ライフサイエンスコーパス: subfornical organ

1 proinflammatory cytokine IL-1beta within the subfornical organ.

2 ctivity (with a peak at 7 days) in the mouse subfornical organ.

3 hypothalamic paraventricular nucleus and the subfornical organ.

4 electrical or optogenetic stimulation of the subfornical organ.

5 ity was sparse like in the area postrema and subfornical organ.

6 strocytes, but was present in neurons in the subfornical organ.

7 glial markers displayed similarities to the subfornical organ.

8 lei, amygdaloid complex, piriform cortex and subfornical organ.

9 in the ventromedial hypothalamic nucleus and subfornical organ.

10 id and mineral homeostasis, most notably the subfornical organ.

11 leus (MnPO) receives afferent input from the subfornical organ, a circumventricular organ that has be

12 e neurons in the median preoptic nucleus and subfornical organ and 14% of the neurons in the fusiform

13 reases AT(1) binding in brain areas outside (subfornical organ and area postrema) and inside (paraven

14 f circulating origin has ready access to the subfornical organ and area postrema, where it can bind t

15 he osmosensitive median preoptic nucleus and subfornical organ and from the fusiform nucleus of the b

16 , including regions of the brain such as the subfornical organ and hypothalamus, could potentially us

17 vasculosum of the lamina terminalis and the subfornical organ and increased Fos-ir in the lateral pa

18 general categories: humeral sensory-related (subfornical organ and median preoptic nucleus, involved

19 The subfornical organ and organum vasculosum lamina terminal

20 ng binding of angiotensin II (ANG II) at the subfornical organ and organum vasculosum of the lamina t

21 omotes acute satiation of thirst through the subfornical organ and other downstream targets.

22 (1) receptor expression was increased in the subfornical organ and periventricular nucleus of the hyp

23 binding and mRNA expression not only in the subfornical organ and the median eminence, situated outs

24 ayer of the olfactory bulb, medial habenula, subfornical organ, and area postrema.

25 nucleus of the thalamus, supraoptic nucleus, subfornical organ, and paraventricular hypothalamic nucl

26 eral septum, nucleus of the stria terminals, subfornical organ, and periaqueductal gray.

27 paraventricular nucleus of the hypothalamus, subfornical organ, and the area postrema.

28 g Fluorogold in the median preoptic nucleus, subfornical organ, and the fusiform nucleus were all sig

29 rojections from the median preoptic nucleus, subfornical organ, and the fusiform nucleus.

30 ventricular nucleus of the hypothalamus, the subfornical organ, and the organum vasculosum of the lam

31 t, Y1-R mRNA expression was also seen in the subfornical organ, anterior hypothalamic area, dorsal hy

32 The subfornical organ, dorsal hypothalamic, perifornical, an

33 Stimulation of glutamatergic neurons in the subfornical organ drives drinking behavior, but the brai

34 We show that optogenetic activation of subfornical organ excitatory neurons, marked by the expr

35 is-particularly glutamatergic neurons of the subfornical organ expressing CaMKIIa (SFO(CaMKIIa)).

36 data suggest that ACE2 overexpression in the subfornical organ impairs Ang II-mediated pressor and dr

37 ypothesize that glutamatergic neurons in the subfornical organ in lamina terminalis continuously comp

38 appetite of angiotensin II generated in the subfornical organ in the brain.

39 ngs altered along the vessels such as in the subfornical organ indicating altering gliovascular relat

40 tarius, and circumventricular organs such as subfornical organ, median eminence, and area postrema.

41 ventricular organs including choroid plexus, subfornical organ, median eminence, and area postrema.

42 The most intensely labeled CVOs include the subfornical organ, median eminence, area postrema and ch

43 These areas included the subfornical organ, median preoptic nucleus, organum vasc

44 We show that thirst-promoting subfornical organ neurons are negatively reinforcing and

45 CO2-evoked neuronal firing in patch-clamped subfornical organ neurons was dependent on acid sensor T

46 ntrast, activation of a second population of subfornical organ neurons, marked by expression of the v

47 ular regions), rostral forebrain structures (subfornical organ, organum vasculosum of the lamina term

48 oughout the CNS, including areas such as the subfornical organ, pineal gland, neurohypophysis, and hy

49 Recently, ATII-responsive neurons in the subfornical organ (SFO) and aldosterone-sensitive neuron

50 emide-treated rats showed Fos-IR in both the subfornical organ (SFO) and around the organum vasculosu

51 The subfornical organ (SFO) and the area postrema (AP), two

52 the mesencephalic trigeminal nucleus (meV), subfornical organ (SFO) and the external lateral parabra

53 The subfornical organ (SFO) and the organum vasculosum lamin

54 sculosum of the lamina terminalis (OVLT) and subfornical organ (SFO) became infected.

55 The subfornical organ (SFO) has been suggested to be importa

56 ted that angiotensinergic stimulation in the subfornical organ (SFO) has effects on the anterior thir

57 -devoid sensory circumventricular organ, the subfornical organ (SFO) in CO(2)-evoked fear.

58 Here we reveal an unexpected role for the subfornical organ (SFO) in the anticipatory regulation o

59 The subfornical organ (SFO) is a circumventricular organ rec

60 The subfornical organ (SFO) is a forebrain structure that co

61 The subfornical organ (SFO) of the brain has long been consi

62 Here we show that the subfornical organ (SFO) of the brain is a nucleus for pa

63 of angiotensin Type 1 (AT1) receptors in the subfornical organ (SFO) on this effect.

64 lamic nucleus (PVH), peri-subfornical organ, subfornical organ (SFO) or hippocampus (dentate gyrus an

65 tions in O2*- production specifically in the subfornical organ (SFO), a brain region lying outside th

66 This study examined the hypothesis that the subfornical organ (SFO), a circumventricular organ with

67 gical abnormalities in the circumventricular subfornical organ (SFO), a region outside the blood-brai

68 c paraventricular and supraoptic nuclei, the subfornical organ (SFO), and the organum vasculosum of t

69 anum vasculosum lamina terminalis (OVLT) and subfornical organ (SFO), are potential sites that could

70 lis, including organum vasculosum (OVLT) and subfornical organ (SFO), as well as in the magnocellular

71 V3V), paraventricular hypothalamus (PVN) and subfornical organ (SFO), but unchanged in anterior pitui

72 Renin induced Fos-ir in the subfornical organ (SFO), median preoptic (MnPO), supraop

73 thors examined the effects of lesions of the subfornical organ (SFO), median preoptic nucleus (MnPO),

74 hypertension, free radical signaling in the subfornical organ (SFO), one of the forebrain circumvent

75 d along the lamina terminalis (LT) (i.e. the subfornical organ (SFO), organum vasculosum (OV) and the

76 Fos-positive cells than control rats in the subfornical organ (SFO), organum vasculosum lamina termi

77 cell nuclei than vehicle-treated rats in the subfornical organ (SFO), organum vasculosum lamina termi

78 nucleus (SON), median preoptic area (MePO), subfornical organ (SFO), organum vasculosum of the lamin

79 alis (OVLT), medial preoptic nucleus (MNPO), subfornical organ (SFO), supraoptic (SON) and paraventri

80 tified in the paraventricular nucleus (PVN), subfornical organ (SFO), supraoptic nucleus (SON), nucle

81 mic ANGII mediates stress responding via the subfornical organ (SFO), we first found that the timing

82 dian preoptic nucleus (MnPO), but not in the subfornical organ (SFO).

83 munoreactivity was markedly increased in the subfornical organ (SFO).

84 ut did not influence c-fos expression in the subfornical organ (SFO).

85 ts with intact brains or with lesions of the subfornical organ (SFO).

86 paraventricular (PVN) nuclei, but not in the subfornical organ (SFO).

87 he median preoptic nucleus (MnPO) and/or the subfornical organ (SFO); are required for the developmen

88 ventricular hypothalamic nucleus (PVH), peri-subfornical organ, subfornical organ (SFO) or hippocampu

89 are much more extensive than those from the subfornical organ, suggesting that the MnPO/OVLT serves

90 Furthermore, subfornical organ-targeted ACE2 overexpression dramatica

91 etically separable neural populations in the subfornical organ that trigger or suppress thirst.

92 In the CVOs, DEPTOR was expressed in the subfornical organ, the median eminence, and the area pos

93 ject detectably to Barrington's nucleus, the subfornical organ, the median preoptic and parastrial nu

94 ay structures such as the area postrema, the subfornical organ, the paraventricular hypothalamic nucl

95 ateral septum, the medial preoptic area, the subfornical organ, the paraventricular thalamus, the sub

96 ns that contain neuronal elements, i.e., the subfornical organ, the vascular organ of the lamina term

97 to AT(1) receptors in the pituitary and the subfornical organ was measured following estrogen treatm