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1 ) and regions (preganglionic, ganglionic and postganglionic).
2             Contractions were antagonized by postganglionic action of guanethidine, but not by phento
3 rgic receptor agonist) on muscle sympathetic postganglionic action potential (AP) discharge, recruitm
4                                     Complete postganglionic arbors (n = 154) in the muscle wall were
5  these fibers were identified as sympathetic postganglionic axons based on their disappearance in org
6 ves in reporter mice to further clarify that postganglionic axons connect to iWAT via lateral cutaneo
7        Electrical stimulation of sympathetic postganglionic axons evoked inhibitory postsynaptic pote
8                 The ability of adult injured postganglionic axons to reinnervate cerebrovascular targ
9                                          The postganglionic axons within the ganglion showed less VAC
10 ase (marker of catecholaminergic sympathetic postganglionic axons), or calcitonin gene-related peptid
11      Unilateral preganglionic denervation or postganglionic axotomy causes declines in alpha3, beta4,
12  prolonged activation of STAT proteins after postganglionic axotomy in vivo is loss of target-derived
13 he loss of target-derived NGF resulting from postganglionic axotomy in vivo, SCG were explanted into
14                                         Like postganglionic axotomy in vivo.
15 onal fibers and a subpopulation of intrinsic postganglionic cardiac neurons.
16 , and cardiopulmonary information to produce postganglionic cardiac sympathetic inputs.
17               Only an occasional sympathetic postganglionic cell in the stellate ganglion complex exh
18 ivity so far identified in preganglionic and postganglionic cells of the ciliary ganglion in differen
19 nst M(3) acetylcholine receptors cause acute postganglionic cholinergic dysautonomia.
20 g cells were used to label preganglionic and postganglionic cholinergic neurons and their projections
21    The inhibitory effect of adenosine on the postganglionic compound action potential (CAP) was antag
22                                          The postganglionic compound action potential (CAP), made sub
23 he amplitude of the extracellularly recorded postganglionic compound action potential.
24 493 and PF 05089771, significantly inhibited postganglionic compound action potentials by approximate
25  physiological evidence indicates that vagal postganglionic control of left ventricular contractility
26                                    The vagal postganglionic controls of cardiac rate and left ventric
27 tral neural mechanisms governing sympathetic postganglionic discharge remain unclear.
28   The extent of the sprouting of sympathetic postganglionic fibers in the dorsal root ganglion (DRG)
29                                              Postganglionic fibers projected into the wall of the ren
30 ear to be a conduit by which pterygopalatine postganglionic fibers reach the choroid.
31                      The distribution of the postganglionic fibers was investigated by means of the c
32                          The pterygopalatine postganglionic fibers were also seen to innervate the Ha
33                              The sympathetic postganglionic fibers were visualized by immunostaining
34                                  Sympathetic postganglionic fibers, as identified by electron microsc
35 ntinuing belief that cardiac parasympathetic postganglionic fibres are sparse or absent from the vent
36 lls were most likely cardiac parasympathetic postganglionic fibres.
37                                 Asynchronous postganglionic firing mediated by peptidergic cotransmis
38 ., approximately 60%) of all individual CSMG postganglionics formed mixed, heterotypic arbors that co
39 opographical distribution of the sympathetic postganglionic innervation in whole atria of C57Bl/6 J m
40 ecise anatomical extent of preganglionic and postganglionic inputs to the inguinal white adipose tiss
41 d tissue was collected to assess sympathetic postganglionic intracellular calcium transients ([Ca(2+)
42         Acetylcholine, released from gastric postganglionic intramural neurons, stimulates the pariet
43         Acetylcholine, released from gastric postganglionic intramural neurons, stimulates the pariet
44                                    While the postganglionic motoneurons in the CG are cholinergic, as
45 of synaptic potentials evoked by stimulating postganglionic motor nerves.
46                                     Efferent postganglionic muscle SNA, BP, and central venous pressu
47 ulatory function and the role of sympathetic postganglionic nerve traffic in maintaining the pain in
48                  Retrograde stimulation of a postganglionic nerve trunk evoked direct, all-or-none ac
49 lowing electrical activation of the pre- and postganglionic nerve trunks and used genetic strategies
50 ally evoked compound action potential in the postganglionic nerve; it also desynchronized the firing
51 of the right atrial fat pad, containing both postganglionic nerves and terminals of preganglionic neu
52 after local application of colchicine to the postganglionic nerves, which blocks fast transport witho
53 at is, in part, dependent on the sympathetic postganglionic neuron (SPGN) terminal, we tested the hyp
54 d neuronal loss but only impaired inhibitory postganglionic neuron function; it is often associated w
55        We therefore examined function of the postganglionic neuron in the paced canine model of HF as
56  central nervous system modulate sympathetic postganglionic neuronal discharge, recruitment and laten
57                                  Sympathetic postganglionic neuronal subpopulations innervating the h
58 ion of cutaneous vasoconstrictor sympathetic postganglionic neurones (PGNs) in anaesthetized rats.
59 ctivity was recorded from single sympathetic postganglionic neurones innervating the caudal ventral a
60 ctivity was recorded from single sympathetic postganglionic neurones innervating the lateral tail vei
61 sed rats, activity recorded from sympathetic postganglionic neurones innervating the tail circulation
62 P)-induced depolarization of parasympathetic postganglionic neurones of the cardiac ganglion.
63 ges of fourteen out of seventeen sympathetic postganglionic neurones were rhythmic.
64 in the myenteric plexus and from sympathetic postganglionic neurones.
65 c rhythms and promote summation of inputs to postganglionic neurones.
66 cal ganglia, whereas immunoreactivity in the postganglionic neurons and small diameter cells remained
67          Receptors for IL-17 were present on postganglionic neurons from superior mesenteric ganglia
68 e P2X receptor expression within sympathetic postganglionic neurons from the superior cervical gangli
69 neurons (CVMs) are mediated by activation of postganglionic neurons in the epicardial ganglia which h
70 Here we imaged the synapses between pre- and postganglionic neurons in the mouse submandibular gangli
71 green fluorescent pseudorabies virus labeled postganglionic neurons in the pelvic ganglion that inner
72 n human colon to investigate how sympathetic postganglionic neurons modulate colon function.
73 togenetic features that distinguish pre- and postganglionic neurons of the cranial parasympathetic ou
74 e presence of collateral projections between postganglionic neurons of the stellate ganglia.
75                                              Postganglionic neurons of the superior cervical and othe
76 asket-like terminals surrounding many of the postganglionic neurons of the superior cervical, stellat
77                                              Postganglionic neurons of the sympathetic chain ganglia
78 vival and proliferation of preganglionic and postganglionic neurons of the sympathetic system, respec
79 f vagal preganglionic neurons that innervate postganglionic neurons of the upper gastrointestinal tra
80 rmal levels of NGF in targets of sympathetic postganglionic neurons prior to the period of programmed
81  and sufficient to relay allergen signals to postganglionic neurons that directly drive airway constr
82 ly, the number of double-labeled sympathetic postganglionic neurons was greatly increased after spina
83 the presence of cholinergic collaterals from postganglionic neurons within the stellate ganglion, we
84 mpathetic preganglionic neurons, sympathetic postganglionic neurons, and dorsal motor nucleus of the
85 make up a small subpopulation of cholinergic postganglionic neurons.
86 P peptides elicited primary responses in the postganglionic neurons.
87 e pool of negative inotropic parasympathetic postganglionic neurons.
88 r nucleus of the vagus nerve, and the second postganglionic, originating in the celiac-superior mesen
89 electrophysiological tests revealed that the postganglionic parasympathetic fibers travel to the faci
90  possibility of electrically stimulating the postganglionic parasympathetic ganglia to improve cereba
91  the SP-induced depolarization in guinea-pig postganglionic parasympathetic neurones of the cardiac g
92 that PACAP-containing fibers innervating the postganglionic parasympathetic neurons in guinea pig car
93 channels subserving transmitter release from postganglionic parasympathetic neurons in the bladder an
94                  The SSN, in turn, activates postganglionic parasympathetic neurons in the sphenopala
95  electrical stimulation of preganglionic and postganglionic parasympathetic neurons innervating the s
96 us to confirm the extensive heterogeneity of postganglionic parasympathetic neurons.
97 s serving as local reflex inputs to modulate postganglionic parasympathetic output within the cardiac
98 tions whose time course mirrored that of the postganglionic peptidergic after-discharge.
99 ory ganglia and reduced number of NC-derived postganglionic (PG) neurons.
100                                              Postganglionic rat sympathetic neurons formed extensive
101 ference in MTR between the preganglionic and postganglionic regions in all lumbar segments.
102 s with subthreshold nicotinic EPSPs and that postganglionic release of NPY shifts frequency tuning of
103 ndamine, suggesting a role for both pre- and postganglionic signals in regulating NE release.
104                      Under these conditions, postganglionic stimulation showed smaller changes in sin
105       Similar depolarizations were evoked by postganglionic stimulation.
106 ity occurs in the presynaptic portion of the postganglionic sudomotor axon.
107 scular and pupillary impairments, 7 of 8 had postganglionic sudomotor dysfunction, 9 of 11 had urinar
108 esions of mixed nerves or of the sympathetic postganglionic supply.
109  cell bridge was enriched in both markers of postganglionic sympathetic and vagal afferents neurons.
110  continuous wavelet transform to investigate postganglionic sympathetic AP firing during a baseline c
111 Action potential-evoked Ca(2+) transients in postganglionic sympathetic axon bundles in mouse vas def
112 pressing neurons prior to the arrival of the postganglionic sympathetic axons from the superior cervi
113 ne release from adrenal chromaffin cells and postganglionic sympathetic axons.
114                                              Postganglionic sympathetic axotomy leads to a prolonged
115                                              Postganglionic sympathetic fibers also showed abnormal r
116 factor (LIF) in axotomy-induced sprouting of postganglionic sympathetic fibres into the dorsal root g
117 of central pre-ganglionic but not peripheral postganglionic sympathetic innervation to the spleen.
118 m the iWAT, we defined the preganglionic and postganglionic sympathetic input to iWAT.
119 s revealed an enhancement of cardiac-related postganglionic sympathetic nerve discharge (SND) in resp
120 he cardiac-related burst of inferior cardiac postganglionic sympathetic nerve discharge (SND) relativ
121 study neurotransmitter release mechanisms in postganglionic sympathetic nerve terminals in the guinea
122 study neurotransmitter release mechanisms in postganglionic sympathetic nerve terminals of the rat is
123 voked neurotransmitter release mechanisms in postganglionic sympathetic nerve terminals.
124  Na(V)1.7 in conducting action potentials in postganglionic sympathetic nerves and in the sympathetic
125                                 In contrast, postganglionic sympathetic nerves arrive late in salivar
126 ckers inhibit action potential conduction in postganglionic sympathetic nerves.
127  suggesting that NA induces NPY release from postganglionic sympathetic nerves.
128 the NGF-TrkA effector protein, Coronin-1, on postganglionic sympathetic neuron final target innervati
129                                          The postganglionic sympathetic neuron has been an amenable m
130 aracteristic rhythmical discharges of single postganglionic sympathetic neurones (PSNs) innervating t
131 IF is associated with sprouting of uninjured postganglionic sympathetic neurones around sensory neuro
132 and functionally precise connections between postganglionic sympathetic neurons and peripheral organs
133                    The results indicate that postganglionic sympathetic neurons are severely depleted
134 ic studies of key events in the formation of postganglionic sympathetic neurons during embryonic and
135  II selectively activates a subpopulation of postganglionic sympathetic neurons in aortic-renal and c
136 asympathetic neurons in the bladder and from postganglionic sympathetic neurons in the vas deferens o
137                           The cell bodies of postganglionic sympathetic neurons innervating the heart
138 y regulatory component in the heart, cardiac postganglionic sympathetic neurons residing in the stell
139                The potential contribution of postganglionic sympathetic neurons to sustained sympathe
140 reganglionic neurons are thought to activate postganglionic sympathetic neurons.
141  it contained a mixed of vagal afferents and postganglionic sympathetic neurons.
142 otransmitter metabolism and cell survival in postganglionic sympathetic neurons.
143 suggesting that Ang II may directly activate postganglionic sympathetic neurons.
144 ensory fibers, but not with the terminals of postganglionic sympathetic neurons.
145                          Because PD involves postganglionic sympathetic noradrenergic lesions, the di
146  noradrenergic tone at rest and by a blunted postganglionic sympathetic response to standing, with a
147 epithelial potentiation (TEP) after pre- and postganglionic sympathetic stimulation in the bullfrog,
148 to pharmacologically replace lower-extremity postganglionic sympathetics is an appropriate overall go
149 se is induced by both presynaptic inputs and postganglionic target tissues but does not occur until t
150 nce of regulatory signals from both pre- and postganglionic tissues.
151                                              Postganglionic vagal stimulation (PGVS) by short bursts

 
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