ライフサイエンスコーパス: stretch receptor

1 e; rapidly and slowly adapting low-threshold stretch receptors).

2 ubset of vagal tension receptors but not any stretch receptors.

3 opic neurotransmitter receptors and putative stretch receptors.

4 climbed to new levels); or altered pulmonary stretch receptor activity (major breathing frequency and

5 When the phase of stretch receptor activity was set to 90-150 degrees by c

6 ed chemoreceptor, baroreceptor, or pulmonary stretch receptor activity.

7 activation of the slowly adapting pulmonary stretch receptor afferents (SARs), which monosynapticall

8 ion of ATP into the NTS site where pulmonary stretch receptor afferents terminate produced central ap

9 e NTS from the central terminals of the lung stretch receptor afferents, activate the second-order re

10 nt of precursors of both chordotonal organs (stretch receptors) and photoreceptors.

11 Vertebrate muscle spindle stretch receptors are important for limb position sensat

12 at feedback from baroreceptors and pulmonary stretch receptors are the dominant determinants of the r

13 The structurally complex stretch receptor arises from a single myotube, which is

14 ormones modulate initiation of swimming; (2) stretch receptors associated with longitudinal muscles i

15 Among the eight pairs of putative stretch receptors associated with longitudinal muscles i

16 Classically recognized as the cutaneous stretch receptors associated with the slowly adapting ty

17 We found that the stretch receptors associated with ventral longitudinal m

18 ilar to the profile of rats and suggest that stretch receptor-associated expression of alpha(3) Na(+)

19 scle fascicles are monitored by at least two stretch receptor cells covering ventral, lateral, and do

20 omoting cellular calcium influx, silence the stretch receptor cells.

21 ion channel complex that is unique to insect stretch receptor cells.

22 into intrafusal muscle fibers that form the stretch receptor core.

23 has a skeletal muscle autonomous function in stretch receptor development.

24 Muscle spindles are commonly considered as stretch receptors encoding movement, but the functional

25 The forewing stretch receptor (fSR) makes direct cholinergic synapses

26 refore, the rhythmic activity of the ventral stretch receptor generated during swimming can change in

27 fied proprioceptor, the gastropyloric muscle stretch receptor (GPR) neuron, regulates the gastric mil

28 Stretch receptors had currents that differed from those

29 ments of medicinal leeches, only the ventral stretch receptor has been characterized in detail.

30 of Cajal as pacemakers, neuromodulators and stretch receptors has been revealed and their dysfunctio

31 In particular, no stretch receptors have been identified in C. elegans, ra

32 Thus spindle afferents responded as stretch receptors, i.e. impulse rates increased with len

33 At the wing hinges are stretch receptors important in generating and controllin

34 the dorsal body wall and hence is a putative stretch receptor in dorsal longitudinal muscle.

35 , mechanosensory structures that function as stretch receptors in insects.

36 of chordotonal organs (CHOs), which serve as stretch receptors in the body wall and joints and as aud

37 Stretch receptors in the fundus are more relevant than t

38 in the ER-rich cell cortex and is linked to stretch receptors in the plasma membrane.

39 the well-defined rapidly and slowly adapting stretch receptors innervating the airways and lungs.

40 anges of chemoreceptor, baroreceptor or lung stretch receptor inputs.

41 Afferent input from pulmonary stretch receptors is important in the control of the tim

42 These stretch receptors may set the optimal intersegmental pha

43 in C. elegans, raising the issue of whether stretch-receptor-mediated proprioception is used by C. e

44 motion, suggesting that TRP-4 is involved in stretch-receptor-mediated proprioception.

45 tic transmission between the locust forewing stretch receptor neuron (fSR) and the first basalar moto

46 Thus, DVA represents a stretch receptor neuron that regulates sensory-motor int

47 stsynaptic potentials (IPSPs) in intraspinal stretch receptor neurons (edge cells).

48 In lampreys, stretch receptor neurons (SRNs) are located at the margi

49 ] inserts to examine the axon projections of stretch receptor neurons and an engrailed-lacZ construct

50 eurons have the characteristic morphology of stretch receptor neurons and that they form a circumfere

51 he channel gating, which acts on chordotonal stretch receptor neurons, is based on a mechanical direc

52 ination and hearing by acting on chordotonal stretch receptor neurons.

53 Sensory feedback from stretch receptors, neurons that detect position or tensi

54 Body size is sensed by either stretch receptors or oxygen restriction, depending on th

55 rn of an original sensory afferent to muscle stretch receptors or the inappropriate recruitment of a

56 urons that are part of the Chordotonal (Cho) stretch receptor organs.

57 ive an inhibitory input from myelinated lung stretch receptors, presumably SARs.

58 is expressed in sensory neurons of internal stretch receptors previously implicated in temperature s

59 spinal cord, while those innervating muscle stretch receptors project to the ventral horn.

60 bitory activity of slowly adapting pulmonary stretch receptors (PSRs) as EEVL was lowered.

61 h-pulp afferent) and non-nociceptive (muscle-stretch receptor) rat sensory neurons.

62 he IMAs were consonant with the hypothesized stretch receptor roles of the afferents.

63 eive an input from slowly adapting pulmonary stretch receptors (SARs) in halothane-anaesthetized vent

64 nlike sensory bristles, SOPs of chordotonal (stretch receptor) sense organs are tightly clustered.

65 Stretch-receptor (SR) axons form a parallel array of 20

66 ts from the enteric nervous system, and (iv) stretch receptors that modulate membrane potential and e

67 ppear to satisfy structural requirements for stretch receptors tuned to tonic or more aperiodic event

68 ubsequently modified the activity of ventral stretch receptors (VSRs) by injecting rhythmic current a

69 nal arborizations of two additional putative stretch receptors with axons in anterior nerve roots and

70 olization, increased stimulation of arterial stretch receptors with resultant coronary vasoconstricti