ライフサイエンスコーパス: mediobasal

1 The mediobasal hypothalami from adult male rats were incubat

2 or hypothalamic-retrochiasmatic area and the mediobasal hypothalamic arcuate nucleus independently ge

3 alamus, estradiol increases spine density in mediobasal hypothalamic nuclei that regulate reproductio

4 e PERIOD2::LUCIFERASE (PER2::LUC) rhythms in mediobasal hypothalamic nuclei, which influence these be

5 nar thalamic nuclei, the supramammillary and mediobasal hypothalamic nuclei.

6 Ex vivo biochemical studies of mediobasal hypothalamic tissue revealed that insulin sti

7 obesity and diabetes, and downregulation of mediobasal hypothalamic TXNIP expression prevents diet-i

8 Thus, mediobasal hypothalamic TXNIP plays a critical role in n

9 f thyrotropin-releasing hormone (TRH) in the mediobasal hypothalamus (MBH) and thyroid-stimulating ho

10 The mediobasal hypothalamus (MBH) contains neurons capable o

11 In response to nutrient stimuli, the mediobasal hypothalamus (MBH) drives multiple neuroendoc

12 diet stimulates microglial reactivity in the mediobasal hypothalamus (MBH) in association with decrea

13 receptors located more ventrally within the mediobasal hypothalamus (MBH) may inhibit the behavior o

14 In the current study, we examined the mediobasal hypothalamus (MBH) of 57 obese human subjects

15 xamine extracellular serotonin (5-HT) in the mediobasal hypothalamus (MBH) of male and female Fischer

16 Here we show that leptin infused into the mediobasal hypothalamus (MBH) of rats inhibits white adi

17 Previous studies on the mediobasal hypothalamus (MBH) of rats, rhesus monkeys an

18 Because the arcuate nucleus in the mediobasal hypothalamus (MBH) plays a pivotal role in in

19 we demonstrate that Socs3 deficiency in the mediobasal hypothalamus (MBH) reduces food intake, prote

20 The metabolism of lactate to pyruvate in the mediobasal hypothalamus (MBH) regulates hepatic glucose

21 Opioid activity within the mediobasal hypothalamus (MBH) regulates suckling-induced

22 Here, we investigated the role of the mediobasal hypothalamus (MBH), a key center involved in

23 n in forebrain neurons, dominantly targeting mediobasal hypothalamus (MBH), display impaired fasting-

24 ose and long-chain fatty acids (LCFA) by the mediobasal hypothalamus (MBH).

25 actions that include nutrient sensing in the mediobasal hypothalamus (MBH).

26 sulin signaling and activation of S6K in the mediobasal hypothalamus (MBH).

27 ty in the third cerebral ventricle or in the mediobasal hypothalamus (MBH).

28 odothyronine deiodinase (D2) activity in the mediobasal hypothalamus (MBH).

29 ene expression patterns in the preoptic area/mediobasal hypothalamus (POA/MBH) of male rat brain 7 h

30 e of long-chain fatty acyl-coenzyme A in the mediobasal hypothalamus and blunted the hypothalamic res

31 euromedin B, which are found in axons in the mediobasal hypothalamus and may also be released from th

32 e Y (NPY) gene and protein expression in the mediobasal hypothalamus and that central administration

33 A expression of Cav3.1 alpha1 subunit in the mediobasal hypothalamus and the pituitary.

34 ther showed that NF-kappaB inhibition in the mediobasal hypothalamus counteracted obesity-related hyp

35 beta-endorphinergic neuronal activity in the mediobasal hypothalamus during pregnancy in the rat.

36 D61A)-expressing adeno-associated virus into mediobasal hypothalamus elicited a similar antiobese eff

37 sults show activation of POMC neurons in the mediobasal hypothalamus following general arousal but no

38 genetic inhibition of HDAC5 activity in the mediobasal hypothalamus increases food intake and modula

39 s that activation of 5-HT1A receptors in the mediobasal hypothalamus inhibits lordosis behavior.

40 ling in WAT, but it abolished the ability of mediobasal hypothalamus insulin to suppress WAT lipolysi

41 sensitive potassium (K(ATP)) channels in the mediobasal hypothalamus is sufficient to lower blood glu

42 sensing of circulating nutrients within the mediobasal hypothalamus may be critical for energy homeo

43 (Pomc) in a group of neurons located in the mediobasal hypothalamus of all vertebrates.

44 owed that autophagy was highly active in the mediobasal hypothalamus of normal mice.

45 e found evidence of increased gliosis in the mediobasal hypothalamus of obese humans, as assessed by

46 enzyme A) were injected bilaterally into the mediobasal hypothalamus of rats.

47 ts of either surgical deafferentation of the mediobasal hypothalamus or administration of a kappa opi

48 s accumbens; surgical deafferentation of the mediobasal hypothalamus prevented the effect of quinelor

49 ase-beta (IKK-beta, encoded by Ikbkb) in the mediobasal hypothalamus rapidly elevated blood pressure

50 The mediobasal hypothalamus regulates functions necessary fo

51 Our results indicate that astrocytes in the mediobasal hypothalamus respond rapidly and robustly to

52 Here, we report that astrocytes in the mediobasal hypothalamus respond robustly and rapidly to

53 the third cerebral ventricle (icv) or in the mediobasal hypothalamus stimulated GP independent of cha

54 that most kiss1 mRNA-containing cells of the mediobasal hypothalamus strongly express ERalpha and sli

55 he ventromedial nucleus (VMN), a part of the mediobasal hypothalamus that regulates sexual behavior i

56 an adipose-derived hormone, acts within the mediobasal hypothalamus to control food intake and energ

57 ulations of leptin-responsive neurons in the mediobasal hypothalamus to MCH and ORX cells in the LHA

58 developed with autophagic inhibition in the mediobasal hypothalamus using site-specific delivery of

59 talk" between leptin and insulin within the mediobasal hypothalamus via the intracellular enzyme, ph

60 Hypocretin cells innervate the mediobasal hypothalamus where they can potentially influ

61 e (GnIH-ir) cell bodies are clustered in the mediobasal hypothalamus with pronounced projections and

62 lso been observed among cells located in the mediobasal hypothalamus, a brain area that exerts centra

63 he hindbrain, including the hippocampus, the mediobasal hypothalamus, and the circumventricular organ

64 minent in the lateral septum, preoptic area, mediobasal hypothalamus, and tuberomammillary nucleus, w

65 tivity of beta-endorphinergic neurons in the mediobasal hypothalamus, as measured by Fos immunoreacti

66 livery of constitutively active FoxO1 to the mediobasal hypothalamus, but not to the suprachiasmatic

67 In the mediobasal hypothalamus, DEPTOR was expressed in neurons

68 ith specialized neurons within nuclei of the mediobasal hypothalamus, namely the arcuate (ARC) and ve

69 oadly across the brain or locally within the mediobasal hypothalamus, or specifically in hypothalamic

70 the infusion of a K(ATP) blocker within the mediobasal hypothalamus, or the surgical resection of th

71 expressed in nutrient-sensing neurons of the mediobasal hypothalamus, responds to hormonal and nutrie

72 hroughout the CNS but highly enriched in the mediobasal hypothalamus, sense hormonal, nutrient and ne

73 activation of IKK-beta and NF-kappaB in the mediobasal hypothalamus--particularly in the hypothalami

74 in mature males and females, in the rostral mediobasal hypothalamus.

75 uated outside the blood-brain barrier in the mediobasal hypothalamus.

76 tion and gliosis returned permanently to the mediobasal hypothalamus.

77 fusion of either insulin or vehicle into the mediobasal hypothalamus.

78 as associated with autophagic decline in the mediobasal hypothalamus.

79 y increased GnRH secretion from the preoptic-mediobasal hypothalamus.

80 hibits cyclic AMP (cAMP) accumulation in the mediobasal hypothalamus.

81 determining the distribution of cells in the mediobasal hypothalamus.

82 out the brain as well as in tanycytes in the mediobasal hypothalamus.