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1 t from the cortex or the orexin group of the lateral hypothalamus.
2 in-concentrating hormone in the perifornical lateral hypothalamus.
3 of the stria terminalis, and densely to the lateral hypothalamus.
4 decreasing GABAergic tone within the rostral lateral hypothalamus.
5 he orexin-2-saporin conjugate (OXSAP) in the lateral hypothalamus.
6 ss by blunting serotonergic signaling in the lateral hypothalamus.
7 in the cat to electrical stimulation of the lateral hypothalamus.
8 reactive astrocytes and microglia within the lateral hypothalamus.
9 slices or minislices consisting only of the lateral hypothalamus.
10 datory attack elicited by stimulation of the lateral hypothalamus.
11 c-Fos immunoreactivity in the medial but not lateral hypothalamus.
12 the arcuate nucleus, and occasionally in the lateral hypothalamus.
13 cular (PVN), supraoptic, arcuate nuclei, and lateral hypothalamus.
14 ere seen in the ventromedial nucleus and the lateral hypothalamus.
15 nervous system exclusively by neurons of the lateral hypothalamus.
16 and lateral septum) and both the medial and lateral hypothalamus.
17 l region) and electrodes in the perifornical lateral hypothalamus.
18 ry amino acid agonists administered into the lateral hypothalamus.
19 neurons whose cell bodies are located in the lateral hypothalamus.
20 n the cord originate from the neurons in the lateral hypothalamus.
21 rect GABAergic projection from the medial to lateral hypothalamus.
22 hypothalamus, ventromedial hypothalamus, and lateral hypothalamus.
23 predatory attack behavior elicited from the lateral hypothalamus.
24 ventromedial and dorsomedial nuclei, and in lateral hypothalamus.
25 d GABA labeled cells, were identified in the lateral hypothalamus.
26 c inhibitory pathways between the medial and lateral hypothalamus.
27 not the posterior VTA, substantia nigra, or lateral hypothalamus.
28 and 4) a meager bilateral projection to the lateral hypothalamus.
29 suppress predatory attack elicited from the lateral hypothalamus.
30 odes were implanted into both the medial and lateral hypothalamus.
31 affinity binding for GABAA receptors in the lateral hypothalamus.
32 H are located in the zona incerta and in the lateral hypothalamus.
33 edial hypothalamus and which projects to 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 straddling its border and extending into the lateral hypothalamus.
40 hypocretin (orexin)-producing neurons in the lateral hypothalamus.
41 c-Fos in the perifornical, dorsomedial, and lateral hypothalamus.
42 onal subcortical target regions, such as the lateral hypothalamus.
43 rded, and neurobiotin-labeled neurons in the lateral hypothalamus, 11 were immunohistochemically iden
44 ral preoptic area (VLPO) [1] arises from the lateral hypothalamus [2], a brain area associated with a
45 synapses on hypocretin/orexin neurons in the lateral hypothalamus, a well-established arousal/wake-pr
46 areas, and infected neurons also appeared in lateral hypothalamus, A7 region, locus coeruleus, subcoe
48 th Fluoro-Gold and CRH mRNA were seen in the lateral hypothalamus after injections in the lateral and
50 As gamma-aminobutyric-acid (GABA) within the lateral hypothalamus also mediates feeding, we sought to
51 d viral vector delivery of syndecan-3 to the lateral hypothalamus also reduces motivation for cocaine
52 ental area (VTA), subthalamic nucleus (STN), lateral hypothalamus, among others, and the roles of the
53 cue-induced overeating in sated rats include lateral hypothalamus, amygdala, and medial prefrontal co
54 rats and included neurons in the medial and lateral hypothalamus, amygdala, bed nucleus of the stria
55 n had greater connectivity between the right lateral hypothalamus and a reward-related brain region a
57 pocretin neuropeptides are restricted to the lateral hypothalamus and contiguous perifornical area bu
58 to the mesolimbic dopamine circuit from the lateral hypothalamus and dorsal raphe nucleus and define
59 in (orexin) is synthesized by neurons in the lateral hypothalamus and has been reported to increase f
60 located only in the perifornical area of the lateral hypothalamus and heavily innervate the cholinerg
61 nin-concentrating hormone, and orexin in the lateral hypothalamus and in the corticotrophin-releasing
63 attack behavior projects from the medial to lateral hypothalamus and its functions are mediated by G
65 identify some specific projections from the lateral hypothalamus and midbrain, we analyzed the distr
66 in the control of food intake, including the lateral hypothalamus and nucleus accumbens shell, sugges
67 a and dorsal hypothalamus (VLG and IGL); the lateral hypothalamus and perifornical area (VLG); and th
69 active hypocretin and GABAergic cells in the lateral hypothalamus and receive inputs from multiple sl
70 lanted with cannulae directed to the rostral lateral hypothalamus and saclofen (GABA-B receptor antag
71 (hypocretin) are located exclusively in the lateral hypothalamus and send axons to numerous regions
72 rease HS content and sulfation levels in the lateral hypothalamus and that HS contributes to the regu
73 ct with hypocretin-expressing neurons in the lateral hypothalamus and that numerous hypocretinergic n
74 d AVP producing cells were also found in the lateral hypothalamus and the bed nucleus of the stria te
76 implanted with stimulating electrodes to the lateral hypothalamus and trained to perform intracranial
77 dinated gamma (30-90 Hz) oscillations in the lateral hypothalamus and upstream brain regions organize
78 of subcortical limbic areas (e.g., amygdala, lateral hypothalamus), and influenced functional connect
81 natal loss of orexin-positive neurons in the lateral hypothalamus, and orexin-containing projections
82 was increased in ventromedial hypothalamus, lateral hypothalamus, and parabrachial nucleus, identify
85 a terminalis, the anterior hypothalamus, the lateral hypothalamus, and the ventral premamillary nucle
86 gray, dorsomedial hypothalamus, dorsolateral lateral hypothalamus, and ventral portion of the medial
89 inputs to orexin-A-containing neurons in the lateral hypothalamus are altered in obesity and how this
90 so known as orexin)-producing neurons in the lateral hypothalamus are important for arousal stability
91 ventromedial hypothalamic nuclei(VMH)and the lateral hypothalamus are sensitive to a number of circul
92 in levels and orexin-positive neurons in the lateral hypothalamus are substantially reduced, suggesti
94 tor 1-expressing neurons that project to the lateral hypothalamus as mediating rapid control over fee
95 rtle Fos-IR increased in the dorsomedial and lateral hypothalamus as well as in the lateral septum.
96 ic mice that overexpress MCH (MCH-OE) in the lateral hypothalamus at approximately twofold higher lev
97 paracentral nucleus, central medial nucleus, lateral hypothalamus, basal nucleus of the amygdala, and
98 ment with bicuculline microinjected into the lateral hypothalamus blocked the suppressive effects of
99 ar nucleus of the hypothalamus; anterior and lateral hypothalamus (both posterior portion); ventromed
100 jections to the preoptic-basal forebrain and lateral hypothalamus, but not to the thalamus, mediate P
101 In addition, there were differences in the lateral hypothalamus, but the PE group had higher recept
102 trema, VRC, dorsolateral pons, raphe nuclei, lateral hypothalamus, central amygdala, and insular cort
103 ntralateral frontal cortex, basal forebrain, lateral hypothalamus, centrolateral, mediodorsal, ventro
104 t behaviorally critical neurocircuits of the lateral hypothalamus contain glucose detectors that exhi
105 he anterior hypothalamus and fornical in the lateral hypothalamus contain large neurons that synthesi
107 t from the ventral pallidal-lateral preoptic-lateral hypothalamus continuum is strong in the RMTg and
108 rious species have indeed confirmed that the lateral hypothalamus contributes to reward mechanisms.
109 Other connections include projections to lateral hypothalamus, dorsal raphe, periaqueductal gray
110 ron was distributed over wide regions of the lateral hypothalamus, extending from the area immediatel
111 Cannula electrodes were implanted into the lateral hypothalamus for elicitation of predatory attack
113 Hypocretin neurons are located only in the lateral hypothalamus from where they innervate virtually
114 ine, was microinjected into sites within the lateral hypothalamus from which predatory attack was eli
115 on of SCH23390 (100 nM in 200 nL) into rats' lateral hypothalamus greatly reduced sodium appetite.
117 ventral tegmental area > putamen > caudate > lateral hypothalamus > accumbens > linear/interfascicula
118 on of muscimol into adjoining regions of the lateral hypothalamus had no effect upon defensive rage,
122 hormone (MCH) and orexins/hypocretins in the lateral hypothalamus have received attention because the
123 arkers for wake-promoting cell groups in the lateral hypothalamus (Hcrt), tuberomammillary nuclei (hi
125 normalized perfusion in the amygdala and the lateral hypothalamus in Fmr1 KO mice and furthermore dec
129 tricular nucleus of the hypothalamus and the lateral hypothalamus in the social isolates than in the
130 rom both embryonic chick and postnatal mouse lateral hypothalamus in vitro reveal robust stimulus-evo
132 orexin (Hcrt)-containing neurones within the lateral hypothalamus integrate nutritional, energetic an
133 tioned stimulus (CS), the model amygdala and lateral hypothalamus interact to calculate the expected
136 synthesized exclusively in the perifornical/lateral hypothalamus, is critical for drug seeking and r
137 ections between basolateral amygdala and the lateral hypothalamus, is crucial for allowing learned cu
138 t, elicited by electrical stimulation of the lateral hypothalamus, is suppressed following activation
139 downstream from the stimulated fibers of the lateral hypothalamus--is more critically involved in wan
140 e is little leptin receptor expressed in the lateral hypothalamus, it is likely that any observed lep
141 ed to the posterior thalamic nucleus and the lateral hypothalamus (lateral torus, lateral recess nucl
142 cleus, paraventricular hypothalamic nucleus, lateral hypothalamus, lateral parabrachial nucleus, dors
143 er injections of the DLAA threonine into the lateral hypothalamus (LH) alter intake of a threonine-de
144 of electrolytic lesions at the level of the lateral hypothalamus (LH) and by correlating these effec
146 ess-responsive orexin gene expression in the lateral hypothalamus (LH) and medial hypothalamus (MH, i
147 , which sends GABAergic projections into the lateral hypothalamus (LH) and receives extensive glutama
148 icted rats with ibotenic acid lesions of the lateral hypothalamus (LH) and sham controls were trained
149 istinct population of neurons located in the lateral hypothalamus (LH) and zona incerta (ZI), but MCH
150 xin (hypocretin)-containing projections from lateral hypothalamus (LH) are thought to play an importa
157 nd orexin/hypocretin types of neurons of the lateral hypothalamus (LH) exert opposing effects on arou
158 ntly reported that activation of a subset of lateral hypothalamus (LH) GABAergic neurons induced both
159 Massive damage to the MFB in the rostral lateral hypothalamus (LH) generally had little effect on
169 we show that depolarization of perifornical lateral hypothalamus (LH) neurons elicits a CB1R-mediate
170 sculosum of the lamina terminalis (OVLT) and lateral hypothalamus (LH) of rats with coronary artery l
171 into the perifornical hypothalamus (PFH) or lateral hypothalamus (LH) of satiated rats, suggesting t
174 of N-methyl-D-aspartic acid (NMDA) into the lateral hypothalamus (LH) on feeding and other behaviors
176 ysis probes in the NAc and electrodes in the lateral hypothalamus (LH) or medial hypothalamus (MH).
182 , central nucleus of the amygdala (CeA), and lateral hypothalamus (LH) send projections to the nucleu
184 its emanating from the septal nucleus to the lateral hypothalamus (LH) that contribute to neural regu
186 e (MCH) and hypocretin/orexin neurons in the lateral hypothalamus (LH) together with neuropeptide Y (
187 l cortex (PFC), nucleus accumbens (NAC), and lateral hypothalamus (LH) were evaluated by using retrog
188 ential AcbSh outputs, including those to the lateral hypothalamus (LH), a target region known to infl
189 refrontal cortex, nucleus accumbens, septum, lateral hypothalamus (LH), amygdala, and ventral tegment
190 cular nucleus (PVN) of the hypothalamus, the lateral hypothalamus (LH), amygdaloid complex (AD) and t
191 limbic information is integrated within the lateral hypothalamus (LH), and excitability of LH neuron
192 ch includes the perifornical area (PeF), the lateral hypothalamus (LH), and lateral portions of the m
193 ei including the lateral habenula (LHb), the lateral hypothalamus (LH), and the midbrain are not only
194 l bands of Broca (VDB and HDB), perifornical lateral hypothalamus (LH), and ventrolateral, medial, an
195 subset of these cells, specifically those in lateral hypothalamus (LH), are involved in reward proces
196 ns is found within the dorsomedial (DMH) and lateral hypothalamus (LH), areas of the brain that conta
197 of these VLPO-projecting neurons within the lateral hypothalamus (LH), as well as their function in
198 was effective when infused directly into the lateral hypothalamus (LH), but not the ventral tegmental
199 SS and CRF in tissue sections containing the lateral hypothalamus (LH), central nucleus of the amygda
200 c nucleus (MPN), medial preoptic area (MPO), lateral hypothalamus (LH), central nucleus of the amygda
201 ed into the perifornical hypothalamus (PFH), lateral hypothalamus (LH), hypothalamic paraventricular
202 l amygdala (BLA), mediodorsal thalamus (MD), lateral hypothalamus (LH), mediolateral septum, dorsolat
203 he thalamus (Sm), parabrachial nucleus (PB), lateral hypothalamus (LH), or medial ventroposterior tha
205 rebrain regions including the PVN, amygdala, lateral hypothalamus (LH), ventral medial hypothalamus (
206 increased Fos-like immunoreactivity (FLI) in lateral hypothalamus (LH), ventral tegmentum (VTA) and m
219 to be identified.SIGNIFICANCE STATEMENT The lateral hypothalamus (LHA) regulates motivated feeding b
222 ns in the juxtaparaventricular region of the lateral hypothalamus (LHAjp) which were stimulated by th
223 wheel on electrical self-stimulation of the lateral hypothalamus (LHSS), a measure of hedonic state,
224 that WIN55,212,2 acted on axons arising from lateral hypothalamus local inhibitory cells that innerva
225 mmunoreactive terminals originating from the lateral hypothalamus make direct synaptic contact with n
228 that NF-kappa B expressing cells within the lateral hypothalamus may be important in the maintenance
230 ling pathway via which signals acting on the lateral hypothalamus may influence the activity of the L
231 unning, Fos was higher in S than in C in the lateral hypothalamus, medial frontal cortex, and striatu
232 l to arousal, including the basal forebrain, lateral hypothalamus, midline thalamus, and cerebral cor
233 llidum (VP) receives orexin projections from lateral hypothalamus neurons (LH), and orexin terminals
234 lateral septum enable separate signalling by lateral hypothalamus neurons according to their feeding-
239 halamus, dorsal ventricular ridge, habenula, lateral hypothalamus, nucleus rotundus, nucleus sphericu
243 NPY-immunoreactivity was not elevated in the lateral hypothalamus or the tissue bordering the anterov
244 liosis was seen in the ventromedial nucleus, lateral hypothalamus, or anterior hypothalamic area.
245 implanting bundles of microelectrodes in the lateral hypothalamus, orbitofrontal cortex, insular cort
249 ddition, we show that chemical activation of lateral hypothalamus orexin neurons reinstates an exting
250 nterodorsal BNST efferent projections-to the lateral hypothalamus, parabrachial nucleus and ventral t
251 rior hypothalamus, dorsomedial hypothalamus, lateral hypothalamus, paraventricular nucleus, supraopti
252 ptal nucleus, ventromedial preoptic nucleus, lateral hypothalamus, perifornical area and in the periv
253 ntricular nucleus of the hypothalamus (PVH), lateral hypothalamus/perifornical area (LH/PFA), and ant
254 rexin, produced by a group of neurons in the lateral hypothalamus/perifornical area, enhances cogniti
256 scharge patterns of neurons in the posterior lateral hypothalamus (PLH) were investigated in the rat.
257 retin/orexin (Hcrt)-producing neurons in the lateral hypothalamus project throughout the brain, inclu
258 Hypocretinergic (orexinergic) neurons in the lateral hypothalamus project to motor columns in the lum
259 Orexin/hypocretin-containing neurons in the lateral hypothalamus project to the VTA, and behavioral
260 atory attack from the medial amygdala to the lateral hypothalamus projects to the ventromedial hypoth
261 Hypocretin (Hcrt)-expressing neurons in the lateral hypothalamus promote and stabilize wakefulness b
262 Nhlh2 is expressed in the ventral-medial and lateral hypothalamus, Rathke's pouch and in the anterior
263 ng the aNAcSh, medial prefrontal cortex, and lateral hypothalamus) recruited by activation of glutama
264 in function, such that orexin neurons in the lateral hypothalamus regulate reward processing for both
265 inhibitory mechanism from the medial to the lateral hypothalamus, resulting in suppression of predat
268 ve regions, including anterior hypothalamus, lateral hypothalamus, somatosensory cortex, paraventricu
269 p65-IR increased significantly in the caudal lateral hypothalamus, specifically the magnocellular lat
270 us [DLM]); (3) restricted regions within the lateral hypothalamus (stratum cellulare externum [SCE]),
271 mined (prefrontal cortex, nucleus accumbens, lateral hypothalamus, substantia nigra, cuneiform nucleu
272 y of hypocretin, but not MCH, neurons in the lateral hypothalamus, suggesting a role for GLP-1 in the
273 The extension of limbic projections into the lateral hypothalamus, suggests that this region be inclu
274 to the ventral telencephalon, preoptic area, lateral hypothalamus, tectum, and pacemaker nucleus conf
275 othalamus (paraventricular, dorsomedial, and lateral hypothalamus), thalamus (paraventricular and cen
277 he mPFC innervated parts of the amygdala and lateral hypothalamus that contain neurons active during
278 retin-sensitive glutamate neurons within the lateral hypothalamus that modulate the output of the hyp
279 xins) are two neuropeptides expressed in the lateral hypothalamus that play a crucial role in the sta
280 ed in neurons of the dorsal raphe nuclei and lateral hypothalamus that project to the mesolimbic dopa
282 dosomes-lysosomes into dendrites and, in the lateral hypothalamus, the formation of massive, lysosome
283 es; areas consistently labelled included the lateral hypothalamus, the parvocellular region of the pa
284 s in the dorsal horn of the spinal cord, the lateral hypothalamus, the spinal trigeminal nuclei, and
285 the pathway from the medial amygdala to the lateral hypothalamus underlying suppression of predatory
286 dual stimulation of the medial amygdala and lateral hypothalamus upon response latencies for predato
287 e pedunculopontine tegmental nucleus (PPTN), lateral hypothalamus, ventral striatum, and striosomes.
288 ol) of the dorsomedial hypothalamic nucleus, lateral hypothalamus, ventral tegmental area, or the int
289 arcuate nucleus and NE concentrations in the lateral hypothalamus, ventromedial hypothalamus (VMH) an
290 cell bodies, located in the perifornical and lateral hypothalamus, were embedded within a dense plexu
291 xons and receptors have been detected in the lateral hypothalamus, where hypocretin neurons are found
292 The NS has only a minor projection to the lateral hypothalamus, whereas the MA, which receives aff
293 s to salient events; and the latter from the lateral hypothalamus, which may explain their involvemen
294 -aminobutyric-acid)-releasing neurons of the lateral hypothalamus, which promote the transition to wa
295 s of the stria terminalis, dorsal raphe, and lateral hypothalamus, which regulate primitive, yet fund
296 orexin/hypocretin system in the perifornical/lateral hypothalamus, which was discovered 15 years ago,
297 he existence of a pathway from the medial to lateral hypothalamus whose functions are mediated by GAB
298 escued by re-expression of syndecan-3 in the lateral hypothalamus with an adeno-associated viral vect
299 ttack latencies of single stimulation of the lateral hypothalamus with those following dual stimulati
300 dent beta-galactosidase in the magnocellular lateral hypothalamus, zona incerta dorsal, as well as th
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