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  • 1
    ISSN: 1570-7458
    Keywords: Phenylpropanoid ; dillapiol ; tenulin ; phenylheptatriyne (PHT) ; polysubstrate monooxygenases (PSMO) ; European corn borer (ECB) ; growth reduction ; allelochemical interactions
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Description / Table of Contents: Résumé Le dillapiole, un phénylpropanoide monomère d'un lignan et contenant un groupement méthylènedioxyhphényl (MDP), a la capacité d'inhiber in vitro les enzymes d'oxydations multiples à cytochrome P-450 (PSMO) utilisées par la pyrale du maïs (ECB), Ostrinia nubilalis, pour detoxifier les substances allélochimiques. Les composés contenant un groupe MDP comptent parmi les plus nombreux et puissants synergistes d'insecticides. Cependant, aucun synergisme n'est observé lorsque le dillapiole est ingéré par la pyrale en association avec l'une ou l'autre ou les deux substances secondaires insecticides des Astéraceae, la lactone sesquiterpène ténuline ou/et le polyacétylène phénylheptatriyne (PHT). Plutôt, le dillapiole est une toxine qui diminue la prise de poids des larves et retarde leur développement. Les effets toxiques sont plus importants avec le dillapiole seul que lorsque celui-ci est associé à la ténuline ou/et au PHT. Les expications possibles de ces résultats sont discutées.
    Notes: Abstract The phenylpropanoid, dillapiol, a compound capable of inhibiting the activity of cytochrome P-450 epoxidase in microsomal preparations of midguts of the European corn borer (ECB), Ostrinia nubilalis Hubner (Lepidoptera), did not enhance the toxicity of two insecticidal allelochemicals from the Asteraceae: the sesquiterpene lactone, tenulin or the phenylacetylene, phenylheptatriyne, when ingested simultaneously. Dillapiol alone was toxic to ECB larvae, and inhibited their growth. Possible reasons for the lack of synergism or potentiation by dillapiol of the insecticidal activity of the other allelochemicals are considered.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1573-1561
    Keywords: Piperaceae ; botanical insecticide ; isobutyl amides ; lignans ; dillapiol ; conocarpan ; piperlonguminine ; European corn borer
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract Insecticidal and growth-reducing properties of extracts of 14 species of American neotropical Piperaceae were investigated by inclusion in diets of a polyphagous lepidopteran, the European corn borer,Ostrinia nubilalis. Nutritional indices suggested most extracts acted by postdigestive toxicity.Piper aduncum, P. tuberculatum, andP. decurrens were among the most active species and were subjected to bioassay-guided isolation of the active components. Dillapiol was isolated from the active fraction ofP. aduncum, piperlonguminine was isolated fromP. tuberculatum, and a novel neolignan fromP. decurrens. The results support other studies on Asian and AfricanPiper species, which suggest that lignans and isobutyl amides are the active defence compounds in this family.
    Type of Medium: Electronic Resource
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