ライフサイエンスコーパス: preoptic

1 h the pituitary vasculature, suggesting that preoptic AgRP2 neurons are hypophysiotropic.

2 of PR-immunoreactivity (PRir) were found in preoptic and hypothalamic nuclei including the medial pr

3 Numerous BrdU+ cells were located around the preoptic and hypothalamic recesses and few around the th

4 from the PVN in the median preoptic nucleus; preoptic and lateral hypothalamic areas; arcuate, dorsom

5 Enrichment of CART 2 and 4 in the preoptic and tuberal areas emphasizes the importance of

6 both peptides, and dense ir-fibers innervate preoptic and ventral telencephalic nuclei homologous to

7 ocative of affiliative emotion induce septal-preoptic-anterior hypothalamic activity that cannot be e

8 and hypothalamic nuclei including the medial preoptic, anteroventral periventricular, arcuate, and ve

9 the ventrolateral subdivision of the medial preoptic area ('thermoregulatory center'), and the retic

10 ast, c-Fos was absent from the ventrolateral preoptic area (active during sleep).

11 ian preoptic nucleus (MnPO) and dorsolateral preoptic area (DLPO) and in the A7 noradrenergic cell gr

12 atures of AVT neurons in the gigantocellular preoptic area (gPOA) and axon varicosities within the ve

13 ith the highest density in the magnocellular preoptic area (MCPO).

14 in norepinephrine (NE) levels in the medial preoptic area (MPA) of the hypothalamus.

15 the stria terminals (BNST, 59%), and medial preoptic area (MPA, 53%).

16 he hypothalamic nuclei, including the medial preoptic area (MPO) and the suprachiasmatic nucleus (SCN

17 antagonizing GABA(A) receptors in the medial preoptic area (MPO), which is thought to contain neurons

18 fferences were observed in the caudal medial preoptic area (MPO), with significantly more FG+ cells o

19 on, and opioids and kisspeptin in the medial preoptic area (mPOA) and hypothalamic arcuate nucleus (A

20 udies have emphasized the role of the medial preoptic area (MPOA) as an important site for the regula

21 f LS and in cingulate cortex (Cg) and medial preoptic area (MPOA) in female mice.

22 The medial preoptic area (mPOA) is a key site for the dopaminergic

23 Finally, because the medial preoptic area (MPOA) is also important for maternal beha

24 The medial preoptic area (MPOA) is an integral site for male sexual

25 The medial preoptic area (MPOA) is critical for male sexual behavio

26 role of dopamine (DA) release in the medial preoptic area (mPOA) is for the activation of male sexua

27 Nitric oxide in the medial preoptic area (MPOA) is important for the expression and

28 While the medial preoptic area (MPOA) is known to be critical for materna

29 on potential frequency in neighboring medial preoptic area (mPOA) neurons and GABAA receptor-mediated

30 The medial preoptic area (mPOA) of the hypothalamus is involved in

31 ffect of ibotenic acid lesions of the medial preoptic area (mPOA) on the expression of a conditioned

32 of galanin-expressing neurons in the medial preoptic area (MPOA) that are specifically activated dur

33 The medial preoptic area (mPOA), a region in the hypothalamus, is a

34 The medial preoptic area (mPOA), an essential node for social behav

35 he dorsomedial hypothalamus (DMH) and median preoptic area (mPOA), both critical sites to regulate sy

36 cleus of the stria terminalis (BNST), medial preoptic area (MPOA), paraventricular nucleus (PVN), ant

37 ntral periventricular nucleus (AVPV), medial preoptic area (MPOA), ventromedial nucleus (VMN), and ar

38 ptors may contribute to mating is the medial preoptic area (MPOA), which is vital for male sexual beh

39 BAergic synaptic current decay in the medial preoptic area (mPOA).

40 LPH) and adjacent lateral part of the medial preoptic area (MPOA).

41 pus (areas important for memory), and medial preoptic area (mPOA, an area important in display of mat

42 escribed in adult fish as the neurosecretory preoptic area (NPO), this region has not been clearly de

43 t levels of aromatase expression in both the preoptic area (POA) and medial preoptic area/medial bed

44 activity in forebrain regions, including the preoptic area (POA) and ventromedial nucleus of the amyg

45 At a neuroanatomical level, the preoptic area (POA) and ventromedial nucleus of the hypo

46 The preoptic area (POA) controls body temperature by modulat

47 in the medial ganglionic eminence (MGE) and preoptic area (PoA) give rise to GABAergic inhibitory in

48 al steroids in the highly sexually dimorphic preoptic area (POA) is to reduce activity of DNA methylt

49 ntral part of the ventral telencephalon, the preoptic area (POA) of the hypothalamus and the ventral

50 In the present study, the preoptic area (POA) of the hypothalamus was investigated

51 m individual warm-sensitive neurons from the preoptic area (POA) of the hypothalamus, a region involv

52 sity did not differ between the sexes in the preoptic area (POA) or ventromedial nucleus of the amygd

53 The preoptic area (POA) regulates body temperature, but is n

54 n warm sensitive neurons of the hypothalamic preoptic area (POA) which play a critical role in the re

55 n from the skin to a median subregion of the preoptic area (POA), a thermoregulatory centre.

56 nown migratory stream that emanates from the preoptic area (POA), a ventral telencephalic domain adja

57 In the preoptic area (POA), estradiol aromatized from testoster

58 ductive social behavior in this species, the preoptic area (POA), the anterior hypothalamus (AH), sep

59 to the thermoregulatory command center, the preoptic area (POA).

60 he density of dendritic spines in the medial preoptic area (POA).

61 ir nuclear receptors in the hypothalamus and preoptic area (POA).

62 mammalian hippocampus), accumbens, anterior preoptic area (POA; homolog of the mammalian paraventric

63 Medial and lateral septum (SM, SL), medial preoptic area (POM), and n. intercollicularis (ICo) were

64 VT-ir neuronal features in the parvocellular preoptic area (pPOA) should have a negative relationship

65 he paraventricular nucleus (PVN) and rostral preoptic area (rPOA).

66 The sexually dimorphic nucleus of the preoptic area (SDN-POA) has received increased attention

67 sed in the sexually dimorphic nucleus of the preoptic area (SDN-POA), a nucleus in which apoptosis is

68 c input to the sleep-promoting ventrolateral preoptic area (VLPO) [1] arises from the lateral hypotha

69 ve neurons in the hypothalamic ventrolateral preoptic area (VLPO) and the wake-active monoaminergic b

70 ompared to the sleep-promoting ventrolateral preoptic area (VLPO), whereas green light produced great

71 ntral periventricular nucleus [AVPV], median preoptic area [MePO], and medial preoptic nucleus [MPN])

72 RESEARCH DESIGN AND The effect of preoptic area administration of insulin on CBT in mice w

73 O) was of interest because its levels in the preoptic area affect ejaculation, and it could synchroni

74 Suppression of ERalpha in the preoptic area almost completely abolished maternal care,

75 bitory stimulation of neurons in the lateral preoptic area and (2) by return of rats to an environmen

76 that outputs from the rdAcbSh to the lateral preoptic area and anterior and lateral hypothalamic area

77 leptin resistance development in the medial preoptic area and anteroventral periventricular nucleus,

78 the medial zone of the dorsal telencephalon, preoptic area and hypothalamus.

79 rosencephalic neuron groups were seen in the preoptic area and in rostral and caudal periventricular

80 eoptic area, especially in the ventrolateral preoptic area and median preoptic nucleus.

81 thalamic nuclei, including the ventrolateral preoptic area and median preoptic nucleus.

82 v3.1 and -3.2, but not Cav3.3, in the medial preoptic area and the arcuate nucleus.

83 Two brain regions are highlighted: the preoptic area and the cerebellum.

84 band of Broca (DBB), moderate levels in the preoptic area and the hypothalamic lateroanterior (LA),

85 sleep-promoting neurons in the ventrolateral preoptic area and the superior colliculus.

86 sleep-promoting neurons in the ventrolateral preoptic area and the superior colliculus.

87 nuclei, and some scattered cells lie in the preoptic area and ventral part of the ventral telencepha

88 entral medial ganglionic eminence and dorsal preoptic area based on fate mapping using an Shh-Cre all

89 ion, and optrode recording, we show that the preoptic area GABAergic neurons projecting to the tubero

90 The medial preoptic area has been shown to be intricately involved

91 pecific and not reflective of differences in preoptic area height or brain size.

92 impairment, indicating a crucial role of the preoptic area in sleep generation.

93 in magnocellular neurons of the hypothalamic preoptic area including those expressing vasopressin and

94 rginine-vasopressin (AVP) on the activity of preoptic area kisspeptin neurons.

95 expression in the medial amygdala and medial preoptic area may fully mediate the effects of genotype

96 ovide easy genetic access to sleep-promoting preoptic area neurons and a valuable entry point for dis

97 s a promising tool to explore whether medial preoptic area neurons interact with VTA neurons to contr

98 Stimulation of glutamatergic median preoptic area neurons produced a profound hypothermia du

99 ptor-alpha (ERalpha) protein is expressed in preoptic area neurons, and a very dense immunoreactive f

100 lence ERalpha expression specifically in the preoptic area of female mice and measured a variety of b

101 Instead, a connection of the bursa with the preoptic area of Martegiani or its extension, Cloquet's

102 ursa fused broadly with the extension of the preoptic area of Martegiani, namely Cloquet's canal, or

103 ulation of kisspeptin neurons appears in the preoptic area of only the male between E19 and P1.

104 The medial preoptic area of the adult sheep contains an ovine sexua

105 Thermoregulatory neurons in the preoptic area of the anterior hypothalamus (POA) form sy

106 t to be initiated via vagal afferents to the preoptic area of the anterior hypothalamus (POAH), an im

107 bcl-2 and bax mRNA expression in the medial preoptic area of the developing lamb fetus decreased dur

108 5, on thermoregulatory neurons in the medial preoptic area of the hypothalamus (mPOA) of rats while s

109 and other mammalian species, lesions in the preoptic area of the hypothalamus cause profound sleep i

110 Injection of insulin into the preoptic area of the hypothalamus induced a specific and

111 in the dorsal and ventral telencephalon, the preoptic area of the hypothalamus, and the lateral reces

112 observed in the olfactory bulb, pallium, and preoptic area of the telencephalon, and the subpallium i

113 the embryonic medial ganglionic eminence and preoptic area preferentially develop electrical, but not

114 nd neural circuitry through which the medial preoptic area regulates this responsivity is described.

115 The MS, DBB, and preoptic area showed overlaps between GABAergic and CB1-

116 Here we identify a population of preoptic area sleep neurons on the basis of their projec

117 expressed in a small group of neurons in the preoptic area that project directly towards the pituitar

118 POINTS: Glutamatergic neurons in the median preoptic area were stimulated using genetically targeted

119 calizes with isotocin-producing cells in the preoptic area, a critical node in the highly conserved v

120 bens, septum, substantia innominata, lateral preoptic area, and diagonal band nuclei of the basal for

121 us semicircularis); and (4) basal forebrain, preoptic area, and hypothalamic nuclei.

122 rs were distributed throughout the thalamus, preoptic area, and hypothalamus.

123 for E(2) signaling pathways in cells of the preoptic area, and it may thereby mediate E(2) negative

124 (medial septum, diagonal band, magnocellular preoptic area, and substantia innominata).

125 rons in the medial septum, the magnocellular preoptic area, and the substantia innominata.

126 ompassing the medial septal area, the medial preoptic area, and the substantia innominata.

127 an amygdalar complex, hippocampus, striatum, preoptic area, anterior hypothalamus, ventromedial hypot

128 an amygdalar complex, hippocampus, striatum, preoptic area, anterior hypothalamus, ventromedial hypot

129 rtion of pubertally born cells in the medial preoptic area, arcuate nucleus, and medial amygdala diff

130 ucleus of the hypothalamus, arcuate nucleus, preoptic area, bed nucleus of the stria terminalis, para

131 re consistently detected at the level of the preoptic area, but the main kiss2 mRNA-positive populati

132 substantia innominata (SI) and magnocellular preoptic area, but there was no innervation by the choli

133 erminal nerve, ventral telencephalon, caudal preoptic area, dorsal mesencephalic tegmentum, and rostr

134 factory bulbs, ventral telencephalon, caudal preoptic area, dorsal tegmentum and rostral rhombencepha

135 the existence of sleep-active neurons in the preoptic area, especially in the ventrolateral preoptic

136 t brain, the dorsal telencephalon, habenula, preoptic area, hypothalamus, and cerebellum.

137 Key neuroendocrine centers, like the preoptic area, hypothalamus, and pituitary, conspicuousl

138 e sbLPXRFa-ir cells profusely innervated the preoptic area, hypothalamus, optic tectum, semicircular

139 ssociated with AVT-ir neurons throughout the preoptic area, indicating the potential for functional i

140 dotropin-releasing hormone-II neurons in the preoptic area, IPe, arcuate nucleus of hypothalamus, and

141 mygdala, septal territories, medial pallium, preoptic area, lateral hypothalamus, thalamus, and preth

142 nucleus accumbens, ventral pallidum, medial preoptic area, medial amygdala, and the supraoptic nucle

143 o express Fos in response to VCS (the medial preoptic area, MPOA; the ventrolateral portion of the ve

144 arvocellular and magnocellular nuclei of the preoptic area, nucleus preglomerulosus, and posterior, v

145 us, paraventricular nucleus of the thalamus, preoptic area, paraventricular nucleus of the hypothalam

146 gion were heavily concentrated in the medial preoptic area, paraventricular thalamic nucleus, the sub

147 ular thalamic nucleus), hypothalamus (medial preoptic area, perifornical, arcuate, dorsomedial, paras

148 emales exhibited increased metabolism in the preoptic area, primary motor cortex, and the amygdala, a

149 on of the boundary between the telencephalic preoptic area, rich in Nkx2.1 expression, and the pretha

150 sular cortex, lateral septal nucleus, medial preoptic area, rostral linear nucleus, and in the Edinge

151 thalamic paraventricular nucleus, and medial preoptic area, sites strongly implicated in the control

152 ct to a subset of the regions, including the preoptic area, that are innervated by the PMv as a whole

153 bed nucleus of stria terminalis, the lateral preoptic area, the entopeduncular nucleus, and the later

154 RC), the paraventricular nucleus, the medial preoptic area, the lateral septum, and nucleus of the so

155 ar group in the lateral aspect of the medial preoptic area, the magnocellular subdivision of the medi

156 d in groups of neurons in the telencephalon, preoptic area, ventral hypothalamus, thalamus, and pitui

157 not in surrounding sites (thalamus, lateral preoptic area, ventral tegmental area, dorsomedial hypot

158 areas controlling reproductive behaviors-the preoptic area, ventromedial amygdala (AMY), and ventrome

159 nd anatomical deficiency in the diencephalic preoptic area, where the optic chiasm normally forms.

160 posterior ventricular nucleus of the caudal preoptic area, whereas LPXRFa-R-immunoreactive cells are

161 soma and near fiber-fiber appositions in the preoptic area.

162 paraventricular nucleus and the ventromedial preoptic area.

163 and in a dense fiber network throughout the preoptic area.

164 ivation of neurons in the medial part of the preoptic area.

165 to the thermoregulatory command center, the preoptic area.

166 ing the medial ganglionic eminence (MGE) and preoptic area.

167 throughout the hypothalamus and towards the preoptic area.

168 xpression in the hypothalamic neuroendocrine preoptic area.

169 vicinity of GnRH neurons within the rostral preoptic area.

170 alamic nucleus, the arcuate nucleus, and the preoptic area.

171 The preoptic area/anterior hypothalamus, a region that conta

172 n in both the preoptic area (POA) and medial preoptic area/medial bed nucleus of the stria terminalis

173 (LH), and ventrolateral, medial, and median preoptic areas (VLPO, MPA, and MnPO, respectively).

174 grade activation, that PB projections to the preoptic-basal forebrain and lateral hypothalamus, but n

175 ting the critical stimulatory role played by preoptic dopamine on male sexual behavior.

176 truder was not different between control and preoptic ERalpha-silenced mice, demonstrating the remark

177 Here we report peptidergic regulation of preoptic glutamatergic neurons that contributes to tempe

178 he prethalamic zona incerta group (A13), the preoptic groups (A15), and the pretectal group.

179 Our results identify the dorsal half of the preoptic-hypothalamic orthopedia a (otpa) domain as the

180 Circuits within the preoptic hypothalamus regulate temperature, with fine co

181 ify warm-sensitive neurons (WSNs) within the preoptic hypothalamus that orchestrate the homeostatic r

182 oth peptide and receptor are abundant in the preoptic hypothalamus.

183 sm that also involved glutamatergic input to preoptic Kiss1 neurons from Kiss1(ARH) neurons.

184 Whereas <25% of preoptic kisspeptin neurons expressed Cre in Vgat- and V

185 ng ovarian steroids as AVP no longer excited preoptic kisspeptin neurons in ovariectomized mice, an e

186 s found to permit circadian AVP signaling at preoptic kisspeptin neurons rather than dynamically modu

187 he electrical activity and [Ca(2+)]i of most preoptic kisspeptin neurons.

188 e forebrain, mainly to the ventral pallidum, preoptic-lateral hypothalamic continuum, and midline-int

189 Input from the ventral pallidal-lateral preoptic-lateral hypothalamus continuum is strong in the

190 nificantly increased GnRH secretion from the preoptic-mediobasal hypothalamus.

191 ced the spontaneous firing rate of GABAergic preoptic neurons by activating H3 subtype histamine rece

192 To investigate whether individual or common preoptic neurons project to the RMR and DMH/DHA, we inje

193 The activation of kisspeptin signaling in preoptic neurons promotes the activation of nNOS through

194 Reduction of ERalpha expression in preoptic neurons significantly decreased sexual behavior

195 ure by acting at two distinct populations of preoptic neurons that express H1 and H3 receptor subtype

196 re not mediated by ERalpha expression in the preoptic neurons we targeted, as ERalpha-suppressed mice

197 othalamus (DMH), and thence to ventrolateral preoptic nuclei (VLPO) and lateral hypothalamus (LHA).

198 ricular, dorsomedial, supraoptic, and median preoptic nuclei of hypothalamus.

199 ventral pallidum, lateral and magnocellular preoptic nuclei, lateral hypothalamus, and lateral haben

200 ng maternal aggression, including the medial preoptic nucleus (likely to represent an important locus

201 in a subset of neurons in the magnocellular preoptic nucleus (MCPO) and the horizontal limb of the d

202 losum laminae terminalis (OV) and the median preoptic nucleus (MEPO), where most of the somata of the

203 es of projections to the PF/LH is the median preoptic nucleus (MnPN) containing a sleep-active neuron

204 The median preoptic nucleus (MnPN) of the hypothalamus contains sle

205 Also, neurons in the median preoptic nucleus (MnPO) and dorsolateral preoptic area (

206 Neurons in the median preoptic nucleus (MnPO) and organum vasculosum of the la

207 f the third ventricle, containing the median preoptic nucleus (MnPO) and organum vasculosum of the la

208 veral lines of evidence implicate the median preoptic nucleus (MnPO) as a downstream site of activati

209 The median preoptic nucleus (MnPO) holds a strategic position in th

210 The median preoptic nucleus (MnPO) receives afferent input from the

211 Thermoregulatory neurons of the median preoptic nucleus (MnPO) represent a target at which hist

212 ABSTRACT: The median preoptic nucleus (MnPO) serves an important role in the

213 naptic to neurons projecting from the median preoptic nucleus (MnPO) to the dorsomedial hypothalamus.

214 nucleus of the hypothalamus (PVN) and median preoptic nucleus (MnPO), but not in the subfornical orga

215 m of the lamina terminalis (OVLT) and median preoptic nucleus (MnPO).

216 ersed by inhibition of neurons in the median preoptic nucleus (MnPO).

217 water deprivation in the hypothalamic median preoptic nucleus (MnPO).

218 ugh afferents to the thermoregulatory median preoptic nucleus (MnPO).

219 The magnocellular division of the medial Preoptic nucleus (MPN mag) plays a critical role in the

220 the magnocellular subdivision of the medial preoptic nucleus (MPN mag).

221 orylated PAK1 immunoreactivity in the medial preoptic nucleus (MPN) but not the arcuate nucleus.

222 occupies the central division of the medial preoptic nucleus (MPNc) and consists of a cluster of cel

223 ocalization in the medial part of the medial preoptic nucleus (MPNm), where half of the neurons that

224 f forebrain neurons-one in the posterodorsal preoptic nucleus (PdPN) and one in the lateral part of t

225 cur in a variety of mammals, with the medial preoptic nucleus (POM) and the ventromedial hypothalamic

226 for the opioid met-enkephalin in the medial preoptic nucleus (POM) correlates positively with undire

227 The sexually dimorphic medial preoptic nucleus (POM) in Japanese quail has for many ye

228 ser in several regions, including the medial preoptic nucleus (POM) in low singing males.

229 We show here that T implants in the medial preoptic nucleus (POM) of castrated male canaries (Serin

230 The medial preoptic nucleus (POM) regulates male sexual behavior, a

231 xual behavior, including in quail the medial preoptic nucleus (POM).

232 ke-active TMN and sleep-active ventrolateral preoptic nucleus (VLPO) are reciprocally connected, sugg

233 -active neurons located in the ventrolateral preoptic nucleus (VLPO) play a crucial role in the induc

234 Neurons of the ventrolateral preoptic nucleus (VLPO) promote sleep and VLPO loss prod

235 The sleep-promoting ventrolateral preoptic nucleus (VLPO) shares reciprocal inhibitory inp

236 onent of this circuitry is the ventrolateral preoptic nucleus (VLPO), a hypothalamic region containin

237 ated, at least in part, by the ventrolateral preoptic nucleus (VLPO), a key cell group for producing

238 e thought to be located in the ventrolateral preoptic nucleus (VLPO), which receives a dense histamin

239 ctivity in the sleep-promoting ventrolateral preoptic nucleus (VLPO).

240 sleep-promoting neurons in the ventrolateral preoptic nucleus (VLPO).

241 PV], median preoptic area [MePO], and medial preoptic nucleus [MPN]), at young (3 months), middle-age

242 rces of dynorphin input to the magnocellular preoptic nucleus and substantia innominata (MCPO/SI) in

243 the brain areas where in mammals the median preoptic nucleus and the medial amygdala are located.

244 that the EP3R-bearing neurons in the median preoptic nucleus are required for fever responses.

245 s, lesions of the hypothalamic ventrolateral preoptic nucleus cause fragmented sleep.

246 Histamine applied in the median preoptic nucleus induced a robust, long-lasting hyperthe

247 andin E synthase-1 (mPGES-1) into the median preoptic nucleus of fever-refractive mPGES-1 knock-out m

248 genetic deletion of the EP3Rs in the median preoptic nucleus of mice resulted in abrogation of the f

249 din E2 (PGE2) to EP3 receptors in the median preoptic nucleus of the hypothalamus, but the origin of

250 ve fibers were observed in the ventrolateral preoptic nucleus, a known sleep-related structure.

251 receptor (MOR) internalization in the medial preoptic nucleus, an important step for full expression

252 evels in specific cells of the hypothalamus, preoptic nucleus, and circumventricular organs.

253 sed in the RVLM, PVH, choroid plexus, median preoptic nucleus, and organosum vasculosum of the lamina

254 Castration reduced PRir in males' medial preoptic nucleus, anteroventral periventricular nucleus,

255 r olfactory nucleus, piriform cortex, median preoptic nucleus, basolateral amygdala, hippocampus, med

256 ofile, is the homologue of the ventrolateral preoptic nucleus, but physiological data in humans were

257 us (rPH), and to a lesser extent, the median preoptic nucleus, exhibited the highest numbers of retro

258 diol-induced activation of MOR in the medial preoptic nucleus, leading to female sexual receptivity.

259 nteroventral periventricular nucleus, medial preoptic nucleus, paraventricular nucleus, suprachiasmat

260 minantly in the posterior PVN; and 3) medial preoptic nucleus-derived inputs to the PVN are not gluta

261 related positively with pTH-ir in the medial preoptic nucleus.

262 n the ventrolateral preoptic area and median preoptic nucleus.

263 g the ventrolateral preoptic area and median preoptic nucleus.

264 n of POMC neurons that project to the medial preoptic nucleus.

265 reased c-Fos expression in the ventrolateral preoptic nucleus.

266 ing the human homologue of the ventrolateral preoptic nucleus.

267 cleus of the stria terminalis and the medial preoptic nucleus.

268 rogradely labeled from the PVN in the median preoptic nucleus; preoptic and lateral hypothalamic area

269 en lean and obese animals include the medial preoptic, paraventricular, and dorsomedial nuclei.

270 Kiss1 neurons were scattered throughout the preoptic periventricular areas (PV), but the vast majori

271 , Vv, Vc, and Vl, respectively]), as well as preoptic (PPa, PPp, and PM), pretectal (PPd, PPv, PCN, P

272 needed if sleep-regulatory mechanisms in the preoptic region are continuously modulated by the hormon

273 NOS or its pharmacological inhibition in the preoptic region blunted the stimulatory action of exogen

274 For histologically-confirmed bilateral preoptic region cannula placements (N=7), effects of T3

275 eral lateral ventricle cannulae or bilateral preoptic region cannulae, and were given 0.02% n-propyth

276 ures were seen in both lateral ventricle and preoptic region groups, but these effects did not intera

277 anteroventral periventricular nucleus of the preoptic region of the hypothalamus (AVPV) develops post

278 inated fertility by acting on neurons in the preoptic region of the hypothalamus and inducing the syn

279 nd microinjection including a T3 dose to the preoptic region or lateral ventricle.

280 injections of l-triiodothyronine (T3) to the preoptic region significantly influence EEG-defined slee

281 gaseous transmitter nitric oxide (NO) in the preoptic region to coordinate the progression of the ova

282 These effects of T3 microinjection to the preoptic region were demonstrated after acute injections

283 rsal thalamus, posterior tuberculum, and the preoptic region, and this corresponded with a higher spa

284 projections from the arcuate nucleus to the preoptic region, but it does not result in alterations i

285 express the kisspeptin receptor GPR54 in the preoptic region, but not in the tuberal region of the hy

286 ntral) regions, and limits dorsally with the preoptic region, caudally with the prethalamic eminence

287 a mRNA-containing cells were observed in the preoptic region, habenula, and hypothalamus, whereas the

288 s of different regions of the telencephalon, preoptic region, hypothalamus, and thalamus at all stage

289 cells in the olfactory bulb, telencephalon, preoptic region, hypothalamus, mesencephalon, and rhombe

290 striatopallidum, extended amygdala, septum, preoptic region, lateral, paraventricular and posterior

291 croinjection sites bilaterally placed in the preoptic region, slow-wave sleep time was significantly

292 (T3) to a sleep-regulatory brain region, the preoptic region, was examined in hypothyroid rats.

293 factory bulb, telencephalic hemispheres, and preoptic region.

294 unoreactive field of ERalpha is found in the preoptic region.

295 projections from the arcuate nucleus to the preoptic region.

296 ugh the activation of nNOS in neurons of the preoptic region.

297 eurotensinergic VTA afferents in the lateral preoptic-rostral lateral hypothalamic continuum (LPH) an

298 ade labeling suggests that telencephalic and preoptic sbLPXRFa cells might represent the source of pi

299 H/RFRP-3-immunoreactive fibres also abut the preoptic-septal gonadotropin-releasing hormone (GnRH) ne

300 n between the retrolental and premacular and preoptic spaces already existent in the eyes of young ad