ライフサイエンスコーパス: antidromic

1 tagonists, kainate lowered the threshold for antidromic action potential generation, suggesting that

2 The dorsal root reflex (DRR) is an antidromic action potential originating in the spinal co

3 ould be recorded at the granule cell soma as antidromic action potentials and from the axons with a n

4 However, antidromic action potentials are recruited at lower thre

5 ilaments were determined either by recording antidromic action potentials from the tooth or by using

6 Kainate application also induced spontaneous antidromic action potentials.

7 on was demonstrated by somatic recordings of antidromic action potentials.

8 However, antidromic activation (mossy fiber stimulation) evoked a

9 Recorded neurons were classified by their antidromic activation and by their changes in firing rat

10 Neurons were identified by their antidromic activation from contralateral facial and acce

11 Neurons were identified by their antidromic activation from facial nucleus (FN) or red nu

12 latencies to trigeminal ganglion shocks and antidromic activation from thalamus or cerebellum were a

13 Neurones were tested for antidromic activation from the contra- and ipsilateral v

14 Neurones were identified by antidromic activation from the contralateral thalamus, a

15 The rmPFC neurons were identified by their antidromic activation from the mediodorsal nucleus and/o

16 ially by driving recurrent inhibition though antidromic activation of corticostriatal axon collateral

17 ations in the orbitofrontal cortex (OFC) via antidromic activation of corticostriatal recurrent inhib

18 Furthermore, antidromic activation of electrical activity in the cell

19 Antidromic activation of ganglion cell axons also increa

20 Previous studies show that antidromic activation of sensory fibers is an important

21 s mediated by peripheral release of CGRP via antidromic activation of sensory fibers.

22 lation through sympathetic inhibition and/or antidromic activation of sensory fibers.

23 sodilation at >or=90% of MT may also involve antidromic activation of some unmyelinated C-fibers.

24 cartwheel cells were recorded to ortho- and antidromic activation of the granule cells (i.e., by sti

25 r were further identified as mitral cells by antidromic activation of the lateral olfactory tract and

26 e if SCS produces cutaneous vasodilation via antidromic activation of the unmyelinated C-fibers and/o

27 ere located and identified by the electrical antidromic activation of their constituent motoneurons.

28 Our previous studies show that antidromic activation of transient receptor potential va

29 Retrograde and anterograde labeling and antidromic activation of vBNST neurons by VTA stimulatio

30 In antidromic activation studies, mu-opioids inhibited a su

31 ic tract (STT) neurons were identified using antidromic activation techniques and examined for their

32 this projection in rats using the method of antidromic activation to map the axon terminals of neuro

33 entified as NTS or DMN using orthodromic and antidromic activation, respectively, following vagal sti

34 injured neuronal circuits is the same during antidromic activation, stimulation of granule cell axons

35 urons were identified as septohippocampal by antidromic activation.

36 reflex (DRR) and the axonal reflex (AR) are antidromic activities in primary afferents and are invol

37 striatal stimulus current necessary to evoke antidromic activity.

38 linked micropipette-microwire recording, and antidromic and orthodromic activation from the ventral t

39 ey rats demonstrated reciprocal interinsular antidromic and orthodromic activation, elicited with sim

40 ypoxia and 1 hour wash-out of the inhibitors antidromic and orthodromic responses were still blocked

41 Antidromic block can cause acceleration due to double-wa

42 riod, and was associated with unidirectional antidromic block of the paced impulse.

43 Antidromic CAPs of C-fibers in dorsal roots were evoked

44 In Protocol 3, antidromic CAPs of the dorsal root were measured in resp

45 Antidromic (centrifugal) conduction of these spikes may

46 h participate with substrate glutamine in an antidromic circular arrangement of hydrogen bonds, cause

47 In Protocol 2, antidromic compound action potentials (CAPs) of the tibi

48 p junctions between AVA and A-MNs only allow antidromic current, but, curiously, disrupting them inhi

49 ger at shorter V1V2 intervals, but a shorter antidromic delay in the area of unidirectional block for

50 Bursts of spontaneous antidromic dorsal root action potentials, and evoked dor

51 nerve to block both orthodromic signals and antidromic DRRs without affecting ARs.

52 We used antidromic electrical stimulation to identify V1 neurons

53 Finally, the antidromic ERG recordings obtained in our implanted volu

54 were recorded using 16 scalp electrodes, and antidromic ERGs were obtained using DTL electrodes while

55 ese responses could not be attributed to the antidromic firing of corticothalamic cells, intrathalami

56 The possible effects of antidromic firing on synaptic strength are unknown.

57 Synaptic stimulation delivered after antidromic firing, which was otherwise too weak to induc

58 glutamate released from its own dendrites by antidromic impulse invasion, or/and lateral excitation b

59 this site was likely to produce block of an antidromic impulse, which may initiate double-wave reent

60 There was no significant difference in antidromic latencies between Type I (m = 1.47 msec) and

61 The mean antidromic latency from the L1 level was 42.8 +/- 4.4 ms

62 on site and distally through orthodromic and antidromic mechanisms for several stimulation frequencie

63 ng neuroendocrine GABA neurons identified by antidromic median eminence stimulation.

64 Antidromic (n=35), monosynaptic (n=2), di-or tri-synapti

65 Both during normal bursting activity and antidromic nerve stimulation, the conduction delay over

66 A mechanism of antidromic passage of depolarizing current from a neuron

67 Antidromic population events in subiculum were single sp

68 for 35 min after trauma injury, improved CA1 antidromic population spike (PS) recovery to 91 +/- 2%,

69 Antidromic population spikes confirmed projections from

70 Antidromic potentials are larger if the afferent is clos

71 pagation of V2 around the line of block, and antidromic propagation through the original location of

72 ion of the lateral olfactory tract evoked an antidromic pulse followed by a short EPSP, which could a

73 The use of antidromic-rectifying gap junctions to amplify chemical

74 so released from sensory-motor nerves during antidromic reflex activity, to produce relaxation of som

75 flammation is believed to originate with the antidromic release of substance P, and of other neurokin

76 The proportion of antidromic responses consisting of full spikes from anti

77 hose neurons projecting to MT, identified by antidromic responses to electrical stimulation of MT.

78 Reciprocal antidromic responses were absent.

79 h could also be elicited independently of an antidromic spike in the recorded cell.

80 Although the antidromic spike latency of the single-spiking and burst

81 m depression between synaptically evoked and antidromic spike trains emphasize that the properties of

82 s was compared quantitatively to that during antidromic spike trains evoked by electrical stimulation

83 naptic spike width that did not occur during antidromic spike trains under physiological calcium conc

84 kes in a burst could be made to collide with antidromic spike.

85 generated rhythmic barrages (up to 25 Hz) of antidromic spikes during BMPs.

86 During BMPs the soma received antidromic spikes generated in processes in the buccal g

87 , we used optogenetic stimulation to trigger antidromic spikes in a local region of primary visual co

88 lation of the medial forebrain bundle evoked antidromic spikes in both burst-firing neurones and in s

89 firing neurones and classical 5-HT neurones, antidromic spikes made collisions with spontaneously occ

90 Plateau potentials after the antidromic spikes or local cerebral inputs will locally

91 During the barrage of antidromic spikes, high-frequency firing will produce st

92 curred spontaneously (53%) or in response to antidromic stimulation (81%).

93 ses in Ca(2+) transients evoked by light and antidromic stimulation are blocked by the purinergic ant

94 r pharmacological gap junction blockade, but antidromic stimulation could not drive activity in contr

95 in a small number of burst-firing neurones, antidromic stimulation evoked spike doublets, similar to

96 ioid, GABA(A), and NK1 receptor antagonists, antidromic stimulation of a population of striatal proje

97 Antidromic stimulation of cardiac sensory C fibers relea

98 rneurons in the medial prefrontal cortex via antidromic stimulation of cortico-accumbal afferents.

99 Skin blood flow was monitored during antidromic stimulation of identified cutaneous C fibres

100 dromic stimulation of the olfactory nerve or antidromic stimulation of mitral and tufted (M/T) cells.

101 Here, we show that antidromic stimulation of motor axons evokes depolarizin

102 ntial [total motor activity (TMA)] evoked by antidromic stimulation of the distal ventral root.

103 In bicuculline (10 microM) and 6 mM [K +]o, antidromic stimulation of the granule cells evoked burst

104 es on granule cells that can be activated by antidromic stimulation of the lateral olfactory tract (L

105 ith extracellular field potentials following antidromic stimulation of the lateral olfactory tract (L

106 ing bursts of action potentials generated by antidromic stimulation of the mossy fibers.

107 They can be activated by antidromic stimulation of the trigeminal nerve, as well

108 furcating axon collaterals in the chicken by antidromic stimulation of two sites along each branch an

109 ctivation of sensory nerve fibers, either by antidromic stimulation or capsaicin, depolarized these n

110 ive green fluorescent protein expression and antidromic stimulation or retrograde Evans blue dye trac

111 ptic to local glutamatergic neurons, we used antidromic stimulation to reveal that many of these cell

112 Furthermore, such antidromic stimulation was adequate to rescue "tagged" s

113 s activation of a pool of identified SPNs by antidromic stimulation.

114 eutic NAc-DBS might exert its effect through antidromic stimulation.

115 he contralateral thalamus were determined by antidromic stimulation.

116 +) activity were recorded in area CA3 during antidromic stimulation.

117 ic transmission are much more effective than antidromic stimuli that do not.

118 In antidromic studies, NA dose-dependently increased firing

119 e refractoriness followed by resetting of an antidromic tachycardia (AT) in patients with decremental

120 rats was significantly greater, and the mean antidromic threshold was significantly lower than in con

121 tion requires a sufficient excitable gap and antidromic unidirectional block of the paced impulse in

122 res were tested for their ability to produce antidromic vasodilatation.

123 These effects were potent: the area of the antidromic volley evoked in the sural nerve by intraspin