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  • Artikel: DFG Deutsche Nationallizenzen  (5)
  • Dytiscidae  (3)
  • gyrinidione  (3)
Datenquelle
  • Artikel: DFG Deutsche Nationallizenzen  (5)
Materialart
Erscheinungszeitraum
  • 1
    Digitale Medien
    Digitale Medien
    Springer
    Journal of chemical ecology 9 (1983), S. 1449-1464 
    ISSN: 1573-1561
    Schlagwort(e): Coleoptera ; Dytiscidae ; Agabus seriatus ; Agabus obtusatus ; defensive secretions ; steroids ; regeneration ; pygidial glands ; prothoracic glands ; cholesterol
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Biologie , Chemie und Pharmazie
    Notizen: Abstract The defensive secretions of the dytiscid species,Agabus seriatus (Say) andAgabus obtusatus (Say), were qualitatively and quantitatively analyzed by high-pressure liquid chromatography. The intrinsic ability ofA. Seriatus andA. Obtusatus to regenerate their prothoracic gland defensive secretions under laboratory conditions was determined by analyzing the secretions every seventh day for five weeks. Both beetles regenerated ∼ 80% of their prothoracic gland components within two weeks.A. seriatus was injected with [4-14C]cholesterol and after a three-week regeneration period 7.5% of the14Clabel was found in the steroidal defensive secretion from the prothoracic glands.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    ISSN: 1573-1561
    Schlagwort(e): Dytiscidae ; Gyrinidae ; chemical defense ; 4-pregnen-3-ones ; gyrinidal ; gyrinidione ; gyrinidone ; steroids ; norsesquiterpenes
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Biologie , Chemie und Pharmazie
    Notizen: Abstract By means of a bioassay employing the minnowPimephales promelas, the anesthetic activities and toxicities of various defensive steroids and norsesquiterpenes produced by the Dytiscidae and Gyrinidae were compared with those of a wide selection of steroid standards. The most widely occurring major components of dytiscid secretions, 4-pregnen-3-ones and related derivatives, were among those compounds most active in minnow bioassays. The norsesquiterpenes gyrinidal and gyrinidione were among the most toxic compounds tested but they possessed little anesthetic action. The anesthetic activity of gyrinidone was comparable to that of testosterone. Steroid activity in the minnow bioassay was highly related to the degree of oxygenation; steroids oxygenated only at the termini of the molecule were most active. Less or additional oxygenation resulted in a loss of activity. When steroids were rapidly administered to minnows the activities of many of them were similar, suggesting they share a common mode of action.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 3
    ISSN: 1573-1561
    Schlagwort(e): Coleoptera ; Dytiscidae ; high-pressure liquid chromatography ; Acilius semisulcatus ; Acilius sylvanus ; Acilius mediatus ; quantitation ; defensive secretions ; steroids ; benzoic acid ; methylp-hydroxybenzoate ; p-hydroxybenzaldehyde
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Biologie , Chemie und Pharmazie
    Notizen: Abstract A rapid, sensitive, stable, and quantitative high-pressure liquid chromatographic technique was developed for the analysis of defensive secretions obtained from the pygidial and prothoracic glands of dytiscids. Methods were developed for both normal phase (μPorasil) and reverse phase (μBondapak C18) columns. The applicability of this technique was demonstrated when defensive compounds ofAcilius semiculcatus, A. sylvanus andA. mediatus were isolated, identified, and quantitated. No major differences were found in the composition of the defensive secretions between the three species. The seasonal defensive titer ofA. semisulcatus was determined from June through October 1977. The pygidial defensive agents (benzoic acid,p-hydroxybenzaldehyde, and methylp-hydroxybenzoate varied from 9.0 to 67.8 μg and exhibited a maximum in July, and a steroid from the prothoracic gland varied from 7.1 to 33.2 μg and was maximum in October.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 4
    Digitale Medien
    Digitale Medien
    Springer
    Journal of chemical ecology 4 (1978), S. 503-510 
    ISSN: 1573-1561
    Schlagwort(e): Gyrinidae ; high-pressure liquid chromatography ; norsesquiterpenes ; Gyrinus frosti ; Dineutus assimilis ; gyrinidal ; isogyrinidal ; gyrinidione ; gyrinidone
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Biologie , Chemie und Pharmazie
    Notizen: Abstract A rapid, sensitive, stable, and quantitative high-pressure liquid chromatographic technique was developed for the analysis of the norsesquiterpenes, gyrinidal, isogyrinidal, gyrinidone, and gyrinidione. Methods were developed for both normal-phase (μPorasil) and reverse-phase (μBondapak) columns. The applicability of this technique was demonstrated when the norsesquiterpenes of the defensive secretions of the water beetleGyrinus frosti Fall were isolated and identified as gyrinidal and isogyrinidal. This method was then used for the quantification of the norsesquiterpene titer ofG. frosti andDineutus assimilis (Kirby).
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 5
    Digitale Medien
    Digitale Medien
    Springer
    Journal of chemical ecology 1 (1975), S. 59-82 
    ISSN: 1573-1561
    Schlagwort(e): biocommunication ; defensive secretions ; Gyrinidae ; norsesquiterpenes ; gyrinidal ; isogyrinidal ; gyrinidone ; gyrinidione ; steroid anesthesia
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Biologie , Chemie und Pharmazie
    Notizen: Abstract By use of a minnow bioassay, toxins were detected in the pygidial secretions of the gyrinid beetlesDineutus assimilis (Kirby) andDineutus nigrior Roberts. The active agents, which may be largely responsible for the relative immunity of the Gyrinidae from predation, were isolated and identified as the norsesquiterpenesgyrinidione [(E)-1-methyl-2-formyl-3-(1′-methylhex-3′-ene-2′,5′-dione)-cyclopentane],gyrinidone [(E,Z)-2-hydroxy-5,9-dimethyl-4-(but-1′-ene-3′-one)-3-oxo-bicyclo[4.3.0]-non-4-ene],gyrinidal [(E,E,E)-3,7-dimethyl-8,11-dioxo-2,6,9-dodecatrienal], andisogyrinidal[(E,E,Z)-3,7-dimethyl-8,11-dioxo-2,6,9-dodecatrienal]. Since gyrinidione and isogyrinidal are being reported for the first time, their physical and chemical properties are presented and biosynthetic relationships of the four norsesquiterpene structures are discussed. About 50% of the beetle defensive material was norsesquiterpenes, 25% polar lipids, and 20% could not be extracted from water into chloroform. As quantified by gas-liquid chromatography,D. assimilis contained 245±73 μg andD. nigrior 144±64 μg norsesquiterpenes per individual. The average relative composition of norsesquiterpenes in the pygidial secretions of both beetle species was constant: isogyrinidal, 6%; gyrinidone, 7%; gyrinidione, 36%; and gyrinidal, 48%. When administered externally in solution to fish, isolated norsesquiterpenes possessed narcotic and toxic activity similar to that of the anesthetic steroids deoxycorticosterone (DOC) and testosterone. Minnow dose-response curves demonstrated that gyrinidione and gyrinidal (LC100=ca. 2 μg/ml) were as toxic to fish as was DOC (LC100=ca. 3 μg/ml). Gyrinidone was less toxic (LC100=ca. 15 μg/ml) while isogyrinidal was relatively inactive (LC100=ca. 90 μg/ml).
    Materialart: Digitale Medien
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