ライフサイエンスコーパス: -projecting neuron

1 aBST-projecting neurons in limbic sites implicated in HPA axi

2 th significantly more c-fos expression in BA-projecting neurons in the VH and PL than that induced by

3 rograde tracer into the amygdala to label BA-projecting neurons in VH and PL.

4 of Fluorogold into the BA, the number of BA-projecting neurons in the mPFC remained stable between P

5 caused a greater inhibition in NAc- than BLA-projecting neurons.

6 bunit, evoked significant currents in caecum-projecting neurones that were previously exposed to alph

7 ard rectification was present only in caecum-projecting neurones, for example.

8 g current (270 pA) when compared with caecum-projecting neurones (302 +/- 22 Momega; 23.5 +/- 0.87 mV

9 ion factor Phox2b would identify oral cavity-projecting neurons in the geniculate ganglion.

10 restingly, more than half of the PGi and CNA-projecting neurons in the NTS expressed TH immunoreactiv

11 Of the few core-projecting neurons that remained in the ventral mesencep

12 auses, whereas signaling is uniform for core-projecting neurons; this difference is amplified by coca

13 Among prefrontal cortex-projecting neurons, quinpirole sensitivity, but not AP d

14 (> 75%) triggered action potentials in CVLM-projecting neurons but spike output was uniformly low (<

15 polysynaptic responses not observed in CVLM-projecting neurons.

16 ore elaborate dendritic morphology than CVLM-projecting neurons.

17 In contrast, DM-projecting neurons exhibited responses to a more structu

18 Although IS does not activate DRN-projecting neurons from the PL, IS did so after ketamine

19 In general, basal forebrain-projecting neurons were distributed throughout the entir

20 al forelimb-projecting and proximal forelimb-projecting neurons are intermingled within motor cortex,

21 %), many of which were identified as forward-projecting neurons.

22 amine (BDA) to identify dendrites of forward-projecting neurons (i.e., from V1 to LM) and postembeddi

23 ent labeling of local collaterals of forward-projecting neurons in V1 and feedback connections from e

24 nection, and that feedback-recipient forward-projecting neurons are strongly interconnected.

25 provide strong monosynaptic input to forward-projecting neurons in V1.

26 on to their relationship with gastric fundus-projecting neurons.

27 Gamma-aminobutyric acid (GABA)-projecting neurons in the paraventricular nucleus (PVN)

28 gate: (1) the response of identified gastric-projecting neurones of the dorsal motor nucleus of the v

29 part from a smaller soma diameter in gastric-projecting neurons, morphological differences were not f

30 the somata and the dendritic tree of gastric-projecting neurons were smaller than intestinal-projecti

31 sponses to depolarizing stimuli than gastric-projecting neurons.

32 d that high-grade lesions of the hippocampal-projecting neurons of the CBF were not sufficient to imp

33 ded beyond the region of mMAN defined by HVC-projecting neurons into the immediately surrounding cort

34 ion neurons surrounded by a shell of non-HVC-projecting neurons, both of which receive input from the

35 The percentages of IML-projecting neurons containing 5-HT(1A)R-ir were 49% in R

36 Moreover, some IML-projecting neurons in the PPR and RPa were doubly immuno

37 eled for 5-HT(1A)R-ir and 5-HT, and some IML-projecting neurons in the RVLM were doubly immunolabeled

38 lized 5-HT(1A)R immunoreactivity (ir) to IML-projecting neurons that were retrogradely labeled with r

39 both planes of section, that is, intestinal-projecting neurons had larger and longer afterhyperpolar

40 jecting neurons were smaller than intestinal-projecting neurons.

41 we show that local circuit and deeper-layer-projecting neurons in layer 1, as well as tuft dendrites

42 We surveyed mouse forebrain LC-projecting neurons by examining retrogradely labeled cel

43 immunoreactivity was never identified in LES-projecting neurons.

44 In the rostral DMN, 15 +/- 4% of LES-projecting neurons also contained NADPH-diaphorase activ

45 The neurochemistry of LES-projecting neurons was also investigated using two marke

46 mine), is synthesized by a population of LES-projecting neurons.

47 The presence of NOS in some LES-projecting neurons may contribute to LES relaxation, as

48 we found that antidromically identified LHb-projecting neurons were distributed mainly in the dorsal

49 distinct subset of vHC neurons onto midbrain-projecting neurons in the central amygdala is necessary

50 Layer 6 middle temporal area (MT)-projecting neurons are particularly interesting, as they

51 MT-projecting neurons in two primate species, bush babies a

52 In both primate species, MT-projecting neurons in layer 3C were unevenly distributed

53 cytochrome oxidase blobs, indicating that MT-projecting neurons of both types restrict their dendrite

54 Regardless of cell type, MT-projecting neurons have larger cell bodies, more dendrit

55 ering the channel on pallidal- versus nigral-projecting neurons.

56 Effects on nigrostriatal-projecting neurons were examined using a retrograde trac

57 ic phenotypes, distinct from GABAergic olive-projecting neurons.

58 ting neurons and the laterally positioned OT-projecting neurons, there was also a slight overlap betw

59 By labelling the OT-projecting and OV-projecting neurons in the same owl, it was confirmed tha

60 ical tuning properties indicate that many OV-projecting neurons are within the area containing space-

61 observed between the medially positioned OV-projecting neurons and the laterally positioned OT-proje

62 Pa-projecting neurons were localized in the same nuclei of

63 lamp techniques on identified vagal pancreas-projecting neurones, we studied the effects of metabotro

64 ed presynaptically on certain vagal pancreas-projecting neurons.

65 pDMS-projecting neurons showed a transient increase in pERK e

66 nt data also suggest that relatively few PVH-projecting neurons in ascending raphe nuclei, nucleus of

67 forebrain distribution of glutamatergic PVH-projecting neurons.

68 ese findings support the conclusion that PVN-projecting neurones in the DC and LM of OVLT could parti

69 PVN-projecting neurons had larger cell bodies with more elab

70 ectrophysiologically similar neurons and PVN-projecting neurons are less excitable than neurons of un

71 Both CVLM- and PVN-projecting neurons had similar, tetraethylammonium-sensi

72 However, fewer PVN-projecting neurons in the C1 and C3 regions expressed DB

73 However, PVN-projecting neurons (n=32) had higher action potential (A

74 pike output was uniformly low (< 20%) in PVN-projecting neurons.

75 d adult rats, as were the proportions of PVN-projecting neurons in each region that were PNMT-positiv

76 The numbers of PVN-projecting neurons in the A1, C1, A2/C2, C3, or A6 catec

77 y retrograde FluoroGold (FG) labeling of PVN-projecting neurons was combined with in situ hybridizati

78 Spontaneous PVN-projecting neurons (n=20) also fired APs at lower rates

79 RA-projecting neurons exhibited purely depolarizing subthre

80 NF expression in HVC occurs mainly in the RA-projecting neurons.

81 nd glutamatergic inputs into identified RVLM-projecting neurons of the hypothalamic paraventricular n

82 N, overlapping with the distribution of RVLM-projecting neurons.

83 MT were remarkably similar to the layer 6 SC-projecting neurons.

84 Surprisingly, optogenetic activation of SC-projecting neurons in V1 or their axon terminals in SC s

85 Sensory-projecting neurons are suppressed by attentional states,

86 positively correlates with arousal, sensory-projecting neurons participate in spindles and show elev

87 depolarization, indicating that duodenum-SO-projecting neurons could be capable of detecting CCK rel

88 The duodenum-SO-projecting neurons were immunoreactive (IR) for choline

89 wn, and until now death of axotomized spinal-projecting neurons has not been described in the lamprey

90 pressed in spinal cord neurons and in spinal-projecting neurons of the brainstem.

91 induces delayed cell death in lamprey spinal-projecting neurons and suggest that the reason why some

92 aventricular nucleus (PVN) contains spinally-projecting neurons implicated in fine-tuning the cardiov

93 y by increasing the excitability of spinally-projecting neurons and identifies NK1 receptors as poten

94 art by the subsequent activation of spinally-projecting neurons in the RVM.

95 ygdala (BLA) receives input from subcortical-projecting neurons in the medial prefrontal cortex (mPFC

96 er pERK-expressing neurons are supraspinally-projecting neurons, we injected Fluorogold (FG) into the

97 kx2.1, but these do not include any thalamus-projecting neurons, suggesting that the projection cells

98 similar to the primate GPi, and non-thalamus-projecting neurons that exhibit activity similar to the

99 tive pallidal cell types in area X: thalamus-projecting neurons that exhibit activity similar to the

100 RFs (upper arm/shoulder) and pyramidal tract-projecting neurons (PTNs) with fast-conducting axons ten

101 targeting the nucleus accumbens; and triple-projecting neurons, targeting the prefrontal cortex, amy

102 V2-projecting neurons were concentrated in the superficial

103 of information from the M pathway, while V2-projecting neurons are likely to mediate slower computat

104 ose occurred in gastric- than in portal vein-projecting neurons, the latter having a higher incidence

105 Herein we describe a population of VLPO-projecting neurons in the LH that express the vesicular

106 mical identity of the majority of these VLPO-projecting neurons within the lateral hypothalamus (LH),

107 Most VPM-projecting neurons examined did not show Fos-like immuno

108 VTA-projecting neurons in subregions of medial accumbens she

109 ly adult brains, had significantly fewer VTA-projecting neurons preferentially within an interconnect

110 n several structures containing NTergic, VTA-projecting neurons, including the LPH-MPOA, nucleus accu

111 ement of excitatory neurotransmission on VTA-projecting neurons, and that this pathway is engaged by

112 radely labeled neurons in the sense that VTA-projecting neurons were present at all of the same rostr

113 We have identified Area X-projecting neurons as belonging to the thick dendrite cl

114 ss FnTm2 include the nucleus HVC (its Area X-projecting neurons), Area X, and LMAN (core and shell).

115 In contrast, subthreshold responses of X-projecting neurons included less-selective depolarizing

116 different subthreshold processes, and only X-projecting neurons appear to be sites for auditory refin

117 Previous studies indicated that only X-projecting neurons have auditory responses, leaving open

118 c interneurons make restricted inputs onto X-projecting neurons.