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  • 1985-1989  (2)
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  • 1
    ISSN: 1432-1955
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract The effects of the amphiphilic cationic drugs chlorpromazine, imipramine, amitriptyline, propranolol and fluoxetine and praziquantel were investigated on glucose uptake and lactate excretion ofSchistosoma mansoni. While praziquantel enhances glucose uptake and lactate excretion at a concentration of 10−7 M, all the other drugs exert the same effects at concentrations above 10−5 M. Generally, a constant molar ratio of 1∶2 is found between glucose uptake and lactate excretion. Above 10−5 M, praziquantel inhibits glucose uptake and lactate excretion. Similar effects are caused by amphiphilic cationic drugs at 10−3 M. Pre-incubation ofS. mansoni with 10−5 M praziquantel completely abolish the stimulation of carbohydrate metabolism by serotonin and by 5×10−5 M chlorpromazine or fluoxetine. The action of praziquantel onS. mansoni resembles that of amphiphilic cationic drugs with respect to their influence on carbohydrate metabolism. This, together with data obtained from electrophysiological and electron microscopic studies, provides evidence for the hypothesis that praziquantel exerts its effect by interacting with membrane structures.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-1955
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract Praziquantel (PZQ) (Droncit, Biltricide) at 10 ΜM completely abolishes the stimulatory effect of serotonin on glucose uptake and lactate excretion of Schistosoma mansoni. Fluoxetine (FXT) exerts similar effects on the serotonin-induced stimulation of glucose uptake and lactate excretion, however, at 100-fold higher concentrations. In comparison with PZQ, which is inhibitory at 10 ΜM, FXT and other amphiphilic cationic drugs (amitriptyline, propranolol, imipramine, chlorpromazine) inhibit glucose uptake or lactate excretion in schistosomes at 1 mM; the strongest inhibitor is FXT. Glycogen breakdown is maximally stimulated by PZQ in the absence or presence of serotonin. There is an additive effect of 50 ΜM chlorpromazine or FXT and 0.01 to 0.1 ΜM PZQ on glycogen breakdown. The rate of sodiumsensitive or insensitive serotonin uptake in Schistosoma mansoni is reduced by 10 ΜM PZQ by about 40%, as is the sodium-sensitive excretion of serotonin. The results show that PZQ interferes with the ability of serotonin to stimulate carbohydrate metabolism. The possibility that PZQ may act through an effect on tegumental integrity is discussed.
    Type of Medium: Electronic Resource
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