Laurasian migration explains Gondwanan disjunctions: evidence from Malpighiaceae.
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Explanations for biogeographic disjunctions involving South America and Africa typically invoke vicariance of western Gondwanan biotas or long distance dispersal. These hypotheses are problematical because many groups originated and diversified well after the last known connection between Africa and South America (approximately 105 million years ago), and it is unlikely that "sweepstakes" dispersal accounts for many of these disjunctions. Phylogenetic analyses of the angiosperm clade Malpighiaceae, combined with fossil evidence and molecular divergence-time estimates, suggest an alternative hypothesis to account for such distributions. We propose that Malpighiaceae originated in northern South America, and that members of several clades repeatedly migrated into North America and subsequently moved via North Atlantic land connections into the Old World during episodes starting in the Eocene, when climates supported tropical forests. This Laurasian migration route may explain many other extant lineages that exhibit western Gondwanan distributions. (+info)
Glochidiolide, isoglochidiolide, acuminaminoside, and glochidacuminosides A-D from the leaves of Glochidion acuminatum MUELL.
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The dimeric butenolides glochidiolide and isoglochidiolide, a new glucoside of a nitrogen-containing C(8) dimer, acuminaminoside, and glucosides of C(8) compounds, designated glochidacuminosides A-D, were isolated from the leaves of Glochidion acuminatum. The structures of glochidionolactone and acuminaminoside were determined by X-ray analyses, and those of the remaining C(8) glucosides by NMR spectroscopic analyses, chemical conversion, and a modified Mosher's method. (+info)
Pollination and reproductive biology of twelve species of neotropical Malpighiaceae: stigma morphology and its implications for the breeding system.
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BACKGROUND AND AIMS: This study on reproductive biology examines the stigmatic morphology of 12 Brazilian Malpighiaceae species with regard to their pollination and breeding system. METHODS: The species were studied in natural populations of a semi-deciduous forest fragment. Style tips were processed for observation by SEM and pollen-tube growth was analyzed under fluorescence microscopy. The breeding system was investigated by isolating flowers within waterproof bags. Floral visitors were recorded through notes and photographs. KEY RESULTS: Flowers are yellow, pink or white, protogynous, herkogamous and sometimes lack oil glands. While Banisteriopsis pubipetala has functional female flowers (with indehiscent anthers), 11 species present hermaphrodite flowers. Stigmas of these species may be terminal, with a slightly concave surface, or internal, consisting of a circular cavity with a large orifice, and are covered with a thin, impermeable cuticle that prevents pollen from adhering, hydrating, or germinating. Malpighiaceae have a special type of 'wet' stigma, where a secretion accumulates under the cuticle and is released by mechanical means-mainly rupture by pollinators. Even though six species show a certain degree of self-compatibility, four of them present a form of late-acting self-incompatibility, and the individual of B. pubipetala is agamospermous. Species of Centris, Epicharis and Monoeca bees pollinate these flowers, mainly collecting oil. Some Epicharis and Monoeca species collected pollen by vibration. Paratetrapedia and Tetrapedia bees are pollen and oil thieves. CONCLUSIONS: The Malpiguiaceae species studied are pollinator-dependent, as spontaneous self-pollination is limited by herkogamy, protogyny and the stigmatic cuticle. Both the oil- and pollen-collecting behaviours of the pollinators favour the rupture of the stigmatic cuticle and the deposition of pollen on or inside the stigmas. As fruit-set rates in natural conditions are low, population fragmentation may have limited the sexual reproduction of these species. (+info)
Structural and functional characterization of polyphenols isolated from acerola (Malpighia emarginata DC.) fruit.
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Two anthocyanins, cyanidin-3-alpha-O-rhamnoside (C3R) and pelargonidin-3-alpha-O-rhamnoside (P3R), and quercitrin (quercetin-3-alpha-O-rhamnoside), were isolated from acerola (Malpighia emarginata DC.) fruit. These polyphenols were evaluated based on the functional properties associated with diabetes mellitus or its complications, that is, on the radical scavenging activity and the inhibitory effect on both alpha-glucosidase and advanced glycation end product (AGE) formation. C3R and quercitrin revealed strong radical scavenging activity. While the inhibitory profiles of isolated polyphenols except quercitrin towards alpha-glucosidase activity were low, all polyphenols strongly inhibited AGE formation. (+info)
Cytotoxic constituents from the stem bark of Dichapetalum gelonioides collected in the Philippines.
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Fractionation of an ethyl acetate-soluble extract of the stem bark of Dichapetalum gelonioides, collected in the Philippines, using the LNCaP (hormone-dependent human prostate) cell line as a monitor, led to the purification of three dichapetalin-type triterpenoids [dichapetalins A (1), I (2), and J (3)], along with two dolabrane norditerpenoids (6, 7), and the additional triterpenoids zeylanol (8), 28-hydroxyzeylanol (9), and betulinic acid. Since compounds 1-3 exhibited promising selectivity against the SW626 (human ovarian cancer) cell line, a re-collection of the plant material was carried out, to obtain more of these compounds for additional biological testing. Two further phenylpyranotriterpenoids [dichapetalins K (4) and L (5)] were isolated from the re-collected plant material. The structures of the new compounds 2-5 and 9 were determined on the basis of spectroscopic data interpretation, and the relative configuration of 6 was confirmed using X-ray crystallography. Compounds 4-6 and the methyl ester, 6a, exhibited broad cytotoxic activity when tested against a panel of human tumor cell lines. Dichapetalin A (1) was not active when evaluated in an in vivo hollow fiber assay in the dose range 1-6 mg/kg. (+info)
Antihyperglycemic effect of polyphenols from Acerola (Malpighia emarginata DC.) fruit.
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A crude acerola polyphenol fraction (C-AP) was prepared by subjecting an acerola extract to a C18 cartridge column, and eluting the adsorbed fraction with ethanol containing 10% of acetic acid. C-AP appeared in a previous study to have an inhibitory effect on alpha-glucosidase and particularly on maltase activities. To elucidate the antihyperglycemic effect of C-AP further, we examined the regulation by C-AP of glucose uptake in Caco-2 cell; this resulted in the inhibition of glucose uptake. We next conducted single administration tests of glucose and maltose to ICR mice to investigate whether C-AP really controlled the intestinal glucose absorption in an animal body. The results showed that C-AP significantly suppressed the plasma glucose level after administering both glucose and maltose, suggesting that C-AP had a preventive effect on hyperglycemia in the postprandial state. The mechanism for this effect is considered to have been both suppression of the intestinal glucose transport and the inhibition of alpha-glucosidase. Despite such a preventive effect, the therapeutic effect of C-AP on hyperglycemia appeared to be low from the experiment with KKAy mice. (+info)
A novel chlorinated diphenyl ether from Byrsonima microphylla (Malpighiaceae).
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The isolation is described of an unusual chlorinated diphenyl ether named methyl 3,5-dichloro-6-(6-hydroxy-4-methoxy-3-methoxycarbonyl-2-methylphenoxy)-2-hydroxy- 4-methylbenzoate that was obtained from the trunk of Byrsonima microphylla (Malpighiaceae). The structure was elucidated by a spectroscopic data analysis, and the presence of this compound in heartwood was confirmed by HPLC and HPTLC analyses. (+info)
Isolation and characterization of a novel flavonoid possessing a 4,2''-glycosidic linkage from green mature acerola (Malpighia emarginata DC.) fruit.
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The novel flavonoid, leucocyanidin-3-O-beta-D-glucoside, possessing a 4,2''-glycosidic linkage was isolated from green mature acerola (Malpighia emarginata DC.) puree and given the trivial name "aceronidin." To examine the functions of aceronidin, its antioxidative activity and both its alpha-glucosidase and alpha-amylase inhibition activities, as a potential inhibitor of the sugar catabolic enzyme, were evaluated against those of taxifolin, catechin, isoquercitrin and quercitrin which each have a similar structure. The 1,1-diphenyl-2-picrylhydrazyl (DPPH) radical quenching activity of aceronidin was stronger than that of alpha-tocopherol and comparable to that of flavonoids. In the yeast alpha-glucosidase inhibitory assay, aceronidin showed significantly greater inhibition than the other flavonoids tested. In the human salivary alpha-amylase inhibitory assay, aceronidin showed inhibition activity. Taken together, these results indicate aceronidin to be a potent antioxidant that may be valuable as an inhibitor of sugar catabolic enzymes. (+info)