The Curculigo pilosa total extract, its butanolic fraction (0.5 microg-100 mg/kg) and the most active in vitro compound structurally similar to adrenaline, pilosidine (10 ng-l mg/kg), caused a reversible and dose-dependent increase in blood pressure in anaesthetized rat. This hypertensive effect is partially reversed (90%) by the prior administration of phentolamine (1 mg/kg) and abolished by pre-treatment with phentolamine (1 mg/kg) and atenolol (100 microg/kg). Neither tachiphylaxis nor any toxic effects were observed. These experimental findings suggest an interaction between C. pilosa and the peripheral adrenergic system (particularly with alpha1 and beta1 receptors); the structure of the bioactive glucosides could be important in evoking this effect.

Africa↗

PubMedDate not supplied

[Effect of lipophilic ortho-naphthoquinones on the growth of and production of peroxides by Leptomonas seymouri and Crithidia fasciculata].

The lipophilic o-naphthoquinones CG 8-935, CG 9-442, CG 10-248 and mansonones A, C, E and F inhibit growth of the trypanosomatids Leptomonas seymouri (LS) and Crithidia fasciculata (CF). The most active mansonones were E and F (I50, 0.1-0.4 microM with LS; 0.3-1.2 microM with CF) with cytotoxic activities equal to or higher than quinones CG, as reported previously. Incubation of LS or CF with the CG-quinones and mansonones E and F caused the release of H2O2 and O2-. from the whole cells to the suspending medium, as detected by the microperoxidase and adrenochrome assays, respectively. Lower O2-. and H2O2 production values were obtained with perezone and primine, two p-benzoquinones used as controls. Quinones effect on O2-. and H2O2 production was closely related to their concentration and with mansonones E and F, O2-. production was 4-5-fold higher than H2O2 production. Smaller differences were observed with the CG-quinones. Peroxide production in the assayed organisms was the result of quinone redox-cycling, which involved an anaerobic, reductive phase producing quinols, and an aerobic phase (II), in which quinol oxidation and peroxide production (O2-., H2O2) occurred. With mansonones E and F, and quinone CG, phase II rate was faster than or similar to phase I rate, but with mansonones A and C, the quinols oxidation rate was 8-10-fold slower than the quinones reduction rate. These differences fit in well with a) the quinol oxidation rates, measured in vitro; b) O2-. production by quinols oxidation and c) quinols capability for producing lucigenin chemiluminescence. These results support the assumption that oxyradicals play a relevant role in o-naphthoquinones cytotoxic action, despite the presence of catalase and other protective enzymes in CF and LS. Other effects are not, however, ruled out. CF and LS sensitivity towards the assayed o-quinones was similar or higher than that of Trypanosoma cruzi, thus allowing the use of those organisms for preliminary screening of antichagasic drugs.

Animals↗

PubMedDate not supplied

[On some 16-alkoxy-strychnines].

Explore the source record for details and available documents.

Chemical Phenomena↗