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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

136 In the medial preoptic area, periventricular regions, including

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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