Selected Publication:
Maggi, CA; Patacchini, R; Santicioli, P; Lippe, IT; Giuliani, S; Geppetti, P; Del Bianco, E; Selleri, S; Meli, A.
The effect of omega conotoxin GVIA, a peptide modulator of the N-type voltage sensitive calcium channels, on motor responses produced by activation of efferent and sensory nerves in mammalian smooth muscle.
Naunyn Schmiedebergs Arch Pharmacol. 1988; 338(2):107-113
Doi: 10.1007/BF00174856
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- Co-authors Med Uni Graz
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Lippe Irmgard Theresia
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- Abstract:
- 1. The effect of omega-conotoxin (CTX) GVIA, a peptide which blocks neuronal calcium channels, were investigated on nerve-mediated motor responses in a variety of isolated smooth muscle preparations from rats and guinea-pigs. 2. In the rat or guinea-pig isolated vas deferens CTX (1 nM-1 microM) produced a concentration and time-related inhibition of the response to field stimulation, while the responses to KCl, noradrenaline or adenosine triphosphate were unaffected. In the presence of CTX a series of tetrodotoxin-resistant contractions could be elicited by field stimulation by increasing pulse width and/or voltage. 3. In the rat or guinea-pig isolated urinary bladder, CTX produced a concentration and time-dependent inhibition of twitch responses to field stimulation without affecting the response to exogenous acetylcholine. In the rat bladder the maximal effect did not exceed 25% inhibition while a much larger fraction of the response (about 70%) was inhibited in the guinea-pig bladder. The CTX-resistant response was abolished, in both tissues, by tetrodotoxin. 4. The effects of CTX in the rat bladder were also studied with a whole range of frequencies of field stimulation (0.1-50 Hz). Maximal inhibition was observed toward contractions elicited at frequencies of 2-5 Hz. At low frequencies the inhibitory effects of CTX and atropine were almost additive while at high frequencies of stimulation a large component of the atropine-sensitive response was CTX-resistant. 5. In the rat isolated proximal duodenum, field stimulation in the presence of atropine and guanethidine produced a primary relaxation followed by a rebound contraction.(ABSTRACT TRUNCATED AT 250 WORDS)
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Animals -
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Calcium Channel Blockers - pharmacology
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Capsaicin - pharmacology
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Duodenum - drug effects
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Guinea Pigs - drug effects
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Male - drug effects
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Mollusk Venoms - pharmacology
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Muscle Contraction - drug effects
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Muscle, Smooth - drug effects
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Neuroeffector Junction - drug effects
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Neurons, Afferent - drug effects
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Neurons, Efferent - drug effects
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Rats - drug effects
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Rats, Inbred Strains - drug effects
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Substance P - metabolism
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Urinary Bladder - drug effects
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Vas Deferens - drug effects
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omega-Conotoxin GVIA - drug effects