Search for tsetse attractants:a structure-activity study on 1-Octen-3-Ol in Glossina fuscipes fuscipes (Diptera: Glossinidae).

Trapping tsetse flies belonging to the palpalis group still relies totally upon luring by visual cues even though odor-baited trapping is used effectively against the morsitans-group species. Forty-three percent of the antennal olfactory cells of Glossina f. fuscipes, a member of the palpalis group, respond to 1-octen-3-ol. For this species we report a structure-activity relationship between 1-octen-3-ol analogs, in which carbon chain length and the configuration of the hydroxyl and pi-bond moieties are varied, and biological activity. Although the optimum chain length for all cells sensitive to 1-octen-3-ol is eight and most cells give lower responses when the hydroxyl function is omitted, there is a clear division into two groups. One group is diverse and represents cells that appear indifferent to the presence or position of the pi bond; many will respond to such disparate structures as acetone and 3-methylphenol as well as to 1-octen-3-ol. In the other group, the structural requirements for the stimulus are more stringent; the cells appear to be specifically tuned to 1-octen-3-ol. Their thresholds are three orders of magnitude lower than those of the former group. The existence of two clusters points to a functional division in the olfactory sense. We suggest that the latter low-threshold group is involved in host detection from a distance while the former diverse group is involved in host discrimination at close range. Trap harvests with 1-octen-3-ol as a bait may have been disappointing because the appropriate mixture for generating a landing response on the traps is still lacking.</p

Evaluation of the Bronchorelaxant, Genotoxic, and Antigenotoxic Effects of Cassia alata L.

International audienceAqueous-ethanolic extract of Cassia alata (AECal) and its derived fractions obtained through liquid-liquid fractionation were evaluated for their bronchorelaxant, genotoxic, and antigenotoxic effects. Contractile activity of rats' tracheas in the presence of tested materials, as well as its modifications with different inhibitors and blockers, was isometrically recorded. The antigenotoxic potential of AECal was evaluated on cyclophosphamide- (CP-) induced genotoxicity in the rat. Animals were pretreated with the extract, then liver comet assay was performed. AECal and its chloroformic fractions (CF-AECal) relaxed the contraction induced by Ach, but both were significantly less potent in inhibiting contraction induced by KCl (30 mM; 80 mM). Propranolol, indomethacin, L-NAME, methylene blue, and glibenclamide did not modify the relaxant effect of CF-AECal. TEA altered the response of trachea to CF-AECal. CF-AECal caused a rightward shift without affecting the E-max in cumulative concentration-response curves of Ach only at low concentrations. In animals pretreated with the extract, the percentage of CP-induced DNA damage decreased. Our results suggest that (1) muscarinic receptors contribute at least in part to the relaxant effects of CF-AECal; (2) CF-AECal interferes with membrane polarization; and (3) AECal is not genotoxic in vivo and contains chemopreventive phytoconstituents offering protection against CP-induced genotoxicity

Effects of two medicinal plants Psidium guajava L. (Myrtaceae) and Diospyros mespiliformis L. (Ebenaceae) leaf extracts on rat skeletal muscle cells in primary culture

Crude decoction, aqueous and ethanolic extracts of two medicinal plants (Psidium guajava and Diospyros mespiliformis), widely used in the central plateau of Burkina Faso to treat many diseases were evaluated for their antagonistic effects on caffeine induced calcium release from sarcoplasmic reticulum of rat skeletal muscle cells. These different extracts showed a decrease of caffeine induced calcium release in a dose dependent manner. Comparison of the results showed that Psidium guajava leaf extracts are more active than extracts of Diospyros mespiliformis and that crude decoctions show better inhibitory activity. The observed results could explaine their use as antihypertensive and antidiarrhoeal agents in traditional medicine, by inhibiting intracellular calcium release