ライフサイエンスコーパス: spinothalamic

1 entation of selectively nociceptive lamina I spinothalamic activity.

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

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

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

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

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

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

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

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

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

11 The spinothalamic input was directed mostly to the ventral p

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

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

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

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

16 Spinothalamic lamina I neurons differed from those label

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

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

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

20 Spinothalamic neurons have generally been associated wit

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

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

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

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

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

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

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

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

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

30 Moreover, these spinothalamic neurons were not activated by vaginocervic

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

32 mation conveyed by both these populations of spinothalamic neurons.

33 more ventrally located within lamina I than spinothalamic neurons.

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

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

36 Intact crossed spinothalamic pathways are unable to support the normal

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

74 The spinothalamic tract projects to the medial and lateral t

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

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

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

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

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

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

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

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