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1 on in vasopressin neurons within the PVN and supraoptic nucleus.
2 on the properties of neurons in the OVLT and supraoptic nucleus.
3 ate of identified oxytocin neurones from the supraoptic nucleus.
4 cin (OT)- and (VP)-containing neurons of the supraoptic nucleus.
5 n the lateral hypothalamic are dorsal to the supraoptic nucleus.
6 and the parallel-projecting dendrites of the supraoptic nucleus.
7 t naloxone was effective when given into the supraoptic nucleus.
8 n-1) onto the exposed ventral surface of the supraoptic nucleus.
9 s along the ventral lamina terminalis to the supraoptic nucleus.
10 en glial coverage of synapses and LTP in the supraoptic nucleus.
11 and somata of magnocellular neurones in the supraoptic nucleus.
12 AHP currents in oxytocin (OT) neurons of the supraoptic nucleus.
13 gest in neostriatum, olfactory tubercle, and supraoptic nucleus.
14 localized in the paraventricular nucleus and supraoptic nucleus.
15 ventricular nucleus of the hypothalamus, and supraoptic nucleus.
16 d with 5-min sampling frequency from the rat supraoptic nucleus.
17 cleus, paraventricular hypothalamic nucleus, supraoptic nucleus, accessory neurosecretory nuclei, per
19 ry tract, the ventrolateral medulla, and the supraoptic nucleus, all showed increases in cFos-IR in t
20 e in the number of Fos-positive cells in the supraoptic nucleus and a 3.4-fold increase in the latera
21 expression of tenascin by astrocytes in the supraoptic nucleus and associated ventral glial limitans
24 ediated glutamate excitatory function in the supraoptic nucleus and paraventricular nucleus of hypert
26 lamic regions outside the SCN, including the supraoptic nucleus and the subparaventricular region.
27 Targets included the lateral nucleus, peri-supraoptic nucleus, and subparaventricular zone of the h
28 regulate hemodynamic processes including the supraoptic nucleus, and the magnocellular division of hy
29 areas, notably the POA, SCN, PVN, DMH, VMH, supraoptic nucleus, and the ventral and dorsal premammil
30 e, piriform cortex, paraventricular nucleus, supraoptic nucleus, arcuate nucleus, and hippocampal CA
31 aventricular nucleus of the hypothalamus and supraoptic nucleus, as well as in the cortex, septal nuc
32 e neurons in the paraventricular nucleus and supraoptic nucleus at 2 and 4 weeks after MI compared wi
33 e neurons in the paraventricular nucleus and supraoptic nucleus at 2 weeks after MI compared with mic
34 ures, including the paraventricular nucleus, supraoptic nucleus, bed nucleus of the stria terminalis
35 microscopic level, labeled fibers within the supraoptic nucleus branched frequently, were punctuated
36 s induced oxytocin release from the isolated supraoptic nucleus, but only allopregnanolone induced si
37 urosteroids induce oxytocin release from the supraoptic nucleus by a mechanism that partly depends on
39 ged in most nuclei, but had increased in the supraoptic nucleus by the end of pregnancy and remained
40 paraventricular nucleus of the hypothalamus, supraoptic nucleus, central amygdala, nucleus tractus so
41 paraventricular nucleus of the hypothalamus, supraoptic nucleus, central nucleus of amygdala, lateral
42 ncreased bilaterally in the piriform cortex, supraoptic nucleus, central nucleus of the amygdala, and
43 alysis administration of kisspeptin into the supraoptic nucleus consistently increased the action pot
44 mble of hypothalamic neurons in and near the supraoptic nucleus, consisting primarily of neuroendocri
45 t on to directly measure GABA release in the supraoptic nucleus during hypertonic infusion, confirmin
46 )) to VP and OT neurones of the hypothalamic supraoptic nucleus elicited by repetitive extracellular
47 , most vasopressin cells of the hypothalamic supraoptic nucleus fire action potentials in a 'phasic'
48 and AVP deficits mapped specifically in the supraoptic nucleus->LS pathway of Magel2KO mice disrupti
49 agonists of GluK1-containing KARs in the rat supraoptic nucleus has an opposite action on glutamaterg
50 ocellular neurosecretory cells (MNCs) of the supraoptic nucleus has been attributed mainly to synapti
51 A1, CA2, and CA3 regions, the dentate gyrus, supraoptic nucleus, hypothalamus, and cortical layers II
52 burst firing in oxytocin (OT) neurons in the supraoptic nucleus in brain slices from lactating rats.
54 cordings from magnocellular cells of the rat supraoptic nucleus in vivo and in vitro and between oxyt
56 and the total number of GABA synapses in the supraoptic nucleus is substantially higher in lactating
57 opioid agonists primarily occurs within the supraoptic nucleus itself, since the antagonist naloxone
58 he highest levels of immunostaining were the supraoptic nucleus, magnocellular PVH, ARH, and suprachi
59 ime points, but not at 6 hours, included the supraoptic nucleus, magnocellular regions of the paraven
60 Here we analysed the discharge patterning of supraoptic nucleus neurones in vivo, to infer the charac
61 alamic slices did not affect the activity of supraoptic nucleus neurones or the strength of local syn
66 t both oxytocin and vasopressin cells in the supraoptic nucleus of normal rats respond to intravenous
67 ecretory cells (MNCs) were isolated from the supraoptic nucleus of rat hypothalamus, and properties o
68 (0.1-10.0 micrograms microliter-1) onto the supraoptic nucleus of rats made dependent by intracerebr
69 osecretory cells (MNCs) dissociated from the supraoptic nucleus of the adult guinea-pig were identifi
70 cation of N-methyl-D-aspartate (NMDA) to the supraoptic nucleus of the hypothalamus (SON) generates c
71 sopressin from magnocellular neurones in the supraoptic nucleus of the hypothalamus has important aut
76 ole-cell patch clamp recordings were made in supraoptic nucleus OT neurons in brain slices from male
77 isspeptin fibre density increases around the supraoptic nucleus over pregnancy and intracerebroventri
82 c area, bed nucleus of the stria terminalis, supraoptic nucleus, paraventricular nucleus, zona incert
83 organum vasculosum of the lamina terminalis, supraoptic nucleus, periaqueductal gray, and medial nucl
84 in select groups of nuclei (e.g., habenula, supraoptic nucleus, pontine nucleus) contained pronounce
85 measurements of SK channel subunits mRNA in supraoptic nucleus punches revealed a diminished express
87 benoxathian directly onto the surface of the supraoptic nucleus reduced the activity of oxytocin neur
88 The central nucleus of the amygdala and the supraoptic nucleus, regions that are involved in autonom
89 ular regions of the paraventricular nucleus, supraoptic nucleus, septohypothalamic nucleus, medial se
90 s, medial septum, and cortex, but not in the supraoptic nucleus, septohypothalamic nucleus, or organu
91 eurons in the paraventricular nucleus (PVN), supraoptic nucleus (SON) and accessory neurosecretory nu
92 d Fos-like immunoreactivity (Fos-LIR) in the supraoptic nucleus (SON) and paraventricular nucleus (PV
93 late AVP steady-state gene expression in the supraoptic nucleus (SON) and PVN, and/or CRF mRNA in the
94 logical functions of PRR were studied in the supraoptic nucleus (SON) because this brain region showe
96 (VP)-secreting magnocellular neurons of the supraoptic nucleus (SON) display calcium-dependent after
97 sured expression of the oxytocin gene in the supraoptic nucleus (SON) during pregnancy, parturition a
98 rosecretory cells (MNCs) of the hypothalamic supraoptic nucleus (SON) generate afterhyperpolarization
100 ministration of hypertonic saline to the rat supraoptic nucleus (SON) increases the expression of sev
101 ted in the paraventricular nucleus (PVN) and supraoptic nucleus (SON) is coordinated by the combined,
102 recordings were obtained from sixty-five rat supraoptic nucleus (SON) neurones in brain slices to inv
103 ole-cell patch recordings were obtained from supraoptic nucleus (SON) neurones in horizontal brain sl
105 ergic and excitatory glutamatergic inputs to supraoptic nucleus (SON) neurons can influence the relea
106 release pathway is activated by hypothalamic supraoptic nucleus (SON) neurons early in the torpor-aro
107 e appearance of Fos and Jun in the nuclei of supraoptic nucleus (SON) neurons following intraperitone
108 g direct olfactory (glutamatergic) inputs to supraoptic nucleus (SON) neurons increases interneuronal
110 nd adenosine receptors (AR) are expressed in supraoptic nucleus (SON) neurons, we postulated that con
113 ower subparaventricular zone, LSPV), and the supraoptic nucleus (SON) of grass rats (Arvicanthis nilo
114 in the paraventricular nucleus (PVN) and the supraoptic nucleus (SON) of the hypothalamus are activat
118 rom the suprachiasmatic nucleus (SCN) to the supraoptic nucleus (SON) of the hypothalamus were charac
119 was used to assess the relative responses of supraoptic nucleus (SON) oxytocin- (OX) and vasopressin-
120 the hypothalamic paraventricular nucleus and supraoptic nucleus (SON) respond to glucocorticoids by r
121 nvestigated in magnocellular neurones of rat supraoptic nucleus (SON) using whole-cell patch recordin
122 ion in the paraventricular nucleus (PVN) and supraoptic nucleus (SON) was evaluated by real time RT-P
123 nohistochemically identified neurones in the supraoptic nucleus (SON) was investigated in the hypotha
124 nearby forebrain cholinergic neurons to the supraoptic nucleus (SON) were used to study synaptic pot
125 lateral amygdaloid nucleus, 1.2-times in the supraoptic nucleus (SON), 1.6-times in the magnocellular
126 in areas receiving input from the SFO is the supraoptic nucleus (SON), a source of vasopressin synthe
127 f neurosecretory neurons in the hypothalamic supraoptic nucleus (SON), a well studied model of struct
128 ensin (Ang)-(1-7)-IR cells were found in the supraoptic nucleus (SON), and in the anterior (ap-), med
129 in 3 receptors (NK3-Rs) are expressed in the supraoptic nucleus (SON), and SON is innervated by subst
130 ral superfusion of 3 microM TTX into the rat supraoptic nucleus (SON), delivered with the use of a mi
131 ocellular neurosecretory system (MNS) of the supraoptic nucleus (SON), in which dendritic release of
132 duces structural changes in the hypothalamic supraoptic nucleus (SON), including increased glutamate
133 urons were particularly abundant in the PVN, supraoptic nucleus (SON), infundibular nucleus, and prem
134 rtion of the paraventricular nucleus (PVNp), supraoptic nucleus (SON), magnocellular PVN and suprachi
135 organum vasculosum lamina terminalis (OVLT), supraoptic nucleus (SON), magnocellular region of the pa
136 e measured in paraventricular nucleus (PVN), supraoptic nucleus (SON), median preoptic area (MePO), s
137 served in the paraventricular nucleus (PVN), supraoptic nucleus (SON), median preoptic nucleus (MnPO)
138 ular nucleus (PVN), subfornical organ (SFO), supraoptic nucleus (SON), nucleus accumbens (NAc) shell
139 hypothalamus, suprachiasmatic nucleus (SCN), supraoptic nucleus (SON), paraventricular nucleus (PVN),
140 significant Fos expression in neurons of the supraoptic nucleus (SON), paraventricular nucleus (PVN),
142 in the rat paraventricular nucleus (PVN) and supraoptic nucleus (SON), regions which lack ERalpha.
143 that VRACs are absent in neurons of the rat supraoptic nucleus (SON), suggesting that glial cells ar
144 ch as the paraventricular nucleus (PVH), the supraoptic nucleus (SON), the lateral hypothalamic area
145 ipRGCs also project to nuclei such as the supraoptic nucleus (SON), which is involved in systemic
157 nuates that of neurosecretory neurons in the supraoptic nucleus (SON; which secrete oxytocin and vaso
158 tify oxytocin neurons in the retrochiasmatic supraoptic nucleus (SOR(OXT)) and oxytocin-receptor-expr
159 gly stained, whereas in the hypothalamus the supraoptic nucleus stood out with strong immunoreactivit
160 ior paraventricular nucleus of the thalamus, supraoptic nucleus, subfornical organ, and paraventricul
161 eceptors (MC4Rs) are highly expressed in the supraoptic nucleus, suggesting that alpha-MSH and oxytoc
162 um, diagonal band, pallidum, preoptic areas, supraoptic nucleus, suprachiasmatic nucleus, paraventric
163 e prominently localized to astrocytes in the supraoptic nucleus, the neurons of which contain only sm
164 e anorectic TB rats, most prominently in the supraoptic nucleus, the parvocellular portion of the par
165 nterior and retrochiasmatic divisions of the supraoptic nucleus, the suprachiasmatic nucleus, the ven
166 lular neurosecretory cells (MNCs) in the rat supraoptic nucleus to different osmotic milieus by salt-
167 teral hypothalamus, paraventricular nucleus, supraoptic nucleus, ventromedial hypothalamus) and two h
169 that alpha-MSH induces Fos expression in the supraoptic nucleus when injected centrally and demonstra