ライフサイエンスコーパス: supraoptic

1 ocellular neurosecretory cells (MNCs) in the supraoptic and paraventricular (PVN) nuclei are regulate

2 ystem, and is essential for formation of the supraoptic and paraventricular (PVN) nuclei of the hypot

3 dependent somatodendritic release within the supraoptic and paraventricular hypothalamic nuclei.

4 hiasmatic, and in magnocellular parts of the supraoptic and paraventricular hypothalamic nucleus (PVH

5 ornical organ (SFO), median preoptic (MnPO), supraoptic and paraventricular nuclei (SON and PVN), are

6 on in the median preoptic nucleus (MPN), the supraoptic and paraventricular nuclei (SON and PVN), but

7 ior third ventricle (AV3V) region and in the supraoptic and paraventricular nuclei (SON and PVN).

8 region and in the vasopressin neurons of the supraoptic and paraventricular nuclei (SON and PVN).

9 In the hypothalamus, the supraoptic and paraventricular nuclei demonstrated the d

10 lusion, increased GPCR101 mRNA expression in supraoptic and paraventricular nuclei from late pregnanc

11 n the nuclei of magnocellular neurons in the supraoptic and paraventricular nuclei of the hypothalamu

12 nd vasopressin-containing neurons within the supraoptic and paraventricular nuclei of the hypothalamu

13 observed among urocortin-ir perikarya in the supraoptic and paraventricular nuclei, in the central an

14 rm layer of the olfactory bulb, hypothalamic supraoptic and paraventricular nuclei, the medial habenu

15 orebrain regions, including the hypothalamic supraoptic and paraventricular nuclei, the thalamic para

16 habenula, cerebral cortex, and hypothalamic supraoptic and paraventricular nuclei.

17 is in part through direct connections to the supraoptic and paraventricular nucleus.

18 teroventral periventricular nucleus, and the supraoptic and suprachiasmatic nuclei as well as the arc

19 entral tegmental area and bilaterally in the supraoptic and tuberomammillary nuclei.

20 i.e., hypothalamic nuclei (paraventricular, supraoptic, and arcuate), major cholinergic and monoamin

21 area; and the paraventricular, dorsomedial, supraoptic, and median preoptic nuclei of hypothalamus.

22 n mRNA were detected in the paraventricular, supraoptic, and reticular thalamic nuclei and in the ven

23 as present within the paraventricular (PVN), supraoptic, arcuate nuclei, and lateral hypothalamus.

24 terminalis; preoptic area; paraventricular, supraoptic, arcuate, and dorsomedial nuclei of the hypot

25 eminence, periventricular, suprachiasmatic, supraoptic, arcuate, paraventricular, ventromedial, and

26 nuclear translocation in closely associated supraoptic astrocytes.

27 s were used to characterize the responses of supraoptic cells to osmotic stimulation.

28 In supraoptic, circular, and ventral tuberomammillary nucle

29 commissural, magnocellular paraventricular, supraoptic, circularis in the anterior hypothalamus and

30 entromedial hypothalamus through the ventral supraoptic commissural pathway to the peripeduncular are

31 the tectobulbar projection, and the ventral supraoptic decussation of the pigeon.

32 the fornix from the hypothalamus, along the supraoptic decussations or the inferior thalamic peduncl

33 ia terminalis, hypothalamic paraventricular, supraoptic, dorsomedial, infundibular (IN), lateral hypo

34 ptidergic neurons in the paraventricular and supraoptic hypothalamus.

35 generated by repetitive action potentials in supraoptic magnocellular neurons regulate repetitive fir

36 e arcuate, periventricular, paraventricular, supraoptic, medial preoptic, anterior, ventromedial, and

37 These data suggest that in supraoptic MNCs classical Ca(2+)-insensitive, delayed re

38 neuroendocrine neurones of the hypothalamic supraoptic neucleus.

39 l amounts, and to have inhibitory actions on supraoptic neuronal activity.

40 lusion, we have characterized BK channels in supraoptic neuronal cell bodies, and demonstrated that t

41 tive Ca2+ channels in isolated magnocellular supraoptic neurones (MNCs).

42 tory postsynaptic currents (sIPSCs) from rat supraoptic neurones in hypothalamic slices in vitro.

43 o difference in preproCCK mRNA levels within supraoptic neurones of (i.c.v.) morphine-treated compare

44 s were identified in freshly dissociated rat supraoptic neurones using patch clamp techniques.

45 i, we measured [Ca2+]i responses in isolated supraoptic neurons and found that MC4R ligands induce a

46 ated with electrophysiological excitation of supraoptic neurons because central injection of alpha-MS

47 tterns of vasopressin (VP) and oxytocin (OT) supraoptic neurons in coronal slices from virgin female

48 re obtained from immunochemically identified supraoptic neurons of diestrous or lactating female rats

49 esults suggest that the cellular response of supraoptic neurons to osmotic stimuli require inputs fro

50 n the synaptic contacts between the MnPo and supraoptic neurons were investigated in rats by ultrastr

51 hybridisation was seen over the cytoplasm of supraoptic neurons, but no differences were measured bet

52 the effects of alpha-MSH on the activity of supraoptic neurons.

53 cid (mRNA) levels in the paraventricular and supraoptic nuclei (PVN and SON) of the ovariectomized ra

54 were found in the paraventricular (PVN) and supraoptic nuclei (SON) and VP-ir projections from these

55 Injection of AdAVP into the supraoptic nuclei (SON) of the hypothalamus resulted in

56 organum vasculosum lamina terminalis (OVLT), supraoptic nuclei (SON), and magnocellular region of the

57 ng the LT and hypothalamic areas such as the supraoptic nuclei (SON), is unclear.

58 cells that have anatomic projections to the supraoptic nuclei (SON).

59 n the hypothalamic paraventricular (PVN) and supraoptic nuclei (SON).

60 Fos in the paraventricular nuclei (PVN) and supraoptic nuclei (SON).

61 xpression in parallel with AVP expression in supraoptic nuclei (SONs) and paraventicular nuclei (PVNs

62 y expressed in the mouse paraventricular and supraoptic nuclei after 10 days of drinking 2% saline, o

63 and vasopressin release from intact isolated supraoptic nuclei and from the neurophypophyses in rats

64 edian and anteroventral preoptic nuclei, and supraoptic nuclei as well as the magnocellular portion o

65 nt variation in PAC1 mRNA within the SCN and supraoptic nuclei during the light-dark cycle and in con

66 By contrast, in supraoptic nuclei from adult rats allopregnanolone-induc

67 In supraoptic nuclei from rats of 3-4 weeks old or less, al

68 Using supraoptic nuclei in brain slices from lactating rats, w

69 muscimol also induced oxytocin release from supraoptic nuclei in young rats, but had no effect in ad

70 S binding was significantly increased in the supraoptic nuclei of both morphine-dependent and salt-lo

71 ls within the dorsal (oxytocin neurone-rich) supraoptic nuclei of rats given an intracerebroventricul

72 s, most prominently, the paraventricular and supraoptic nuclei of the hypothalamus (13-fold and 80-fo

73 the inferior olive, the paraventricular and supraoptic nuclei of the hypothalamus, and in the ventra

74 a, the zona incerta, the paraventricular and supraoptic nuclei of the hypothalamus, the substantia ni

75 he surviving vasopressinergic neurons in the supraoptic nuclei of the ST + CISL group was significant

76 Studies of the paraventricular and supraoptic nuclei revealed induction of the chaperone pr

77 ific subdivisions of the paraventricular and supraoptic nuclei, and in the arcuate and ventromedial n

78 e (VP-ir) neurons in the paraventricular and supraoptic nuclei, as well as an unusually extensive dis

79 ber of CFLI cells in the Paraventricular and Supraoptic nuclei, but preloads of mineral oil did not.

80 tary tract, hypothalamic paraventricular and supraoptic nuclei, central nucleus of amygdala, lateral

81 , neuroendocrine system (paraventricular and supraoptic nuclei, hypothalamic visceromotor pattern gen

82 raventricular, accessory magnocellulary, and supraoptic nuclei, in the retrochiasmatic part of the su

83 diagonal band of Broca, paraventricular and supraoptic nuclei, suprachiasmatic nucleus, and dorsomed

84 s IR in the hypothalamic paraventricular and supraoptic nuclei, the subfornical organ (SFO), and the

85 lease of oxytocin from dendrites in isolated supraoptic nuclei.

86 thalamus, dorsolateral to the borders of the supraoptic nuclei.

87 oid receptors in the rat paraventricular and supraoptic nuclei.

88 ry system, including the paraventricular and supraoptic nuclei.

89 al (EW), lateral superior olivary (LSO), and supraoptic nuclei; lower levels of expression are seen i

90 ampal, periventricular, suprachiasmatic, and supraoptic nuclei; Purkinje cells in the cerebellum; and

91 eptor immunoreactivity decreased 13% only in supraoptic nucleus (P < 0.05).

92 eurons in the paraventricular nucleus (PVN), supraoptic nucleus (SON) and accessory neurosecretory nu

93 d Fos-like immunoreactivity (Fos-LIR) in the supraoptic nucleus (SON) and paraventricular nucleus (PV

94 late AVP steady-state gene expression in the supraoptic nucleus (SON) and PVN, and/or CRF mRNA in the

95 logical functions of PRR were studied in the supraoptic nucleus (SON) because this brain region showe

96 Magnocellular neurons of the supraoptic nucleus (SON) can differentially control pept

97 (VP)-secreting magnocellular neurons of the supraoptic nucleus (SON) display calcium-dependent after

98 sured expression of the oxytocin gene in the supraoptic nucleus (SON) during pregnancy, parturition a

99 We explored this issue using the supraoptic nucleus (SON) in lactating rats.

100 ministration of hypertonic saline to the rat supraoptic nucleus (SON) increases the expression of sev

101 recordings were obtained from sixty-five rat supraoptic nucleus (SON) neurones in brain slices to inv

102 ole-cell patch recordings were obtained from supraoptic nucleus (SON) neurones in horizontal brain sl

103 Unlike many neuron populations, supraoptic nucleus (SON) neurons are rich in both nitric

104 ergic and excitatory glutamatergic inputs to supraoptic nucleus (SON) neurons can influence the relea

105 e appearance of Fos and Jun in the nuclei of supraoptic nucleus (SON) neurons following intraperitone

106 g direct olfactory (glutamatergic) inputs to supraoptic nucleus (SON) neurons increases interneuronal

107 Supraoptic nucleus (SON) neurons possess a prominent aft

108 nd adenosine receptors (AR) are expressed in supraoptic nucleus (SON) neurons, we postulated that con

109 ted by activation of eNMDARs in hypothalamic supraoptic nucleus (SON) neurons.

110 ower subparaventricular zone, LSPV), and the supraoptic nucleus (SON) of grass rats (Arvicanthis nilo

111 in the paraventricular nucleus (PVN) and the supraoptic nucleus (SON) of the hypothalamus are activat

112 The paraventricular nucleus (PVN) and supraoptic nucleus (SON) of the hypothalamus are importa

113 The paraventricular nucleus (PVN) and supraoptic nucleus (SON) of the hypothalamus are importa

114 The supraoptic nucleus (SON) of the hypothalamus contains ma

115 rom the suprachiasmatic nucleus (SCN) to the supraoptic nucleus (SON) of the hypothalamus were charac

116 was used to assess the relative responses of supraoptic nucleus (SON) oxytocin- (OX) and vasopressin-

117 the hypothalamic paraventricular nucleus and supraoptic nucleus (SON) respond to glucocorticoids by r

118 nvestigated in magnocellular neurones of rat supraoptic nucleus (SON) using whole-cell patch recordin

119 ion in the paraventricular nucleus (PVN) and supraoptic nucleus (SON) was evaluated by real time RT-P

120 nohistochemically identified neurones in the supraoptic nucleus (SON) was investigated in the hypotha

121 nearby forebrain cholinergic neurons to the supraoptic nucleus (SON) were used to study synaptic pot

122 lateral amygdaloid nucleus, 1.2-times in the supraoptic nucleus (SON), 1.6-times in the magnocellular

123 in areas receiving input from the SFO is the supraoptic nucleus (SON), a source of vasopressin synthe

124 f neurosecretory neurons in the hypothalamic supraoptic nucleus (SON), a well studied model of struct

125 ensin (Ang)-(1-7)-IR cells were found in the supraoptic nucleus (SON), and in the anterior (ap-), med

126 in 3 receptors (NK3-Rs) are expressed in the supraoptic nucleus (SON), and SON is innervated by subst

127 ral superfusion of 3 microM TTX into the rat supraoptic nucleus (SON), delivered with the use of a mi

128 ocellular neurosecretory system (MNS) of the supraoptic nucleus (SON), in which dendritic release of

129 duces structural changes in the hypothalamic supraoptic nucleus (SON), including increased glutamate

130 urons were particularly abundant in the PVN, supraoptic nucleus (SON), infundibular nucleus, and prem

131 rtion of the paraventricular nucleus (PVNp), supraoptic nucleus (SON), magnocellular PVN and suprachi

132 organum vasculosum lamina terminalis (OVLT), supraoptic nucleus (SON), magnocellular region of the pa

133 e measured in paraventricular nucleus (PVN), supraoptic nucleus (SON), median preoptic area (MePO), s

134 served in the paraventricular nucleus (PVN), supraoptic nucleus (SON), median preoptic nucleus (MnPO)

135 ular nucleus (PVN), subfornical organ (SFO), supraoptic nucleus (SON), nucleus accumbens (NAc) shell

136 hypothalamus, suprachiasmatic nucleus (SCN), supraoptic nucleus (SON), paraventricular nucleus (PVN),

137 significant Fos expression in neurons of the supraoptic nucleus (SON), paraventricular nucleus (PVN),

138 Vasopressin was localized in the supraoptic nucleus (SON), paraventricular nucleus, amygd

139 in the rat paraventricular nucleus (PVN) and supraoptic nucleus (SON), regions which lack ERalpha.

140 that VRACs are absent in neurons of the rat supraoptic nucleus (SON), suggesting that glial cells ar

141 ch as the paraventricular nucleus (PVH), the supraoptic nucleus (SON), the lateral hypothalamic area

142 eurosecretory cells (MNCs) isolated from rat supraoptic nucleus (SON).

143 nucleus (TM) project monosynaptically to the supraoptic nucleus (SON).

144 ith an increased synaptic innervation of the supraoptic nucleus (SON).

145 erior periventricular nucleus (aPV), and the supraoptic nucleus (SON).

146 pothalamic paraventricular nucleus (PVN) and supraoptic nucleus (SON).

147 icular nucleus of the hypothalamus (PVN) and supraoptic nucleus (SON).

148 pothalamic paraventricular nucleus (PVN) and supraoptic nucleus (SON).

149 us system (CNS) plasticity: the hypothalamic supraoptic nucleus (SON).

150 only neuronal phenotypes present in the rat supraoptic nucleus (SON).

151 nce of constitutive NO production within the supraoptic nucleus (SON).

152 nuates that of neurosecretory neurons in the supraoptic nucleus (SON; which secrete oxytocin and vaso

153 e in the number of Fos-positive cells in the supraoptic nucleus and a 3.4-fold increase in the latera

154 expression of tenascin by astrocytes in the supraoptic nucleus and associated ventral glial limitans

155 c nuclei, in the retrochiasmatic part of the supraoptic nucleus and in the median eminence.

156 the cell bodies of oxytocin neurones in the supraoptic nucleus and in their noradrenergic input.

157 ediated glutamate excitatory function in the supraoptic nucleus and paraventricular nucleus of hypert

158 served in other brain regions, including the supraoptic nucleus and piriform cortex.

159 lamic regions outside the SCN, including the supraoptic nucleus and the subparaventricular region.

160 e neurons in the paraventricular nucleus and supraoptic nucleus at 2 and 4 weeks after MI compared wi

161 e neurons in the paraventricular nucleus and supraoptic nucleus at 2 weeks after MI compared with mic

162 microscopic level, labeled fibers within the supraoptic nucleus branched frequently, were punctuated

163 urosteroids induce oxytocin release from the supraoptic nucleus by a mechanism that partly depends on

164 ist bicuculline to the dendritic zone of the supraoptic nucleus by microdialysis.

165 ged in most nuclei, but had increased in the supraoptic nucleus by the end of pregnancy and remained

166 t on to directly measure GABA release in the supraoptic nucleus during hypertonic infusion, confirmin

167 )) to VP and OT neurones of the hypothalamic supraoptic nucleus elicited by repetitive extracellular

168 , most vasopressin cells of the hypothalamic supraoptic nucleus fire action potentials in a 'phasic'

169 agonists of GluK1-containing KARs in the rat supraoptic nucleus has an opposite action on glutamaterg

170 ocellular neurosecretory cells (MNCs) of the supraoptic nucleus has been attributed mainly to synapti

171 burst firing in oxytocin (OT) neurons in the supraoptic nucleus in brain slices from lactating rats.

172 alamus, apparently no longer confined to the supraoptic nucleus in mutants.

173 cordings from magnocellular cells of the rat supraoptic nucleus in vivo and in vitro and between oxyt

174 and the total number of GABA synapses in the supraoptic nucleus is substantially higher in lactating

175 opioid agonists primarily occurs within the supraoptic nucleus itself, since the antagonist naloxone

176 Here we analysed the discharge patterning of supraoptic nucleus neurones in vivo, to infer the charac

177 2/SK3 channel subunit mRNA expression in the supraoptic nucleus of HF rats.

178 t both oxytocin and vasopressin cells in the supraoptic nucleus of normal rats respond to intravenous

179 ecretory cells (MNCs) were isolated from the supraoptic nucleus of rat hypothalamus, and properties o

180 (0.1-10.0 micrograms microliter-1) onto the supraoptic nucleus of rats made dependent by intracerebr

181 osecretory cells (MNCs) dissociated from the supraoptic nucleus of the adult guinea-pig were identifi

182 cation of N-methyl-D-aspartate (NMDA) to the supraoptic nucleus of the hypothalamus (SON) generates c

183 sopressin from magnocellular neurones in the supraoptic nucleus of the hypothalamus has important aut

184 arterioles in two brain regions (cortex and supraoptic nucleus of the hypothalamus).

185 es, c-fos expression was elevated within the supraoptic nucleus of the hypothalamus.

186 uclei, the accessory olfactory bulb, and the supraoptic nucleus of the hypothalamus.

187 dial preoptic area, medial amygdala, and the supraoptic nucleus of the hypothalamus.

188 ole-cell patch clamp recordings were made in supraoptic nucleus OT neurons in brain slices from male

189 Morphine inhibits supraoptic nucleus oxytocin neurones directly and presyn

190 Supraoptic nucleus oxytocin neurones were identified ant

191 Thus, the acute inhibition of supraoptic nucleus oxytocin neurones which results from

192 measurements of SK channel subunits mRNA in supraoptic nucleus punches revealed a diminished express

193 ectrical activity of oxytocin neurons in the supraoptic nucleus recorded in vivo.

194 benoxathian directly onto the surface of the supraoptic nucleus reduced the activity of oxytocin neur

195 gly stained, whereas in the hypothalamus the supraoptic nucleus stood out with strong immunoreactivit

196 lular neurosecretory cells (MNCs) in the rat supraoptic nucleus to different osmotic milieus by salt-

197 Single neurones of the rat supraoptic nucleus were recorded during microdialysis of

198 that alpha-MSH induces Fos expression in the supraoptic nucleus when injected centrally and demonstra

199 cleus, paraventricular hypothalamic nucleus, supraoptic nucleus, accessory neurosecretory nuclei, per

200 ry tract, the ventrolateral medulla, and the supraoptic nucleus, all showed increases in cFos-IR in t

201 Targets included the lateral nucleus, peri-supraoptic nucleus, and subparaventricular zone of the h

202 regulate hemodynamic processes including the supraoptic nucleus, and the magnocellular division of hy

203 e, piriform cortex, paraventricular nucleus, supraoptic nucleus, arcuate nucleus, and hippocampal CA

204 aventricular nucleus of the hypothalamus and supraoptic nucleus, as well as in the cortex, septal nuc

205 ures, including the paraventricular nucleus, supraoptic nucleus, bed nucleus of the stria terminalis

206 s induced oxytocin release from the isolated supraoptic nucleus, but only allopregnanolone induced si

207 paraventricular nucleus of the hypothalamus, supraoptic nucleus, central amygdala, nucleus tractus so

208 paraventricular nucleus of the hypothalamus, supraoptic nucleus, central nucleus of amygdala, lateral

209 ncreased bilaterally in the piriform cortex, supraoptic nucleus, central nucleus of the amygdala, and

210 A1, CA2, and CA3 regions, the dentate gyrus, supraoptic nucleus, hypothalamus, and cortical layers II

211 In the supraoptic nucleus, in situ hybridisation revealed that

212 he highest levels of immunostaining were the supraoptic nucleus, magnocellular PVH, ARH, and suprachi

213 ime points, but not at 6 hours, included the supraoptic nucleus, magnocellular regions of the paraven

214 c area, bed nucleus of the stria terminalis, supraoptic nucleus, paraventricular nucleus, zona incert

215 organum vasculosum of the lamina terminalis, supraoptic nucleus, periaqueductal gray, and medial nucl

216 in select groups of nuclei (e.g., habenula, supraoptic nucleus, pontine nucleus) contained pronounce

217 The central nucleus of the amygdala and the supraoptic nucleus, regions that are involved in autonom

218 ular regions of the paraventricular nucleus, supraoptic nucleus, septohypothalamic nucleus, medial se

219 s, medial septum, and cortex, but not in the supraoptic nucleus, septohypothalamic nucleus, or organu

220 ior paraventricular nucleus of the thalamus, supraoptic nucleus, subfornical organ, and paraventricul

221 eceptors (MC4Rs) are highly expressed in the supraoptic nucleus, suggesting that alpha-MSH and oxytoc

222 um, diagonal band, pallidum, preoptic areas, supraoptic nucleus, suprachiasmatic nucleus, paraventric

223 e prominently localized to astrocytes in the supraoptic nucleus, the neurons of which contain only sm

224 e anorectic TB rats, most prominently in the supraoptic nucleus, the parvocellular portion of the par

225 nterior and retrochiasmatic divisions of the supraoptic nucleus, the suprachiasmatic nucleus, the ven

226 teral hypothalamus, paraventricular nucleus, supraoptic nucleus, ventromedial hypothalamus) and two h

227 on the properties of neurons in the OVLT and supraoptic nucleus.

228 ventricular nucleus of the hypothalamus, and supraoptic nucleus.

229 d with 5-min sampling frequency from the rat supraoptic nucleus.

230 AHP currents in oxytocin (OT) neurons of the supraoptic nucleus.

231 ate of identified oxytocin neurones from the supraoptic nucleus.

232 cin (OT)- and (VP)-containing neurons of the supraoptic nucleus.

233 n the lateral hypothalamic are dorsal to the supraoptic nucleus.

234 and the parallel-projecting dendrites of the supraoptic nucleus.

235 t naloxone was effective when given into the supraoptic nucleus.

236 n-1) onto the exposed ventral surface of the supraoptic nucleus.

237 s along the ventral lamina terminalis to the supraoptic nucleus.

238 en glial coverage of synapses and LTP in the supraoptic nucleus.

239 and somata of magnocellular neurones in the supraoptic nucleus.

240 gest in neostriatum, olfactory tubercle, and supraoptic nucleus.

241 localized in the paraventricular nucleus and supraoptic nucleus.

242 (10 microM), on glutamate-induced firing in supraoptic oxytocin (OT) and vasopressin (VP) neurones i

243 r electrical activity of paraventricular and supraoptic oxytocin cells was recorded in lactating rats

244 alpha-MSH induces Fos expression in supraoptic oxytocin neurons, and alpha-MSH melanocortin-

245 ensely rCRMP-4-labeled neurons populated the supraoptic, paraventricular, and periventricular nuclei

246 immunostained cell bodies were found in the supraoptic, paraventricular, and ventromedial hypothalam

247 Neurons of the olfactory bulb, supraoptic, paraventricular, suprachiasmatic, and tubera

248 ascicular nuclei, the hypothalamus including supraoptic, periventricular, paraventricular (PVN), arcu

249 c nucleus, dorsomedial hypothalamic nucleus, supraoptic retrochiasmatic nucleus, lateral hypothalamic

250 s, irBC was concentrated in perikarya of the supraoptic (SO), paraventricular (PVH) and accessory neu

251 C-fos expression was also suppressed in the supraoptic (SON) and (less completely) in the paraventri

252 hy of galanin expression in the hypothalamic supraoptic (SON) and paraventricular (PVN) nuclei neuron

253 tic nucleus (MNPO), subfornical organ (SFO), supraoptic (SON) and paraventricular (PVN) nuclei of for

254 organ (SFO), as well as in the magnocellular supraoptic (SON) and paraventricular hypothalamic (PVN)

255 are expressed in vasopressin neurones of the supraoptic (SON) and paraventricular nuclei (PVN).

256 osecretory cells located in the hypothalamic supraoptic (SON) and paraventricular nuclei.

257 ctivity of magnocellular cells (MNCs) in the supraoptic (SON) and paraventricular nuclei.

258 P) magnocellular neurons in the hypothalamic supraoptic (SON) and paraventricular nuclei.

259 ocellular neuroendocrine cells (MNCs) of the supraoptic (SON) and paraventricular nucleus of the hypo

260 ir) were found in the paraventricular (PVN), supraoptic (SON) and suprachiasmatic nuclei (SCN) of the

261 irmed that IL-6 is robustly expressed in the supraoptic (SON) and the paraventricular (PVN) nuclei of

262 on factor, Fos, by paraventricular (PVN) and supraoptic (SON) magnocellular neurons.

263 ain, including the paraventricular (PVN) and supraoptic (SON) nuclei of the hypothalamus.

264 entricular (aPV), paraventricular (PVN), and supraoptic (SON) nuclei strongly express the homeobox ge

265 on of hypothalamic paraventricular (PVN) and supraoptic (SON) nuclei, as well as OT and VP neurons pr

266 nd in hypothalamic paraventricular (PVN) and supraoptic (SON) nuclei.

267 is observed in the paraventricular (PVN) and supraoptic (SON) nuclei.

268 y the hypothalamic paraventricular (PVN) and supraoptic (SON) nuclei.

269 the depletion period showed no Fos-IR in the supraoptic (SON) or paraventricular hypothalamic nuclei

270 nd the anterior hypothalamus, as well as the supraoptic (SON), paraventricular (PVH), ventromedial, d

271 e hypothalamus (i.e., paraventricular [PVN], supraoptic [SON], and suprachiasmatic [SCN]) and extende

272 particularly the preoptic, periventricular, supraoptic, suprachiasmatic, and arcuate nuclei; and in

273 The cellular regions of the paraventricular, supraoptic, suprachiasmatic, arcuate, and mammillary nuc