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1.
Indian J Biochem Biophys ; 1992 Aug; 29(4): 360-3
Article in English | IMSEAR | ID: sea-27151

ABSTRACT

Quassin, a mosquito larvicide isolated from Quassia amara, inhibits tyrosinase activity in the larvae of Culex quinquefasciatus. Since tyrosinase is directly involved in sclerotisation of the cuticle, it is suggested that quassin, as a larvicide, inhibits development of the cuticle. In presence of quassin phenylalanine, tyrosine and L-dopa levels were increased in larvae. In the larval stages, mosquitoes have a high concentration of phenylalanine and tyrosine with the level of the latter being very high just before pupation and then declines sharply. Monoamine oxidase (MAO), an enzyme directly involved in the metabolism of catecholamines, remained unaffected by quassin, in fact the level of adrenaline also remained unchanged in larvae during quassin poisoning. MAO showed high variation in its activity between synthetic and natural substrates. Tyramine is not a substrate for MAO. Tyrosinase activity was high in developing stages and negligibly low in adults and showed specificity to L-dopa. Phenylalanine and tyramine are unaffected by tyrosinase. Blood feeding did not influence the activity of both these enzymes.


Subject(s)
Animals , Catecholamines/metabolism , Culex/metabolism , Female , Glaucarubin/analogs & derivatives , Insecticides/pharmacology , Male , Monoamine Oxidase/analysis , Monophenol Monooxygenase/analysis , Quassins
2.
Article in English | IMSEAR | ID: sea-25645

ABSTRACT

Crushed aqueous extracts of leaf, wood, bark and flowers of Quassia amara showed antilarval activity against C quinquefasciatus. Quassin has been identified to be the antilarval principle present in this plant and was effective against mosquito larvae at a concentration of 6 ppm. Quassin was present to the extent of 0.1 to 0.14 per cent (average 0.12%) on a dry weight basis in wood of Q. amara. This compound is an unsaturated lactone and it gave a positive response to the Legal test, characteristic of unsaturated lactones. Quassin lost its antilarval activity on treatment with strong alkalies. Quassin was over five times as active as carbaryl, a synthetic antilarval agent.


Subject(s)
Animals , Culex , Glaucarubin/analogs & derivatives , Insecticides , Larva , Molecular Structure , Mosquito Control , Plants , Quassins
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