ライフサイエンスコーパス: mechanoreceptive

1 owing peripheral nerve injury, low threshold mechanoreceptive Abeta-fibers sprout from their normal t

2 correlation between functional properties of mechanoreceptive afferent fibers and intrinsic discharge

3 tunity to bridge the gap between first-order mechanoreceptive afferent input codes and their spatial,

4 To examine the contribution of low threshold mechanoreceptive afferent input to the development of al

5 sults support the idea that each of the four mechanoreceptive afferent systems innervating the hand s

6 ht of similar studies of other low-threshold mechanoreceptive afferent terminals in the rat and cat a

7 ntraneural microstimulation (INMS) of single mechanoreceptive afferent units in the median nerve, in

8 We record the responses of mechanoreceptive afferents and of neurons in areas 3b an

9 raditionally, different classes of cutaneous mechanoreceptive afferents are ascribed different and la

10 tile stimuli conveyed in Abeta low threshold mechanoreceptive afferents become capable of activating

11 Mechanoreceptive afferents innervating the glabrous skin

12 In contrast, myelinated hair mechanoreceptive afferents proportionally increased thei

13 across one of three populations of cutaneous mechanoreceptive afferents that innervate the fingertips

14 ion with periodic microstimulation of single mechanoreceptive afferents whose receptive fields occupi

15 at stimulus intensities that activated large mechanoreceptive afferents, and grew as additional affer

16 n additional function to vibration-sensitive mechanoreceptive afferents.

17 We show that CTs are unique among mechanoreceptive afferents: they discharged preferential

18 urvival of subpopulations of proprioceptive, mechanoreceptive and nociceptive sensory neurons, where

19 ions for, and possible interactions between, mechanoreceptive and nociceptive signals.

20 Interestingly, Cbln2 is expressed by mechanoreceptive and proprioceptive neurons and in regio

21 tions between low-threshold primary afferent mechanoreceptive axons and dorsal horn cells are invaria

22 hydroxylase (Th), specific to low-threshold mechanoreceptive C-fibers, which was shown previously to

23 tegories included a variety of low threshold mechanoreceptive classes, innocuous thermoreceptive and

24 assively, influence GG EMG activity; and (3) mechanoreceptive control of GG EMG can fully explain all

25 ring rates of low-threshold Abeta and D-hair mechanoreceptive fibers were also altered.

26 cting the high innervation density and small mechanoreceptive fields in this area [1, 2].

27 stical model of the excitatory low threshold mechanoreceptive fields of spinocervical, postsynaptic d

28 ent of the trigeminal and cervical cutaneous mechanoreceptive fields was observed in 71% of neurons.

29 eociliary bundles as an essential element of mechanoreceptive function.

30 cture of Eimer's organs is consistent with a mechanoreceptive function.

31 The mechanoreceptive hair bundles of hair cells in the bullf

32 annels that open following the deflection of mechanoreceptive hair bundles that reside on top of thes

33 that impose complex mechanical loads on the mechanoreceptive hair bundles.

34 The regeneration of mechanoreceptive hair cells occurs throughout life in no

35 ed amplification by an active process in the mechanoreceptive hair cells.

36 Positive C-fibre high threshold mechanoreceptive (HTM) units had receptive fields in der

37 uli as nociceptive (including high-threshold mechanoreceptive (HTM) units), and non-nociceptive (incl

38 Here, we reported the cross-inhibition of mechanoreceptive information in DRG under peripheral inf

39 ts to convey proprioceptive, nociceptive and mechanoreceptive information to the spinal cord.

40 ntation, the pretectum receives electro- and mechanoreceptive inputs in addition to retinal input.

41 Tapping into the mechanoreceptive interface between the animal and the en

42 and non-nociceptive (including low-threshold mechanoreceptive (LTM) and cooling units).

43 proportion of nociceptive than low threshold mechanoreceptive (LTM) neurons showed Nav1.8-LI, and noc

44 ding nociceptive and cutaneous low-threshold mechanoreceptive (LTM) neurons, 50 had no discernable ri

45 characterized as nociceptive, low- threshold mechanoreceptive (LTM) or unresponsive according to thei

46 mal stimuli, as a nociceptive, low threshold mechanoreceptive (LTM) or unresponsive unit.

47 ies were characterized as: (a) low-threshold mechanoreceptive (LTM) units (5 C-, 10 Adelta- and 57 Aa

48 sensitive (n = 4) nor C-fibre low threshold mechanoreceptive (LTM) units (n = 3) had CGRP-LI.

49 after peripheral injury, some low-threshold mechanoreceptive (LTMR) afferents "sprout" into pain-spe

50 channel, we analyzed Drosophila melanogaster mechanoreceptive mutants for defects in mechanosensory p

51 ype I (RAs) and slowly adapting type I (SAs) mechanoreceptive nerve fibers.

52 e system of the channel catfish is formed by mechanoreceptive neuromasts located within five pairs of

53 Spike trains from primary mechanoreceptive neurons did not predict choices about i

54 xhibit numerical expansion of large-diameter mechanoreceptive neurons expressing the mechano-gated io

55 l eleven types: three distinct low-threshold mechanoreceptive neurons, two proprioceptive, and six pr

56 s known, however, about the possible role of mechanoreceptive or other somatosensory feedback in the

57 actin-filled stereocilia that serves as the mechanoreceptive organelle of each hair cell in the inne

58 The hair cell's mechanoreceptive organelle, the hair bundle, is highly s

59 in the hair bundle, the sensory hair cell's mechanoreceptive organelle.

60 ignaling molecules define common features of mechanoreceptive processing across sensory systems.

61 emic episodes that excite chemosensitive and mechanoreceptive receptors in the heart.

62 l activation, probably representing a robust mechanoreceptive reflex.

63 vity is modulated by both chemoreceptive and mechanoreceptive reflexes that help stabilize airway pat

64 To determine the contribution of ongoing mechanoreceptive reflexes to phasic activity of airway d

65 ve shown that non-physiological upper airway mechanoreceptive stimuli (e.g. rapidly imposed pulses of