ライフサイエンスコーパス: spinothalamic

1 However, we found that spinothalamic ablation in humans, whilst profoundly impa

2 entation of selectively nociceptive lamina I spinothalamic activity.

3 Thus, the overlapping spinothalamic and cerebellar inputs may provide a substr

4 rns and corresponding nerves, atrophy of the spinothalamic and spinocerebellar tracts and posterior c

5 The question whether the spinothalamic and spinoreticular fibres cross the cord t

6 is then transmitted to brain regions via the spinothalamic and thalamocortical pathways.

7 n C7 and over one-fourth of those in L4 were spinothalamic, and at each level some projected to both

8 dial SPFp receives unique inputs from lumbar spinothalamic cells and brain regions involved in proces

9 d the significance of a population of lumbar spinothalamic cells for male sexual behavior in rats.

10 hese results suggest that this population of spinothalamic cells plays a pivotal role in generation o

11 lamina I projection cells per side, and that spinothalamic cells therefore make up approximately 42%

12 ounted for only on the assumption that these spinothalamic fibres are crossing the cord transversely.

13 The spinothalamic input was directed mostly to the ventral p

14 lls were distinguished from other classes of spinothalamic lamina I neurones by their peripheral inpu

15 racteristics of warming-specific lumbosacral spinothalamic lamina I neurones.

16 We have shown that spinothalamic lamina I neurons are infrequent in rat lum

17 Virtually all spinothalamic lamina I neurons at both levels were label

18 Spinothalamic lamina I neurons differed from those label

19 p of their collaterals that results in every spinothalamic neurone receiving an input from several do

20 olecystokinin as a marker for this subset of spinothalamic neurons and Fos-immunoreactivity as a mark

21 PAG and LPb, to determine the proportion of spinothalamic neurons at lumbar and cervical levels that

22 Spinothalamic neurons have generally been associated wit

23 mina I and lamina III/IV NK1r-immunoreactive spinothalamic neurons in cervical and lumbar segments co

24 investigate the involvement of these lumbar spinothalamic neurons in conveying copulation-related in

25 into the thalamus to estimate the number of spinothalamic neurons in each of these two populations,

26 This pathway originates from a population of spinothalamic neurons in the lumbar spinal cord containi

27 esults demonstrated that activation of these spinothalamic neurons is triggered by stimuli associated

28 The numbers of spinomedullary and spinothalamic neurons on the left side were comparable,

29 r results suggest that there are 90 lamina I spinothalamic neurons per side in C7 and 15 in L4 and th

30 demonstrate that a specific subpopulation of spinothalamic neurons signals information associated wit

31 Second, spinomedullary and spinothalamic neurons were compared in retrograde double

32 Moreover, these spinothalamic neurons were not activated by vaginocervic

33 urons with collaterals to the medulla and 2) spinothalamic neurons with collaterals to the midbrain.

34 mation conveyed by both these populations of spinothalamic neurons.

35 more ventrally located within lamina I than spinothalamic neurons.

36 ly, the recent identification of a candidate spinothalamic pathway involved in relay of ejaculation-s

37 ding the Neurologic Pain Signature (NPS) and spinothalamic pathway regions, with strong support for n

38 d others has demonstrated the existence of a spinothalamic pathway that is a candidate to relay infor

39 thalamic and cortical organoids to model the spinothalamic pathway.

40 Intact crossed spinothalamic pathways are unable to support the normal

41 ately 1%, indicating that spinomedullary and spinothalamic pathways arise from separate subpopulation

42 th other unmyelinated afferents, in lamina I-spinothalamic pathways.

43 nd that this projection is distinct from the spinothalamic projection.

44 dings preclude privileged C-tactile-lamina I-spinothalamic projections and imply integrated hedonic a

45 risingly, placebo increased activity in some spinothalamic regions for unconditioned mechanical pain.

46 (spectral phase-coherence) between the main spinothalamic sensory area (posterior insula) and 12 oth

47 Classically, the spinothalamic (ST) system has been viewed as the major p

48 us results in monkeys show that mid-cervical spinothalamic (STT) neurons are activated by groups II a

49 ion of rat lumbar laminae VII and X putative spinothalamic (STT) neurons that co-contain cholecystoki

50 otopically organized lamina I trigemino- and spinothalamic terminations in a cytoarchitectonically di

51 In addition, the patches of spinothalamic terminations intermingled and partly overl

52 al spinal cord to inhibit activity of lumbar spinothalamic tract (SST) cells and dorsal horn (DH) cel

53 ed neuron, indicating the termination of the spinothalamic tract (STT) axon.

54 oposed to contribute to the sensitization of spinothalamic tract (STT) cells and hyperalgesia.

55 ted NR1 subunits (pNR1) are expressed in the spinothalamic tract (STT) cells and immunohistochemistry

56 The responses of spinothalamic tract (STT) cells were recorded before and

57 The spinothalamic tract (STT) is an integral pathway in the

58 Nociceptive spinothalamic tract (STT) neurones in lamina I of the lu

59 Central sensitization of spinothalamic tract (STT) neurons in anesthetized monkey

60 ogy and distribution of retrogradely labeled spinothalamic tract (STT) neurons in lamina I (the margi

61 c pain, central sensitization of dorsal horn spinothalamic tract (STT) neurons is a major underlying

62 mine the effects of central sensitization of spinothalamic tract (STT) neurons produced by intraderma

63 perior sagittal sinus (SSS) can excite C1-C2 spinothalamic tract (STT) neurons receiving thoracic vis

64 Spinothalamic tract (STT) neurons respond to itch-produc

65 We found a class of lamina I spinothalamic tract (STT) neurons selectively excited by

66 The distribution of retrogradely labeled spinothalamic tract (STT) neurons was analyzed in macaqu

67 The distribution of retrogradely labeled spinothalamic tract (STT) neurons was analyzed in monkey

68 Lamina I spinothalamic tract (STT) neurons were identified by ret

69 Fifty-seven primate spinothalamic tract (STT) neurons were identified using

70 by disruption of the DC pathway, but not the spinothalamic tract (STT).

71 in the pain-signaling pathway to the brain [spinothalamic tract (STT)] that respond only to painful

72 ing peripheral nociceptive sensation via the spinothalamic tract and brainstem nuclei to the thalamus

73 ll tissues caudal to the neck eliminates the spinothalamic tract and the transmission of somatosensor

74 Excitation of spinothalamic tract cells in the upper thoracic and lowe

75 la and then descend to excite upper cervical spinothalamic tract cells.

76 Our results demonstrate that the spinothalamic tract contains mutually exclusive populati

77 07, P = 0.0440, R2 = 0.20) and cervical cord spinothalamic tract fractional anisotropy associated wit

78 width of ventral tissue bridges-a proxy for spinothalamic tract function-at 1 month post-spinal cord

79 tic or demyelinating lesions centered on the spinothalamic tract in rats.

80 ntact animals, electrical stimulation of the spinothalamic tract induces increases in thalamic CCL21

81 st that GRPR+ neurons are different from the spinothalamic tract neurons that have been the focus of

82 We examined the responses of spinothalamic tract neurons to histaminergic and, for th

83 pinocervical, postsynaptic dorsal column and spinothalamic tract neurons was used to simulate the pop

84 The spinothalamic tract projects to the medial and lateral t

85 ified itch-specific neuronal pathways in the spinothalamic tract that are distinct from pain pathways

86 ensory neuronal circuits of nociception (the spinothalamic tract) and proprioception (the dorsal spin

87 s in C6 and 17% of those in L5 belong to the spinothalamic tract, and these apparently project exclus

88 This review focuses on the spinothalamic tract, but other pathways are excited as w

89 n of the sensory component of pain along the spinothalamic tract, or stereotactic cingulotomy (n = 7)

90 s in each of these populations belong to the spinothalamic tract, which conveys nociceptive informati

91 he DC at T10, but not by interruption of the spinothalamic tract.

92 influenced by interfering with the ascending spinothalamic tract.

93 hose in the cervical cord also belong to the spinothalamic tract.

94 linical outcome groups in the left and right spinothalamic tracts (p = 0.003 and 0.020) and MTRh (p =

95 prion protein in the substantia gelatinosa, spinothalamic tracts, posterior columns and nuclei and i

96 icroscope to examine lamina I trigemino- and spinothalamic (TSTT) terminations in the posterior part

97 PHA-L-labeled trigemino- and spinothalamic (TSTT) terminations were identified immuno