ライフサイエンスコーパス: ventromedial hypothalamus

1 -receptive neurons, primarily located in the ventromedial hypothalamus.

2 responsive neurons, primarily located in the ventromedial hypothalamus.

3 ed neurones contained in slices from the rat ventromedial hypothalamus.

4 labeled for both Fluoro-Gold and GABA in the ventromedial hypothalamus.

5 rcuate nucleus, paraventricular nucleus, and ventromedial hypothalamus.

6 and alpha7-nAChR binding in the lateral and ventromedial hypothalamus.

7 le) were found in both female groups only in ventromedial hypothalamus.

8 spectively, to a point of convergence in the ventromedial hypothalamus.

9 ent manner when infused bilaterally into the ventromedial hypothalamus.

10 (25%) and significantly lower uptake in the ventromedial hypothalamus (-20%) compared with females t

11 ng the perifornical hypothalamus (PFH; 30%), ventromedial hypothalamus (34%), paraventricular hypotha

12 atio(s) are: dorsomedial hypothalamus (9.3), ventromedial hypothalamus (4.9), superior colliculis (2.

13 We tested the hypothesis that the ventromedial hypothalamus, a key area in the integration

14 ion with FG neurons was most abundant in the ventromedial hypothalamus after anterior PVN FG injectio

15 ricular nucleus, between the dorsomedial and ventromedial hypothalamus and between the ventromedial a

16 , and decreased DAT sites in the lateral and ventromedial hypothalamus and dentate gyrus.

17 to the lateral hypothalamus projects to the ventromedial hypothalamus and its functions are mediated

18 rease in the mRNA level of Rfrp in the dorso/ventromedial hypothalamus and Kiss1, Pomc, and Somatosta

19 contrast, mice with collateral damage to the ventromedial hypothalamus and paraventricular nucleus sh

20 In this study we measured the size of the ventromedial hypothalamus and preoptic area-anterior hyp

21 nding to receptors in the arcuate nucleus or ventromedial hypothalamus and regulating release of prod

22 olves a GABAergic pathway originating in the ventromedial hypothalamus and which projects to the late

23 paraventricular nucleus, supraoptic nucleus, ventromedial hypothalamus) and two hindbrain sites (nucl

24 d in the regulation of energy balance (e.g., ventromedial hypothalamus), and stimulate SNS outflow to

25 gh densities of substance P receptors in the ventromedial hypothalamus, and (2) neurons that are posi

26 lateral preoptic area/anterior hypothalamus, ventromedial hypothalamus, and lateral hypothalamus.

27 leus, anteroventral periventricular nucleus, ventromedial hypothalamus, and posterodorsal medial amyg

28 g the retrochiasmatic area, arcuate nucleus, ventromedial hypothalamus, and tuber cinereum), and the

29 iatum, preoptic area, anterior hypothalamus, ventromedial hypothalamus, and ventral tegmental area.

30 iatum, preoptic area, anterior hypothalamus, ventromedial hypothalamus, and ventral tegmental area/su

31 xytocin neurons are found ectopically in the ventromedial hypothalamus, apparently no longer confined

32 ergic neurons that project to the medial and ventromedial hypothalamus are required for sympathoadren

33 Neurons in the ventromedial hypothalamus are thought to mediate counter

34 study, including the lateral septum and the ventromedial hypothalamus, are known to express high lev

35 that project from the medial amygdala to the ventromedial hypothalamus as demonstrated by retrograde

36 d showed CCK-B antagonist profile in the rat ventromedial hypothalamus assay with a Ke of 34 nM.

37 e number of nNOS-immunolabelled cells in the ventromedial hypothalamus compared to chow-fed controls.

38 cleus [PVN]) but not in the pituitary gland, ventromedial hypothalamus, dorsal hippocampus, ventral s

39 at glucose-receptive neurones within the rat ventromedial hypothalamus exhibit a KATP channel current

40 Nuclei within the ventromedial hypothalamus, extended amygdala and limbic

41 limbic core of the brain prevent starvation (ventromedial hypothalamus), heighten reward (ventral teg

42 REB signal in the paraventricular nuclei and ventromedial hypothalamus in comparison to rats fed ad l

43 e targeted to glucose-sensing neurons in the ventromedial hypothalamus in glucokinase-Cre mice, which

44 e in the volume of the preoptic area and the ventromedial hypothalamus in males, but not in females.

45 NMU is expressed in the ventromedial hypothalamus in the rat brain, and its leve

46 erminalis, medial preoptic area, lateral and ventromedial hypothalamus), in the central amygdala and

47 Thus, activation of protein kinase G in the ventromedial hypothalamus is necessary for the expressio

48 des, c-Fos immunoreactivity was increased in ventromedial hypothalamus, lateral hypothalamus, and par

49 d/magnocellular preoptic area, zona incerta, ventromedial hypothalamus, lateral mammillary nuclei, ve

50 teral hypothalamus (both posterior portion); ventromedial hypothalamus; lateral periaqueductal gray;

51 Therefore, the ventromedial hypothalamus may be a central site coordina

52 Therefore, glucose-responsive neurons in the ventromedial hypothalamus may play a role in the synchro

53 Neurons in the ventromedial hypothalamus mediate some counterregulatory

54 mented in regions regulating energy balance (ventromedial hypothalamus), neuroendocrine function (pre

55 In the present study, ventromedial hypothalamus neurons were identified on the

56 ver tones only in the lateral portion of the ventromedial hypothalamus, not in the rest of the networ

57 n the anterior hypothalamus of males, in the ventromedial hypothalamus of both males and females from

58 Glucose-inhibited neurons in the ventromedial hypothalamus of NIRKO mice displayed signif

59 of gold-thioglucose-sensitive neurons in the ventromedial hypothalamus prevent metabolic regulation o

60 -releasing factor receptor-2 agonist) to the ventromedial hypothalamus reduces the glucose counterreg

61 he same subnuclei of the medial amygdala and ventromedial hypothalamus, regions implicated in fear, a

62 livery of a potassium-channel blocker to the ventromedial hypothalamus reversed the effects of system

63 affect spine density in the dentate gyrus or ventromedial hypothalamus, suggesting specific effects o

64 nucleus, basolateral amygdala, hippocampus, ventromedial hypothalamus, superior colliculi, ventrolat

65 eoptic area, the lateral ventral septum, the ventromedial hypothalamus, the bed nucleus of the stria

66 parse in the septum and was prominent in the ventromedial hypothalamus, the caudal portion of the per

67 the amygdala, the anterior hypothalamus, the ventromedial hypothalamus, the premammillary nucleus, an

68 associated with attack was the path from the ventromedial hypothalamus through the ventral supraoptic

69 ts of substance P, that was infused into the ventromedial hypothalamus, upon predatory attack.

70 The ventromedial hypothalamus, ventrolateral area (VMHvl) wa

71 ot electrical, stimulation of neurons in the ventromedial hypothalamus, ventrolateral subdivision (VM

72 To assess the role of ventromedial hypothalamus (VMH) (arcuate plus ventromedi

73 tereotaxically into three brain regions--the ventromedial hypothalamus (VMH) (bilaterally, n = 6), th

74 Metabolic sensing neurons in the ventromedial hypothalamus (VMH) alter their activity whe

75 concentrations in the lateral hypothalamus, ventromedial hypothalamus (VMH) and suprachiasmatic nucl

76 responses to hypoglycemia is located in the ventromedial hypothalamus (VMH) and that local VMH gluco

77 The ventromedial hypothalamus (VMH) and the brain melanocort

78 The ventromedial hypothalamus (VMH) and the central melanoco

79 t specialized glucose-sensing neurons in the ventromedial hypothalamus (VMH) are able to detect falli

80 Noradrenergic and GABAergic systems in the ventromedial hypothalamus (VMH) are activated during hyp

81 itive K(+) channels (K(ATP) channels) in the ventromedial hypothalamus (VMH) are mediated by changes

82 Glucose-responsive neurons in the ventromedial hypothalamus (VMH) are stimulated when gluc

83 levels of H1R were seen in arcuate (Arc) and ventromedial hypothalamus (VMH) as well as the area post

84 of the role of CD36 in neuronal FA sensing, ventromedial hypothalamus (VMH) CD36 was depleted using

85 esponses seen were in part due to changes in ventromedial hypothalamus (VMH) exposure to insulin, bil

86 Given the similarities between islet and ventromedial hypothalamus (VMH) glucose sensing, we test

87 ic failure (HAAF) and impaired activation of ventromedial hypothalamus (VMH) glucose-inhibited (GI) n

88 The ventromedial hypothalamus (VMH) has been proposed to be

89 The activity of neurons in the ventromedial hypothalamus (VMH) important for initiating

90 P-activated protein kinase (AMPK) within the ventromedial hypothalamus (VMH) in glucose sensing durin

91 le of glutamatergic neurotransmission in the ventromedial hypothalamus (VMH) in response to hypoglyce

92 A5 receptor-ephrinA5 interactions within the ventromedial hypothalamus (VMH) influence counterregulat

93 The ventromedial hypothalamus (VMH) is a distinct morphologi

94 ession of GABAergic neurotransmission in the ventromedial hypothalamus (VMH) is crucial for full acti

95 nf promoter 1, and TrkB transcription in the ventromedial hypothalamus (VMH) of adult mice, consisten

96 er of PR-immunoreactive (PR-IR) cells in the ventromedial hypothalamus (VMH) of C57 and C57X129 mice

97 viously that selective BDNF depletion in the ventromedial hypothalamus (VMH) of mice resulted in hype

98 Electrolytic lesions placed in the ventromedial hypothalamus (VMH) of rats induce instant h

99 plays a role in hypoglycemia sensing in the ventromedial hypothalamus (VMH) of the Sprague-Dawley ra

100 n action, whether because of ablation of the ventromedial hypothalamus (VMH) or a loss-of-function mu

101 -expressing (SF-1-expressing) neurons in the ventromedial hypothalamus (VMH) play an important role i

102 The ventromedial hypothalamus (VMH) plays a central role in

103 Previous studies have demonstrated that the ventromedial hypothalamus (VMH) plays a critical role in

104 the sodium-glucose transporter SGLT1 in the ventromedial hypothalamus (VMH) plays a role in glucose

105 rone receptor (PR)-expressing neurons in the ventromedial hypothalamus (VMH) that are critical for ma

106 The ventromedial hypothalamus (VMH) was thought to be essent

107 that BDNF is expressed at high levels in the ventromedial hypothalamus (VMH) where its expression is

108 The ventromedial hypothalamus (VMH), a critical node in the

109 Norepinephrine is locally released into the ventromedial hypothalamus (VMH), a key brain glucose-sen

110 y rat that direct in vivo application to the ventromedial hypothalamus (VMH), a key glucose-sensing r

111 t from gamma-aminobutyric acid (GABA) in the ventromedial hypothalamus (VMH), a major glucose-sensing

112 , a brain region rich in CCKA receptors, the ventromedial hypothalamus (VMH), a region rich in CCKB r

113 total neuron number in the POA, AMY, and the ventromedial hypothalamus (VMH), a region typically invo

114 1 cell-surface expression in the BDNF mutant ventromedial hypothalamus (VMH), an energy balance-regul

115 nobutyric acid (GABA) inhibitory tone in the ventromedial hypothalamus (VMH), an important glucose-se

116 ation on cell proliferation in the amygdala, ventromedial hypothalamus (VMH), and dentate gyrus of th

117 rdosis behavior have been located within the ventromedial hypothalamus (VMH), and several hormone-res

118 Excitation of neurons in the ventromedial hypothalamus (VMH), especially those residi

119 ceptor immunoreactivity were examined in the ventromedial hypothalamus (VMH), medial tuberal region (

120 o effect on fever when administered into the ventromedial hypothalamus (VMH), organum vasculosum lami

121 regions included the arcuate nucleus (Arc), ventromedial hypothalamus (VMH), paraventricular nucleus

122 glucose-sensing region within the brain, the ventromedial hypothalamus (VMH), plays an important role

123 erone (P) on serotonin (5HT) overflow in the ventromedial hypothalamus (VMH), preoptic area (POA) and

124 ver longer periods of time, possibly via the ventromedial hypothalamus (VMH), to increase leptin sign

125 ulin-induced hypoglycemia is mediated by the ventromedial hypothalamus (VMH), which contains speciali

126 transmission in the rat arcuate nucleus and ventromedial hypothalamus (VMH).

127 xpressing neuronal population located in the ventromedial hypothalamus (VMH).

128 optic area, ventromedial amygdala (AMY), and ventromedial hypothalamus (VMH).

129 reciprocal pathways between the MAN and the ventromedial hypothalamus (VMH).

130 rminal differentiation of neurons within the ventromedial hypothalamus (VMH).

131 ressed in other sites as well, including the ventromedial hypothalamus (VMH).

132 trogen receptor alpha (ER alpha) mRNA in the ventromedial hypothalamus (VMH).

133 ypothalamic nucleus (VMN) neurons or primary ventromedial hypothalamus (VMH; VMN plus arcuate nucleus

134 The ventrolateral subdivision of the murine ventromedial hypothalamus (VMHvl) contains neurons whose

135 rons in the ventrolateral subdivision of the ventromedial hypothalamus (VMHvl) control mating and fig

136 that cells in the ventrolateral part of the ventromedial hypothalamus (VMHvl) that express estrogen

137 we found that the ventrolateral part of the ventromedial hypothalamus (VMHvl), an area with a known

138 in and around the ventrolateral part of the ventromedial hypothalamus (VMHvl)-a region required for

139 tion of the ventrolateral subdivision of the ventromedial hypothalamus (VMHvl).

140 Lesions of the ventromedial hypothalamus (VMN) depress lordosis but inc

141 n-induced increase in PPE mRNA levels in the ventromedial hypothalamus was diminished by coadministra

142 nsing of glucose-inhibitory neurons from the ventromedial hypothalamus was impaired in BG4KO mice.

143 CRF2 binding in the ventromedial hypothalamus was the same in juveniles, but

144 ) receptor binding in the lateral septum and ventromedial hypothalamus were increased.

145 hypothalamus and the dorsomedial half of the ventromedial hypothalamus, while GnRH neurons were obser

146 Male and female meadow voles differed in the ventromedial hypothalamus, with females expressing more