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  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Science Ltd
    European journal of neuroscience 21 (2005), S. 0 
    ISSN: 1460-9568
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Ionotropic nicotinic acetylcholine (ACh) receptors have been shown to be modulated by protein kinase-mediated phosphorylation in vitro. Here we demonstrate that 5-hydroxytryptamine (5-HT) can downregulate postsynaptic nicotinic ACh responses, elicited in an identified arthropod motoneuron in situ, by a mechanism dependent on protein kinase activity. Serotonergic modulation can be mimicked by perfusion with membrane-permeable analogues of either adenine (cAMP) or guanine (cGMP) cyclic nucleotides, and is prolonged in the presence of phosphodiesterase inhibitors. Furthermore, suppression of the ACh response by 5-HT is blocked by specific competitive inhibitors of protein kinase A and G, as well as the broad specificity protein kinase inhibitor staurosporine. The protein phosphatase inhibitor cantharidin similarly blocks recovery of the ACh response from suppression mediated by 5-HT. Thus, it appears that the nicotinic ACh response is modulated by a cAMP-mediated phosphorylation-dependent intracellular signalling pathway that is distinct from the direct block of mammalian nicotinic ACh receptors by 5-HT previously reported in vitro.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 222 (1969), S. 1075-1076 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Until recently it has been difficult to penetrate the neurones in the insect central nervous system with micro-electrodes and obtain stable membrane potentials and action potentials. There is now, however, considerable evidence that microelectrode recordings can be obtained from insect central ...
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Journal of comparative physiology 172 (1993), S. 359-368 
    ISSN: 1432-1351
    Keywords: Acetylcholine receptors ; Muscarinic ; Nicotinic ; Cockroach ; Periplaneta americana
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract The effects of a number of cholinergic agonists and antagonists have been examined on the cell body of the fast coxal depressor (Df) of the cockroach Periplaneta americana using voltage-clamp techniques. Acetylcholine (ACh), when applied to this neurone voltage-clamped at its normal resting potential, results in the generation of an inward current through the activation of receptors which are blocked by α-bungarotoxin (α-bgt). At more depolarized membrane potentials acetylcholine induces an inward current which is strongly voltage-dependent and which is insensitive to α-bgt. An α-bgt-resistant current is also induced by the application of a number of cholinergic agonists. In order of potency these are: decamethonium〉oxotremorine = McN-A-343 = (+)-muscarine = arecaidine propargyl ester 〉nicotine 〉ACh. This α-bgt-resistant response to cholinergic agonists is blocked by a range of antagonists. In order of potency these are : decamethonium 〉pirenzipine 〉quinuclidinyl benzilate = atropine = p-f-hexahydro-sila-difenidol = dexetimide 〉scopolamine = methoctramine. The receptors mediating this response have been termed ‘mixed cholinergic’ due to their sensitivity to both nicotinic and muscarinic ligands. Pharmacological similarities between these ‘mixed’ receptors and binding components found in high speed supernatant fractions of insect nervous tissue are discussed.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1573-7381
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The post-embryonic development of the non-rectifying septate synapse between homologous lateral giant (LG) fibre segments has been investigated using electron microscopy and electrophysiology. In adults, the LG-LG synapse is characterized by closely apposed membranes (approximately 4 nm separation) traversed by regularly spaced particles, and large (60–80 nm) spherical vesicles on both sides of the junction. In newly hatched crayfish the junction between lateral giant fibre segments comprises regions of close membrane apposition as seen in the adult along with non-specialized areas of wide (10–15 nm) membrane separation. Vesicles associated with these junctions are small (25–40 nm) and pleomorphic. The number of vesicles is low by comparison with adult junctions; in most sections of hatchling junctions there are normally fewer than five vesicles, although as many as 30 have occasionally been seen. During development the non-specialized areas of wide membrane separation become rare and the vesicle population changes to a mixture of small pleomorphic forms and larger (60–80 nm) spherical ones. However even at two months the number of large spherical vesicles is markedly less than that at the adult synapse, while small pleomorphic vesicles are still abundant. Despite the difference between the adult and hatchling vesicle populations, intracellular recordings have shown that the synapse is fully functional as a non-rectifying electrical junction on hatching and that the intracellular marker Lucifer Yellow can pass between adjacent lateral giant fibre neurons.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Journal of neurocytology 20 (1991), S. 109-123 
    ISSN: 1573-7381
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary In a previous paper we showed that the ultrastructure of the giant fibre to motor giant synapse of crayfish changes in the first few weeks after hatching from having predominantly the appearance of a chemical synapse to having the appearance of an electrical synapse. This is parallelled by a behavioural change from non-giant fibre-mediated to giant fibre-mediated tailflips. In this paper we describe the physiology of the giant fibre to motor giant synapse over this period. We find the following: (1) The giant fibre to motor giant synapse usually transmits spikes 1∶1 from the day of hatching. (2) The synapse operates by electrical transmission from the day of hatching, when no connexons are apparent at the ultrastructural level. (3) The synapse has no detectable chemical component, even at an age when the predominant type of junctional apposition has the ultrastructural appearance of a chemical synapse. (4) Inhibitory chemical synapses occur onto the motor giant at the day of hatching, and these show similar physiological characteristics to those which occur onto the motor giant in adults. (5) In some preparations, the giant fibre to motor giant electrical synapse shows rectification similar to that in the adult, but in most cases both depolarizing and hyperpolarizing current injected into the medial giant spreads to the motor giant. (6) Current spread from the medial giant to the motor giant is increased by hyperpolarizing the motor giant neuron, even when medial giant to motor giant transmission is apparently non-rectifying. (7) Both the giant fibre and the motor giant have resting potentials of about −90 mV. There is no standing difference in resting potential as there is in the adult. This may explain the apparent lack of medial giant to motor giant rectification observed in most preparations.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Journal of neurocytology 18 (1989), S. 749-761 
    ISSN: 1573-7381
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The post-embryonic development of the rectifying Giant Fibre-Motor Giant (GF-MoG) synapse and the Giant Fibre-Segmental Giant (GF-SG) synapse has been investigated using electron-microscopy. In adults, the MoG and SG neurons make contact with the GFs by sending narrow ‘finger-like’ processes through the glial and connective tissue sheath surrounding each GF. The junctional region is characterized by closely apposed membranes (approximately 4 nm separation) traversed by regularly spaced connections, and large (60–80 nm) spherical vesicles in the presynaptic fibre. In newly hatched crayfish junctional contact is made over extensive areas of flat membrane apposition, due to the absence of a thick connective sheath around the giant fibres. Initially the junctional region is dominated by contacts which are morphologically indistinguishable from chemical synapses, i.e. 1. The apposed membranes are separated by a cleft of approximately 20–30 nm (an order of magnitude larger than the cleft distance at electrotonic synapses). 2. There is pre- and post-synaptic thickening of the junctional membranes with a dense cytoplasmic material. 3. Small (25–40nm) pleomorphic vesicles are found on the presynaptic side of the junction, commonly in association with a dense presynaptic bar. Regions of junctional contact displaying the adult electrotonic-type morphology first appear at approximately one week post-hatching. At this age they are limited in distribution and occupy a central position in the area of contact surrounded by a broad ‘chemical-like’ annulus. During subsequent development these sites with electrotonic-type morphology grow in relative size, so that the ‘chemical-like’ sites become compressed towards the edges of the regions of contact. The adult type of morphology, in which the ‘chemical-like’ regions are vestigial, is achieved approximately two months after hatching.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1573-7381
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Antibodies raised against gamma-aminobutyric acid (GABA) were used to stain sections from the crayfish abdominal nervous system, and the sections were examined under the electron microscope using a protein-A/gold conjugate secondary label. Sections were taken through the third ganglionic root, and through the interganglionic connective at the base of the third root posterior to the ganglia. The third root contains two very large motor axons, a non-GABAergic excitor (Motor Giant; MoG), and a GABAergic inhibitor (Flexor Inhibitor; FI). Only one of the two large axons stained positively for GABA, confirming that the antibody has high specificity for GABAergic neurones. The MoG is driven by powerful electrical synapses from the giant fibres, but also receives inhibitory chemical synaptic input which can gate the excitatory input. There is no physiological evidence for any other form of chemical input. However, at the ultrastructural level, the MoG is postsynaptic to three types of chemical profiles; SE-type containing round agranular vesicles, SI-type containing pleomorphic vesicles, and SM-type containing a mixture of round agranular and dense-cored vesicles. There is a highly differentiated staining pattern of these three synaptic types. Only the SI-type profiles stain positively with the GABA antibody, while the SE- and SM-type do not show significant staining. This suggests that the MoG can under some circumstances receive chemical input other than GABAergic inhibitory input. These other types of input have yet to be physiologically identified.
    Type of Medium: Electronic Resource
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