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 synthesised by magnocellular neurones of the supraoptic and paraventricular nuclei and is released fr

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

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

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

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

14 n magnocellular neurones of the hypothalamic supraoptic and paraventricular nuclei to induce uterine

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

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

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

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

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

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

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

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

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

24 triggers activation of the suprachiasmatic, supraoptic, and paraventricular nuclei of the hypothalam

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

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

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

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

29 nuclear translocation in closely associated supraoptic astrocytes.

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

31 In supraoptic, circular, and ventral tuberomammillary nucle

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

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

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

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

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

37 ptidergic neurons in the paraventricular and supraoptic hypothalamus.

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

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

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

41 neuroendocrine neurones of the hypothalamic supraoptic neucleus.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

88 lease of oxytocin from dendrites in isolated supraoptic nuclei.

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

90 oid receptors in the rat paraventricular and supraoptic nuclei.

91 ry system, including the paraventricular and supraoptic nuclei.

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

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

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

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

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

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

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

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

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

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

102 rosecretory cells (MNCs) of the hypothalamic supraoptic nucleus (SON) generate afterhyperpolarization

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

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

105 ted in the paraventricular nucleus (PVN) and supraoptic nucleus (SON) is coordinated by the combined,

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

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

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

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

110 release pathway is activated by hypothalamic supraoptic nucleus (SON) neurons early in the torpor-aro

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

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

113 Supraoptic nucleus (SON) neurons possess a prominent aft

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

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

116 Within the supraoptic nucleus (SON) of a 35-day-old rat, we previou

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

149 ipRGCs also project to nuclei such as the supraoptic nucleus (SON), which is involved in systemic

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

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

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

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

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

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

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

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

158 c innervation of the CeA originated from the supraoptic nucleus (SON).

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

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

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

162 tify oxytocin neurons in the retrochiasmatic supraoptic nucleus (SOR(OXT)) and oxytocin-receptor-expr

163 Here, we show that intra-supraoptic nucleus administration of kisspeptin increase

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

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

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

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

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

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

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

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

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

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

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

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

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

177 alysis administration of kisspeptin into the supraoptic nucleus consistently increased the action pot

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

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

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

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

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

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

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

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

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

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

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

189 alamic slices did not affect the activity of supraoptic nucleus neurones or the strength of local syn

190 or the strength of local synaptic inputs to supraoptic nucleus neurones.

191 rents or inhibitory postsynaptic currents in supraoptic nucleus neurones.

192 frequency or baseline membrane potential in supraoptic nucleus neurones.

193 2/SK3 channel subunit mRNA expression in the supraoptic nucleus of HF rats.

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

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

196 (0.1-10.0 micrograms microliter-1) onto the supraoptic nucleus of rats made dependent by intracerebr

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

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

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

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

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

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

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

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

205 isspeptin fibre density increases around the supraoptic nucleus over pregnancy and intracerebroventri

206 Morphine inhibits supraoptic nucleus oxytocin neurones directly and presyn

207 Supraoptic nucleus oxytocin neurones were identified ant

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

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

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

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

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

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

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

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

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

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

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

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

220 areas, notably the POA, SCN, PVN, DMH, VMH, supraoptic nucleus, and the ventral and dorsal premammil

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

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

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

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

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

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

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

228 mble of hypothalamic neurons in and near the supraoptic nucleus, consisting primarily of neuroendocri

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

230 In the supraoptic nucleus, in situ hybridisation revealed that

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

246 and AVP deficits mapped specifically in the supraoptic nucleus->LS pathway of Magel2KO mice disrupti

247 on in vasopressin neurons within the PVN and supraoptic nucleus.

248 localized in the paraventricular nucleus and supraoptic nucleus.

249 ventricular nucleus of the hypothalamus, and supraoptic nucleus.

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

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

252 ate of identified oxytocin neurones from the supraoptic nucleus.

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

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

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

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

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

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

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

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

261 and somata of magnocellular neurones in the supraoptic nucleus.

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

263 (10 microM), on glutamate-induced firing in supraoptic oxytocin (OT) and vasopressin (VP) neurones i

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

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

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

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

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

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

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

271 In contrast, Oxt neurons in the supraoptic (SO) and accessory (AN) nuclei have limited c

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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