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  • 1990-1994  (11)
  • 1985-1989  (10)
  • Enteric nervous system  (20)
  • 5-HT receptors
  • 1
    Electronic Resource
    Electronic Resource
    Evidence for two types of 5-hydroxytryptamine receptor on secretomotor neurons of the guinea-pig ileum (1989)
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 339 (1989), S. 409-414 
    Details
    ISSN: 1432-1912
    Keywords: Enteric nervous system ; 5-Hydroxytryptamine ; Electrolyte transport ; Small intestine ; Secretomotor neurons
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Flat sheet preparations of the mucosa plus submucosa from the guinea-pig ileum were placed in Ussing chambers so that short circuit currrent (I sc), an index of electrolyte movement across the mucosa, could be measured. In these preparations, 5-hydroxytryptamine (5-HT) increasesI sc indirectly by stimulating both cholinergic and non-cholinergic secretomotor neurons. The 5-HT3 receptor antagonist, ICS 205–930 (10−13–10−5 M), substantially depressed the secretory response due to 5-HT (10−6 M), but not that produced by direct activation of muscarinic receptors on the mucosal epithelium with carbachol (10−6 M), or by stimulation of secretomotor neurons with substance P (10−8 M) or 1,1-dimethyl-4-phenylpiperazinium (10−5 M). The residual response to 5-HT, after the addition of a maximally effective concentration of ICS 205–930 (10−6 M), was further reduced by hyoscine (10−7M). When that part of the 5-HT response attributable to the release of acetylcholine was blocked by hyoscine (10−7M), ICS 205–930 did not further modify the response to 5-HT. The hyoscine-resistant component was, however, sustantially depressed by tetrodotoxin (3.5 × 10−7 M). The response remaining after ICS 205–930 and hyoscine was not affected by methysergide (2 × 10− 5 M) or cyproheptadine (10−7 M). We conclude that there are ICS 205–930 sensitive 5-HT receptors on cholinergic secretomotor neurons, and ICS 205–930, methysergide, and cyproheptadine insensitive 5-HT receptors on non-cholinergic secretomotor neurons.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00736055
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  • 2
    Electronic Resource
    Electronic Resource
    Characterization of 5-HT receptors mediating contraction and relaxation of the longitudinal muscle of guinea-pig distal colon in vitro (1994)
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 349 (1994), S. 455-462 
    Details
    ISSN: 1432-1912
    Keywords: 5-HT receptors ; Guinea-pig colon ; Longitudinal muscle ; Tachykinins ; Enteric neurons
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract A range of agonists and antagonists were used to characterize the receptors through which 5-hydroxytryptamine (5-HT) contracts and relaxes the longitudinal muscle of segments of guinea-pig distal colon, in vitro. 5-HT contracted the longitudinal muscle over the concentration range 10−9 to 10−4 mol/l. The 5-HT3 receptor agonist, 2-methyl-5-HT, produced concentration dependent contractions over the range 10−6 to 10−4 mol/l. 5-methoxytryptamine, an agonist at 5-HT4 receptors, caused contractions over a concentration range of 10−8 to 10−4 mol/l. The 5-HT4 antagonist, SDZ 205-557 (5 × 10−7 mol/l) substantially suppressed the responses to low concentrations of 5-HT and to 5-methoxytryptamine, but had no effect on the responses to higher concentrations of 5-HT. In contrast, the 5-HT3 antagonist, granisetron (10−6 mol/l), blocked the effect of 2-methyl-5-HT and substantially depressed responses to high concentrations of 5-HT, but had no effect on lower concentrations of 5-HT. Granisetron produced a small reduction in the response to 5-methoxytryptamine. Tetrodotoxin (TTX) (3 × 10−7 mol/l) almost abolished the response to 5-methoxytryptamine and markedly suppressed the response to 2-methyl-5-HT, but the responses to 5-HT were only partially reduced. The 5-HT, antagonist, methiothepin 10−6 mol/l. depressed the response to 5-HT 10−7 to 10−4 mol/l. and blocked its TTX insensitive component. The 5-HT2 antagonist, ketanserin, in concentrations up to 10−5 mol/l, had no effect on the contractions evoked by 5-HT. The response to 5-HT was substantially depressed by hyoscine (3 × 10−6 mol/l. The tachykinin antagonist, spantide 10−5 mol/l. depressed the response to 5-HT but to a lesser extent than hyoscine. Spantide and hyoscine combined completely blocked the contractile responses to 5-HT Responses to 2-methyl-5-HT were partially suppressed by hyoscine (3 x 10−6 mol/l. and spantide (10−5 mol/l) and completely blocked when both byoscine and spantide were present. Contractions evoked by 5-methoxytryptamine were partially blocked by hyoscine (3 × 10−6 mol/l) and were unaffected by spantide (10−5 mol/l), but a combination of hyoscine and spantide completely blocked such responses. When the excitatory transmission was blocked with hyoscine (3 × 10−6 mol/l) and spantide 10−5 mol/l) and the tone of the muscle raised, an inhibitory response to 5-HT was revealed that had a threshold concentration between 10−7 mol/l) and 3 × 10−7 mol/l, and a maximum effect at 10−4 mol/l. It was blocked by TTX (3 × 10−7 mol/l) and granisetron 10−6 mol/l. while N-nitro-l-arginine (NOLA) (10−4 mol/l) and SDZ 205-557 (5 × 10−7 mol/l) had no effect. Apamin A 10−6 mol/l. partially suppressed this response. It is concluded that 5-HT3, 5-HT4 and 5-HT1-like receptors mediate contraction of the longitudinal muscle of the distal colon. The 5-HT3 and 5-HT4 receptors are located on the excitatory motor neurons innervating the longitudinal muscle and the 5-HT1-like receptor is located on the muscle. 5-HT3 receptors are also found on inhibitory neurons to the muscle.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00169133
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  • 3
    Electronic Resource
    Electronic Resource
    Charybdotoxin and iberiotoxin but not apamin abolish the slow after-hyperpolarization in myenteric plexus neurons (1994)
    Springer
    Pflügers Archiv 428 (1994), S. 300-306 
    Details
    ISSN: 1432-2013
    Keywords: Potassium channels ; Enteric nervous system ; After-hyperpolarization ; Toxins
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Myenteric neurons of guinea-pig ileum were studied with intracellular microelectrodes. The specific toxins charybdotoxin, iberiotoxin and apamin were used to characterize the prolonged after-hyperpolarizations of AH neurons in this preparation. Charybdotoxin and iberiotoxin blocked prolonged after-hyperpolarizations in 23 of 24 AH neurons, but apamin had no effect on 5 of 5 AH neurons. Abolition of the after-hyperpolarizations was accompanied by depolarization and increases in input resistances of those AH neurons affected, but the shapes of action potentials were unchanged. The excitability of the AH neurons was enhanced as shown by an increase in the number of action potentials evoked by a 500-ms depolarizing current pulse or by a train of 15 ms depolarizing current pulses (10Hz). The other class of myenteric neurons, S neurons, was also investigated. The 19 S neurons studied fired action potentials only at the start of a 500 ms depolarization, but the toxins had no effect on this behaviour or on their other properties. Intracellular injection of Neurobiotin into the neurons studied and subsequent immunohistochemical staining to localise the calcium-binding protein, calretinin, indicated that all major classes of S neurons were included in the sample. Thus, the prolonged after-hyperpolarizations in AH neurons may be due to opening of a large-conductance (BK) calcium-dependent potassium channel, but similar channels play little or no role in regulation of the excitability of S neurons.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00724511
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  • 4
    Electronic Resource
    Electronic Resource
    Calbindin neurons of the guinea-pig small intestine: quantitative analysis of their numbers and projections (1990)
    Springer
    Cell & tissue research 260 (1990), S. 261-272 
    Details
    ISSN: 1432-0878
    Keywords: Calbindin ; Enteric nervous system ; Intestine, small ; Sensory neurons ; Guinea-pig
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary The distribution of nerve cells with immunoreactivity for the calcium-binding protein, calbindin, has been studied in the small intestine of the guinea-pig, and the projections of these neurons have been analysed by tracing their processes and by examining the consequences of nerve lesions. The immunoreactive neurons were numerous in the myenteric ganglia; there were 3500±100 reactive nerve cells per cm2 of undistended intestine, which is 30% of all nerve cells. In contrast, reactive nerve cells were extremely rare in submucous ganglia. The myenteric nerve cells were oval in outline and gave rise to several long processes; this morphology corresponds to Dogiel's type-II classification. Processes from the cell bodies were traced through the circular muscle in perforating nerve fibre bundles. Other processes ran circumferentially in the myenteric plexus. Removal of the myenteric plexus, allowing time for subsequent fibre degeneration, showed that reactive nerve fibres in the submucous ganglia and mucosa came from the myenteric cell bodies. Operations to sever longitudinal or circumferential pathways in the myenteric plexus indicated that most reactive nerve terminals in myenteric ganglia arise from myenteric cell bodies whose processes run circumferentially for 1.5 mm, on average. It is deduced that the calbindin-reactive neurons are multipolar sensory neurons, with the sensitive processes in the mucosa and with other processes innervating neurons of the myenteric plexus.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00318629
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  • 5
    Electronic Resource
    Electronic Resource
    Distribution of enteric nerve cells projecting to the superior and inferior mesenteric ganglia of the guinea-pig (1993)
    Springer
    Cell & tissue research 271 (1993), S. 333-339 
    Details
    ISSN: 1432-0878
    Keywords: Enteric nervous system ; Prevertebral ganglia ; Retrograde tracing ; Calbindin ; Vasoactive intestinal peptide (VIP) ; Intestine ; Guinea-pig
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract Retrograde tracing, using Fast Blue dye, was employed to determine the distribution of enteric nerve cells that project to the superior mesenteric and inferior mesenteric ganglia of the guinea-pig. Retrogradely labelled neurons were found in the myenteric but not submucous ganglia. When the superior mesenteric ganglion was injected, labelled neurons were found in low frequencies (less than 5 nerve cell bodies/cm2) in the duodenum, jejunum, ileum, caecum and proximal colon. The distal colon was analysed in five segments of equal length (1–5; oral to anal). Segment 1 had about 4 labelled nerve cells/cm2, whereas segments 2 to 5 displayed an average of about 25 nerve cells/cm2. The rectum contained about 36 labelled neurons/cm2. After injection of the inferior mesenteric ganglia with Fast Blue, no labelled neurons were found in the duodenum, jejunum, ileum or caecum. No labelled cells were observed in the gallbladder. A small number of labelled cells occurred in the proximal colon and in segment 1 of the distal colon. The frequency of labelled cells increased markedly in the more anal regions of the distal colon, and reached a peak in the rectum (138 cells/cm2). Both nerve lesions and immersion of the cut nerve in Fast Blue solution showed that the superior mesenteric nerve carries the axons of neurons located in the middle distal colon to the superior mesenteric ganglion. Almost half of the neurons in the rectum that project to the inferior mesenteric ganglia do so via the hypogastric nerves. Of neurons that projected to the inferior or superior mesenteric ganglia from the colon or rectum, similar proportions (about 75–80%) showed immunoreactivity for calbindin or VIP. For each of the prevertebral ganglia (coeliac, superior mesenteric and inferior mesenteric) the great majority of peripheral inputs arise from the large intestine.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00318620
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  • 6
    Electronic Resource
    Electronic Resource
    Light- and electron-microscopic immunochemical analysis of nerve fibre types innervating the taenia of the guinea-pig caecum (1992)
    Springer
    Cell & tissue research 270 (1992), S. 125-137 
    Details
    ISSN: 1432-0878
    Keywords: Enteric nervous system ; Caecum ; Neurochemistry ; Neuropeptides ; Nitric oxide synthase ; Chemical coding ; Guinea-pig
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary The present work was undertaken to determine by immunocytochemical methods which of the putative enteric neurotransmitters are contained in axons supplying the guinea-pig taenia coli and what proportion of axons is accounted for by the presence of these substances. Numerous fibres displayed immunoreactivity for dynorphin (DYN), enkephalin (ENK), γ-aminobutyric acid (GABA), nitric oxide synthase (NOS), substance P (SP) and vasoactive intestinal peptide (VIP), but, in contrast to other gut regions, fibres showing immunoreactivity for gastrin-releasing peptide, galanin and neuropeptide Y were rare in the taenia. Fibres reactive for calbindin, calcitonin gene-related peptide, cholecystokinin, 5-hydroxytryptamine and somatostatin were also rare. Tyrosine hydroxylase-like immunoreactivity (TH-LI) was present in numerous fibres that disappeared after extrinsic denervation, a procedure that did not detectably affect any of the other major groups of fibres. Simultaneous staining of extrinsically denervated preparations revealed that SP-LI and VIP-LI were located in separate fibres, and ultrastructural studies showed these to be 58% and 33% of intrinsic fibres supplying the muscle. Immunoreactivity for the general marker, neuron-specific enolase, was located in 95–98% of axons. ENK-LI and DYN-LI were in the same axons, and similar proportions of the fibres with either SP-LI or VIP-LI, about 85%, contained immunoreactivity for ENK and DYN. All VIP-LI fibres, but no SP-LI fibres, were reactive for NOS. The results imply that the taenia of the guinea-pig caecum is innervated by two major groups of enteric neurons: (i) excitatory neurons that contain ACh, SP, other tachykinins, and, in most cases, DYN-LI and ENK-LI; and (ii) inhibitory neurons that contain NOS-LI, VIP-LI, in most cases, the two opioids and, quite probably, ATP as a transmitter. GABA-LI is contained in a smaller population of intrinsic axons. Even though the taenia represents one of the simplest tissues for examining transmission from enteric neurons to intestinal muscle, it shares some of the complexity of other regions, in that four major axon types supply the muscle and both the enteric excitatory and enteric inhibitory neurons contain multiple transmitters.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00381887
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  • 7
    Electronic Resource
    Electronic Resource
    Neurochemically similar myenteric and submucous neurons directly traced to the mucosa of the small intestine (1985)
    Springer
    Cell & tissue research 241 (1985), S. 155-163 
    Details
    ISSN: 1432-0878
    Keywords: Calcitonin gene-related peptide ; Cholecystokinin ; Choline acetyltransferase ; Neuropeptide Y ; Somatostatin ; Enteric nervous system ; Intestine, small ; Guinea-pig
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Antisera to neuropeptide Y (NPY) gave an intense immunohistochemical reaction of certain nerve cells in the myenteric and submucous plexuses of the guinea-pig small intestine. Each nerve cell had up to 20 branching, tapering processes that were less than ∼50 μm long and a long process that could be followed for a considerable distance. This morphology corresponds to that of the type-III cells of Dogiel. The long process of each myenteric cell ran through the circular muscle to the submucosa, and in most cases the process could be traced to the mucosa. The submucous nerve cell bodies also had processes that extended to the mucosa. These cell bodies, in both plexuses, also stained with antisera raised against calcitonin generelated peptide (CGRP), cholecystokinin (CCK), choline acetyltransferase (ChAT) and somatostatin (SOM), but did not stain with antibodies against enkephalin, substance P or vasoactive intestinal peptide. Thus, it has been possible for the first time to trace the processes of chemically specified neurons through the layers of the intestinal wall and to show by a direct method that CGRP/CCK/ChAT/NPY/ SOM myenteric and submucous nerves cells provide terminals in the mucosa.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00214637
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  • 8
    Electronic Resource
    Electronic Resource
    The source of the nerve fibres forming the deep muscular and circular muscle plexuses in the small intestine of the guinea-pig (1987)
    Springer
    Cell & tissue research 247 (1987), S. 497-504 
    Details
    ISSN: 1432-0878
    Keywords: Enteric nervous system ; Intestine, small ; Nerves, degeneration ; Neuronal connections ; Guinea-pig
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary A quantitative ultrastructural study was made of the neuntes forming the deep muscular and circular muscle plexuses of the guinea-pig small intestine following microsurgical lesions designed to interrupt intrinsic and extrinsic nerve pathways within the intestinal wall. Removal of a collar of longitudinal muscle with attached myenteric plexus from the circumference of a segment of small intestine resulted in the subsequent disappearance of 99.3% of neurites in the underlying circular muscle. The few surviving neurites in the deep muscular plexus and circular muscle disappeared completely from lesioned segments that were, in addition, extrinsically denervated surgically. These results indicate that the majority of nerve fibres in the deep muscular and circular muscle plexuses of the guinea-pig small intestine is intrinsic to the intestine and originates from nerve cell bodies located in the overlying myenteric plexus. At the light-microscopic level, nerve bundles were traced from the myenteric plexus to the circular muscle.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00215742
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  • 9
    Electronic Resource
    Electronic Resource
    Shapes of nerve cells in the myenteric plexus of the guinea-pig small intestine revealed by the intracellular injection of dye (1988)
    Springer
    Cell & tissue research 254 (1988), S. 561-571 
    Details
    ISSN: 1432-0878
    Keywords: Enteric nervous system ; Intestine, small ; Neurons, types ; Myenteric plexus ; Intracellular dye injection (Lucifer yellow) ; Guinea pig
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary The shapes of myenteric neurons in the guineapig small intestine were determined after injecting living neurons with the dye Lucifer yellow via a microelectrode. The cells were fixed and the distribution of Lucifer yellow rendered permanent by an immunohistochemical method. Each of 204 nerve cells was examined in whole-mount preparations of the myenteric plexus and drawn using a camera lucida at 1250 x magnification. Four cell shapes were distinguished: (1) neurons with several long processes corresponding to type II of Dogiel; (2) neurons with a single long process and lamellar dendrites corresponding to type I of Dogiel; (3) neurons with numerous filamentous dendrites; and (4) small neurons with few processes. About 15% of the neurons could not be placed into these classes or into any single class. The type II neurons (39% of the sample) had generally smooth somata and up to 7 (average 3.3) long processes, most of which ran circumferentially. Dogiel type I neurons (34% of sampled neurons) had characteristic lamellar dendrites, i.e., broad dendrites that were flattened in the plane of the plexus. The filamentous neurons (7% of the sample), had, on average, 14 fine processes up to about 50 μm in length. Small neurons with smooth outlines and a few fine processes made up 5% of the neurons encountered. We conclude that myenteric neurons that have been injected with dye can be separated into morphologically distinct classes and that the different morphological classes probably correspond to different functional groupings of neurons.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00226506
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  • 10
    Electronic Resource
    Electronic Resource
    Projections of neurons with neuromedin U-like immunoreactivity in the small intestine of the guinea-pig (1989)
    Springer
    Cell & tissue research 257 (1989), S. 415-422 
    Details
    ISSN: 1432-0878
    Keywords: Neuromedin U ; Enteric nervous system ; Intestine, small ; Immunohistochemistry ; Neuropeptides ; Guinea-pig
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Neuromedin U immunoreactivity was located histochemically in the guinea-pig small intestine. Projections of immunoreactive neurons were determined by analysing patterns of degeneration following nerve lesions. The co-localization of neuromedin U immunoreactivity with immunoreactivity for substance P, neuropeptide Y, vasoactive intestinal peptide and calbindin was also investigated. Neuromedin U immunoreactivity was found in nerve cells in the myenteric and submucous plexuses and in nerve fibres in these ganglionated plexuses, around submucous arterioles and in the mucosa. Reactive fibres did not supply the muscle layers. Most reactive nerve cells in the myenteric ganglia had Dogiel type-II morphology and in many there was co-localization of calbindin, although some Dogiel type-II neuromedin U neurons were calbindin negative. Lesion studies suggest that these myenteric neurons project circumferentially to local myenteric ganglia. Projections from myenteric neurons also run anally in the myenteric plexus, while other projections extend to submucous ganglia, and still further projections run from the intestine to provide terminals in the coeliac ganglia. In the submucous ganglia neuromedin U was co-localized in three populations of nerve cells: (i) those with vasoactive intestinal peptide immunoreactivity, (ii) neurons containing neuropeptide Y, and (iii) neurons containing substance P. Each of these populations sends nerve fibres to the mucosa. Neuromedin U immunoreactivity is thus located in a variety of neurons serving different functions in the intestine and therefore probably does not have a single role in intestinal physiology.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00261844
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