[Effects of cervical epidural block and stellate ganglion block on short latency somatosensory evoked potentials].
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Neurons lying in the white matter of the upper cervical spinal cord become transneuronally labelled following pseudorabies virus injections into the kidney or stellate ganglion, suggesting that they project directly to sympathetic preganglionic neurons. In the present study, we extend these findings and report here that i) neurons in both the lateral spinal nucleus and lateral funiculus become transneuronally labelled after pseudorabies virus injections into the superior cervical ganglion, stellate ganglion, celiac ganglion, or adrenal gland and ii) both of these two cell groups project directly to the sympathetic preganglionic neurons as demonstrated with the Phaseolus vulgaris leuco-agglutinin axonal tracing method. In addition, lateral funiculus neurons project to the cervical and upper thoracic dorsal horn (lamina V), intermediate gray matter (laminae VII and X), and ventral horn. The lateral spinal nucleus also projects to the medial part of laminae I and II, V, VII. To verify that pseudorabies virus-infected lateral funiculus and lateral spinal nucleus cells have a neuronal phenotype, we demonstrated that these cells also can be immunostained with antibodies directed against a neuron specific marker, neuronal nuclear protein called NeuN, but not with antibodies against glial acidic fibrillary protein or oligodendroglia. In summary, this report provides the first evidence that two descending sympathetic projection systems arise from neurons lying within the white matter of the cervical spinal cord.
The viral transneuronal labeling method was used to localize sympathetic-related neurons in the preoptic region following pseudorabies virus (PRV) injections into either the superior cervical ganglion, stellate ganglion, celiac ganglion, or adrenal gland of rats. A general pattern of infection was detected. First, neuronal labeling was found in the medial preoptic area, medial preoptic nucleus, median preoptic nucleus, and lateral preoptic area, and then it spread to the anteroventral periventricular, anteroventral preoptic, and parastrial nuclei. Finally, the forebrain circumventricular organs: organum vasculosum of the lamina terminalis (OVLT) and subfornical organ (SFO) became infected. Neuropeptide-containing preoptic neurons were analyzed following PRV injections in the stellate ganglion. Some thyrotropin-releasing hormone and neurotensin neurons were labeled, but none of the calcitonin gene-related peptide, cholecystokinin, corticotropin-releasing factor, galanin, luteinizing hormone-releasing hormone, enkephalin, substance P, or tyrosine hydroxylase neurons were PRV infected. Two major sympathetic networks appear to be represented in the preoptic region. One is linked to the OVLT, SFO, and anteroventral third ventricular (AV3V) region, sites previously implicated in fluid and electrolyte balance as well as cardiovascular control. The other descending sympathetic pathway appears to target the medial preoptic nucleus as its key nodal point, receiving inputs from infralimbic cortex and limbic regions, such as the lateral septum, medial nucleus of the amygdala, subiculum, and amygdalohippocampal area, and then, projecting caudally to the hypothalamus and brainstem. This second sympathetic network may subserve affiliative, defensive and sexual behaviors.
The content of LDH isozymes was studied in extramural ganglions (superior cervical ganglion, stellate ganglion and symphathetic chain at the level of the 4th--6th thoracic segments) of the sympathetic nervous system, of the nodosal ganglion of the vagus nerve, working myocardium and conductive system of the heart of rabbits with acute experimental emotional stress provoked by simultaneous electric stimulation of the negative emotiogenic area of the hypothalamus, ventromedial nuclei, and skin. Under conditions of emotional stress no changes could be recorded in the ratio of LDH isozymic fractions in the ganglions as compared with control. No changes were found in LDH content of the working myocardium in rabbits exposed to stress. The conductive system of the heart (atrioventricular node and His' bundle) demonstrated a certain sensitivity to stress, manifesting in the increased activity of fast-moving fractions in the spectrum of LDH isozymes. The modulated electromagnetic field that exerts a protective action against an adverse effect of emotional stress produced significant shifts in LDH spectrum in the ganglions of the autonomous nervous system. No changes were detected in the spectrum of LDH isozymes in the conductive system. The results obtained suggest that the above structures of the autonomous nervous system are an important link in the bodily response to the concomitant action of the two stressors.
We analyzed the activities of acetylcholinesterase and butyrylcholinesterase, and of the metabolic enzymes enolase and lactate dehydrogenase, in the superior cervical ganglion, ciliary ganglion, dorsal root ganglion, stellate ganglion, and caudate nucleus of the cat; we found that these tissues possess very different levels of enzymic activities. The proportions of the alpha alpha, alpha gamma, and gamma gamma enolase isozymes are also quite variable. We particularly studied the molecular forms of acetylcholinesterase and butyrylcholinesterase, in normal tissues and in preganglionically denervated SCG, in comparison with earlier histochemical findings. The results are consistent with the premise that the G1 (globular monomer) forms of both enzymes are located in the cytoplasm, the G4 (globular tetramer) forms are at the plasma membranes, and the A12 (collagen-tailed, asymmetric dodecamer) form of acetylcholinesterase is at synaptic sites.
In anesthetized cats, the preganglionic input to the stellate ganglion involved Th3 and Th4 white rami. The chronotropic influences to the heart travelled through caudal anastomose whereas inotropic those--through inferior cardiac nerve. Neurons of these nerves are distributed over the ganglion stellate in different sites. The data obtained suggest that the pathways relating central sympathetic influences, are specialized.
In the present study, we investigated the immunohistochemical localization of the two-pore K+ channels, TASK-3 and TRAAK, in paraganglionic cells within the superior cervical ganglion, stellate ganglion, and aortic body in comparison with membrane channels in chief cells of the carotid body. TASK-3 immunoreactivity was observed in the paraganglionic cells in all tissues examined. TRAAK immunoreactivity was observed in the chief cells of the aortic body as well as these of the carotid body, but not in the paraganglionic cells in the sympathetic (superior cervical and stellate) ganglia. Our findings indicate that sympathetic paraganglionic cells and glossopharyngeal/vagal paraganglionic cells were different from each other in the expression patterns of TASK-3 and TRAAK to result in the different chemoreception properties of sympathetic paraganglionic cells from those of chief cells of the aortic and carotid bodies.
The occurrence of CGRP-immunoreactive neurons in human paravertebral sympathetic ganglia was investigated and CGRP-immunoreactive perikarya correlated with the distribution of structures which were immunoreactive to other peptides and tyrosine hydroxylase, the key enzyme of catecholamine-synthesis. CGRP-immunoreactive neurons were present in all investigated ganglia (superior cervical ganglion, stellate ganglion, thoracic ganglia IV and VII). Most of the CGRP-immunolabelled cell bodies contained also vasoactive intestinal polypeptide-as well as somatostatin-immunoreactivity. Approximately 40 per cent of the CGRP-immunoreactive neurons were weakly tyrosine hydroxylase-immunolabelled. CGRP-immunoreactive cell bodies appear to be neither identical with the large population of neuropeptide Y-labelled perikarya nor with the large group of cell bodies which were surrounded by leuenkephalin-immunoreactive nerve fibres. Colocalization of CGRP- with vasoactive intestinal polypeptide- and somatostatin-immunoreactivity in postganglionic sympathetic neurons substantiates the suggestion of sympathetic origin of respective peptidergic nerve fibres in sweat glands.
Changes in the duration of monophasic action potentials on the anterior and posterior walls of the dog ventricle were correlated with changes in T wave polarity and duration of the Q-T interval after (1) left stellate ganglion transection, (2) right stellate ganglion stimulation, and (3) administration of isoproterenol before or after these procedures. Left stellate ganglion transection and right stellate ganglion stimulation produced similar changes in T wave polarity, but the former prolonged and the latter shortened the Q-T interval. All procedures changed the duration of the monophasic action potential and the Q-T interval in the same direction. The reversal of T wave polarity induced by left stellate ganglion transection, right stellate ganglion stimulation or administration of isoproterenol after left stellate ganglion transection was associated with an average change of 13 to 17 msec in the difference between the monophasic action potential durations on the anterior and posterior ventricular walls. Isoproterenol restored to normal the neurogenic T wave abnormalities produced by left stellate ganglion transection and right stellate ganglion stimulation. The drug shortened the previously prolonged monophasic action potential more than the normal monophasic action potential, and the normal monophasic action potential more than the previously shortened monophasic action potential. This study confirms that the T wave is a sensitive indicator of relatively small changes (less than 20 msec) in the sequence of ventricular repolarization and explains the mechanism by which isoproterenol "normalizes" the primary T wave abnormalities.
Indirect immunofluorescence methods using a mouse monoclonal antibody raised to rat choline acetyltransferase (ChAT) revealed dense networks of ChAT-immunoreactive fibers in the superior cervical ganglion, the stellate ganglion, and the celiac superior mesenteric ganglion of the rat. Numerous and single ChAT-immunoreactive cell bodies were observed in the stellate and superior cervical ganglia, respectively. The majority of ChAT-immunoreactive fibers in the stellate and superior cervical ganglia were nitric oxide synthase (NOS) positive. Some ChAT-immunoreactive fibers contained enkephalin-like immunoreactivity. Virtually all ChAT-positive cell bodies in the stellate ganglion were vasoactive intestinal polypeptide (VIP)-positive, and some were calcitonin gene-related peptide (CGRP)-positive. After transection of the cervical sympathetic trunk almost all ChAT- and NOS-positive fibers and most enkephalin- and CGRP-positive fibers disappeared in the superior cervical ganglion. The results suggest that most preganglionic fibers are cholinergic and that the majority of these in addition can release nitric oxide, some enkephalin, and a few CGRP. Acetylcholine, VIP, and CGRP are coexisting messenger molecules in some postganglionic sympathetic neurons.
Correlative quantitative analyses were performed on the rat comparing the number of fibers in the cervical sympathetic trunk (CST) and the horseradish peroxidase (HRP)-labeled neurons in the superior cervical sympathetic ganglion (SCG), stellate ganglion, as well as in the spinal cord. The total number of nerve fibers in the left CST was 4180 +/- 169 (mean +/- S.E.M.) among which 92 +/- 3 (mean +/- S.E.M.) were myelinated. The diameter of unmyelinated fibers was 0.68 +/- 0.22 (mean +/- S.D.) microns and showed single-peaked distribution. After the application of HRP to the proximal cut end of the CST, labeled neurons were found in the stellate ganglion as well as in the ipsilateral spinal cord from C7 to T4 segments. The total number of HRP-labeled neurons in the spinal cord was 1334 +/- 45 (mean +/- S.E.M.) with the range between 844 and 1808. Ninety-nine percent of labeled neurons were located in the intermediolateral column and in the lateral funiculus while 1% were in the intercalated region and central autonomic area. Labeled neurons were encountered only sporadically in the dorsal root ganglia (DRG) from C8 to T3 level. After the application of HRP to the distal cut end of the CST, about 200 labeled neurons were observed in the caudal part of the SCG. The present results were discussed with special reference to the organization of the CST of the rat.