ライフサイエンスコーパス: raphe nucleus

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

2 dunculopontine tegmental nucleus, and dorsal raphe nucleus.

3 haviors after microinjection into the median raphe nucleus.

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

5 l reticular nucleus, hypoglossal nucleus and raphe nucleus.

6 et of serotonergic neurons within the dorsal raphe nucleus.

7 5-HT transmission at the level of the dorsal raphe nucleus.

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

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

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

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

12 activity of serotonergic cells of the dorsal raphe nucleus.

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

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

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

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

17 omedial subregion of the intermediate dorsal raphe nucleus.

18 dinal fasciculi and extended into the median raphe nucleus.

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

20 any serotonergic group other than the dorsal raphe nucleus.

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

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

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

24 of the serotonergic perikarya in the dorsal raphe nucleus.

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

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

27 R translocation were performed in the dorsal raphe nucleus.

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

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

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

31 reticular formation, including the inferior raphe nucleus.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

90 ; 1 microgram) microinjected into the dorsal raphe nucleus (DRN) 15 min before IS.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

107 (5-HT) from neurons within the caudal dorsal raphe nucleus (DRN) both at the time of IS and later beh

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

123 5-HT(7) receptors in the dorsal raphe nucleus (DRN) influence circadian rhythms, sleep,

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

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

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

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

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

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

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

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

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

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

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

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

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

137 5-HT neurons in the dorsal raphe nucleus (DRN) often fire locked to sensory stimuli

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

156 7, t = 2.57, df = 7, P = 0.04) in the dorsal raphe nucleus (DRN), and not different between suicides

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

173 (5-HT) neurons in the female macaque dorsal raphe nucleus (DRN).

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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