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  • 1
    ISSN: 1573-1561
    Keywords: Dytiscidae ; Gyrinidae ; chemical defense ; 4-pregnen-3-ones ; gyrinidal ; gyrinidione ; gyrinidone ; steroids ; norsesquiterpenes
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: 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.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of chemical ecology 1 (1975), S. 59-82 
    ISSN: 1573-1561
    Keywords: biocommunication ; defensive secretions ; Gyrinidae ; norsesquiterpenes ; gyrinidal ; isogyrinidal ; gyrinidone ; gyrinidione ; steroid anesthesia
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: 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).
    Type of Medium: Electronic Resource
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