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Neuromuscular effects and acute toxicity of an ethyl acetate extract of Spigelia anthelmia Linn

An ethyl acetate extract of Spigelia anthelmia (EASa), with validated anthelmintic activity, was evaluated for its acute toxicity and general effects in albino Swiss mice and for neuromuscular relaxant activity in the frog sciatic-gastrocnemius and rectus abdominis preparation. The extract induced a...

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Bibliographic Details
Published in:Journal of ethnopharmacology 2004-06, Vol.92 (2), p.257-261
Main Authors: Camurça-Vasconcelos, A.L.F., Nascimento, N.R.F., Sousa, C.M., Melo, L.M., Morais, S.M., Bevilaqua, C.M.L., Rocha, M.F.G.
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Language:English
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Summary:An ethyl acetate extract of Spigelia anthelmia (EASa), with validated anthelmintic activity, was evaluated for its acute toxicity and general effects in albino Swiss mice and for neuromuscular relaxant activity in the frog sciatic-gastrocnemius and rectus abdominis preparation. The extract induced a dose-related myotonia and muscular paralysis of rapid onset at higher doses. The calculated LD 50 after oral and intraperitoneal administration was 345.9 [241.4–484.7] mg/kg and 60.8 [47.4–80] mg/kg, respectively. In broilers, intramuscullar injection of EASa-induced spastic paralysis qualitatively similar to that obtained after succinylcholine administration and contrasting to the flaccid paralysis induced by d-tubocurarine. The contraction elicited by direct stimulation of the gastrocnemius was blocked by EASa by 54.3±4.7% (IC 50 = 21.4 [11.2–35.8] μg/ml) and the twitches evoked by stimulation of the sciatic nerve were blocked by 69.1±7.4% (IC 50 = 17.9 [4.5–34.23] μg/ml). EASa also blocked acetylcholine-induced contractions in the frog rectus abdominis by 58.6±7.4% (IC 50 = 7.4 [1.7–15.28] μg/ml) but did not decrease tonic contractions induced by a high-potassium Ringer solution. In summary, the ethyl acetate extract of Spigelia anthelmia induces tonic paralysis in vivo, and decreases amplitudes of twitches and increases tonus of skeletal muscle in vitro.
ISSN:0378-8741
1872-7573
DOI:10.1016/j.jep.2004.03.005