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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 349 (1994), S. 455-462 
    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
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Experimental brain research 42 (1981), S. 158-170 
    ISSN: 1432-1106
    Keywords: Spinal cord ; Excitation ; Presynaptic ; Inhibition ; Baclofen ; Glutamergic ; Aspartergic ; Gabergic
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary When ejected microelectrophoretically near spinal interneurones of cats anaesthetised with pentobarbitone and under conditions where postsynaptic excitability was maintained artificially at a constant level, (−), but not (+), -baclofen selectively reduced monosynaptic excitation by impulses in low threshold muscle (Ia and Ib) and cutaneous (Aα) afferents. Polysynaptic excitation of interneurones and Renshaw cells by impulses in higher threshold afferents was less affected, and baclofen had little or no effect on the cholinergic monosynaptic excitation of Renshaw cells. Glycinergic and gabergic inhibitions of spinal neurones were relatively insensitive to baclofen. These stereospecific actions of baclofen, produced by either a reduction in the release of excitatory transmitter or postsynaptic antagonism, suggest that Ia, Ib, and Aα afferents may release the same excitatory transmitter which differs from that of spinal excitatory interneurones. Microelectrophoretic (−), but not (+), -baclofen also reduced primary afferent depolarization of ventral horn Ia extensor afferent terminations produced by impulses in low threshold flexor afferents, without altering either the electrical excitability of the terminations or their depolarization by electrophoretic GABA or L-glutamate. This stereospecific action of baclofen is interpreted as a reduction in the release of GABA at depolarizing axo-axonic synapses on Ia terminals.
    Type of Medium: Electronic Resource
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