ライフサイエンスコーパス: preoptic nucleus

1 leus of the diagonal band, and magnocellular preoptic nucleus.

2 gnature of estrogen activation of the medial preoptic nucleus.

3 n the ventrolateral preoptic area and median preoptic nucleus.

4 found in many hypothalamic nuclei including preoptic nucleus.

5 Neurons in these areas project to the medial preoptic nucleus.

6 sleep-promoting neurons of the ventrolateral preoptic nucleus.

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

8 ing the human homologue of the ventrolateral preoptic nucleus.

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

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

11 g the ventrolateral preoptic area and median preoptic nucleus.

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

13 entrolateral preoptic area and dorsal median preoptic nucleus.

14 RPP-32 immunoreactivity by 92% in the medial preoptic nucleus, 134% in the caudal ventromedial hypoth

15 Sniffer cells placed on the median preoptic nucleus (a presumptive site of angiotensin rele

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

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

18 ERalphaKO mouse brain regions including the preoptic nucleus and arcuate nucleus of the hypothalamus

19 Ucn III neurons were observed in the median preoptic nucleus and in the rostral perifornical area la

20 the lamina terminalis (containing the median preoptic nucleus and organum vasculosum of the lamina te

21 ression in the central portion of the medial preoptic nucleus and posterodorsal medial amygdala at PN

22 at at least 30% of the neurons in the median preoptic nucleus and subfornical organ and 14% of the ne

23 a direct input from the osmosensitive median preoptic nucleus and subfornical organ and from the fusi

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

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

26 late motivation and reward (i.e., the medial preoptic nucleus and ventral tegmental area) related pos

27 id regulation of OFQ/N and NOP in the medial preoptic nucleus and VMH is consistent with emerging dat

28 jection to the sleep-promoting ventrolateral preoptic nucleus, and a mainly glutamate-thyrotropin-rel

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

30 eoptic area, medial preoptic nucleus, median preoptic nucleus, and lateral preoptic area, and then it

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

32 bed nucleus of stria terminalis, left medial preoptic nucleus, and right tubero-mammillary hypothalam

33 he ventromedial preoptic nucleus, the median preoptic nucleus, and the paraventricular hypothalamic n

34 rs included the ventromedial nucleus, medial preoptic nucleus, and ventral premammillary nucleus.

35 ntral periventricular nucleus (AVPV), median preoptic nucleus, and VMH.

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

37 othalamic area, medial preoptic area, median preoptic nucleus, anteroventral periventricular nucleus,

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

39 athetic pathway appears to target the medial preoptic nucleus as its key nodal point, receiving input

40 in (DAMGO) or endomorphin-1, into the medial preoptic nucleus attenuated lordosis, and their effects

41 fibers in the anteroventral periventricular preoptic nucleus (AVPV) and the central and medial divis

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

43 ing neurons were most abundant in the medial preoptic nucleus, bed nucleus of the stria terminalis, a

44 rons in multiple sites, including the medial preoptic nucleus, bed nucleus of the stria terminalis, a

45 ion; after small lesions of the ventromedial preoptic nucleus, body temperature showed normal circadi

46 A expression was only seen within the median preoptic nucleus but Fos-IR showed little coexpression w

47 uced expression of NOP mRNA in VMH or median preoptic nucleus but reduced expression in the AVPV.

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

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

50 In the medial preoptic nucleus (central aspect) and ventromedial nucle

51 The ventrolateral preoptic nucleus contains GABAergic and galaninergic neu

52 icular nucleus; reproductive: lateral medial preoptic nucleus; defensive: anterior hypothalamic nucle

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

54 medial and lateral preoptic areas and medial preoptic nucleus), diencephalon (viz., subincertal nucle

55 rminalis, ventral aspect (INSTv), the medial preoptic nucleus, dorsomedial aspect (MPNdm) and the ven

56 e, whereas, in the medial part of the medial preoptic nucleus, estrogen and progesterone were needed

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

58 imary somatosensory cortex and magnocellular preoptic nucleus increased on the IL1beta-injected side.

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

60 ensory-related (subfornical organ and median preoptic nucleus, involved in initiating drinking behavi

61 om hypothalamic regions including the median preoptic nucleus, lateral hypothalamic area, and dorsome

62 in the lateral septal nucleus, ventromedial preoptic nucleus, lateral hypothalamus, perifornical are

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

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

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

66 of day or day of estrous cycle in the medial preoptic nucleus, median eminence, ventromedial nucleus,

67 as found in the medial preoptic area, medial preoptic nucleus, median preoptic nucleus, and lateral p

68 The median preoptic nucleus (MePO) has been suggested to be an impo

69 SFO), organum vasculosum (OV) and the median preoptic nucleus (MePO)) and in the hypothalamus, have b

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

71 The median preoptic nucleus (MnPN) and the ventral lateral preoptic

72 Neurones in the median preoptic nucleus (MnPN) and the ventrolateral preoptic a

73 The median preoptic nucleus (MnPN) and the ventrolateral preoptic a

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

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

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

77 Fos immunoreactivity was found in the median preoptic nucleus (MnPN).

78 receptors expressed by neurons in the median preoptic nucleus (MnPO(EP3R) neurons).

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

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

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

82 te neuronal subpopulations within the median preoptic nucleus (MnPO) and ventrolateral preoptic nucle

83 of the lamina terminalis (OVLT), the median preoptic nucleus (MnPO) and/or the subfornical organ (SF

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

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

86 The median preoptic nucleus (MnPo) is critical for normal fluid bal

87 ( c) Dehydration is aversive, and median preoptic nucleus (MnPO) neuron activity is proportional

88 r (EP3R) marks a unique population of median preoptic nucleus (MnPO) neurons that are required for bo

89 Previous studies suggest that the median preoptic nucleus (MnPO) of the hypothalamus plays an imp

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

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

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

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

94 ne whether individual neurones of the median preoptic nucleus (MnPO) with axonal projections to the h

95 leus (PVN), supraoptic nucleus (SON), median preoptic nucleus (MnPO), anterior hypothalamus (AH) and

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

97 osum of the lamina terminalis (OVLT), median preoptic nucleus (MNPO), hypothalamic paraventricular nu

98 sions of the subfornical organ (SFO), median preoptic nucleus (MnPO), lateral preoptic area (LPO), or

99 icular nucleus of the thalamus (PVA), median preoptic nucleus (MnPO), periventricular nucleus (Pe), c

100 osum of the lamina terminalis (OVLT), medial preoptic nucleus (MNPO), subfornical organ (SFO), suprao

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

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

103 gulated by the neurons located in the median preoptic nucleus (MnPO).

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

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

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

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

108 The medial preoptic nucleus (MPN) and ventrolateral part of the ven

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

110 The medial preoptic nucleus (MPN) of the medial preoptic area (MPOA

111 receptor (PR) immunoreactivity in the medial preoptic nucleus (MPN) of the rat brain is due to the in

112 ition altered c-Fos expression in the medial preoptic nucleus (MPN) or the arcuate nucleus (ARH).

113 We then compared the medial preoptic nucleus (MPN) within the MPA of Etruscan shrew

114 ntral periventricular nucleus (AVPV), medial preoptic nucleus (MPN), arcuate nucleus (ARH), and ventr

115 hat a select subset of neurons in the medial preoptic nucleus (MPN), lateral hypothalamic area (LHA),

116 r levels of V(1a)R binding within the medial preoptic nucleus (MPN), medial preoptic area (MPO), late

117 ir were colocalized in neurons of the medial preoptic nucleus (MPN), the dorsal medial amygdala (dMEA

118 ression induced by dehydration in the median preoptic nucleus (MPN), the supraoptic and paraventricul

119 ol column (RBCC), which comprises the medial preoptic nucleus (MPN), the ventrolateral part of the ve

120 s of the stria terminalis (BNST), the medial preoptic nucleus (MPN), the ventromedial nucleus (VMN),

121 ventromedial hypothalamus (VMHvl) and medial-preoptic nucleus (MPN), we test whether CART-signalling

122 of mu-opioid receptors (MORs), in the medial preoptic nucleus (MPN).

123 munoreactive (bNOS-ir) neurons in the medial preoptic nucleus (MPN).

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

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

126 SDN-POA, the central division of the medial preoptic nucleus (MPNc), over the first 13 days postnata

127 e central and medial divisions of the medial preoptic nucleus (MPNc, MPNm, respectively) revealed uni

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

129 state and with opioid markers in the medial preoptic nucleus (mPOA).

130 ate the magnocellular division of the medial preoptic nucleus of castrates.

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

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

133 Stimulation of the medial preoptic nucleus of the hypothalamus (MPO) has been show

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

135 xual interaction with a female in the medial preoptic nucleus only, while visual access to a female l

136 areas included the subfornical organ, median preoptic nucleus, organum vasculosum of the lamina termi

137 tricular nucleus of the hypothalamus, median preoptic nucleus, organum vasculosum of the lamina termi

138 bed nucleus of the stria terminalis, medial preoptic nucleus, paraventricular nucleus, medial amygda

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

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

141 The posterodorsal preoptic nucleus (PdPN) and the lateral part of the post

142 l medial amygdala (MeApd), the posterodorsal preoptic nucleus (PdPN), and the medial cell group of th

143 ed with ejaculation, i.e., the posterodorsal preoptic nucleus (PdPN), the lateral part of the postero

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

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

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

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

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

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

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

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

152 dial preoptic area and nucleus, ventromedial preoptic nucleus, retrochiasmatic nucleus, paraventricul

153 ens, FS, substantia innominata/magnocellular preoptic nucleus (SI/MA), and bed nucleus of the stria t

154 eurons accumulating Fluorogold in the median preoptic nucleus, subfornical organ, and the fusiform nu

155 t and functional projections from the median preoptic nucleus, subfornical organ, and the fusiform nu

156 s within the AV3V region (the ventral median preoptic nucleus) suppressed water intake following 24 h

157 ar paraventricular nucleus, arcuate nucleus, preoptic nucleus, suprachiasmatic nucleus).

158 is, paraventricular hypothalamus, and median preoptic nucleus than did rats fed either mid- or high-N

159 zed neuronal populations in the hypothalamic preoptic nucleus that are activated during either social

160 subunit mRNA included the septum, the median preoptic nucleus, the anteroventral periventricular nucl

161 kg), Fos-IR was observed in the ventromedial preoptic nucleus, the median preoptic nucleus, and the p

162 24 hr after estrogen treatment in the medial preoptic nucleus, the principal part of the bed nucleus,

163 -positive cells was identified in the medial preoptic nucleus, the suprachiasmatic nucleus, and the s

164 d cAMP concentrations in the SCN and rostral preoptic nucleus throughout the day in young and middle-

165 of the magnocellular division of the medial preoptic nucleus to pheromones.

166 trol (subparaventricular zone, ventrolateral preoptic nucleus, tuberomammillary nucleus, supramammill

167 bed nucleus of the stria terminalis, medial preoptic nucleus, ventrolateral portion of the ventromed

168 he visceromotor (infralimbic) cortex, median preoptic nucleus, ventromedial preoptic area, bed nucleu

169 masking, and the sleep-active ventrolateral preoptic nucleus (VLPO) and determined the subsets of me

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

171 -positive during sleep) in the ventrolateral preoptic nucleus (VLPO) decreases non-rapid eye movement

172 Neurons in the ventrolateral preoptic nucleus (VLPO) in rats show c-fos activation af

173 rats where the sleep-promoting ventrolateral preoptic nucleus (VLPO) is lesioned (male Sprague-Dawley

174 an preoptic nucleus (MnPO) and ventrolateral preoptic nucleus (VLPO) of the hypothalamus would modula

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

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

177 at sleep-active neurons in the ventrolateral preoptic nucleus (VLPO) provide a major input to the TMN

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

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

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

181 , we examined afferents to the ventrolateral preoptic nucleus (VLPO), an area critically implicated i

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

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

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

185 that induce sleep such as the ventrolateral preoptic nucleus (VLPO).

186 expression in sites such as the ventromedial preoptic nucleus (VMPO) and the hypothalamic paraventric

187 A projection from the BSTp to the medial preoptic nucleus was also weaker in females but was much

188 he stria terminalis (BNST) and to the medial preoptic nucleus, whereas MeA projects to adjacent subnu

189 The second includes neurons in the preoptic nucleus, which send long-range projections to t