Austroplenckia Populnea Research Articles

Toxic effects of the crude methanolic extract of <i>Austroplenckia populnea</i> leaves and fractions on the growth of <i>Spodoptera frugiperda</i>

The aim of the current study is to assess the toxicity of <i>Austroplenckia populnea</i> leaf extracts towards the <i>Spodoptera frugiperda</i> population in laboratory conditions. Initially, a crude methanolic extract was obtained from dried leaves of <i>A. populnea</i>. This extract was fractionated using hexane, ethyl acetate, and then methanol. Neonate <i>S. frugiperda</i> larvae were isolated in plastic containers and fed (once) on corn leaf fragments treated with crude and fractions of the investigated plant extracts. The life cycle of the larvae treated with the extracts was monitored. In addition to the intake of leaves treated with the plant extracts, such variables as larval and pupal mortality rate, larval and pupal weight, and larval, pupal, and adult stage duration were evaluated. The crude, hexane, and methanol extract fractions exerted an antixenosis effect on the feeding behaviour of neonate <i>S. frugiperda</i> larvae. A significant antibiosis effect was observed for the hexane fraction of the <i>A. populnea</i> extract, since all of its concentrations promoted a <i>S. frugiperda</i> larval mortality rate differing from that observed for the control. The pupal mortality rate was low, but it did not differ significantly from the mortality rate observed for the control treatment, which was nil. The larvicidal effect of the <i>A. populnea</i> leaf extract, mainly of its hexane fraction, has indicated its potential to be used in integrated <i>S. frugiperda</i> management programs.

Evaluation of anti-inflammatory and antinociceptive activities of the Austroplenckia populnea extract in topical formulations

Austroplenckia populnea (Reiss.) Lundell is a Brazilian Cerrado plant that has been widely used in folk medicine and has many therapeutic properties. The aim of this study is to evaluate the anti-inflammatory and antinociceptive properties of a raw hydroalcoholic wood extract of A. populnea in semi-solid formulations administered topically in rats. The extract of A. populnea was administrated topically in male and female Wistar rats using cream and gel (4.0 and 8.0%) in the paw edema test induced by carrageenan and in the formalin test. Creams remained stable, and the gels showed syneresis. In the paw edema test induced by carrageenan, the gels and creams showed a significant effect compared to the control group. Only 4.0% cream showed swelling inhibition at the 3rd hour compared to the Piroxicam gel. Likewise, in the formalin test, the 4.0% cream had an effect similar to the methyl salicylate, showing a significant anti-inflammatory effect. Based in these results, there was antinociceptive effect with 4.0% cream. We conclude that topical preparations with extract of A. populnea may generate new methods for the treatment of local inflammation. Key words: Analgesia, inflammation, topical administration, formalin test.

Effect of constituents from samaras of Austroplenckia populnea (Celastraceae) on human cancer cells.

Background:Aiming the continuity of the studies of Austroplenckia populnea, Brazilian species of the Celastraceae family, in the present study, it was investigated the effect of crude extracts obtained with ethanol, ethyl acetate and chloroform and two purified constituents, proanthocyanidin A and 4’-O-methylepigallocatechin, both isolated from its samaras, on cancer cell proliferation assays.Materials and Methods:The human cancer cells lines MCF-7 (ductal breast carcinoma), A549 (lung cancer), HS578T (ductal breast carcinoma) and non-cancer HEK293 (embryonic kidney cells) were treated with different concentrations of extracts and constituents and the effect was observed through the acid phosphatase method. The chemical structures of the purified compounds were identified by the respective IR and 1H and 13C nuclear magnetic resonance spectral data.Results:While crude extracts from samaras of the folk medicine A. populnea can trigger cell proliferative effects in human cell lines, the purified compounds (proanthocyanidin A and 4’-O-methyl-epigallocatechin) isolated from the same extracts can have an opposite (anti-proliferative) effect.Conclusion:Based on the results, it was possible to suggest that extracts from samaras of A. populnea should be further investigated for possible cancer-promoting activities; and the active extracts can also represent a source of compounds that have anti-cancer properties.

Evaluation of the genotoxic potential of Austroplenckia populnea (Reiss) Lundell chloroform fraction from barkwood extract in rodent cells in vivo

The genotoxic effect of the Austroplenckia populnea chloroform fraction from barkwood extract was tested in vivo on peripheral blood cells of Swiss mice with the comet assay (SCGE), and the clastogenic effect was investigated on peripheral blood cells of Swiss mice and bone marrow cells of Wistar rats, with the micronucleus and chromosome aberrations tests. The animals were treated by gavage with 3 concentrations of the extract: 300, 600 and 900 mg.kg-1. Peripheral blood cells of Swiss mice were collected 4 and 24 hours after the treatment to the SCGE assay and 48 and 72 hours to the micronucleus test. Bone marrow cells of Wistar rats were collected 24 hours after the treatment to the micronucleus and chromosome aberration tests. The results showed that the A. populnea chloroform fraction induced an increase in the average number of DNA damage in peripheral blood cells at the three concentrations tested, but this increase was not statistically significant. In the micronucleus and chromosome aberrations test, no significant increase was observed in the mean number of micronucleated polychromatic erythrocytes (MNPCE) of Swiss mice or MNPCE or chromosome aberrations for the rat bone marrow cells, for any of the tested doses. Our findings enable us to conclude that by the comet assay, A. populnea chloroform fraction from barkwood extract showed no genotoxic effects, and by the micronucleus and chromosome aberration tests, the extract fraction showed no clastogenic/aneugenic effects on the rodent cells tested.

Evaluation of antibacterial activity of "Mangabarana" Austroplenckia populnea Reissek (Celastraceae)

Austroplenckia populnea (Mangabarana) is popularly used by people from Minas Gerais, Brazil for dysenteries diseases treatment. Antitumor and antiulcer activities were also attributed to this plant. Extracts obtained using solvents of different polarities and pentacyclic triterpenes (PCTTs) isolated from these extracts through phytochemical methods were submitted to antibacterial assays. The results showed the existence of this activity and open perspectives for news studies with other organic compounds isolated from this plant.

Antileishmanial, Antimalarial and Antimicrobial Activities of the Extract and Isolated Compounds from Austroplenckia populnea (Celastraceae)

Austroplenckia populnea (Celastraceae), known as "marmelinho do campo", is used in Brazilian folk medicine as antimicrobial, anti-inflammatory, and antitumoural agent. The aim of the present work was to evaluate the antimicrobial, antileishmanial and antimalarial activities of the crude hydroalcoholic extract of A. populnea (CHE) and some of its isolated compounds. The phytochemical study of the CHE was carried out affording the isolation of methyl populnoate (1), populnoic acid (2), and stigmast-5-en-3-O-beta-(D-glucopyranoside) (3). This is the first time that the presence of compound 3 in A. populnea is reported. The results showed that the CHE presents antifungal and antibacterial activities, especially against Candida glabrata and Candida albicans, for which the CHE showed IC50 values of 0.7 microg mL(-1) and 5.5 microg mL(-1), respectively, while amphotericin B showed an IC50 value of 0.1 microg mL(-1) against both microorganisms. Compounds 1-3 were inactive against all tested microorganisms. In the antileishmanial activity test against Leishmania donovani, the CHE showed an IC50 value of 52 microg mL(-1), while compounds 2 and 3 displayed an IC50 value of 18 microg mL(-1) In the antimalarial assay against Plasmodium falciparum (D6 and W2 clones), it was observed that all evaluated samples were inactive. In order to compare the effect on the parasites with the toxicity to mammalian cells, the cytotoxicity activity of the isolated compounds was evaluated against Vero cells, showing that all evaluated samples exhibited no cytotoxicity at the maximum dose tested.

Anti-inflammatory and antinociceptive activities of extract, fractions and populnoic acid from bark wood of Austroplenckia populnea

Austroplenckia populnea (Reiss) Lund is a Brazilian plant from “cerrado”, which belongs to Celastraceae family, popularity know as “marmelinho-do campo, mangabeira-brava, mangabarana, vime and maria-mole”. This plant is used in folk medicine to treat dysenteries and inflammatory disorders, such as rheumatism. Austroplenckia populnea bark hydroalcoholic crude extract, and its hexane, chloroform and ethyl acetate fractions, obtained by partition, as well as the isolated populnoic acid were investigated for their anti-inflammatory (carrageenan, dextran and histamine-induced rat paw oedema, histamine-induced increase in vascular permeability, and granulomatous tissue induction) and analgesic activities (writhing and hot plate tests). The ED 50 (oral) of the crude extract for the inhibition of carragenan-induced rat paw oedema assay was determined to be 200 mg/kg, which was also used in the assays with the extract and its fractions in all other experiments. Populnoic acid was administered in the dose of 50 mg/kg. Crude extract, hexane and chloroform fractions (200 mg/kg), and indomethacin (10 mg/kg) inhibited significantly ( p < 0.05) the formation of the carrageenan-induced rat paw oedema, measured in third hour of experiment (peak of oedema formation) by 43.2%, 37.3%, 31.1% and 59.3%, respectively. There was a significant reduction ( p < 0.05) in dextran-induced rat paw oedema in all groups, while in the assay using histamine as the oedematogenic agent, only the groups treated with populnoic acid (50 mg/kg) and cyproheptadine (10 mg/kg) displayed significant reduction ( p < 0.05). The populnoic acid and cyproheptadine reduced the peak of oedema formation (1st hour) by 41.3% and 34.7%, respectively. Only for the groups treated with populnoic acid (50 mg/kg) and cyproheptadine (10 mg/kg) it was observed a significant ( p < 0.05) reduction in histamine-induced increase in vascular permeability (44.8% and 80.3%, respectively). Granulomatous tissue formation was significantly inhibited ( p < 0.05) by both hexane fraction (46.0%) and dexamethasone (66.2%). In the analgesic assays, the crude extract and its hexane and chloroform fractions, as well as indomethacin diminished significantly the number of writhings ( p < 0.05) by 69.6%, 47.2%, 44.8% and 62.8%, respectively. On the other hand, none assayed sample displayed significant result in the hot plate test. Based on the obtained results it is suggested that extracts of Austroplenckia populnea bark and populnoic acid display anti-inflammatory activity, supporting its folkloric use to treat inflammatory disorders.

Constituents of the Root Wood of Austroplenckia populnea var. ovata

The root wood of Austroplenckia populnea var. ovata was extracted successively with chloroform and methanol. Lapachol and dehydro-beta-lapachone were isolated from the chloroform extract, and euonine, alatusinine, wilfordine, 2-O-deacetyleuonine (1), 7-O-deacetyleuonine (2), and austronine (3) from the methanol extract. The structures of the new compounds 1-3 were elucidated by spectroscopic data interpretation. Lapachol, dehydro-beta-lapachone, euonine, alatusinine, and wilfordine are known compounds that are newly identified from root wood of Austroplenckia populnea.

Antiulcerogenic Activity of Crude Extract, Fractions and Populnoic Acid Isolated from Austroplenckia populnea (Celastraceae)

Many plant crude extracts and their isolated compounds are the most attractive sources of new drugs and show promising results for the treatment of gastric ulcers. Austroplenckia populnea is commonly known as "marmelinho-do campo, mangabeira-brava, mangabarana and vime" and it has been used in folk medicine as anti-dysenteric and anti-rheumatic. Powdered bark wood (3.25 kg) was macerated with aqueous ethanol (96%) and the extract was concentrated under reduced pressure to yield 406 g of crude hydralcoholic extract. The hydralcoholic extract was suspended in aqueous methanol and partitioned with hexane, chloroform and ethyl acetate (EtOAc) in sequence, yielding 8.0 g, 9.5 g and 98.17 g of crude extracts, respectively. Chromatography of the hexane extract over a silica gel column led to the isolation of the triterpene populnoic acid. The oral administration of hydralcoholic, hexane, chloroform and EtOAc extracts (200 mg/kg) decreased the ulcer lesion index (ULI) by 83.15%, 46.87%, 32.2%, 68.12%, respectively. Oral administration of populnoic acid (100 mg/kg) diminished the ULI by 55.29%. All the obtained results were significant in comparison with the negative control, with exception of the chloroform extract.

3β‐(Stearyloxy)olean‐12‐ene from Austroplenckia populnea: Structure Elucidation by 2D‐NMR and Quantitative 13C‐NMR Spectroscopy

Abstract3β‐(Stearyloxy)olean‐12‐ene was isolated from a hexane extract of Austroplenckia populnea Reiss (Celastraceae) leaves. The structure was solved by means of quantitative 13C‐NMR, HMBC, HMQC, COSY, NOESY, and NOE difference spectra. The mass spectrum showed an [M+1]+ ion peak at m/z 693, and the molecular formula C48H84O2 was confirmed by combustion analysis.

3-Oxoolean-12-en-20-yl α-methylcarboxylate

The title compound, C31H48O3, was obtained by methyl­ation of 3-oxoolean-12-en-20-α-oic acid, isolated from the root bark of Austroplenckia populnea (Celastraceae). Rings A, B, D and E are in chair conformations and ring C is in an envelope conformation.

Effects of the hydromethanolic extract of Austroplenckia populnea (Celastraceae) on reproductive parameters of male rats

Austroplenckia populnea (Reiss.) Lundell. was selected for this study because it has been shown that some plants from the Celastraceae family have antifertility effects. Twelve adult male rats were treated with hydromethanolic extract made from the leaves, 500 mg/kg/day, orally, for 70 days. Distilled water was administered to the control animals (n = 10). At the end of the experiment, and before killing the rats, their sexual behavior was evaluated. The number of intromissions, latencies to first mount and ejaculation, and first intromission after ejaculation were significantly reduced in the treated group, but the total number of ejaculations did not differ from the control group. The weight and histology of the reproductive organs, sperm production, spermatogenesis, prostate fructose content, cauda epidydimides duct diameter, and sperm morphology were not affected. Sperm concentration in cauda epidydimides was significantly decreased. The results showed that A. populnea has effects on male rat reproduction, affecting the sexual behavior and epididymal sperm concentration.

Anti-trypanosomal activity of pentacyclic triterpenes isolated from Austroplenckia populnea (Celastraceae).

Four pentacyclic triterpenes isolated from Austroplenckia populnea and four compounds of known anti T. cruzi or anti-malarial activity were tested. Of those triterpenes tested 20alpha-hydroxy-tingenone showed high activity, epikatonic acid was less active, while populnilic and populninic acids were inactive against the trypanosome of the subgenus Schizotrypanum tested. Benzonidazole, nifurtimox, ketoconazole and primaquine presented a remarkable dose-dependent inhibitory effect reaching practically to a total growth inhibition of the parasite at the end of incubation time. The trypanosome tested appear to be a suitable model for preliminary screen for anti T. (S.) cruzi compounds.

Epikatonic acid from Austroplenckia populnea: structure elucidation by 2D NMR spectroscopy and X‐ray crystallography

AbstractFrom the chloroform extract of Austroplenckia populnea, epikatonic acid, friedelin, populnonic acid, abruslactone A, salaspermic acid and 22β‐epi‐maytenfolic acid were isolated. The structure and stereochemistry of epikatonic acid were established by two‐dimensional NMR spectroscopic techniques (HMQC, HMBC and NOESY) and later confirmed by single crystal X‐ray diffraction as 3β‐hydroxy‐olean‐12‐en‐29‐oic acid, which unambiguously established the configuration of the hydroxyl group at C‐3 as 3β‐OH and the carboxyl group at C‐20 as 20α‐COOH. The crystal structure shows two independent molecules in the asymmetric unit. The crystal packing is stabilized by four O–H·O intermolecular hydrogen bonds, which give rise to infinite double chains along the c axis. Copyright © 2002 John Wiley &amp; Sons, Ltd.

Antiulcerogenic and analgesic effects of the Austroplenckia populnea extracts in mice.

Austroplenckia populnea (Reiss.) Lund. is a Brazilian Cerrado plant belonging to the Celastraceae family. Hexane and methanol extracts of leaves were investigated for their antiulcerogenic (ethanol and indomethacin/bethanecol induced gastric damage) and analgesic (writhing and tail-flick tests) activities in mice. Acute toxic effects also were evaluated. Oral administration of both extracts at a dose of 1000 mg/kg significantly reduced the total area of the lesion, the relative area of lesion and the ulcerative index in ethanol-induced gastric damage, but both extracts were inactive in the indomethacin/bethanecol-induced gastric damage test. A dose dependent effect was determined with the hexane extract in the ethanol-induced lesions test. The hexane and methanol extracts reduced the number of contortions in the writhing test, but both extracts were inactive in the tail-flick immersion test.

Total assignment of 1H and 13C NMR spectra of two 3,4‐secofriedelanes from Austroplenckia populnea

AbstractTwo new 3,4‐secofriedelanes, 3,4‐seco‐28‐hydroxyfriedelan‐3‐oic acid (1) and 3,4‐secofriedelan‐3‐oic acid (2), were isolated from the leaves of Austroplenckia populnea (Celastraceae). The structures were established by 2D NMR spectroscopic techniques (COSY, HMQC, HMBC and NOESY). Copyright © 2001 John Wiley &amp; Sons, Ltd.

Decrease in sperm number after treatment of rats with Austroplenckia populnea

The purpose of this study was to evaluate the effects of a hexanic extract (HE) made from leaves of A. populnea collected in Botucatu, State of São Paulo, and Nova Lima, State of Minas Gerais, Brazil, at a range of doses during 7 and 14 days, on the male reproductive system of rats. The treatment did not affect the body weight, nor absolute organ weight. The serum testosterone levels, testicular sperm head counts, daily sperm production, and sperm morphology did not differ from that of the control groups. The spermatogenesis and the morphometric parameters of cauda epididymidis were not affected by the treatment. Cauda epididymis sperm number was significantly reduced in the group that received HE of Nova Lima, 1 g/kg/day, during 14 days, from the control group.

3-Epiabruslactone A, a New Triterpene Lactone Isolated from Austroplenckia populnea

A new lactonic triterpene isolated from the heartwood of Austroplenckia populnea (Celastraceae) was characterized as 3a-hydroxyolean-12-en-29,22a-olide (the g-lactone of the 3a,22a-dihydroxyolean-12-en-29a-oic acid), the 3-epimer of the abruslactone A, on the basis of its spectral data, chemical transformations, and single crystal X-ray analysis.

Friedelane and oleanane triterpenoids from bark wood of Austroplenckia populnea

The bark wood of Austroplenckia populnea afforded, in addition to 3-hydroxy-2-oxofriedelan- 3-ene-20α-methylcar☐ylate, methyl populnonate, 3-hydroxy-2-oxofriedelan-3-ene-20α-car☐ylic acid, populnonic acid, epikatonic acid, dispermoquinone, β-sitosterol, β-sitostenone and dulcitol, two new pentacyclic triterpenes: 3-oxoolean-12-ene-20α-car☐ylic acid and 3β-hydroxy-2- oxofriedelan-20α-car☐ylic acid. The structures of these have been established from spectral studies and structural correlations, and single-crystal X-ray analysis of 3β-hydroxy-2-oxofriedelan- 20α-car☐ylic acid.

Polyhydroxyagarofuran derivatives from Austroplenckia populnea

The larvicidal extract of Austroplenckia populnea leaves gave two new polyesters of 8-oxo-1,2,3,4,9,14-hexahydroxydihydroagarofuran, a compound which is typical of Celastraceae species.