ライフサイエンスコーパス: postganglionic

1 Contractions were antagonized by postganglionic action of guanethidine, but not by phento

2 Complete postganglionic arbors (n = 154) in the muscle wall were

3 these fibers were identified as sympathetic postganglionic axons based on their disappearance in org

4 Electrical stimulation of sympathetic postganglionic axons evoked inhibitory postsynaptic pote

5 The ability of adult injured postganglionic axons to reinnervate cerebrovascular targ

6 The postganglionic axons within the ganglion showed less VAC

7 ase (marker of catecholaminergic sympathetic postganglionic axons), or calcitonin gene-related peptid

8 Unilateral preganglionic denervation or postganglionic axotomy causes declines in alpha3, beta4,

9 prolonged activation of STAT proteins after postganglionic axotomy in vivo is loss of target-derived

10 he loss of target-derived NGF resulting from postganglionic axotomy in vivo, SCG were explanted into

11 Like postganglionic axotomy in vivo.

12 onal fibers and a subpopulation of intrinsic postganglionic cardiac neurons.

13 Only an occasional sympathetic postganglionic cell in the stellate ganglion complex exh

14 ivity so far identified in preganglionic and postganglionic cells of the ciliary ganglion in differen

15 g cells were used to label preganglionic and postganglionic cholinergic neurons and their projections

16 The inhibitory effect of adenosine on the postganglionic compound action potential (CAP) was antag

17 The postganglionic compound action potential (CAP), made sub

18 he amplitude of the extracellularly recorded postganglionic compound action potential.

19 physiological evidence indicates that vagal postganglionic control of left ventricular contractility

20 The vagal postganglionic controls of cardiac rate and left ventric

21 The extent of the sprouting of sympathetic postganglionic fibers in the dorsal root ganglion (DRG)

22 Postganglionic fibers projected into the wall of the ren

23 ear to be a conduit by which pterygopalatine postganglionic fibers reach the choroid.

24 The distribution of the postganglionic fibers was investigated by means of the c

25 The pterygopalatine postganglionic fibers were also seen to innervate the Ha

26 The sympathetic postganglionic fibers were visualized by immunostaining

27 Sympathetic postganglionic fibers, as identified by electron microsc

28 ntinuing belief that cardiac parasympathetic postganglionic fibres are sparse or absent from the vent

29 lls were most likely cardiac parasympathetic postganglionic fibres.

30 Asynchronous postganglionic firing mediated by peptidergic cotransmis

31 ., approximately 60%) of all individual CSMG postganglionics formed mixed, heterotypic arbors that co

32 d tissue was collected to assess sympathetic postganglionic intracellular calcium transients ([Ca(2+)

33 Acetylcholine, released from gastric postganglionic intramural neurons, stimulates the pariet

34 Acetylcholine, released from gastric postganglionic intramural neurons, stimulates the pariet

35 While the postganglionic motoneurons in the CG are cholinergic, as

36 of synaptic potentials evoked by stimulating postganglionic motor nerves.

37 Efferent postganglionic muscle SNA, BP, and central venous pressu

38 ulatory function and the role of sympathetic postganglionic nerve traffic in maintaining the pain in

39 ally evoked compound action potential in the postganglionic nerve; it also desynchronized the firing

40 of the right atrial fat pad, containing both postganglionic nerves and terminals of preganglionic neu

41 after local application of colchicine to the postganglionic nerves, which blocks fast transport witho

42 at is, in part, dependent on the sympathetic postganglionic neuron (SPGN) terminal, we tested the hyp

43 d neuronal loss but only impaired inhibitory postganglionic neuron function; it is often associated w

44 We therefore examined function of the postganglionic neuron in the paced canine model of HF as

45 ion of cutaneous vasoconstrictor sympathetic postganglionic neurones (PGNs) in anaesthetized rats.

46 ctivity was recorded from single sympathetic postganglionic neurones innervating the caudal ventral a

47 ctivity was recorded from single sympathetic postganglionic neurones innervating the lateral tail vei

48 sed rats, activity recorded from sympathetic postganglionic neurones innervating the tail circulation

49 P)-induced depolarization of parasympathetic postganglionic neurones of the cardiac ganglion.

50 ges of fourteen out of seventeen sympathetic postganglionic neurones were rhythmic.

51 in the myenteric plexus and from sympathetic postganglionic neurones.

52 c rhythms and promote summation of inputs to postganglionic neurones.

53 cal ganglia, whereas immunoreactivity in the postganglionic neurons and small diameter cells remained

54 Receptors for IL-17 were present on postganglionic neurons from superior mesenteric ganglia

55 e P2X receptor expression within sympathetic postganglionic neurons from the superior cervical gangli

56 neurons (CVMs) are mediated by activation of postganglionic neurons in the epicardial ganglia which h

57 Here we imaged the synapses between pre- and postganglionic neurons in the mouse submandibular gangli

58 green fluorescent pseudorabies virus labeled postganglionic neurons in the pelvic ganglion that inner

59 togenetic features that distinguish pre- and postganglionic neurons of the cranial parasympathetic ou

60 Postganglionic neurons of the superior cervical and othe

61 asket-like terminals surrounding many of the postganglionic neurons of the superior cervical, stellat

62 f vagal preganglionic neurons that innervate postganglionic neurons of the upper gastrointestinal tra

63 rmal levels of NGF in targets of sympathetic postganglionic neurons prior to the period of programmed

64 ly, the number of double-labeled sympathetic postganglionic neurons was greatly increased after spina

65 mpathetic preganglionic neurons, sympathetic postganglionic neurons, and dorsal motor nucleus of the

66 make up a small subpopulation of cholinergic postganglionic neurons.

67 P peptides elicited primary responses in the postganglionic neurons.

68 e pool of negative inotropic parasympathetic postganglionic neurons.

69 r nucleus of the vagus nerve, and the second postganglionic, originating in the celiac-superior mesen

70 possibility of electrically stimulating the postganglionic parasympathetic ganglia to improve cereba

71 the SP-induced depolarization in guinea-pig postganglionic parasympathetic neurones of the cardiac g

72 that PACAP-containing fibers innervating the postganglionic parasympathetic neurons in guinea pig car

73 channels subserving transmitter release from postganglionic parasympathetic neurons in the bladder an

74 The SSN, in turn, activates postganglionic parasympathetic neurons in the sphenopala

75 electrical stimulation of preganglionic and postganglionic parasympathetic neurons innervating the s

76 s serving as local reflex inputs to modulate postganglionic parasympathetic output within the cardiac

77 tions whose time course mirrored that of the postganglionic peptidergic after-discharge.

78 ory ganglia and reduced number of NC-derived postganglionic (PG) neurons.

79 Postganglionic rat sympathetic neurons formed extensive

80 s with subthreshold nicotinic EPSPs and that postganglionic release of NPY shifts frequency tuning of

81 ndamine, suggesting a role for both pre- and postganglionic signals in regulating NE release.

82 Under these conditions, postganglionic stimulation showed smaller changes in sin

83 Similar depolarizations were evoked by postganglionic stimulation.

84 ity occurs in the presynaptic portion of the postganglionic sudomotor axon.

85 esions of mixed nerves or of the sympathetic postganglionic supply.

86 Action potential-evoked Ca(2+) transients in postganglionic sympathetic axon bundles in mouse vas def

87 ne release from adrenal chromaffin cells and postganglionic sympathetic axons.

88 Postganglionic sympathetic axotomy leads to a prolonged

89 factor (LIF) in axotomy-induced sprouting of postganglionic sympathetic fibres into the dorsal root g

90 of central pre-ganglionic but not peripheral postganglionic sympathetic innervation to the spleen.

91 s revealed an enhancement of cardiac-related postganglionic sympathetic nerve discharge (SND) in resp

92 he cardiac-related burst of inferior cardiac postganglionic sympathetic nerve discharge (SND) relativ

93 study neurotransmitter release mechanisms in postganglionic sympathetic nerve terminals in the guinea

94 study neurotransmitter release mechanisms in postganglionic sympathetic nerve terminals of the rat is

95 voked neurotransmitter release mechanisms in postganglionic sympathetic nerve terminals.

96 the NGF-TrkA effector protein, Coronin-1, on postganglionic sympathetic neuron final target innervati

97 The postganglionic sympathetic neuron has been an amenable m

98 aracteristic rhythmical discharges of single postganglionic sympathetic neurones (PSNs) innervating t

99 IF is associated with sprouting of uninjured postganglionic sympathetic neurones around sensory neuro

100 The results indicate that postganglionic sympathetic neurons are severely depleted

101 II selectively activates a subpopulation of postganglionic sympathetic neurons in aortic-renal and c

102 asympathetic neurons in the bladder and from postganglionic sympathetic neurons in the vas deferens o

103 otransmitter metabolism and cell survival in postganglionic sympathetic neurons.

104 suggesting that Ang II may directly activate postganglionic sympathetic neurons.

105 ensory fibers, but not with the terminals of postganglionic sympathetic neurons.

106 Because PD involves postganglionic sympathetic noradrenergic lesions, the di

107 noradrenergic tone at rest and by a blunted postganglionic sympathetic response to standing, with a

108 epithelial potentiation (TEP) after pre- and postganglionic sympathetic stimulation in the bullfrog,

109 to pharmacologically replace lower-extremity postganglionic sympathetics is an appropriate overall go

110 se is induced by both presynaptic inputs and postganglionic target tissues but does not occur until t

111 nce of regulatory signals from both pre- and postganglionic tissues.

112 Postganglionic vagal stimulation (PGVS) by short bursts