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dc.typeArtigo de periódicopt_BR
dc.titlePyrrolizidine Alkaloids In The Arctiid Mothhyalurga Syma.pt_BR
dc.contributor.authorTrigo, J Rpt_BR
dc.contributor.authorWitte, Lpt_BR
dc.contributor.authorBrown, K Spt_BR
dc.contributor.authorHartmann, Tpt_BR
dc.contributor.authorBarata, L Ept_BR
unicamp.authorJ R Trigo, Laboratório de Ecologia Química Departamento de Zoologia, Instituto de Biologia, UNICAMP, Caixa Postal 6109, 13081, Campinas, S.P., Brazil.pt_BR Witte,pt S Brown,pt Hartmann,pt E Barata,pt
dc.description.abstractThe arctiid mothHyalurga syma (subfamily Pericopinae) sequesters pyrrolizidine alkaloids (PAs) from its larval food plantHeliotropium transalpinum (Boraginaceae). Colorimetric quantification of total PAs in the larvae, pupae, and adults ofHyalurga revealed mean values of about 286-445μg per individual (1.4-2.6% of dry weight). The PA mixtures found in the moth and its larval food plant were evaluated by GC-MS. Food-piant leaves were found to contain the diastereoisomeric retronecine esters indicine (IIIa), intermedine (IIIb), and lycopsamine (IIIc), and the heliotridine ester rinderine (IIId) only as minor constituents, whereas 3'-acetylrinderine (IVc) (68% of total PAs) and the respective 3'-acetyl esters of indicine (IVa) and intermedine (IVb) (both 17%) were the major alkaloids. Supinine (IIa) is detectable in traces only. The PA mixtures in eggs, larvae, pupae, and imagines ofHyalurga were identical: indicine, intermedine, and lycopsamine accompanied by considerable amounts of supinine and amabiline or coromandalinine (IIb/IIc) were the major components. Only larvae were found to store small quantities of a 3'-acetyl derivative. Rinderine and its 3'-acetyl ester were never found in the insects. Low concentrations of the arctiidspecific PA callimorphine (I) were present in larvae, pupae, and imagines. The differences in the PA patterns of the insects and their larval food plant suggest thatHyalurga is capable of modifying plant-derived PAs by inversion of the 7-OH configuration (conversion of the necine base heliotridine into retronecine), and perhaps the inversion of the 3'-OH [conversion of (+)-trachelanthic acid into (-)-viridifloric acid], although the possibility of a selective sequestration of the respective retronecine esters cannot be excluded. Some trials with the orb-weaving spiderNephila clavipes, a common neotropical predator, showed that both freshly emerged and field-caught adults ofHyalurga syma are liberated unharmed by the spider. The liberation could be related to the presence of PAs in the moths.en
dc.relation.ispartofJournal Of Chemical Ecologypt_BR
dc.relation.ispartofabbreviationJ. Chem. Ecol.pt_BR
dc.identifier.citationJournal Of Chemical Ecology. v. 19, n. 4, p. 669-79, 1993-Apr.pt_BR
dc.description.provenanceMade available in DSpace on 2015-11-27T12:18:25Z (GMT). No. of bitstreams: 1 pmed_24249009.pdf: 580714 bytes, checksum: e93cc8a116307c3976b64694a569beb0 (MD5) Previous issue date: 1993en
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