the dorsal raphe nucleus-serotonin (DRN-5-HT) system during stress

272 nergic neurons in the locus ceruleus, dorsal raphe nucleus, substantia nigra, and ventral tegmental a

273 development of ruminations, while the dorsal raphe nucleus system is engaged by distal cues predictiv

274 ce of serotonergic neurons within the median raphe nucleus that have a unique response profile.

275 de within serotonergic neurons of the dorsal raphe nucleus that mediates depressive and drug-seeking

276 tivation of serotonergic cells in the dorsal raphe nucleus that would normally be produced by uncontr

277 one in anterior insula and one in the dorsal raphe nucleus, that track global reward state as well as

278 orks for the medial reticular formation, the raphe nucleus, the glossopharyngeal nuclei, and the Purk

279 eA is reciprocally connected with the dorsal raphe nucleus, the main source of serotonin (5-HT) in th

280 A receives dense innervation from the dorsal raphe nucleus, the major source of 5-HT, and expresses 5

281 cular nucleus of the hypothalamus and dorsal raphe nucleus to increase anxiety-like behavior during t

282 otonergic neurons projecting from the dorsal raphe nucleus to pontine cholinergic/cholinoceptive cell

283 inobutyric acidergic pathway from the dorsal raphe nucleus to the NAcSh to influence behavioral respo

284 urons to serotonergic neurons in the ventral raphe nucleus (vRN).

285 uccessful loss-avoidance although the median raphe nucleus was not found to be underactive.

286 rter mRNA hybridization signal in the dorsal raphe nucleus was only slightly reduced after 5,7-dihydr

287 rter by 62-96% whereas binding in the dorsal raphe nucleus was preserved.

288 Levels of mRNA for the SERT in the raphe nucleus were also unaltered by chronic paroxetine

289 gantocellularis, pars alpha, and the pontine raphe nucleus were labeled.

290 in the ventral portion of the caudal dorsal raphe nucleus were markedly potentiated in slices prepar

291 lar levels of serotonin (5-HT) in the dorsal raphe nucleus were measured by in vivo microdialysis.

292 oxlyase-immunoreactive neurons in the dorsal raphe nucleus were related to depressive symptoms.

293 thought that the autoreceptors in the dorsal raphe nucleus were solely of the 5-HT(1A) subtype.

294 alR2-binding sites by 50%, in the rat dorsal raphe nucleus, where galanin coexists with serotonin.

295 shock elevated galanin mRNA levels in dorsal raphe nucleus, whereas sleep deprivation increased galan

296 of these receptors specifically from dorsal raphe nucleus, which provides serotonergic (5-hydroxytry

297 on, their close relationship with the dorsal raphe nucleus will require reassessment of previous stud

298 ty of serotonergic neurons in the rat dorsal raphe nucleus with extracellular single unit recording i

299 rder is associated with an overactive dorsal raphe nucleus with overactive projections to the amygdal

300 grey and striatum, and an underactive median raphe nucleus with underactive projections to the hippoc