ライフサイエンスコーパス: paraventricular nucleus

1 -1Rs) in the vagus nerve, area postrema, and paraventricular nucleus.

2 releasing factor immunoreactive cells in the paraventricular nucleus.

3 e number of synapses has been doubled in the paraventricular nucleus.

4 ed c-fos mRNA expression in the hypothalamic paraventricular nucleus.

5 entromedial parvocellular subdivision of the paraventricular nucleus.

6 activity (indicating neuronal excitation) in paraventricular nucleus.

7 as found in the parvocellular portion of the paraventricular nucleus.

8 nd parvocellular neurons of the hypothalamic paraventricular nucleus.

9 elicited by stimulation of the hypothalamic paraventricular nucleus.

10 ventromedial hypothalamus, and hypothalamic paraventricular nucleus.

11 mpaired c-fos activation in the hypothalamic paraventricular nucleus.

12 In the paraventricular nucleus, although temporal changes in ox

13 neurons that express ENK in the hypothalamic paraventricular nucleus and central nucleus of the amygd

14 aled significantly less oxytocin mRNA in the paraventricular nucleus and increased oxytocin receptor

15 ated neuronal activation in the hypothalamic paraventricular nucleus and medial nucleus of the amygda

16 4Rs only in SIM1 neurons in the hypothalamic paraventricular nucleus and neurons in the amygdala was

17 , galanin, enkephalin, and dynorphin, in the paraventricular nucleus and orexin and melanin-concentra

18 s in Arc NPY projections areas (hypothalamic paraventricular nucleus and perifornical area) after Arc

19 ut had normal activation in the hypothalamic paraventricular nucleus and the amygdalar central nucleu

20 er intake, was increased in the hypothalamic paraventricular nucleus and the subfornical organ.

21 amus was measured by c-fos expression in the paraventricular nucleus and the ventromedial preoptic ar

22 action, reduces melanocortin content in the paraventricular nucleus, and markedly increases suscepti

23 of the bed nucleus of the stria terminalis, paraventricular nucleus, and medial amygdala.

24 ary tract, periaqueductal gray, hypothalamic paraventricular nucleus, and medial preoptic area, sites

25 dalar nucleus (CAmy), anterior hypothalamus, paraventricular nucleus, and posterior lateral hypothala

26 and improving mitochondrial function in the paraventricular nucleus, and reveal multiple novel targe

27 ndant in the area postrema, arcuate nucleus, paraventricular nucleus, and ventromedial hypothalamus.

28 lateral hypothalamus, somatosensory cortex, paraventricular nucleus, and zona incerta; no regions we

29 in/proNKB fibers were also identified in the paraventricular nucleus, anterior hypothalamic area, med

30 easing hormone (TRH)-positive neurons in the paraventricular nucleus area of the hypothalamus and thu

31 ry tract and arcuate hypothalamic nucleus -> paraventricular nucleus axonal fiber outgrowth.

32 n carotid bodies, striatum, and hypothalamic paraventricular nucleus, but not in the nucleus tractus

33 nucleus, ventromedial hypothalamic nucleus, paraventricular nucleus, dorsomedial hypothalamic nucleu

34 somatosensory/insular cortex, preoptic area, paraventricular nucleus, dorsomedial nucleus and lateral

35 with RFRP-3 immunoreactivity enhanced in the paraventricular nucleus, dorsomedial nucleus, and Arc of

36 oinjection of muscimol into the hypothalamic paraventricular nucleus failed to reduce changes evoked

37 hanisms of chronic stress integration in the paraventricular nucleus, focusing on the role of glucoco

38 ngle-minded 1 neurons, we show dependence of paraventricular nucleus GLP-1 signaling in the coordinat

39 hypothalamic feeding nuclei/cell types, the paraventricular nucleus (GLP-1RKD(DeltaSim1cre)) and pro

40 The rat paraventricular nucleus has three major divisions: desce

41 n a modest increase in CRH expression in the paraventricular nucleus, hypoplastic adrenal glands and

42 ut of the X-linked Fgf13 in the hypothalamic paraventricular nucleus impairs sympathetic output to br

43 le, the locus coeruleus, medial amygdala and paraventricular nucleus), implicating a prominent role o

44 oss of oxytocin (OT)-containing cells in the paraventricular nucleus in the hypothalamus (PVN; p<0.05

45 terminals, originating from the hypothalamic paraventricular nucleus, in the CA2 of mice.

46 brain barrier, but also in the hypothalamic paraventricular nucleus, located inside the blood brain

47 somatodendritic release of vasopressin from paraventricular nucleus neurones.

48 enetic stimulation of ARC TH axons inhibited paraventricular nucleus neurons by dopamine and GABA co-

49 of their postsynaptic targets (Arc POMC and paraventricular nucleus neurons), where ATP dramatically

50 at increased OT/c-fos colocalizations in the paraventricular nucleus of both sexes.

51 and increased mitochondrial function in the paraventricular nucleus of hypertensive rats by promotin

52 atory function in the supraoptic nucleus and paraventricular nucleus of hypertensive rats that contri

53 se system, and decreased inflammation in the paraventricular nucleus of hypertensive rats.

54 -2 fluorescence in perivascular cells of the paraventricular nucleus of hypothalamus, prostaglandin E

55 ied by reduced GLP-1 immunoreactivity in the paraventricular nucleus of hypothalamus, suggesting rele

56 vation, and proinflammatory cytokines in the paraventricular nucleus of hypothalamus.

57 Application of SP to the paraventricular nucleus of rats increases heart rate and

58 The paraventricular nucleus of thalamus (PVT), which project

59 neurotropic factor-expressing neurons in the paraventricular nucleus of the hypothalamus (BDNF(PVH)).

60 stinct from that of Utx, specifically in the paraventricular nucleus of the hypothalamus (high Uty) a

61 ion between the circumventricular organs and paraventricular nucleus of the hypothalamus (PVH) and th

62 Neurons within the paraventricular nucleus of the hypothalamus (PVH) are a

63 ve absent Crh mRNA and peptide mainly in the paraventricular nucleus of the hypothalamus (PVH) but pr

64 its were identified in subpopulations of the paraventricular nucleus of the hypothalamus (PVH) by dou

65 The paraventricular nucleus of the hypothalamus (PVH) consis

66 The paraventricular nucleus of the hypothalamus (PVH) contai

67 The paraventricular nucleus of the hypothalamus (PVH) coordi

68 ogenetic activation of OT neurons within the paraventricular nucleus of the hypothalamus (PVH) of mal

69 The paraventricular nucleus of the hypothalamus (PVH) plays

70 e mediation of activational responses of the paraventricular nucleus of the hypothalamus (PVH) provok

71 ed mainly to the hypothalamus, including the paraventricular nucleus of the hypothalamus (PVH), later

72 altered POMC projections to the preautonomic paraventricular nucleus of the hypothalamus (PVH), pancr

73 utonomic nervous system, particularly in the paraventricular nucleus of the hypothalamus (PVH), play

74 ons provide a distinctive innervation of the paraventricular nucleus of the hypothalamus (PVH), with

75 tream melanocortin-4 receptors (MC4R) in the paraventricular nucleus of the hypothalamus (PVH).

76 the mouse and send direct projections to the paraventricular nucleus of the hypothalamus (PVH).

77 tion factor necessary for development of the paraventricular nucleus of the hypothalamus (PVH).

78 nd behavioral responses are regulated by the paraventricular nucleus of the hypothalamus (PVH).

79 f serotonin 2C receptors (5-HT(2C)Rs) in the paraventricular nucleus of the hypothalamus (PVH).

80 es in the anterior parvicellular part of the paraventricular nucleus of the hypothalamus (PVHap) and

81 xpression of IRS2 and TRPV1 receptors in the paraventricular nucleus of the hypothalamus (PVN) and do

82 reduced binding of both radioligands in the paraventricular nucleus of the hypothalamus (PVN) and me

83 tressors and are found within neurons of the paraventricular nucleus of the hypothalamus (PVN) and se

84 We tested the hypotheses that (1) the paraventricular nucleus of the hypothalamus (PVN) and th

85 ation of firing activity of neurons from the paraventricular nucleus of the hypothalamus (PVN) by alp

86 d female rats, nanoinjection of NPY into the paraventricular nucleus of the hypothalamus (PVN) dose-d

87 ysiological properties of CRF neurons in the paraventricular nucleus of the hypothalamus (PVN) found

88 is critical for energy homeostasis, and the paraventricular nucleus of the hypothalamus (PVN) is a k

89 ocellular cells and fiber projections of the paraventricular nucleus of the hypothalamus (PVN) of mal

90 d the Cre/lox system to delete AT1a from the paraventricular nucleus of the hypothalamus (PVN) of mic

91 We found that neurons of the paraventricular nucleus of the hypothalamus (PVN) send d

92 ly glutamatergic and send projections to the paraventricular nucleus of the hypothalamus (PVN) that a

93 gly, we found bilateral projections from the paraventricular nucleus of the hypothalamus (PVN) to RAI

94 e hypocretin neurons project directly to the paraventricular nucleus of the hypothalamus (PVN), and S

95 BST), central nucleus of the amygdala (CEA), paraventricular nucleus of the hypothalamus (PVN), and t

96 tal cortex, striatum, nucleus accumbens, and paraventricular nucleus of the hypothalamus (PVN), in bo

97 Within the paraventricular nucleus of the hypothalamus (PVN), OXT-i

98 Bilateral nanoinjection of SHU9119 into the paraventricular nucleus of the hypothalamus (PVN), to bl

99 the hindbrain send robust projections to the paraventricular nucleus of the hypothalamus (PVN), which

100 ropin-releasing hormone (CRH) neurons in the paraventricular nucleus of the hypothalamus (PVN).

101 and oxytocin- (OC) containing neurons of the paraventricular nucleus of the hypothalamus (PVN).

102 mone (ACTH) secretagogue biosynthesis in the paraventricular nucleus of the hypothalamus (PVN).

103 rge part by noradrenergic (NA) inputs to the paraventricular nucleus of the hypothalamus (PVN).

104 the medial parvocellular subdivision of the paraventricular nucleus of the hypothalamus (PVN).

105 : the caudal ventrolateral medulla (CVLM) or paraventricular nucleus of the hypothalamus (PVN).

106 These neurons densely populate the paraventricular nucleus of the hypothalamus (PVN).

107 ith hypothalamic brain nuclei, including the paraventricular nucleus of the hypothalamus (PVN).

108 in G(s)alpha in brain regions outside of the paraventricular nucleus of the hypothalamus (PVN).

109 noreactive cells and OT messenger RNA in the paraventricular nucleus of the hypothalamus and an incre

110 withdrawal induces OT neuroplasticity in the paraventricular nucleus of the hypothalamus and dorsal r

111 uroplasticity in OT-producing neurons in the paraventricular nucleus of the hypothalamus and its effe

112 mmunication in hypertension originating from paraventricular nucleus of the hypothalamus and presenti

113 n releasing factor-containing neurons of the paraventricular nucleus of the hypothalamus and primaril

114 ing was significantly greater in the AH, the paraventricular nucleus of the hypothalamus and the late

115 sympathoexcitatory brain centres such as the paraventricular nucleus of the hypothalamus and the rost

116 found that PACAP increased CRF levels in the paraventricular nucleus of the hypothalamus and, importa

117 c and anorexigenic neural projections to the paraventricular nucleus of the hypothalamus at PN 28.

118 hat knockdown of VP and OT production in the paraventricular nucleus of the hypothalamus exerts diver

119 tivate c-fos expression in the hind brain or paraventricular nucleus of the hypothalamus indicating t

120 in-releasing hormone (CRH) released from the paraventricular nucleus of the hypothalamus is a major r

121 -releasing factor type 1 receptor within the paraventricular nucleus of the hypothalamus is an import

122 ective activation of oxytocin neurons in the paraventricular nucleus of the hypothalamus stimulates i

123 g there make appositions onto neurons in the paraventricular nucleus of the hypothalamus that are als

124 Oxytocinergic neurons in the paraventricular nucleus of the hypothalamus that project

125 ina terminals and vasopressin neurons in the paraventricular nucleus of the hypothalamus, and further

126 tive axonal projections and terminals in the paraventricular nucleus of the hypothalamus, arcuate nuc

127 lateral bed nucleus of the stria terminalis, paraventricular nucleus of the hypothalamus, dorsal late

128 ular nucleus of the thalamus, preoptic area, paraventricular nucleus of the hypothalamus, IPe, arcuat

129 leasing hormone (Crh) gene expression in the paraventricular nucleus of the hypothalamus, the central

130 n type-1a receptor-containing neurons of the paraventricular nucleus of the hypothalamus, the goal be

131 ssion in the brain that was localized to the paraventricular nucleus of the hypothalamus.

132 er, bed nucleus of the stria terminalis, and paraventricular nucleus of the hypothalamus.

133 ely the locus coeruleus, raphe pallidus, and paraventricular nucleus of the hypothalamus.

134 mpanied by increased oxytocin release in the paraventricular nucleus of the hypothalamus.

135 olved in the development and function of the paraventricular nucleus of the hypothalamus.

136 d nucleus of the stria terminalis (BNST) and paraventricular nucleus of the hypothalamus.

137 TS and reduction of GLP-1 innervation to the paraventricular nucleus of the hypothalamus.

138 e stria terminalis, and medial parvocellular paraventricular nucleus of the hypothalamus.

139 parvocellular neurosecretory neurons of the paraventricular nucleus of the hypothalamus.

140 ss responsiveness and transcriptomics of the paraventricular nucleus of the hypothalamus.

141 -releasing factor (CRF) immunodensity in the paraventricular nucleus of the hypothalamus.

142 with high levels of oxidative stress in the paraventricular nucleus of the hypothalamus.

143 effect that is dependent upon VDR within the paraventricular nucleus of the hypothalamus.

144 ntified in 11 of 40 brain regions, including paraventricular nucleus of the hypothalamus; anterior an

145 precursor peptide, prepro-TRH (ppTRH) in the paraventricular nucleus of the rat hypothalamus and the

146 sted that OrxA transmission in the posterior paraventricular nucleus of the thalamus (pPVT) participa

147 ting neurons of the posterior portion of the paraventricular nucleus of the thalamus (pPVT).

148 Recently, we reported that activation of the paraventricular nucleus of the thalamus (PVT) abolished

149 thway from the prelimbic cortex (PrL) to the paraventricular nucleus of the thalamus (PVT) decreases

150 We focus on the temporal recruitment of the paraventricular nucleus of the thalamus (PVT) for the re

151 Here, we show that the paraventricular nucleus of the thalamus (PVT) orchestrat

152 estigated the functional organization of the paraventricular nucleus of the thalamus (PVT), a midline

153 Here we show a key role for the rat paraventricular nucleus of the thalamus (PVT), a nucleus

154 ian brain, one putative stress sensor is the paraventricular nucleus of the thalamus (PVT), an area t

155 The posterior paraventricular nucleus of the thalamus (THPVP) has been

156 entiates excitatory transmission between the paraventricular nucleus of the thalamus and D2-receptor-

157 Here we identify the paraventricular nucleus of the thalamus as a prominent i

158 Activity in the paraventricular nucleus of the thalamus to nucleus accum

159 ay- and cell-type-specific plasticity in the paraventricular nucleus of the thalamus to nucleus accum

160 The Gpr151-expressing neurons in the paraventricular nucleus of the thalamus was primarily co

161 ives dense DA innervation via the fr and the paraventricular nucleus of the thalamus, a stress sensit

162 grade and anterograde tracing identified the paraventricular nucleus of the thalamus, bed nucleus of

163 observed in the cingulate cortex, posterior paraventricular nucleus of the thalamus, periaqueductal

164 lis in the telencephalon; habenular nucleus, paraventricular nucleus of the thalamus, preoptic area,

165 e midbrain periaqueductal gray (PAG) and the paraventricular nucleus of the thalamus, two brain areas

166 and some of which innervate both the PAG and paraventricular nucleus of the thalamus.

167 bed nuclei of the stria terminalis, and the paraventricular nucleus of the thalamus.

168 ation of GLP-1 into the arcuate, but not the paraventricular, nucleus of the hypothalamus reduced hep

169 ARC TH cells project to the hypothalamic paraventricular nucleus; optogenetic stimulation of ARC

170 Intra-paraventricular nucleus oxytocin injections reduced beha

171 Together, our data demonstrate that paraventricular nucleus oxytocin mediates the social buf

172 uropeptide Y (NPY) levels in the DMH and the paraventricular nucleus (P < 0.05).

173 TH+) and somatostatin (SST+) neurons in the paraventricular nucleus (PaVN) of the hypothalamus of ad

174 TH release, in the parvocellular division of paraventricular nucleus (pcPVN), and (2) mFSS-induced ac

175 g hormone (CRH) neurons in the parvocellular paraventricular nucleus (pPVN) play a key role in coordi

176 eurones in the parvocellular division of the paraventricular nucleus (pPVN) via noradrenergic (A2 cel

177 tion of BM-derived cells to the hypothalamic paraventricular nucleus, presumably via a mechanism of d

178 preoptic area (POA; homolog of the mammalian paraventricular nucleus), Purkinje cell layer of the cer

179 tidromically activated from the hypothalamic paraventricular nucleus (PVH) (latency: 10.3+/-1.3 ms, t

180 e Arc and its projection to the hypothalamic paraventricular nucleus (PVH) are both components of the

181 for glutamatergic input to the hypothalamic paraventricular nucleus (PVH) in stress-induced activati

182 ablished orexigenic peptide and hypothalamic paraventricular nucleus (PVH) is one major brain site th

183 ral brain regions including the hypothalamic paraventricular nucleus (PVH), the anteroventral periven

184 and to the medial parvocellular part of the paraventricular nucleus (PVHmp).

185 ey rats with both a push-pull cannula in the paraventricular nucleus (PVN) and a catheter in the jugu

186 ors are highly expressed in the hypothalamic paraventricular nucleus (PVN) and arcuate nucleus (ARC).

187 ssure, and heart rate via projections to the paraventricular nucleus (PVN) and dorsomedial hypothalam

188 by parvocellular neurons of the hypothalamic paraventricular nucleus (PVN) and released into the port

189 ns in other hypothalamic regions such as the paraventricular nucleus (PVN) and rostral preoptic area

190 f E2 exposure, rats were sacrificed, and the paraventricular nucleus (PVN) and rostral ventrolateral

191 opressin (AVP) neurons from the hypothalamic paraventricular nucleus (PVN) and supraoptic nucleus (SO

192 CRF and oxytocin mRNA expression in the paraventricular nucleus (PVN) and supraoptic nucleus (SO

193 The paraventricular nucleus (PVN) and supraoptic nucleus (SO

194 fspring stress regulating brain regions, the paraventricular nucleus (PVN) and the bed nucleus of str

195 These prominently included the hypothalamic paraventricular nucleus (PVN) and the nucleus of the sol

196 t the effects of NPS within the hypothalamic paraventricular nucleus (PVN) are mediated via actions o

197 tagonist) microinjected bilaterally into the paraventricular nucleus (PVN) attenuated the increase in

198 The paraventricular nucleus (PVN) contains spinally-projecti

199 The hypothalamic paraventricular nucleus (PVN) coordinates major neuroend

200 CRH mRNA expression in hypothalamic paraventricular nucleus (PVN) diminished after daily han

201 m laminae terminalis (OVLT) and hypothalamic paraventricular nucleus (PVN) each contribute significan

202 utyric acid (GABA)-projecting neurons in the paraventricular nucleus (PVN) have been shown to inhibit

203 in stimulates VP neurons in the hypothalamic paraventricular nucleus (PVN) in a nutritional state-dep

204 The paraventricular nucleus (PVN) in mammals is the main hyp

205 that NMU microinjected into the hypothalamic paraventricular nucleus (PVN) in rats increases the ener

206 osynthesis, in the arcuate nucleus (Arc) and paraventricular nucleus (PVN) in the hypothalamus.

207 The hypothalamic paraventricular nucleus (PVN) integrates preautonomic an

208 The development of the hypothalamic paraventricular nucleus (PVN) involves several factors t

209 lenges such as dehydration, the hypothalamic paraventricular nucleus (PVN) is activated and drives SN

210 The hypothalamic paraventricular nucleus (PVN) is critically involved in

211 1 receptor (NMDA-NR1) expression within the paraventricular nucleus (PVN) is critically linked to th

212 (NMDA) receptor activity in the hypothalamic paraventricular nucleus (PVN) is crucial for the sympath

213 Increased glutamatergic input in the paraventricular nucleus (PVN) is important for high symp

214 NMDAR activity in the hypothalamic paraventricular nucleus (PVN) is increased and criticall

215 elaxin-3/RXFP3 signaling in the hypothalamic paraventricular nucleus (PVN) is necessary for the expre

216 The hypothalamic paraventricular nucleus (PVN) is responsive to hypoxic s

217 tocin- and arginine-vasopressin-synthesizing paraventricular nucleus (PVN) magnocellular neurosecreto

218 r GABA plays a key role in the modulation of paraventricular nucleus (PVN) neuronal excitability and

219 Despite the fact that paraventricular nucleus (PVN) neurones innervating the r

220 te mechanisms regulating the excitability of paraventricular nucleus (PVN) neurones that project dire

221 oxidase (NOX) in AVP-expressing hypothalamic paraventricular nucleus (PVN) neurons in "menopausal" fe

222 increased by angiotensin II (Ang II) within paraventricular nucleus (PVN) neurons of normotensive ra

223 c stressors via trans-synaptic influences on paraventricular nucleus (PVN) neurons.

224 The paraventricular nucleus (PVN) of the hypothalamus contro

225 The paraventricular nucleus (PVN) of the hypothalamus is a k

226 -aspartate receptor (NMDAR) activity, in the paraventricular nucleus (PVN) of the hypothalamus is clo

227 asing factor (CRF) that is released from the paraventricular nucleus (PVN) of the hypothalamus is ess

228 d-aspartate receptor (NMDAR) activity in the paraventricular nucleus (PVN) of the hypothalamus is inv

229 Glutamatergic inputs in the paraventricular nucleus (PVN) of the hypothalamus mainta

230 rentiated neurons were transplanted into the paraventricular nucleus (PVN) of the hypothalamus of an

231 Preautonomic neurons in the paraventricular nucleus (PVN) of the hypothalamus play a

232 The hyperphagia derived from the paraventricular nucleus (PVN) of the hypothalamus, where

233 sed c-Fos immunoreactivity of neurons in the paraventricular nucleus (PVN) of the hypothalamus.

234 ttributable to global hypocellularity of the paraventricular nucleus (PVN) of the hypothalamus.

235 scription factor abundantly expressed in the paraventricular nucleus (PVN) of the hypothalamus.

236 rticotropin-releasing hormone (CRH) from the paraventricular nucleus (PVN) of the hypothalamus.

237 by microdialysis, either in the hypothalamic paraventricular nucleus (PVN) or in the ventromedial nuc

238 SB334867 microinjected into the hypothalamic paraventricular nucleus (PVN) or into the bed nucleus of

239 During social interactions, activity in paraventricular nucleus (PVN) OXT neurons increased.

240 amatergic synaptic input in the hypothalamic paraventricular nucleus (PVN) plays a critical role in r

241 eceptor (NMDAR) activity in the hypothalamic paraventricular nucleus (PVN) plays a major role in elev

242 thetic drive emanating from the hypothalamic paraventricular nucleus (PVN) plays a major role in the

243 The hypothalamic paraventricular nucleus (PVN) regulates numerous homeost

244 The paraventricular nucleus (PVN) regulates sympathetic outf

245 Hypothalamic projections from the paraventricular nucleus (PVN) release oxytocin (OT) to m

246 rolateral medulla (RVLM) from neurons in the paraventricular nucleus (PVN) that release arginine vaso

247 Whether leptin acts in the paraventricular nucleus (PVN) to increase sympathetic ne

248 supports a contribution of the hypothalamic paraventricular nucleus (PVN) to sympathoexcitation and

249 Tmem18 expression in the murine hypothalamic paraventricular nucleus (PVN) was altered by changes in

250 At the end, the paraventricular nucleus (PVN) was analyzed by Real-time

251 s of the amygdala (CeA) and the hypothalamic paraventricular nucleus (PVN) were evaluated in male rhe

252 ened glutamate signaling in the hypothalamic paraventricular nucleus (PVN), a key central coordinator

253 actions of ANG II that are mediated via the paraventricular nucleus (PVN), an area that serves as a

254 or (CRF) mRNA expression in the hypothalamic paraventricular nucleus (PVN), and plasma cortisol and A

255 minalis (BNST), medial preoptic area (MPOA), paraventricular nucleus (PVN), anterior cortical (AcA),

256 Neuronal activity in the hypothalamic paraventricular nucleus (PVN), as well as sympathetic ou

257 a terminalis, central amygdala, hypothalamic paraventricular nucleus (PVN), Barrington's nucleus and

258 tic nucleus (SCN), supraoptic nucleus (SON), paraventricular nucleus (PVN), dorsomedial nucleus (DM),

259 bited higher expression of 5HT2A mRNA in the paraventricular nucleus (PVN), higher expression of 5HT2

260 development of HPA axis regions, such as the paraventricular nucleus (PVN), in addition to blood pres

261 in neurons of the supraoptic nucleus (SON), paraventricular nucleus (PVN), locus coeruleus (LC), ros

262 in the bed nucleus of the stria terminalis, paraventricular nucleus (PVN), posterior hypothalamus, p

263 Fos-ir activity was quantified in the paraventricular nucleus (PVN), subfornical organ (SFO),

264 Fos-like immunoreactive (IR) neurons in the paraventricular nucleus (PVN), supraoptic nucleus (SON)

265 tor (CRF) mRNA and immunoreactive CRF in the paraventricular nucleus (PVN), the pituitary adrenocorti

266 The rostral region, containing the paraventricular nucleus (PVN), was defined by discrete l

267 ack CREB1 in SIM1-expressing neurons, of the paraventricular nucleus (PVN), which are known to be MC4

268 um intake evoked an endogenous, hypothalamic paraventricular nucleus (PVN)-specific, decrease (sodium

269 -dependent dysregulation of the hypothalamic paraventricular nucleus (PVN).

270 rticotropin releasing hormone neurons in the paraventricular nucleus (PVN).

271 eptors (MC4R) in neurons of the hypothalamic paraventricular nucleus (PVN).

272 on mediated in part through the hypothalamic paraventricular nucleus (PVN).

273 tor blockade in the ipsilateral hypothalamic paraventricular nucleus (PVN).

274 te several hypothalamic areas, including the paraventricular nucleus (PVN).

275 ERbeta immunoreactive cell numbers in ARH or paraventricular nucleus (PVN).

276 elicited by the stimulation of hypothalamic paraventricular nucleus (PVN).

277 ntact neurons projecting to the hypothalamic paraventricular nucleus (PVN).

278 l-regulated kinase (ERK) in the hypothalamic paraventricular nucleus (PVN).

279 or no direct projections to the hypothalamic paraventricular nucleus (PVN).

280 ventromedial (VMN) nucleus and parvocellular paraventricular nucleus (PVN).

281 bition of SNA by neuropeptide Y (NPY) in the paraventricular nucleus (PVN).

282 ate nucleus-median eminence (ARC-ME) and the paraventricular nucleus (PVN).

283 LHA (22%), zona incerta (ZI, 15%), CeA (5%), paraventricular nucleus (PVN, 13%), SLEA (66%), and MPA

284 RVLM-projecting neurons of the hypothalamic paraventricular nucleus (PVN-RVLM) contributes to an imb

285 the dorsomedial hypothalamus (including the paraventricular nucleus [PVN]) but not in the pituitary

286 were counted in the posterior portion of the paraventricular nucleus (PVNp), supraoptic nucleus (SON)

287 ed their projections from the arcuate to the paraventricular nucleus, reduced energy expenditure, and

288 Transcriptomic analysis of the paraventricular nucleus revealed widespread changes in e

289 autonomic brain regions (i.e., hypothalamic paraventricular nucleus, rostral ventrolateral medulla a

290 damage to the ventromedial hypothalamus and paraventricular nucleus showed severe obesity and insuli

291 unexpectedly, emanates from the hypothalamic paraventricular nucleus, specifically from subsets of ne

292 m hypothalamic neuroendocrine neurons in the paraventricular nucleus stimulates neighboring (~100 mum

293 entricular nucleus, medial preoptic nucleus, paraventricular nucleus, suprachiasmatic nucleus, and ve

294 were high in, for example, piriform cortex, paraventricular nucleus, supraoptic nucleus, arcuate nuc

295 ng hormone (CRH) neurons in the hypothalamic paraventricular nucleus that govern neuroendocrine stres

296 ns, including the arcuate nucleus (ARC), the paraventricular nucleus, the medial preoptic area, the l

297 ns from oxytocin neurons in the hypothalamic paraventricular nucleus to midbrain DA regions.

298 nate extract reduces oxidative stress in the paraventricular nucleus to relieve hypertension.

299 rticotrophin releasing factor neurons in the paraventricular nucleus, which when activated result in

300 llular and magnocellular subdivisions of the paraventricular nucleus, with greater increases ipsilate