Inhibition of the lethal and myotoxic activities of Crotalus durissus terrificus venom by Tabernaemontana catharinensis:: Identification of one of the active components

被引:65
作者
Batina, MD
Cintra, ACO
Veronese, ELG
Lavrador, MAS
Giglio, JR [1 ]
Pereira, PS
Dias, DA
França, SC
Sampaio, SV
机构
[1] Univ Sao Paulo, Fac Med, Dept Bioquim, BR-14049900 Ribeirao Preto, Brazil
[2] Univ Sao Paulo, Fac Ciencias Farmaceut, Dept Anal Clin Toxicol & Bromatol, BR-14049 Ribeirao Preto, SP, Brazil
[3] Univ Sao Paulo, Fac Ciencias Farmaceut, Dept Fis & Quim, BR-14049 Ribeirao Preto, SP, Brazil
[4] Univ Ribeirao Preto, Dept Biotecnol Vegetal, Ribeirao Preto, Brazil
[5] Univ Sao Paulo, Fac Filosofia Ciencias & Letras, Dept Quim, BR-14049 Ribeirao Preto, Brazil
关键词
Tabernaemontana catharinensis; Apocynaceae; Crotalus durissus terrificus venom; antiophidian activity; myotoxicity; alkaloid;
D O I
10.1055/s-2000-8577
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
In Brazilian folk medicine, victims of bites by poisonous animals are usually treated with plant extracts derived from the diverse national flora. The chemical and pharmacological properties of most extracts were yet not investigated. In the rural community of Assis-SP, the root bark of Tobernaemontana catharinensis ("leiteiro", "cow milk") is applied to the site of the snake bite and believed to neutralize the effect of the venom. We report here the ability of the lyophilized aqueous extract (AE) and of a pure compound obtained from the ethanolic extract of T. catharinensis to inhibit the lethal and myotoxic activities of C. d. terrificus (South American rattlesnake) venom. Doses of 10 mg AE/100 g, injected (i.m., rat) 20 s after injecting (i.m.) the venom and that of 2.5 mg AE/100 g, incubated for 1 h at 25 degrees C with the venom before injection (i.m.) were able to neutralize the lethal activity of 2LD(50). These data indicate that T. catharinensis could be used as a source of a model molecule able to neutralize the lethality and myotoxicity induced by C. d. terrificus venom. Its ethanolic extract was then fractionated on a silica gel 60 chromatography column affording fractions A to F. Fraction A consisted basically of non-polar compounds, terpenes and sterols. Fraction D showed a pronounced antiophidian activity which was later correlated with the presence of the quaternary alkaloid 12-methoxy-4-methylvoachalotine in this fraction. This alkaloid was isolated and inhibited 100% lethality when injected 20 s after 2 LD50 at 1.7 mg/100 g.
引用
收藏
页码:424 / 428
页数:5
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