ライフサイエンスコーパス: medial preoptic area

1 0, and 90 min after their infusions into the medial preoptic area.

2 gion of the paraventricular nucleus, and the medial preoptic area.

3 ), the nucleus of the diagonal band, and the medial preoptic area.

4 romedial nucleus of the hypothalamus and the medial preoptic area.

5 bed nucleus of the stria terminalis, and the medial preoptic area.

6 ates maternal defense via projections to the medial preoptic area.

7 duces a prolonged inhibitory activity in the medial preoptic area.

8 s behaviour through their projections to the medial preoptic area.

9 terior commissures, and more caudally at the medial preoptic area.

10 ely via activity of nitric oxide (NO) in the medial preoptic area.

11 GnRH injection were combined, but not in the medial preoptic area.

12 regions except for equivalent input from the medial preoptic area.

13 Deletion of Prlr specifically from the medial preoptic area, a brain region associated with mul

14 The medial preoptic area, a region that plays an important r

15 l Nissl-stained coronal sections through the medial preoptic area and anterior hypothalamus were exam

16 delayed leptin resistance development in the medial preoptic area and anteroventral periventricular n

17 companied by increased Fos expression in the medial preoptic area and arcuate nucleus--two reproducti

18 etic rats are increased kappa binding in the medial preoptic area and decreased mu binding in the lat

19 ypothalamus, irNPB cells were present in the medial preoptic area and nucleus, ventromedial preoptic

20 rboxylase (GAD) 65 mRNA was increased in the medial preoptic area and posteromedial bed nucleus of th

21 nt stress decreased GAD65 mRNA levels in the medial preoptic area and posteromedial BST of aged rats.

22 n of Cav3.1 and -3.2, but not Cav3.3, in the medial preoptic area and the arcuate nucleus.

23 ficantly higher specific IMEL binding in the medial preoptic area and the bed nucleus of the stria te

24 caudal to the nucleus, corresponding to the medial preoptic area and the dorsomedial hypothalamus, a

25 n progestin receptor-containing cells in the medial preoptic area and the ventromedial nucleus of the

26 ral hypothalamic and lateral preoptic areas, medial preoptic area, and certain other hypothalamic reg

27 ude the locus coeruleus, medial septal area, medial preoptic area, and substantia innominata.

28 r hypothalamic area, the posterior BNST, the medial preoptic area, and the dorsomedial hypothalamus.

29 bonding, such as ventromedial hypothalamus, medial preoptic area, and the medial amygdala, but that

30 ons encompassing the medial septal area, the medial preoptic area, and the substantia innominata.

31 araventricular area, periventricular nuclei, medial preoptic areas, and between the arcuate and ventr

32 the inferior olive, the retrochiasmatic and medial preoptic areas, and the thalamic posterior parave

33 D67 mRNA increases were only observed in the medial preoptic area, anterior BST, and hippocampus.

34 d paraventricular n), the rostral forebrain (medial preoptic area, anterior olfactory nucleus, island

35 of aromatase activity were found within the medial preoptic area/anterior hypothalamus, periventricu

36 , aromatase was significantly reduced in the medial preoptic area/anterior hypothalamus, periventricu

37 a proportion of pubertally born cells in the medial preoptic area, arcuate nucleus, and medial amygda

38 r, our data illuminate the importance of the medial preoptic area as a brain node which encodes a neg

39 -dependent labeling, we next pin-pointed the medial preoptic area as a brain region strongly activate

40 e nucleus, dorsomedial hypothalamic nucleus, medial preoptic area, bed nucleus of the stria terminali

41 a-expressing cells in the caudal part of the medial preoptic area (cMPOA(Esr1)) to the ventrolateral

42 After retrograde tracer injections in the medial preoptic area, dorsomedial and paraventricular hy

43 Because medial preoptic area galanin-expressing (MPOA(Gal)) neur

44 The medial preoptic area has been shown to be intricately in

45 ntobarbital, ethanol and adenosine, into the medial preoptic area has been shown to increase sleep, s

46 of glutamatergic neurons in the lateral and medial preoptic area increases wakefulness, challenging

47 ompanying paced mating behavior, whereas the medial preoptic area is a critical component of the neur

48 structures (bed nucleus of stria terminalis, medial preoptic area, lateral and ventromedial hypothala

49 Ralpha expression in the medial amygdala and medial preoptic area may fully mediate the effects of ge

50 ing the nucleus accumbens, ventral pallidum, medial preoptic area, medial amygdala, and the supraopti

51 First, neuronal labeling was found in the medial preoptic area, medial preoptic nucleus, median pr

52 retrograde tracing from the locus coeruleus, medial preoptic area, medial septal area, and substantia

53 ation between PnNOS and PIN was found in the medial preoptic area, medial septum, and cortex, and les

54 pression in both the preoptic area (POA) and medial preoptic area/medial bed nucleus of the stria ter

55 ricular nucleus, anterior hypothalamic area, medial preoptic area, median preoptic nucleus, anteroven

56 mediate female preference, and those to the medial preoptic area mediate male preference.

57 re implanted with a push-pull cannula in the medial preoptic area (MPA) and ovariectomized bilaterall

58 Despite the recent identification of medial preoptic area (MPA) as a key brain region to regu

59 Recent advances have revealed the medial preoptic area (MPA) as a key site for the regulat

60 ation in hypothalamus, and they may activate medial preoptic area (MPA) neurons in POA to induce hypo

61 ol, induce sleep when microinjected into the medial preoptic area (MPA) of the anterior hypothalamus.

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

63 o increase sleep when microinjected into the medial preoptic area (MPA) of the rat.

64 e nucleus (AN), median eminence (ME) and the medial preoptic area (MPA) were microdissected and analy

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

66 ed in the hypothalamic nuclei, including the medial preoptic area (MPO) and the suprachiasmatic nucle

67 s and FosB immunoreactivity increased in the medial preoptic area (MPO) and the ventral bed nucleus o

68 r) cells in the medial amygdala (AMYGme) and medial preoptic area (MPO) relative to males that cohabi

69 We have shown recently that the medial preoptic area (MPO) robustly innervates discrete

70 (VMHvl shell) and long-range input from the medial preoptic area (MPO) with functional coupling to n

71 ng within the medial preoptic nucleus (MPN), medial preoptic area (MPO), lateral hypothalamus (LH), c

72 e anteroventral periventricular nucleus, the medial preoptic area (MPO), specific subdivisions of the

73 nate (T) were bilaterally implanted into the medial preoptic area (MPO), the ventral tegmental area (

74 sed by antagonizing GABA(A) receptors in the medial preoptic area (MPO), which is thought to contain

75 Sex differences were observed in the caudal medial preoptic area (MPO), with significantly more FG+

76 pontine neurons excited by activation of the medial preoptic area (MPO).

77 of VPA on GnRH-GABA interactions within the medial preoptic area (mPOA) across pubertal development

78 Neurotoxic lesions involving the medial preoptic area (MPOA) and anterior hypothalamus (n

79 ses in ER-immunoreactivity were noted in the medial preoptic area (MPOA) and bed nucleus of the stria

80 egulation, and opioids and kisspeptin in the medial preoptic area (mPOA) and hypothalamic arcuate nuc

81 nt behavior through their projections to the medial preoptic area (MPOA) and promote dopamine release

82 es was to assess the regulatory roles of the medial preoptic area (MPOA) and the bed nucleus of the s

83 The medial preoptic nucleus (MPN) of the medial preoptic area (MPOA) and the medial amygdala are

84 the basal forebrain region encompassing the medial preoptic area (MPOA) and the substantia innominat

85 IEGs) c-fos, fos B, and egr-1 were mapped in medial preoptic area (MPOA) and ventral bed nucleus of s

86 ion of c-Fos and Fos B within neurons of the medial preoptic area (MPOA) and ventral bed nucleus of t

87 To determine whether the neurons of the medial preoptic area (MPOA) are necessary for pup-induce

88 Studies have emphasized the role of the medial preoptic area (MPOA) as an important site for the

89 n (I) balance, with increased E/I ratios, in medial preoptic area (MPOA) circuits, but through affect

90 This may be due in part to the impairment of medial preoptic area (MPOA) dopamine (DA) release.

91 Dopamine in the medial preoptic area (MPOA) facilitates copulation in ma

92 Increased dopamine (DA) in the medial preoptic area (MPOA) facilitates male sexual beha

93 Here we report that medial preoptic area (MPOA) GABAergic neurons mediate mu

94 Neuronal nitric oxide synthase (nNOS) in the medial preoptic area (MPOA) has been implicated in vario

95 ision of LS and in cingulate cortex (Cg) and medial preoptic area (MPOA) in female mice.

96 The role of the medial preoptic area (mPOA) in regulating female musk sh

97 Dopamine (DA) released from the medial preoptic area (MPOA) in response to a receptive f

98 controls) in both 2-DG and c-fos activity in medial preoptic area (MPOA) indicated an increase in its

99 r intralaminar thalamic nucleus (PIL) to the medial preoptic area (MPOA) involved in the control of s

100 rtant facilitative neurotransmitter, and the medial preoptic area (MPOA) is a critical integrative si

101 The medial preoptic area (MPOA) is a critical integrative si

102 The medial preoptic area (MPOA) is a critical regulatory sit

103 The medial preoptic area (mPOA) is a key site for the dopami

104 Finally, because the medial preoptic area (MPOA) is also important for matern

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

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

107 alanin (Gal)-expressing neurons in the mouse medial preoptic area (MPOA) is critical for pregnancy-in

108 ral the role of dopamine (DA) release in the medial preoptic area (mPOA) is for the activation of mal

109 Nitric oxide in the medial preoptic area (MPOA) is important for the express

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

111 signed to test the hypothesis that bilateral medial preoptic area (MPOA) lesions, which enhance the d

112 ed action potential frequency in neighboring medial preoptic area (mPOA) neurons and GABAA receptor-m

113 oinjecting PGE(2) (3 fmol/1 microl) into the medial preoptic area (mPOA) of conscious, unrestrained r

114 rior lateral hypothalamic area (LHAA) or the medial preoptic area (MPOA) of male rats after ejaculati

115 Dopamine (DA) is released in the medial preoptic area (MPOA) of male rats in the presence

116 extracellular DA levels were assessed in the medial preoptic area (MPOA) of ovariectomized female rat

117 The medial preoptic area (mPOA) of the hypothalamus is invol

118 ofiling of the arcuate nucleus (ARC) and the medial preoptic area (MPOA) of the mouse hypothalamus in

119 the effects of ibotenic acid lesions of the medial preoptic area (mPOA) on the display of partner pr

120 d the effect of ibotenic acid lesions of the medial preoptic area (mPOA) on the expression of a condi

121 olytic and ibotenic acid (IA) lesions of the medial preoptic area (MPOA) on the temporal pattern of f

122 terally (50 microg/0.5 microl/side) into the medial preoptic area (MPOA) or nucleus accumbens (NA), 2

123 or oestrogen receptor 1 (ESR1) in either the medial preoptic area (MPOA) or the ventromedial hypothal

124 er blockade of kappa-opioid receptors in the medial preoptic area (MPOA) prior to the critical period

125 subset of galanin-expressing neurons in the medial preoptic area (MPOA) that are specifically activa

126 nd oestrous state converge on neurons in the medial preoptic area (MPOA) to shape infant-directed beh

127 ity) in the extracellular compartment of the medial preoptic area (MPOA) using microdialysis.

128 ypothalamic nuclei that control mating(7-9) (medial preoptic area (MPOA)) and aggression(9-14) (ventr

129 d competing neural circuits(5,6), we use the medial preoptic area (MPOA), a key site for maternal beh

130 The medial preoptic area (mPOA), a region in the hypothalamu

131 The medial preoptic area (mPOA), an essential node for socia

132 pothalamus (LH), ventral tegmentum (VTA) and medial preoptic area (MPOA), and decreased FLI in the ha

133 Aromatization occurs in the medial preoptic area (MPOA), and this region is critical

134 T), injected either systemically or into the medial preoptic area (MPOA), facilitates ejaculation.

135 thalamus (VMH), medial tuberal region (mTu), medial preoptic area (mPOA), medial nucleus of the amygd

136 bed nucleus of the stria terminalis (BNST), medial preoptic area (MPOA), paraventricular nucleus (PV

137 , injected systemically or directly into the medial preoptic area (MPOA), reduces the ejaculatory thr

138 The medial preoptic area (MPOA), ventral pallidum (VP), and

139 terioventral periventricular nucleus (AVPV), medial preoptic area (MPOA), ventromedial nucleus (VMN),

140 DA receptors may contribute to mating is the medial preoptic area (MPOA), which is vital for male sex

141 e LBN-induced transcriptional changes in the medial preoptic area (mPOA), which underlies male reprod

142 les, dopamine is transiently released in the medial preoptic area (MPOA)-an area that is critical for

143 ponses in glutamatergic neurons of the mouse medial preoptic area (mPOA).

144 ranscriptional signatures that reside in the medial preoptic area (mPOA).

145 and GABAergic synaptic current decay in the medial preoptic area (mPOA).

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

147 la, bed nucleus of the stria terminalis, and medial preoptic area (MPOA).

148 ippocampus (areas important for memory), and medial preoptic area (mPOA, an area important in display

149 shown to express Fos in response to VCS (the medial preoptic area, MPOA; the ventrolateral portion of

150 lofen is a promising tool to explore whether medial preoptic area neurons interact with VTA neurons t

151 ly, we found that chemogenetic activation of medial preoptic area neurons that were active during the

152 in CART peptide distribution, including the medial preoptic area, nucleus accumbens, central amygdal

153 est in brain regions such as the lateral and medial preoptic areas, nucleus of the diagonal band, nuc

154 The medial preoptic area of the adult sheep contains an ovin

155 nd that bcl-2 and bax mRNA expression in the medial preoptic area of the developing lamb fetus decrea

156 thalamic nucleus that nonlinearly integrate medial preoptic area of the hypothalamus (MPOA) and mech

157 A-889425, on thermoregulatory neurons in the medial preoptic area of the hypothalamus (mPOA) of rats

158 Microdialysis experiments in the medial preoptic area of the hypothalamus showed that DVS

159 rachiasmatic nucleus, islands of Calleja and medial preoptic area, olfactory bulb, nucleus accumbens

160 bed nucleus of the stria terminalis and the medial preoptic area on the display of paced mating beha

161 microinjection of prostaglandin E2 into the medial preoptic area or by disinhibition of neurones in

162 stress pathways, such as the lateral septum, medial preoptic area or dorsomedial hypothalamus.

163 Infusing SHBG into the medial preoptic area or medial basal hypothalamus of fem

164 and extrahypothalamic regions, including the medial preoptic area, paraventricular nucleus, and bed n

165 PIN staining was present in neurons of the medial preoptic area, paraventricular nucleus, medial se

166 each region were heavily concentrated in the medial preoptic area, paraventricular thalamic nucleus,

167 ventricular thalamic nucleus), hypothalamus (medial preoptic area, perifornical, arcuate, dorsomedial

168 re found in forebrain regions, including the medial preoptic area, periventricular preoptic area, bed

169 In the medial preoptic area, periventricular regions, including

170 jection of PGE2 (200 pmol in 70 nl) into the medial preoptic area (POA) or microinjection of the GABA

171 n and the density of dendritic spines in the medial preoptic area (POA).

172 Medial and lateral septum (SM, SL), medial preoptic area (POM), and n. intercollicularis (IC

173 nisms and neural circuitry through which the medial preoptic area regulates this responsivity is desc

174 n in insular cortex, lateral septal nucleus, medial preoptic area, rostral linear nucleus, and in the

175 septum, bed nucleus of the stria terminalis, medial preoptic area, several hypothalamic nuclei, centr

176 In contrast, lesions of the medial preoptic area significantly lengthen contact-retu

177 y, hypothalamic paraventricular nucleus, and medial preoptic area, sites strongly implicated in the c

178 rior hypothalamic area, dorsomedial nucleus, medial preoptic area, suprachiasmatic nucleus, anterior

179 were detected in the parastrial nucleus, the medial preoptic area, the anterior hypothalamic area, th

180 leus (ARC), the paraventricular nucleus, the medial preoptic area, the lateral septum, and nucleus of

181 normal animals were examined, including the medial preoptic area, the lateral ventral septum, the ve

182 l nuclear group in the lateral aspect of the medial preoptic area, the magnocellular subdivision of t

183 r olfactory nucleus, the lateral septum, the medial preoptic area, the periventricular preoptic area,

184 infralimbic cortex, the lateral septum, the medial preoptic area, the subfornical organ, the paraven

185 s, the paraventricular thalamic nucleus, the medial preoptic area, the ventromedial, dorsomedial and

186 tion of the ventrolateral subdivision of the medial preoptic area ('thermoregulatory center'), and th

187 the mechanism via which estrogen acts in the medial preoptic area to prevent the display of female re

188 eriventricular nucleus of the preoptic area; medial preoptic area; ventral part of the bed nucleus of

189 tial c-fos induction was not observed in the medial preoptic area (ventrolateral quadrant), paraventr

190 noreactive (-ir) nuclei were observed in the medial preoptic area, ventromedial and arcuate hypothala

191 oreactive positive cells than females in the medial preoptic area, ventromedial nucleus of the hypoth

192 pressing less ERalpha-IR than females in the medial preoptic area, ventromedial nucleus, ventrolatera

193 terized population of neurons in the ventral medial preoptic area (VMPO) of the hypothalamus that are

194 nd excites downstream neurons in the ventral medial preoptic area (vMPO) that mediates body temperatu

195 of inhibitory and excitatory neurons in the medial preoptic area, we revealed that a subset of the n

196 behavior and elevated neural activity in the medial preoptic area, whereas sexual behavior remains no

197 ria terminalis and in the dorsal part of the medial preoptic area with projections to the CTFl were a