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At least 973 records · Page 54Linked to original sources
PubMed1990

Distribution of functional significance of Met-enkephalin-Arg6-Phe7- and Met-enkephalin-Arg6-Gly7-Leu8-like peptides in the blowfly Calliphora vomitoria. II. Immunocytochemical mapping of neuronal pathways in the retrocerebral complex and thoracic ganglion.

Neuronal pathways in the retrocerebral complex and thoracico-abdominal ganglionic mass of the blowfly Calliphora vomitoria have been identified immunocytochemically with antisera against the extended-enkephalins, Met-enkephalin-Arg6-Phe7 (Met-7) and Met-enkephalin-Arg6-Gly7-Leu8 (Met-8). Neurons of the hypocerebral ganglion, immunoreactive to Met-8, have axons in the crop duct nerve and terminals in muscles of the crop and its duct. Certain neurons of the hypocerebral ganglion are also immunoreactive to Met-7, and axons from these cells innervate the heart. Met-8 immunoreactive nerve terminals invest the cells of the corpus allatum. The source of this material is believed to be a single pair of lateral neurosecretory cells in the brain. There is no Met-7 immunoreactive material in the corpus allatum. In the corpus cardiacum neither Met-7 nor Met-8 immunoreactivity is present in the cells. However, in the neuropil of the gland certain fibres, with their origins elsewhere, do contain Met-8 immunoreactivity. The most prominent neurons in the thoracic ganglion are the Met-7 immunoreactive ventral thoracic neurosecretory cells, axons from which project to neurohaemal areas in the dorsal neural sheath and also, via the ventral connective, to the brain. Co-localisation studies show that the perikarya of these cells are immunoreactive to antisera raised against several vertebrate-type peptides, such as Met-7, gastrin/cholecystokinin and pancreatic polypeptide. However, their axons and terminals show varying amounts of the peptides, suggesting differential transport and utilisation. Only a few cells in the thoracic ganglion are immunoreactive to Met-8 antisera. These lie close to the nerve bundles supplying the legs. In the abdominal ganglion, Met-8 immunoreactive neurons project to the muscles of the hindgut. This study suggests that the extended enkephalin-like peptides of Calliphora may have a variety of different roles: as neurotransmitter or neuromodulator substances; in the direct innervation of effector organs; and as neurohormones.

Animals↗
PubMed1986

Initiation of swimming activity by trigger neurons in the leech subesophageal ganglion. I. Output connections of Tr1 and Tr2.

The aim of this study was to identify neurons in the subesophageal ganglion of the medicinal leech which initiate swimming activity and to determine their output connections. We found two bilaterally symmetrical pairs of interneurons, Tr1 and Tr2, located in the first division of the subesophageal ganglion which initiate swimming activity in the isolated nervous system when depolarized with brief (1-3 s) current pulses. Tr1 and Tr2 are considered trigger neurons because elicited swimming episodes outlast the stimulus duration, and because the length of elicited swim episodes is nearly independent of the intensity with which Tr1 and Tr2 are stimulated. Tr1 and Tr2 have similar morphologies. The neurites of both cells cross contralaterally in the subesophageal ganglion, project posteriorly, and exit the subesophageal ganglion in the contralateral connective. The axons of Tr1 and Tr2 extend as far posterior as segmental ganglion 18 of the ventral nerve cord. Tr1 provides direct excitatory drive to three groups of segmental neurons which are capable of initiating swimming: swim-initiating interneurons (cells 204 and 205), serotonin-containing interneurons (cells 61 and 21), and the serotonergic Retzius cells. In addition, all Retzius cells in the subesophageal ganglion are excited directly by Tr1. These three groups of neurons are excited even if Tr1 stimulation is subthreshold for swim initiation. In contrast to Tr1, Tr2 stimulation evokes transient inhibition in swim-initiating and serotonin-containing interneurons, and has little immediate effect on Retzius cells. In addition, Tr2 indirectly inhibits several oscillator neurons, including cells 208, 33, and 60. When Tr1 is stimulated during a swimming episode the swim period decreases for several cycles, while stimulation of Tr2 during swimming episodes reliably resets the ongoing swimming rhythm. Our findings indicate that Tr1 and Tr2 are trigger neurons which initiate swimming activity by different pathways. These neurons also have functional interactions with the swim oscillator network since either Tr1 or Tr2 stimulation during swimming can modulate the ongoing swimming rhythm.

Animals↗
PubMed1982

Catecholamine-containing neurons in Remak's ganglion: a developmental and tissue culture study.

Development and maturation of the catecholamine-containing neurons of the embryonic chick and quail Remak's ganglion were studied, using the glyoxylic acid method. Fluorescent neurons were detected in the pararectal segment of the ganglion from its earliest in vivo formation, and along the whole ganglionic chain in later developmental stages. In tissue culture, a large number of catecholamine-containing neurons matured in explants of both early and more developed ganglia, producing an extensive network of outgrowing fluorescent nerve processes. Pararectal ganglia, cultured in vitro for up to 4 days, gave rise, whatever the developmental stage examined, to fluorescent migratory neurons distributed either in ganglion-like clusters or singly in a large area surrounding the explant. Many non-fluorescent neurons were intermingled with the fluorescent ones in the explants, as well as in the outgrowth. Ganglia from segments adjacent to the small intestine did not give rise to migratory neurons whatever the developmental stage. Regional differences in the development of migratory neurons may be correlated to the mechanism of the in vivo organization of the ganglionic chain. The present observations indicate that catecholamine-containing neurons in Remak's ganglion exhibit the same histochemical features as adrenergic sympathetic neurons and differentiate in short-term cultures.

Animals↗
PubMed1990

An unbiased estimation of the total number of synapses in the superior cervical ganglion of adult rats established by the disector method. Lack of change after long-lasting sodium bromide administration.

Previous physiological and morphological studies suggested that sodium bromide promotes synaptogenesis of implanted cholinergic nerves in the superior cervical ganglion of adult rats. To check whether sodium bromide also modifies synaptic numbers in the intact ganglion, quantitative electron microscopy was used to determine the total number of synaptic junctions in the superior cervical ganglion of adult rats. Untreated controls were compared with animals which drank water containing 280 mg ml-1 sodium bromide for 7 days. The disector method, an unbiased estimator of volume density of certain particles, has been adapted to this particular case. To accomplish the task, an on-line counting procedure was developed, which permitted the efficient adaptation of the disector method for the superior cervical ganglion, in which the synapses are known to be distributed sparsely. Three pairs of (control and treated) ganglia have been completely processed by three independent examiners. The estimated number of synapses in the ganglia ranged from 4 to 8 million while the volumes of the ganglia varied from 0.65 to 0.90 mm3. Evaluation of the results showed that variations in the total number of synapses were in each case proportional to differences in ganglionic volumes. This suggests that: (1) sodium bromide does not lead to changes in density of intrinsic synapses; and (2) the morphogenetic action of sodium bromide on principal ganglion cells previously described is essentially postsynaptic and requires additional presynaptic elements to increase the number of synapses.

Animals↗
PubMed1979

[Morphological changes in ciliary ganglions of healthy subjects and glaucoma patients].

The authors studied morphological changes in eleven ciliary ganglions. Seven ganglions were obtained from four corpses of patients with primary glaucoma in different stages, and four control ganglions were obtained from corpses of healthy people. The ciliary ganglion neurons of healthy subjects demonstrated age-related changes revealing nucleus shift toward the periphery, atypical hairy Kahal neurons, nerve fiber irritation phenomena, and other effects. The stage-dependent changes observed included: devastation areas, reactive proliteration around prolapsed neurons, nerve fiber degeneration, and hemorrhages. Maturing glaucomatous nerve cells and fiber degeneration also grew in proportion. In absolute glaucoma, ganglion cells were not present in ganglions. The authors believe that the existence of age-dependent structural changes in ciliary ganglia shows that ciliary ganglia are responsible for neurotropic innervation of eye membranes and participate in the glaucomatous process.

Age Factors↗
PubMed2004

Neuromodulation for behavior in the locust frontal ganglion.

Neuromodulators orchestrate complex behavioral routines by their multiple and combined effects on the nervous system. In the desert locust, Schistocerca gregaria, frontal ganglion neurons innervate foregut dilator muscles and play a key role in the control of foregut motor patterns. To further investigate the role of the frontal ganglion in locust behavior, we currently focus on the frontal ganglion central pattern generator as a target for neuromodulation. Application of octopamine, a well-studied insect neuromodulator, generated reversible disruption of frontal ganglion rhythmic activity. The threshold for the modulatory effects of octopamine was 10(-6) mol l(-1), and 10(-4) mol l(-1) always abolished the ongoing rhythm. In contrast to this straightforward modulation, allatostatin, previously reported to be a myoinhibitor of insect gut muscles, showed complex, tri-modal, dose-dependent effects on frontal ganglion rhythmic pattern. Using a novel cross-correlation analysis technique, we show that different allatostatin concentrations have very different effects not only on cycle period but also on temporal characteristics of the rhythmic bursts of action potentials. Allatostatin also altered the frontal ganglion rhythm in vivo. The analysis technique we introduce may be instrumental in the study of not fully characterized neural circuits and their modulation. The physiological significance of our results and the role of the modulators in locust behavior are discussed.

Action Potentials↗
PubMed2004

Embryonic development of the ganglion plexuses and the concentric layer structure of human gut: a topographical study.

In this study, we performed a detailed topographical study on the development of ganglion plexuses and the smooth muscle layers of human embryonic and fetal gut. Neuron and glia differentiation was investigated with anti-PGP9.5 and anti-S100 antibodies respectively. The differentiation of smooth muscle and interstitial cells of Cajal (ICC) was studied with anti-smooth muscle alpha-actin and anti-C-Kit antibodies respectively. By week 7, rostro-caudal neural crest cell (NCC) colonization of the gut was complete, and NCCs have differentiated into neurons and glia. At the foregut, neurons and glia were aggregated into ganglion plexus in the myenteric region, and the longitudinal and circular muscle layers have started to differentiate; however, neurons and glia were not found in the submucosa. At the hindgut, neurons and glia were dispersed within the mesenchyme. Myenteric plexus, longitudinal and circular muscle layers formed along the entire gut by week 9. Scattered and individual neurons and glia, and small ganglion plexuses were detected in the foregut and midgut submucosa by week 12. Ganglion plexus was not seen in the hindgut submucosa until week 14. Muscularis mucosae was formed at the foregut and midgut by week 12 but was only discernible at the hindgut 2 weeks later. As the gut wall developed, ganglion plexus increased in size with more neurons and glia, and the formation of intra-plexus nerve fascicle. ICCs were localized in the ganglion plexus as early as week 7. ICCs were initially dispersed in the plexus and were preferentially localized at the periphery of the plexus by week 20. The specification of the annular layers of human embryonic and fetal gut follows a strict spatio-temporal pattern in a rostro-caudal and centripetal manner suggesting that interaction between (1) homotypic and/or heterotypic cells; and (2) cells and the extracellular matrix is critical for the embryonic development of the gut mesenchyme and the enteric nervous system.

Actins↗
PubMed2001

Differences in the distribution and chemical coding between neurons in the inferior mesenteric ganglion supplying the colon and rectum in the pig.

The distribution and chemical coding of neurons in the porcine left and right inferior mesenteric ganglion projecting to the ascending colon and rectum have been investigated by using combined retrograde tracing and double-labelling immunohistochemistry. The ganglion contained many neurons supplying both gut regions. The colon-projecting neurons (CPN) occurred exclusively in the cranial part of the ganglia where they formed a large cluster distributed along the dorso-lateral ganglionic border and a smaller cluster located close to the caudal colonic nerve output. The rectum-projecting neurons (RPN) formed a long stripe along the entire length of the lateral ganglionic border and, within the right ganglion only, a small cluster located close to the caudal colonic nerve output. Immunohistochemistry revealed that the vast majority of the CPN and RPN were noradrenergic (tyrosine-hydroxylase-positive). Many noradrenergic neurons supplying the colon contained somatostatin or, less frequently, neuropeptide Y. In contrast, a significant subpopulation of the noradrenergic RPN expressed neuropeptide Y, whereas only a small proportion contained somatostatin. A small number of the non-adrenergic RPN were cholinergic (choline-acetyltransferase-positive) and a much larger subpopulation of the nerve cells supplying both the colon and rectum were non-adrenergic and non-cholinergic. Many cholinergic neurons contained neuropeptide Y. The non-adrenergic non-cholinergic neurons expressed mostly somatostatin or neuropeptide Y and some of those projecting to the rectum contained nitric oxide synthase, galanin or vasoactive intestinal polypeptide. Many of both the CPN and RPN were supplied with varicose nerve fibres exhibiting immunoreactivity against Leu5-enkephalin, somatostatin, choline-acetyltransferase, vasoactive intestinal polypeptide or nitric oxide synthase The somatotopic and neurochemical organization of this relatively large population of differently coded inferior mesenteric ganglion neurons projecting to the large bowel indicates that these cells are probably involved in intestino-intestinal reflexes controlling peristaltic and secretory activities.

Animals↗
PubMed2001

NADPH-diaphorase histochemistry in the terminal abdominal ganglion of the crayfish.

Nitric oxide (NO) has an important modulatory role on the processing of sensory signals in vertebrates and invertebrates. In this investigation we studied the potential sources of NO in the terminal abdominal ganglion of the crayfish, Pacifastacus leniusculus, using NADPH-diaphorase (NADPHd) histochemistry, with NADPHd acting as a marker for NO synthase (NOS). In the terminal ganglion a mean of 27 strongly labelled NADPHd-positive cell bodies were found, and of these 80% [of stained cell bodies] [corrected] occurred in three regions located in antero-lateral, central and posterior parts of the ganglion. Ventral and antero-ventral commissures as well as specific dorsal and ventral areas of the dendritic neuropil showed positive staining. Intense labelling was seen in the ventro-medial tract, and in the connective between the terminal ganglion and the 5th abdominal ganglion. In addition, some motor neurones and neurones with branches in the sensory commissures were NADPHd positive. Our finding that NADPHd-positive cells occur in consistent patterns in the terminal abdominal ganglion implies that NO may have a role in mechanosensory processing in the crayfish.

Animals↗
PubMed1977

Histochemical and biochemical characterization of the rat paracervical ganglion.

The nature and identity of the catecholamines in the paracervical ganglion and superior cervical ganglion small, intensely fluorescent (SIF) cells were investigated using fluorescence histochemical and immunohistochemical techniques. The paracervical ganglion SIF cells were found to contain norepinephrine and the superior cervical ganglion SIF cells, dopamine. The norepinephrine content of the paracervical ganglion SIF cells averaged about 72 ng/ganglion and did not change during the rat estrus cycle. The activity of the enzyme tyrosine hydroxylase in the PCG was very low (about 0.48 nmoles DOPA formed/h/mg protein) and was about 1/50th of the activity of the enzyme in the SCG, where it averaged about 23.90 nmoles DOPA formed/h/mg protein. These experiments suggested that the paracervical ganglion has large numbers of norepinephrine containing SIF cells with a relatively slow turnover of their catecholamine content.

Adrenal Medulla↗
PubMed1977

Further identification of neurons in the abdominal ganglion of Aplysia using behavioral criteria.

This review is an updating of the paper by Frazier et at. 13 in which 30 individual cells and 8 cell clusters were identified in the abdominal ganglion of of Aplysia californica on the basis of morphological, physiological and pharmacological criteria. Since that time, a number of neurobiological studies have utilized the neurons of the abdominal ganglion for behavioral studies. Based on these new investigations, 32 additional cells and 2 additional cell clusters have been identified, bringing the total of identified cells in the ganglion to 62 individual cells and 10 cell clusters. Additional features of the previously identified cells have also emerged. Much of the new information concerns the role of identified cells in behavior. We have summarized the current list of identified cells in the abdominal ganglion emphasizing these behavioral features. We also review the known synaptic connections made by identified interneurons in the ganglion. Included are descriptions of 6 new interneurons that connect to other cells in the ganglion. A major conclusion from this survey is that behavioral criteria permit resolution between cells in identified cell clusters that could previously not be distinguished using other criteria.

Abdomen↗
PubMed1980

Cobalt and horseradish peroxidase tracer studies in the stellate ganglion of octopus.

The connectivity of the stellate ganglion of Octopus was investigated using cobalt and horseradish peroxidase (HRP) tracers applied to severed preganglionic and postganglionic nerves. Centripetal cells, defined as cells in the ganglion which send their axons back toward the brain, were discovered by both methods. Application of HRP to the pallial (preganglionic) nerve labeled the preganglionic fibers which enter the ganglion and spread widely within the neuropil. Application of either tracer to a single stellar (postganglionic) nerve labeled motor neuron cell bodies spread over 1/4 to 1/3 of the ganglion. Since there are 25-40 such stellar nerves per ganglion, it may be inferred that there is only a limited topographic relationship between the location of motor neuron cell bodies in the stellate ganglion and the segment of mantle muscle which they innervate. The axon and many side branches of these motor neurons were also labeled. The smooth, diffuse form of HRP labeling produced in pre- and portganglionic axotomized neurons in Oct0pus is similar in appearance to that produced in damaged mammalian neurons.

Animals↗
PubMed1981

Growth of adult superior cervical ganglion explants in serum-free media.

Neurite outgrowth from explants of superior cervical ganglion from adult rats can be achieved in a serum-free medium. Extensive neurite outgrowth occurred from ganglion explants maintained in Eagle's minimum essential medium supplemented with either 10% (V/V) fetal calf serum or 1% (W/V) bovine serum albumin and nerve growth factor. After one week in culture, the ATP content of explants maintained in the serum-free medium was slightly higher than that noted in explants cultured in the presence of fetal calf serum and amounts of phosphocreatine were significantly lower. Despite these differences in high energy phosphate content, the abundance and morphology of neuritic outgrowth were essentially the same from explants cultured in the two types of media. Comparable activities of a number of NADP+-dependent dehydrogenases were noted in explants maintained in the two types of media. Increases in the activities of the oxidative enzymes of the pentose pathway, which occur in axotomized ganglia in vivo, were observed in the cultured ganglion explants. NADP+-dependent isocitrate dehydrogenase activity remained constant in ganglion explants in vitro, and measurements of this activity were employed in a new method to quantitate neurite outgrowth. The activity of isocitrate dehydrogenase in lyophilized neurite processes that had grown out onto a Millipore filter substrate correlated well with visual estimates of neuritic outgrowth. Substitution of delipidated for normal bovine serum albumin in the growth medium resulted in a significant decrease in neuritic outgrowth from ganglion explants from both adult and weanling rats. Addition of fatty acids to media containing delipidated bovine serum albumin enhanced neuritic outgrowth in explants of weanling rats. Thus, lipophilic substances bound to bovine serum albumin including fatty acids appear necessary for optimal growth of neurites from explants of the rat superior cervical ganglion.

Animals↗
PubMed1983

Effect of axotomy on the cyclic GMP increase induced by preganglionic stimulation and high extracellular K+ concentration in superior cervical sympathetic ganglion of the rat.

Cyclic GMP generation, induced by preganglionic nerve stimulation or by high extracellular potassium ion concentration (70 mM) in the medium, was studied during aerobic incubation of the excised superior cervical sympathetic ganglion of the rat with and without axotomy, and the results were compared with that of preganglionic denervation. Both axotomy and denervation of the ganglion for a week caused complete loss of increase of cyclic GMP content in the ganglion in response to the preganglionic nerve stimulation. However, the increase of the ganglionic cyclic GMP content evoked by raising the extracellular potassium ion concentration was maintained at a level about two-thirds of the control after axotomy for 1-4 days, while it was abolished within a day after denervation. Ganglionic choline acetyltransferase activity was maintained for several days after axotomy, but it was decreased rapidly by denervation. Acetylcholinesterase, dopamine-beta-hydroxylase and muscarinic cholinergic receptor sites had been lost almost completely a week after axotomy. These results suggest that the increase of ganglionic cyclic GMP content caused by depolarization with high extracellular K+ is associated with the preganglionic nerve terminals rather than with postganglionic receptor.

Acetylcholinesterase↗
PubMed1983

Enteric origin of bombesin immunoreactive fibres in the rat coeliac-superior mesenteric ganglion.

Bombesin-like immunoreactivity occurs in a dense network of nerve fibres in the rat coeliac-superior mesenteric ganglion. No bombesin immunoreactive cell bodies have been observed in this ganglion. An origin outside the ganglion was therefore assumed for the bombesin immunoreactive fibres. Ligation of the mesenteric nerve, between the ganglion and the gut resulted in an accumulation of bombesin immunoreactive material on the distal side, i.e. towards the gut. Transection of the nerve caused a depletion of bombesin immunoreactive fibres in the ganglion. These results suggest that bombesin immunoreactive fibres in the coeliac-superior mesenteric ganglion of the rat originate in neurons in the gastrointestinal wall. Application of colchicine to the stomach wall caused an accumulation of bombesin immunoreactive material in myenteric neurons.

Animals↗
PubMed1985

The density of reinnervation of adult rat superior cervical sympathetic ganglionic neurons is limited by the number of available postsynaptic sites.

The adult rat superior cervical ganglion has about 27,000 neurons and is innervated by about 9000 preganglionic axons which make a total of nearly 11 million synapses. Surgical removal of the upper part of the ganglion, reducing the number of neurons to about 20%, causes an overall reduction of the number of synapses to about 30%, but has no effect on the numbers of preganglionic axons. Thus, a 5-fold increase in the axon/neuron ratio causes an increase of only about 50% in the number of synapses per cell. Axotomy followed by regeneration of the preganglionic axons causes no further increase in the number of synapses per cell, even though the average number of synapses per axon is reduced to about one-quarter of the normal. This suggests that the ganglionic neurons can only accept a limited number of synapses, and that in the normal situation there is only possibility for a relatively minor increase before this limit is reached. This study is complementary to a previous one in which the numbers of preganglionic axons were surgically reduced and it was found that, when allowed to regenerate into an entire denervated ganglion, the remaining axons could not increase their numbers of synapses. Thus, in the normal rat superior cervical sympathetic ganglion the total number of synapses is such that while the preganglionic axons are probably expressing close to their full synaptogenic potential, the ganglionic neurons express only about two-thirds of their ability to receive synapses.

Animals↗
PubMed1985

Placodal sensory neurons in culture: nodose ganglion neurons are unresponsive to NGF, lack NGF receptors but are supported by a liver-derived neurotrophic factor.

Explant and dissociated neuron-enriched cultures of nodose ganglia (inferior or distal sensory ganglion of the Xth cranial nerve) were established from chick embryos taken between embryonic Day 4 (E4) and Day 16 (E16). The response of each type of culture to nerve growth factor (NGF) was examined over this developmental range. At the earliest ages taken (E4-E6), NGF elicited modest neurite outgrowth from ganglion explants cultured in collagen gel for 24 hr, although the effect of NGF on ganglia taken from E4 chicks was only marginally greater than spontaneous neurite extension from control ganglia of the same developmental age. The response of nodose explants to NGF was maximal at E6-E7, but declined to a negligible level in ganglia taken from E9-E10 or older chick embryos. In dissociated neuron-enriched cultures, nodose ganglion neurons were unresponsive to NGF throughtout the entire developmental age range between E5 and E12. In contrast to the lack of effect of NGF, up to 50% of nodose ganglion neurons survived and produced extensive neurites in dissociated cultures, on either collagen- or polylysine-coated substrates, in the presence of extracts of late embryonic or early posthatched chick liver (E18-P7). Antiserum to mouse NGF did not block the neurotrophic activity of chick (or rat or bovine) liver extracts. Whether cultured with chick liver extract alone or with chick liver extract plus NGF, nodose ganglion neurons taken from E6-E12 chick embryos and maintained in culture for 2 days were devoid of NGF receptors, as assessed by autoradiography of cultures incubated with 125I-NGF. Under similar conditions 70-95% of spinal sensory neurons (dorsal root ganglion--DRG) were heavily labeled. 2+

Animals↗
PubMed1986

Enkephalin modulation of neural transmission in the cat stellate ganglion: pharmacological actions of exogenous opiates.

Neural ganglionic transmission was studied in vivo in the cat, using closed chest anesthetized preparations. The right stellate ganglion and its branches were exposed retropleurally and prepared for electrical stimulation of pre- and postganglionic nerve fibers. The axillary artery was cannulated allowing direct administration of drugs in the arterial blood supplying the ganglion. Stimulation of postjunctional receptors could thus be obtained by local administration of selective agents. Local administration of nicotinic, muscarinic or histaminergic agents increased heart rate and blood pressure. Opiates were given either i.v. or locally through the axillary artery: we tested the effects of morphine, Leu-enkephalin (Leu-enk), Met-enkephalin (Met-enk), [D-ala2]-Met-enkephalinamide (DAME) and etorphine. When given locally, Leu-enk (from 10 micrograms), Met-enk (from 20 micrograms), DAME (from 5 micrograms) and etorphine (from 0.2 micrograms) inhibited tachycardia induced by preganglionic stimulation and reduced the amplitude of the compound action potential recorded from the postganglionic nerve. Morphine (10-200 micrograms) had no effect. On the other hand, tachycardia induced by postganglionic nerve stimulation was unaffected by opiates in the same experimental conditions. Intravenous administration of similar doses of opiates had no effect on ganglionic transmission. When tachycardia was induced by chemical stimulation of nicotinic (DMPP), muscarinic (McN-A-343-11) or histamine receptors in the stellate ganglia, opiates were still active in reducing the effect of these chemicals. These data provide evidence that exogenous opiates exert a depressing action on postsynaptic responses of sympathetic ganglia tested in vivo, although an additional action on presynaptic terminals is not excluded. As endogenous opiates are normally present in various sympathetic ganglia, including the stellate ganglion of the cat, it is possible that they play some modulatory role on ganglionic transmission in physiological conditions.

(4-(m-Chlorophenylcarbamoyloxy)-2-butynyl)trimethy↗