ライフサイエンスコーパス: lateral hypothalamus

1 straddling its border and extending into the lateral hypothalamus.

2 hypocretin (orexin)-producing neurons in the lateral hypothalamus.

3 c-Fos in the perifornical, dorsomedial, and lateral hypothalamus.

4 onal subcortical target regions, such as the lateral hypothalamus.

5 t from the cortex or the orexin group of the lateral hypothalamus.

6 in-concentrating hormone in the perifornical lateral hypothalamus.

7 icular focus on accumbens projections to the lateral hypothalamus.

8 decreasing GABAergic tone within the rostral lateral hypothalamus.

9 he orexin-2-saporin conjugate (OXSAP) in the lateral hypothalamus.

10 in the cat to electrical stimulation of the lateral hypothalamus.

11 centrating hormone and orexin neurons in the lateral hypothalamus.

12 reactive astrocytes and microglia within the lateral hypothalamus.

13 slices or minislices consisting only of the lateral hypothalamus.

14 datory attack elicited by stimulation of the lateral hypothalamus.

15 c-Fos immunoreactivity in the medial but not lateral hypothalamus.

16 the arcuate nucleus, and occasionally in the lateral hypothalamus.

17 cular (PVN), supraoptic, arcuate nuclei, and lateral hypothalamus.

18 ergic neurons and through projections to the lateral hypothalamus.

19 ere seen in the ventromedial nucleus and the lateral hypothalamus.

20 in (also known as hypocretin) neurons of the lateral hypothalamus.

21 nervous system exclusively by neurons of the lateral hypothalamus.

22 and lateral septum) and both the medial and lateral hypothalamus.

23 l region) and electrodes in the perifornical lateral hypothalamus.

24 ry amino acid agonists administered into the lateral hypothalamus.

25 neurons whose cell bodies are located in the lateral hypothalamus.

26 n the cord originate from the neurons in the lateral hypothalamus.

27 rect GABAergic projection from the medial to lateral hypothalamus.

28 hypothalamus, ventromedial hypothalamus, and lateral hypothalamus.

29 atory and wake-promoting neuropeptide-in the lateral hypothalamus.

30 projections to the nucleus accumbens and the lateral hypothalamus.

31 n MgRA-driven optogenetic stimulation in the lateral hypothalamus.

32 of the stria terminalis, and densely to the lateral hypothalamus.

33 ss by blunting serotonergic signaling in the lateral hypothalamus.

34 part of the axons known to emanate from the lateral hypothalamus.

35 ST outputs to the ventral tegmental area and lateral hypothalamus.

36 he destruction of orexinergic neurons in the lateral hypothalamus.

37 he disconnection of amygdala pathways to the lateral hypothalamus.

38 retin cells expressing FosB/DeltaFosB in the lateral hypothalamus.

39 rded, and neurobiotin-labeled neurons in the lateral hypothalamus, 11 were immunohistochemically iden

40 ral preoptic area (VLPO) [1] arises from the lateral hypothalamus [2], a brain area associated with a

41 synapses on hypocretin/orexin neurons in the lateral hypothalamus, a well-established arousal/wake-pr

42 areas, and infected neurons also appeared in lateral hypothalamus, A7 region, locus coeruleus, subcoe

43 ed that, in male mice, orexin neurons in the lateral hypothalamus activated a small population of glu

44 hypothalamus, specifically the magnocellular lateral hypothalamus adjacent to the subthalamus.

45 As gamma-aminobutyric-acid (GABA) within the lateral hypothalamus also mediates feeding, we sought to

46 d viral vector delivery of syndecan-3 to the lateral hypothalamus also reduces motivation for cocaine

47 ental area (VTA), subthalamic nucleus (STN), lateral hypothalamus, among others, and the roles of the

48 cue-induced overeating in sated rats include lateral hypothalamus, amygdala, and medial prefrontal co

49 rats and included neurons in the medial and lateral hypothalamus, amygdala, bed nucleus of the stria

50 n had greater connectivity between the right lateral hypothalamus and a reward-related brain region a

51 The lateral hypothalamus and arcuate nucleus of the hypothal

52 pocretin neuropeptides are restricted to the lateral hypothalamus and contiguous perifornical area bu

53 to the mesolimbic dopamine circuit from the lateral hypothalamus and dorsal raphe nucleus and define

54 in (orexin) is synthesized by neurons in the lateral hypothalamus and has been reported to increase f

55 located only in the perifornical area of the lateral hypothalamus and heavily innervate the cholinerg

56 nin-concentrating hormone, and orexin in the lateral hypothalamus and in the corticotrophin-releasing

57 neuromodulator are localized in the postero-lateral hypothalamus and incerto-hypothalamic area.

58 identify some specific projections from the lateral hypothalamus and midbrain, we analyzed the distr

59 in the control of food intake, including the lateral hypothalamus and nucleus accumbens shell, sugges

60 a and dorsal hypothalamus (VLG and IGL); the lateral hypothalamus and perifornical area (VLG); and th

61 europeptides are exclusively produced by the lateral hypothalamus and play important roles in sleep,

62 active hypocretin and GABAergic cells in the lateral hypothalamus and receive inputs from multiple sl

63 lanted with cannulae directed to the rostral lateral hypothalamus and saclofen (GABA-B receptor antag

64 (hypocretin) are located exclusively in the lateral hypothalamus and send axons to numerous regions

65 motivation requires mPFC communications with lateral hypothalamus and showed that disconnection of th

66 rease HS content and sulfation levels in the lateral hypothalamus and that HS contributes to the regu

67 ct with hypocretin-expressing neurons in the lateral hypothalamus and that numerous hypocretinergic n

68 The lateral hypothalamus and the nucleus accumbens shell (Ac

69 implanted with stimulating electrodes to the lateral hypothalamus and trained to perform intracranial

70 dinated gamma (30-90 Hz) oscillations in the lateral hypothalamus and upstream brain regions organize

71 of subcortical limbic areas (e.g., amygdala, lateral hypothalamus), and influenced functional connect

72 Bipolar electrodes were implanted in the lateral hypothalamus, and cannula guides were implanted

73 , lateral and magnocellular preoptic nuclei, lateral hypothalamus, and lateral habenula.

74 lso the hippocampus, anteroventral thalamus, lateral hypothalamus, and nucleus accumbens.

75 natal loss of orexin-positive neurons in the lateral hypothalamus, and orexin-containing projections

76 was increased in ventromedial hypothalamus, lateral hypothalamus, and parabrachial nucleus, identify

77 ding the preoptic area, dorsomedial nucleus, lateral hypothalamus, and posterior hypothalamus.

78 The prefrontal cortex, the lateral hypothalamus, and the periaqueductal gray matter

79 a terminalis, the anterior hypothalamus, the lateral hypothalamus, and the ventral premamillary nucle

80 gray, dorsomedial hypothalamus, dorsolateral lateral hypothalamus, and ventral portion of the medial

81 the hippocampus, amygdala, ventral pallidum, lateral hypothalamus, and ventral tegmental area.

82 ial nuclei to the central extended amygdala, lateral hypothalamus, and ventromedial thalamus.

83 s controlling defensive behaviors, including lateral hypothalamus, anterior hypothalamus, and anterom

84 inputs to orexin-A-containing neurons in the lateral hypothalamus are altered in obesity and how this

85 so known as orexin)-producing neurons in the lateral hypothalamus are important for arousal stability

86 ventromedial hypothalamic nuclei(VMH)and the lateral hypothalamus are sensitive to a number of circul

87 in levels and orexin-positive neurons in the lateral hypothalamus are substantially reduced, suggesti

88 Orexin/hypocretin neurons of the lateral hypothalamus are widely projecting glucose-inhib

89 tor 1-expressing neurons that project to the lateral hypothalamus as mediating rapid control over fee

90 rtle Fos-IR increased in the dorsomedial and lateral hypothalamus as well as in the lateral septum.

91 ic mice that overexpress MCH (MCH-OE) in the lateral hypothalamus at approximately twofold higher lev

92 paracentral nucleus, central medial nucleus, lateral hypothalamus, basal nucleus of the amygdala, and

93 ar nucleus of the hypothalamus; anterior and lateral hypothalamus (both posterior portion); ventromed

94 jections to the preoptic-basal forebrain and lateral hypothalamus, but not to the thalamus, mediate P

95 In addition, there were differences in the lateral hypothalamus, but the PE group had higher recept

96 trema, VRC, dorsolateral pons, raphe nuclei, lateral hypothalamus, central amygdala, and insular cort

97 t behaviorally critical neurocircuits of the lateral hypothalamus contain glucose detectors that exhi

98 he anterior hypothalamus and fornical in the lateral hypothalamus contain large neurons that synthesi

99 The posterior lateral hypothalamus contains orexin/hypocretin neurons

100 t from the ventral pallidal-lateral preoptic-lateral hypothalamus continuum is strong in the RMTg and

101 rious species have indeed confirmed that the lateral hypothalamus contributes to reward mechanisms.

102 Other connections include projections to lateral hypothalamus, dorsal raphe, periaqueductal gray

103 Gamma-rhythmic input to the lateral hypothalamus from somatostatin-positive lateral

104 Hypocretin neurons are located only in the lateral hypothalamus from where they innervate virtually

105 ceptor subunit alpha2 (GABRA2) expression in lateral hypothalamus GABAergic (LH(GABA)) neurons.

106 on of SCH23390 (100 nM in 200 nL) into rats' lateral hypothalamus greatly reduced sodium appetite.

107 In the lateral hypothalamus, groups of functionally related cel

108 ventral tegmental area > putamen > caudate > lateral hypothalamus > accumbens > linear/interfascicula

109 on of muscimol into adjoining regions of the lateral hypothalamus had no effect upon defensive rage,

110 Here, we show that syndecan-3 in the lateral hypothalamus has an unexpected new role in limit

111 The lateral hypothalamus has been long suspected of triggeri

112 hormone (MCH) and orexins/hypocretins in the lateral hypothalamus have received attention because the

113 arkers for wake-promoting cell groups in the lateral hypothalamus (Hcrt), tuberomammillary nuclei (hi

114 Like neurons in the amygdala and lateral hypothalamus, hippocampal neurons discriminated

115 PPn may originate from SPl-ir neurons in the lateral hypothalamus (Hl).

116 normalized perfusion in the amygdala and the lateral hypothalamus in Fmr1 KO mice and furthermore dec

117 n-concentrating hormone, in the perifornical lateral hypothalamus in preweanling offspring.

118 r 30 days (flow rate=0.22 microg/h) into the lateral hypothalamus in rats.

119 The importance of the lateral hypothalamus in the regulation of reward and mot

120 tricular nucleus of the hypothalamus and the lateral hypothalamus in the social isolates than in the

121 rom both embryonic chick and postnatal mouse lateral hypothalamus in vitro reveal robust stimulus-evo

122 al imaging of GABAergic neurons in the mouse lateral hypothalamus in vivo.

123 Although lesions of the lateral hypothalamus induced severe hypodipsia in Experi

124 orexin (Hcrt)-containing neurones within the lateral hypothalamus integrate nutritional, energetic an

125 tioned stimulus (CS), the model amygdala and lateral hypothalamus interact to calculate the expected

126 The lateral hypothalamus is a brain region historically impl

127 The lateral hypothalamus is known to drive food consumption

128 synthesized exclusively in the perifornical/lateral hypothalamus, is critical for drug seeking and r

129 ections between basolateral amygdala and the lateral hypothalamus, is crucial for allowing learned cu

130 downstream from the stimulated fibers of the lateral hypothalamus--is more critically involved in wan

131 e is little leptin receptor expressed in the lateral hypothalamus, it is likely that any observed lep

132 ed to the posterior thalamic nucleus and the lateral hypothalamus (lateral torus, lateral recess nucl

133 cleus, paraventricular hypothalamic nucleus, lateral hypothalamus, lateral parabrachial nucleus, dors

134 ice, we found that inhibitory neurons in the lateral hypothalamus (LH(vgat)) show unique activity pat

135 Activation of LS(Nts) terminals in the lateral hypothalamus (LH) also decreases food intake.

136 er injections of the DLAA threonine into the lateral hypothalamus (LH) alter intake of a threonine-de

137 Here, we studied the role of the lateral hypothalamus (LH) and its forebrain projections

138 ess-responsive orexin gene expression in the lateral hypothalamus (LH) and medial hypothalamus (MH, i

139 , which sends GABAergic projections into the lateral hypothalamus (LH) and receives extensive glutama

140 icted rats with ibotenic acid lesions of the lateral hypothalamus (LH) and sham controls were trained

141 from VP cell types and their projections to lateral hypothalamus (LH) and ventral tegmental area (VT

142 istinct population of neurons located in the lateral hypothalamus (LH) and zona incerta (ZI), but MCH

143 Here, we show that CeA projections to the lateral hypothalamus (LH) are preferentially activated i

144 xin (hypocretin)-containing projections from lateral hypothalamus (LH) are thought to play an importa

145 nto neurons of the zona incerta (ZI), or the lateral hypothalamus (LH) blocked cataplexy.

146 Hcrt neurons are located only in the lateral hypothalamus (LH) but neither electrolytic nor p

147 Lesions of the lateral hypothalamus (LH) cause hypophagia.

148 Damage to the lateral hypothalamus (LH) causes profound physical inact

149 This study investigated whether the lateral hypothalamus (LH) contributes to the depressor r

150 The lateral hypothalamus (LH) controls energy balance.

151 nd orexin/hypocretin types of neurons of the lateral hypothalamus (LH) exert opposing effects on arou

152 ntly reported that activation of a subset of lateral hypothalamus (LH) GABAergic neurons induced both

153 Although the lateral hypothalamus (LH) has long been known to regulat

154 Electrical stimulation of the lateral hypothalamus (LH) has two motivational effects:

155 A pivotal role of the lateral hypothalamus (LH) in regulating appetitive and r

156 The lateral hypothalamus (LH) is a central hub that integrat

157 The lateral hypothalamus (LH) is a crucial neural substrate

158 The lateral hypothalamus (LH) is a key regulator of multiple

159 The lateral hypothalamus (LH) is a neuroanatomical region es

160 The lateral hypothalamus (LH) is a site of integration for c

161 However, the lateral hypothalamus (LH) is also a key reward-control l

162 The lateral hypothalamus (LH) is implicated in the behaviora

163 we show that depolarization of perifornical lateral hypothalamus (LH) neurons elicits a CB1R-mediate

164 sculosum of the lamina terminalis (OVLT) and lateral hypothalamus (LH) of rats with coronary artery l

165 into the perifornical hypothalamus (PFH) or lateral hypothalamus (LH) of satiated rats, suggesting t

166 ) elicit feeding when microinjected into the lateral hypothalamus (LH) of satiated rats.

167 , elicit feeding when microinjected into the lateral hypothalamus (LH) of satiated rats.

168 of N-methyl-D-aspartic acid (NMDA) into the lateral hypothalamus (LH) on feeding and other behaviors

169 leus (MnPO), lateral preoptic area (LPO), or lateral hypothalamus (LH) on the drinking.

170 ysis probes in the NAc and electrodes in the lateral hypothalamus (LH) or medial hypothalamus (MH).

171 Here, we examined inputs to the lateral hypothalamus (LH) orexin cell field from the lat

172 to find that activating the downstream NAc->lateral hypothalamus (LH) pathway also prevents relapse.

173 Stimulation of the lateral hypothalamus (LH) produces antinociception modif

174 Electrical stimulation of the lateral hypothalamus (LH) produces antinociception parti

175 es have shown that increased activity in the lateral hypothalamus (LH) promotes feeding.

176 The lateral hypothalamus (LH) regulates metabolic, behaviora

177 , central nucleus of the amygdala (CeA), and lateral hypothalamus (LH) send projections to the nucleu

178 The lateral hypothalamus (LH) sends a dense glutamatergic an

179 its emanating from the septal nucleus to the lateral hypothalamus (LH) that contribute to neural regu

180 Projections from the lateral hypothalamus (LH) to the ventral tegmental area

181 e (MCH) and hypocretin/orexin neurons in the lateral hypothalamus (LH) together with neuropeptide Y (

182 l cortex (PFC), nucleus accumbens (NAC), and lateral hypothalamus (LH) were evaluated by using retrog

183 r a strong connection between the IC and the lateral hypothalamus (LH) with a monosynaptic relay in t

184 ential AcbSh outputs, including those to the lateral hypothalamus (LH), a target region known to infl

185 refrontal cortex, nucleus accumbens, septum, lateral hypothalamus (LH), amygdala, and ventral tegment

186 cular nucleus (PVN) of the hypothalamus, the lateral hypothalamus (LH), amygdaloid complex (AD) and t

187 limbic information is integrated within the lateral hypothalamus (LH), and excitability of LH neuron

188 ch includes the perifornical area (PeF), the lateral hypothalamus (LH), and lateral portions of the m

189 ei including the lateral habenula (LHb), the lateral hypothalamus (LH), and the midbrain are not only

190 l bands of Broca (VDB and HDB), perifornical lateral hypothalamus (LH), and ventrolateral, medial, an

191 subset of these cells, specifically those in lateral hypothalamus (LH), are involved in reward proces

192 ns is found within the dorsomedial (DMH) and lateral hypothalamus (LH), areas of the brain that conta

193 of these VLPO-projecting neurons within the lateral hypothalamus (LH), as well as their function in

194 was effective when infused directly into the lateral hypothalamus (LH), but not the ventral tegmental

195 SS and CRF in tissue sections containing the lateral hypothalamus (LH), central nucleus of the amygda

196 c nucleus (MPN), medial preoptic area (MPO), lateral hypothalamus (LH), central nucleus of the amygda

197 ed into the perifornical hypothalamus (PFH), lateral hypothalamus (LH), hypothalamic paraventricular

198 l amygdala (BLA), mediodorsal thalamus (MD), lateral hypothalamus (LH), mediolateral septum, dorsolat

199 he thalamus (Sm), parabrachial nucleus (PB), lateral hypothalamus (LH), or medial ventroposterior tha

200 In the lateral hypothalamus (LH), the inhibitory amino acid neu

201 rebrain regions including the PVN, amygdala, lateral hypothalamus (LH), ventral medial hypothalamus (

202 increased Fos-like immunoreactivity (FLI) in lateral hypothalamus (LH), ventral tegmentum (VTA) and m

203 The APC projects to the lateral hypothalamus (LH), where glutamate acts to stimu

204 The NAcSh receives inputs from the lateral hypothalamus (LH), where self-stimulation can be

205 ct line of connection between the IC and the lateral hypothalamus (LH), which engages numerous LH-pro

206 n-concentrating hormone (MCH) neurons in the lateral hypothalamus (LH), which regulate REM sleep init

207 us accumbens medial shell (NAcmSh), and with lateral hypothalamus (LH)-projecting D1-MSN hyperexcitab

208 successfully withheld licking responses, but lateral hypothalamus (LH)-projecting neurons were more a

209 xclusively in dorsomedial, perifornical, and lateral hypothalamus (LH).

210 , central nucleus of the amygdala (CeA), and lateral hypothalamus (LH).

211 ACC may also regulate autonomic flow via the lateral hypothalamus (LH).

212 ber of brain regions, most significantly the lateral hypothalamus (LH).

213 so partially on VTA(Vgat) projections to the lateral hypothalamus (LH).

214 (VPm) and neurons in the VPm project to the lateral hypothalamus (LH).

215 esembling that seen after stimulation of the lateral hypothalamus (LH).

216 uced alterations in sleep, we focused on the lateral hypothalamus (LH).

217 influence feeding via its projections to the lateral hypothalamus (LH).

218 oject from the central amygdala (CeA) to the lateral hypothalamus (LH)] mediates avoidance of stress-

219 send convergent projections into the caudal lateral hypothalamus (LHA) encompassing the parasubthala

220 The lateral hypothalamus (LHA) integrates reward and appetit

221 Additional results show that the lateral hypothalamus (LHA) is a critical downstream subs

222 to be identified.SIGNIFICANCE STATEMENT The lateral hypothalamus (LHA) regulates motivated feeding b

223 to ventrolateral preoptic nuclei (VLPO) and lateral hypothalamus (LHA).

224 AMY) and by disconnection of this region and lateral hypothalamus (LHA).

225 ns in the juxtaparaventricular region of the lateral hypothalamus (LHAjp) which were stimulated by th

226 wheel on electrical self-stimulation of the lateral hypothalamus (LHSS), a measure of hedonic state,

227 that WIN55,212,2 acted on axons arising from lateral hypothalamus local inhibitory cells that innerva

228 mmunoreactive terminals originating from the lateral hypothalamus make direct synaptic contact with n

229 us), and behavioral/homeostatic integration (lateral hypothalamus, mammillary nuclei).

230 A new study suggests that the lateral hypothalamus may also participate in the formati

231 that NF-kappa B expressing cells within the lateral hypothalamus may be important in the maintenance

232 The orexin neurons in the lateral hypothalamus may help stabilize this system by e

233 ling pathway via which signals acting on the lateral hypothalamus may influence the activity of the L

234 unning, Fos was higher in S than in C in the lateral hypothalamus, medial frontal cortex, and striatu

235 l to arousal, including the basal forebrain, lateral hypothalamus, midline thalamus, and cerebral cor

236 llidum (VP) receives orexin projections from lateral hypothalamus neurons (LH), and orexin terminals

237 lateral septum enable separate signalling by lateral hypothalamus neurons according to their feeding-

238 Among those lateral hypothalamus neurons that project to the hypoglo

239 recently identified as neurotransmitters in lateral hypothalamus neurons.

240 Within the lateral hypothalamus, neurons directed to rWAT and iWAT

241 In the lateral hypothalamus, neurotensin, but neither orexin no

242 s--the PV1 nucleus--has been observed in the lateral hypothalamus of rodents.

243 r light deep in the brain, directly into the lateral hypothalamus, of freely moving mice.

244 antial ipsilateral loss of NT-ir in the VTA, lateral hypothalamus or lateral habenula.

245 liosis was seen in the ventromedial nucleus, lateral hypothalamus, or anterior hypothalamic area.

246 implanting bundles of microelectrodes in the lateral hypothalamus, orbitofrontal cortex, insular cort

247 Evidence also indicates roles for lateral hypothalamus orexin neurons and ventral tegmenta

248 These data reveal a new role for lateral hypothalamus orexin neurons in reward-seeking, d

249 Here we show that activation of lateral hypothalamus orexin neurons is strongly linked t

250 ddition, we show that chemical activation of lateral hypothalamus orexin neurons reinstates an exting

251 Then we showed that lateral hypothalamus orexin-producing neurons project to

252 ventricular nucleus, dorsomedial nucleus and lateral hypothalamus, PAG, and LPB.

253 nterodorsal BNST efferent projections-to the lateral hypothalamus, parabrachial nucleus and ventral t

254 rior hypothalamus, dorsomedial hypothalamus, lateral hypothalamus, paraventricular nucleus, supraopti

255 ptal nucleus, ventromedial preoptic nucleus, lateral hypothalamus, perifornical area and in the periv

256 ntricular nucleus of the hypothalamus (PVH), lateral hypothalamus/perifornical area (LH/PFA), and ant

257 rexin, produced by a group of neurons in the lateral hypothalamus/perifornical area, enhances cogniti

258 The perifornical area of the lateral hypothalamus (PF/LH) was recently recognized to

259 Orexin/hypocretin neurons located in the lateral hypothalamus play a critical role in the mainten

260 scharge patterns of neurons in the posterior lateral hypothalamus (PLH) were investigated in the rat.

261 retin/orexin (Hcrt)-producing neurons in the lateral hypothalamus project throughout the brain, inclu

262 Hypocretinergic (orexinergic) neurons in the lateral hypothalamus project to motor columns in the lum

263 Orexin/hypocretin-containing neurons in the lateral hypothalamus project to the VTA, and behavioral

264 These neurons inhibit the lateral hypothalamus-projecting neurons in the ventrolat

265 Hypocretin (Hcrt)-expressing neurons in the lateral hypothalamus promote and stabilize wakefulness b

266 gnaling, mediated through projections to the lateral hypothalamus, promotes selective avoidance of fo

267 ng the aNAcSh, medial prefrontal cortex, and lateral hypothalamus) recruited by activation of glutama

268 in function, such that orexin neurons in the lateral hypothalamus regulate reward processing for both

269 amatergic (VGLUT2-expressing) neurons in the lateral hypothalamus represent a key afferent input for

270 CRH-ir cells were observed in the lateral hypothalamus, retrochiasmatic, and in magnocellu

271 ve regions, including anterior hypothalamus, lateral hypothalamus, somatosensory cortex, paraventricu

272 p65-IR increased significantly in the caudal lateral hypothalamus, specifically the magnocellular lat

273 us [DLM]); (3) restricted regions within the lateral hypothalamus (stratum cellulare externum [SCE]),

274 mined (prefrontal cortex, nucleus accumbens, lateral hypothalamus, substantia nigra, cuneiform nucleu

275 y of hypocretin, but not MCH, neurons in the lateral hypothalamus, suggesting a role for GLP-1 in the

276 The extension of limbic projections into the lateral hypothalamus, suggests that this region be inclu

277 othalamus (paraventricular, dorsomedial, and lateral hypothalamus), thalamus (paraventricular and cen

278 territories, medial pallium, preoptic area, lateral hypothalamus, thalamus, and prethalamus.

279 he mPFC innervated parts of the amygdala and lateral hypothalamus that contain neurons active during

280 retin-sensitive glutamate neurons within the lateral hypothalamus that modulate the output of the hyp

281 xins) are two neuropeptides expressed in the lateral hypothalamus that play a crucial role in the sta

282 ed in neurons of the dorsal raphe nuclei and lateral hypothalamus that project to the mesolimbic dopa

283 n of D1 medium spiny neuron terminals in the lateral hypothalamus that promotes overeating.

284 rojections from the nucleus accumbens to the lateral hypothalamus that regulate feeding.

285 ed that a small, circumscribed region of the lateral hypothalamus, the anterior dorsal region (LHAad)

286 es; areas consistently labelled included the lateral hypothalamus, the parvocellular region of the pa

287 this work has focused on projections to the lateral hypothalamus, the role of NAc projections to the

288 s in the dorsal horn of the spinal cord, the lateral hypothalamus, the spinal trigeminal nuclei, and

289 e pedunculopontine tegmental nucleus (PPTN), lateral hypothalamus, ventral striatum, and striosomes.

290 ol) of the dorsomedial hypothalamic nucleus, lateral hypothalamus, ventral tegmental area, or the int

291 arcuate nucleus and NE concentrations in the lateral hypothalamus, ventromedial hypothalamus (VMH) an

292 cell bodies, located in the perifornical and lateral hypothalamus, were embedded within a dense plexu

293 xons and receptors have been detected in the lateral hypothalamus, where hypocretin neurons are found

294 The NS has only a minor projection to the lateral hypothalamus, whereas the MA, which receives aff

295 s to salient events; and the latter from the lateral hypothalamus, which may explain their involvemen

296 -aminobutyric-acid)-releasing neurons of the lateral hypothalamus, which promote the transition to wa

297 s of the stria terminalis, dorsal raphe, and lateral hypothalamus, which regulate primitive, yet fund

298 orexin/hypocretin system in the perifornical/lateral hypothalamus, which was discovered 15 years ago,

299 escued by re-expression of syndecan-3 in the lateral hypothalamus with an adeno-associated viral vect

300 dent beta-galactosidase in the magnocellular lateral hypothalamus, zona incerta dorsal, as well as th