ライフサイエンスコーパス: solitarii

1 by different regions of the nucleus tractus solitarii.

2 lateral areas of the caudal nucleus tractus solitarii.

3 ntrolateral medulla, and the nucleus tractus solitarii.

4 matergic transmission in the nucleus tractus solitarii abolished rimonabant-induced hypophagia.

5 region to the cardiovascular nucleus tractus solitarii and evaluated the confluence of tracing from t

6 o visceral relay nuclei: the nucleus tractus solitarii and pontine parabrachial complex, and perivent

7 ures: the area postrema, the nucleus tractus solitarii, and the dorsal motor nucleus of the vagus.

8 nucleus raphe obscurus, the nucleus tractus solitarii, and the regions of the retrofacial nucleus, n

9 in the area postrema and the nucleus tractus solitarii, believed to be involved in terminal emetic pa

10 nhibition of the commissural nucleus tractus solitarii (cNTS) significantly reduced tSNA.

11 mmissural subdivision of the nucleus tractus solitarii (cNTS) using in vivo microdialysis during acti

12 rones within the commissural nucleus tractus solitarii (commNTS) with glycine (40 nmol/80 nl) or with

13 ostral and caudal regions of nucleus tractus solitarii did not.

14 )-1beta microinjected in the nucleus tractus solitarii increases fR and the predictability of the ven

15 ularis dorsalis, commissural nucleus tractus solitarii, lateral medulla, A5 area, and internal latera

16 ommissural subnucleus of the nucleus tractus solitarii, lateral medulla, medial facial nucleus, A5 ar

17 Altered nucleus tractus solitarii (nTS) activity contributes to this response.

18 usions of lidocaine into the nucleus tractus solitarii (NTS) and by propranolol infused into the baso

19 comprising the DVC, i.e. the nucleus tractus solitarii (NTS) and the dorsal motor nucleus (DMN).

20 o twenty-two neurones in the nucleus tractus solitarii (NTS) and ventral respiratory group (VRG).

21 of adenosine release in the nucleus tractus solitarii (NTS) and ventrolateral medulla (VLM) during a

22 ateral medulla (VLM) and the nucleus tractus solitarii (NTS) are implicated in the control of a varie

23 e glutamate receptors in the nucleus tractus solitarii (NTS) are necessary for the baroreceptor refle

24 oducing (PPG) neurons in the nucleus tractus solitarii (NTS) are the predominant source of endogenous

25 ltiple mechanisms within the nucleus tractus solitarii (nTS) contribute to functional changes followi

26 s exogenously applied to the nucleus tractus solitarii (NTS) depressed the baroreceptor cardiac refle

27 rainstem and from within the nucleus tractus solitarii (NTS) during the defence response evoked by hy

28 ignalling is critical in the nucleus tractus solitarii (nTS) for cardiorespiratory homeostasis and in

29 ukin-1beta (IL-1beta) in the nucleus tractus solitarii (nTS) from ALI but not sham rats.

30 (caudal C1 area) or into the nucleus tractus solitarii (NTS) greatly attenuated the baroreflex and si

31 al aspect of the commissural nucleus tractus solitarii (NTS) in mediating the peripheral chemorecepto

32 d fibers in subnuclei of the nucleus tractus solitarii (NTS) in the squirrel monkey, Saimuri sciureus

33 e recorded simultaneously in nucleus tractus solitarii (NTS) including the dorsal respiratory group (

34 Electrical stimulation of nucleus tractus solitarii (NTS) induced excitatory postsynaptic currents

35 the fourth ventricle or the nucleus tractus solitarii (NTS) inhibits food intake and weight gain.

36 The nucleus tractus solitarii (NTS) integrates inputs from cardiovascular af

37 The nucleus tractus solitarii (NTS) is essential for coordinating arterial b

38 The nucleus tractus solitarii (NTS) is the first brain site that receives in

39 The nucleus tractus solitarii (nTS) is the first integration site of the per

40 The nucleus tractus solitarii (NTS) is the first site of integration for pri

41 The brainstem nucleus tractus solitarii (nTS) is the first site of visceral sensory af

42 activated by vagal input to nucleus tractus solitarii (NTS) neurones in immature rats.

43 fferent neurotransmission in nucleus tractus solitarii (NTS) neurons, which affect respiratory and au

44 Fos was induced in the nucleus tractus solitarii (NTS) of hypotensive piglets.

45 catecholamine neurons in the nucleus tractus solitarii (NTS) of rat, attenuates arterial baroreflexes

46 hat nitric oxide (NO) in the nucleus tractus solitarii (NTS) participates in modulating cardiovascula

47 edial aspects of commissural nucleus tractus solitarii (NTS) received input from cardiopulmonary C fi

48 se, we hypothesized that the Nucleus Tractus Solitarii (NTS) region of the medulla oblongata, to whic

49 hibitory transmission in the nucleus tractus solitarii (NTS) remain unclear, even though this could b

50 noradrenergic relay from the nucleus tractus solitarii (NTS) to corticotropin releasing hormone neuro

51 of direct pathways from the nucleus tractus solitarii (NTS) to the olfactory tubercle and the midlin

52 f L-S-nitrosocysteine in the nucleus tractus solitarii (NTS) were compared and contrasted with those

53 Vestibular afferents to the nucleus tractus solitarii (NTS) were identified for the first time in th

54 Hd) staining patterns in the nucleus tractus solitarii (NTS) were spatially related to terminal sites

55 , we examined LTD in the rat nucleus tractus solitarii (NTS), a brainstem nucleus that relays homeost

56 egrated within the brainstem nucleus tractus solitarii (nTS), a critical contributor to cardiorespira

57 present on astrocytes in the nucleus tractus solitarii (nTS), an important nucleus in cardiorespirato

58 tors excites neurones in the nucleus tractus solitarii (NTS), but discharge patterns evoked by physio

59 amino acids (EAAs) into the nucleus tractus solitarii (nTS), in a region located immediately rostral

60 ly in the caudal zone of the nucleus tractus solitarii (NTS), mainly within the commissural subnucleu

61 al nucleus, cuneate nucleus, nucleus tractus solitarii (NTS), paraventricular nucleus of the hypothal

62 -fibre-activated neurones in nucleus tractus solitarii (NTS), phrenic nerve activity, tracheal pressu

63 the CNS, particularly in the nucleus tractus solitarii (NTS), the first central site for synaptic con

64 expression increased in the nucleus tractus solitarii (nTS), whereas it decreased in the hypoglossal

65 nds dense projections to the nucleus tractus solitarii (nTS), which exhibits neuronal activation foll

66 on neurotransmission in the nucleus tractus solitarii (nTS).

67 of baroreflex signals in the nucleus tractus solitarii (NTS).

68 entified subdivisions of the nucleus tractus solitarii (NTS).

69 ergic input arising from the nucleus tractus solitarii (NTS).

70 cell group) neurones in the nucleus tractus solitarii (NTS).

71 trointestinal tissues to the nucleus tractus solitarii (NTS).

72 projections to the brainstem nucleus tractus solitarii (NTS).

73 reflex afferent pathway (the nucleus tractus solitarii, NTS; nodose ganglion, NG).

74 tegmentum/substantia nigra, nucleus tractus solitarii, nucleus accumbens, thalamus/subthalamus, pari

75 xydopamine or vitamin C into nucleus tractus solitarii of the rat and evaluated the cardiopulmonary c

76 aroreceptive neurones in the nucleus tractus solitarii of the rat.

77 The cardiovascular nucleus tractus solitarii projected to pontine preganglionic parasympath

78 ntrast, all three regions of nucleus tractus solitarii projected to the nucleus ambiguus and dorsal m

79 and caudal to cardiovascular nucleus tractus solitarii sent projections through the pons medial to th

80 mal and central subnuclei of nucleus tractus solitarii, spinal trigeminal nucleus caudalis, and infer

81 citatory currents (eEPSCs) evoked by tractus solitarii stimulation (TS-eEPSC) of second-order neurons

82 esis that the cardiovascular nucleus tractus solitarii, the site of termination of arterial barorecep

83 cing from the cardiovascular nucleus tractus solitarii to pontine preganglionic neurons labeled retro

84 eurons in the cardiovascular nucleus tractus solitarii to pontine preganglionic parasympathetic neuro

85 cing from the cardiovascular nucleus tractus solitarii to preganglionic parasympathetic neurons in th

86 e exception these cells responded to tractus solitarii (TS) stimulation with a monophasic excitatory

87 p dorsal horn project to the nucleus tractus solitarii via two distinct pathways.

88 ses its neural output to the nucleus tractus solitarii with a subsequent activation of several reflex

89 ateral medulla (CVL) and the nucleus tractus solitarii with immunocytochemical identification of C1 a