RESUMO
In the field of research on medicinal plants from the Armenian flora, the phytochemical study of two Scabiosa L. species, S. caucasica M. Bieb. and S. ochroleuca L. (Caprifoliaceae), has led to the isolation of five previously undescribed oleanolic acid glycosides from an aqueous-ethanolic extract of the roots: 3-O-α-L-rhamnopyranosyl-(1â3)-ß-D-glucopyranosyl-(1â4)-ß-D-glucopyranosyl-(1â4)-ß-D-xylopyranosyl-(1â3)-α-L-rhamnopyranosyl-(1â2)-α-L-arabinopyranosyloleanolic acid 28-O-ß-D-glucopyranosyl-(1â6)-ß-D-glucopyranosyl ester, 3-O-ß-D-xylopyranosyl-(1â2)-[α-L-rhamnopyranosyl-(1â4)]-ß-D-glucopyranosyl-(1â4)-ß-D-glucopyranosyl-(1â4)-ß-D-xylopyranosyl-(1â3)-α-L-rhamnopyranosyl-(1â2)-α-L-arabinopyranosyloleanolic acid 28-O-ß-D-glucopyranosyl-(1â6)-ß-D-glucopyranosyl ester, 3-O-ß-D-xylopyranosyl-(1â2)-[α-L-rhamnopyranosyl-(1â4)]-ß-D-glucopyranosyl-(1â4)-ß-D-glucopyranosyl-(1â4)-ß-D-xylopyranosyl-(1â3)-α-L-rhamnopyranosyl-(1â2)-α-L-arabinopyranosyloleanolic acid, 3-O-ß-D-xylopyranosyl-(1â2)-[α-L-rhamnopyranosyl-(1â4)]-ß-D-xylopyranosyl-(1â4)-ß-D-glucopyranosyl-(1â4)-ß-D-xylopyranosyl-(1â3)-α-L-rhamnopyranosyl-(1â2)-α-L-arabinopyranosyloleanolic acid 28-O-ß-D-glucopyranosyl-(1â6)-ß-D-glucopyranosyl ester, 3-O-α-L-rhamnopyranosyl-(1â4)-ß-D-glucopyranosyl-(1â4)-ß-D-glucopyranosyl-(1â4)-ß-D-xylopyranosyl-(1â3)-α-L-rhamnopyranosyl-(1â2)-α-L-arabinopyranosyloleanolic acid 28-O-ß-D-glucopyranosyl-(1â6)-ß-D-glucopyranosyl ester. Their full structural elucidation required extensive 1D and 2D NMR experiments, as well as mass spectrometry analysis. For the biological activity of the bidesmosidic saponins and the monodesmosidic saponin, their cytotoxicity on a mouse colon cancer cell line (MC-38) was evaluated.
Assuntos
Caprifoliaceae , Dipsacaceae , Ácido Oleanólico , Saponinas , Triterpenos , Animais , Camundongos , Glicosídeos/farmacologia , Glicosídeos/química , Ácido Oleanólico/farmacologia , Ácido Oleanólico/química , Saponinas/química , Caprifoliaceae/química , Triterpenos/farmacologia , Triterpenos/químicaRESUMO
The phytochemical study of Wisteria sinensis (Sims) DC. (Fabaceae), commonly known as the Chinese Wisteria, led to the isolation of seven oleanane-type glycosides from an aqueous-ethanolic extract of the roots. Among the seven isolated saponins, two have never been reported before: 3-O-α-L-rhamnopyranosyl-(1â2)-ß-D-glucopyranosyl-(1â2)-ß-D-glucuronopyranosyl-22-O-acetylolean-12-ene-3ß,16ß,22ß,30-tetrol, and 3-O-ß-D-xylopyranosyl-(1â2)-ß-D-glucuronopyranosylwistariasapogenol A. Based on the close structures between the saponins from W. sinensis, and the glycyrrhizin from licorice, the stimulation of the sweet taste receptor TAS1R2/TAS1R3 by these glycosides was evaluated.
Assuntos
Saponinas , Wisteria , Glicosídeos/farmacologia , Glicosídeos/química , Paladar , Saponinas/químicaRESUMO
Phytochemical investigation of Eryngium creticum L. has resulted in isolation of five compounds, including four compounds that are reported from the plant for the first time. Compound 1 was identified as (E)-rosmarinic acid, meanwhile, compound 2 was isolated as an (E/Z)-rosmarinic acid mixture. Interestingly, the E/Z-isomeric mixture was about 4 times as active as the single E-isomer toward the severe acute respiratory syndrome coronavirus 2 3-chymotrypsin-like protease (3CLpro), IC50 = 6.062 and 25.75 µM, respectively. Utilizing combined molecular docking and molecular dynamics (MD) techniques, the binding affinities and features of the isolated compounds were evaluated against 3CLpro. Compound 2Z demonstrated a higher binding affinity for 3CLpro than 2E , with docking scores of -8.9 and -8.5 kcal/mol and MM-GBSA/150 ns MD binding energies of -26.5 and -22.1 kcal/mol, respectively. This justifies the superior activity of the E/Z-isomeric mixture versus the single E-isomer. Structural and energetic analyses revealed the stability of 2Z and 2E compared to the reference HIV-1 protease inhibitor, lopinavir. Besides, DFT calculations demonstrated the more energetic stability of 2E compared to 2Z , which justifies the difficulty in isolating the Z-isomer in a pure form, where it readily isomerizes to the E-isomer.
RESUMO
Although many natural products have proven their potential to regulate obesity through the modulation of adipocyte biology, none of them has yet been approved for clinical use in obesity therapy. This work aims to isolate valuable secondary metabolites from an orchid species (Dendrobium heterocarpum) and evaluate their possible roles in the growth and differentiation of 3T3-L1 pre-adipocytes. Six compounds were isolated from the orchid's methanolic extracts and identified as amoenylin (1), methyl 3-(4-hydroxyphenyl) propionate (2), 3,4-dihydroxy-5,4'-dimethoxybibenzyl (3), dendrocandin B (4), dendrofalconerol A (5), and syringaresinol (6). Among these phytochemicals, compounds 2, 3, and 6 exhibited lower effects on the viability of 3T3-L1 cells, offering non-cytotoxic concentrations of â²10 µM. Compared to others tested, compound 3 was responsible for the maximum reduction of lipid storage in 3T3-L1 adipocytes (IC50 = 6.30 ± 0.10 µM). A set of protein expression studies unveiled that compound 3 at non-cytotoxic doses could suppress the expression of some key transcription factors in adipocyte differentiation (i.e., PPARγ and C/EBPα). Furthermore, this compound could deactivate some proteins involved in the MAPK pathways (i.e., JNK, ERK, and p38). Our findings prove that D. heterocarpum is a promising source to explore bioactive molecules capable of modulating adipocytic growth and development, which can potentially be assessed and innovated further as pharmaceutical products to defeat obesity.
Assuntos
Dendrobium , Células 3T3-L1 , Adipócitos , Adipogenia , Animais , Diferenciação Celular , Dendrobium/metabolismo , Lipídeos/farmacologia , Metanol/farmacologia , Camundongos , Obesidade/metabolismo , PPAR gama/metabolismo , Extratos Vegetais/químicaRESUMO
Seven previously undescribed oleanane-type glycosides were isolated from the trunk barks of a Central African tree named Millettia laurentii De Wild (Fabaceae). After the extraction from the barks, the isolation and purification of these compounds were achieved using various solid/liquid chromatographic methods. Their structures were established mainly by 1D and 2D NMR (COSY, TOCSY, ROESY, HSQC, HMBC) and mass spectrometry (ESI-MS), as 3-O-ß-D-glucuronopyranosyl-(1 â 2)-ß-D-glucuronopyranosylechinocystic acid, 3-O-ß-D-apiofuranosyl-(1 â 3)-ß-D-glucuronopyranosyl-(1 â 2)-ß-D-glucuronopyranosylechinocystic acid, 3-O-ß-D-apiofuranosyl-(1 â 3)-ß-D-galactopyranosyl-(1 â 2)-ß-D-glucuronopyranosylechinocystic acid, 3-O-ß-D-apiofuranosyl-(1 â 3)-[ß-d-xylopyranosyl-(1 â 2)]-ß-D-galactopyranosyl-(1 â 2)-ß-D-glucuronopyranosylechinocystic acid, 3-O-ß-D-apiofuranosyl-(1 â 3)-[α-L-arabinofuranosyl-(1 â 2)]-ß-D-galactopyranosyl-(1 â 2)-ß-D-glucuronopyranosylechinocystic acid, 3-O-α-L-arabinofuranosyl-(1 â 2)-ß-D-galactopyranosyl-(1 â 2)-ß-D-glucuronopyranosyloleanolic acid, 3-O-ß-D-apiofuranosyl-(1 â 3)-[α-L-arabinofuranosyl-(1 â 2)]-ß-D-galactopyranosyl-(1 â 2)-ß-D-glucuronopyranosyloleanolic acid. In addition, the cytotoxicity of six glycosides among the isolated ones, was evaluated against 4 T1 cell line from a mouse mammary gland tissue, using MTS method.
Assuntos
Millettia , Saponinas , Animais , Glicosídeos/química , Camundongos , Estrutura Molecular , Ácido Oleanólico/análogos & derivados , Saponinas/química , ÁrvoresRESUMO
Harringtonine (HT), produced from Cephalotaxus species, is known to exhibit potent antiproliferative activity against myeloid leukemia cells by inhibiting protein synthesis. A previous study using acute promyelocytic leukemia (HL-60) cells raised the possibility that the C-5' methyl group of HT plays an important role in regulating leukemia cell line antiproliferative activity. In order to investigate the effect of hydrocarbon chains at C-5' on the resultant activity, the C-5' methyl group was replaced with various straight- and branched-chain hydrocarbons using the corresponding alcohols, and their antiproliferative activity against HL-60 and HeLa cells was investigated. As a result, 4'-n-heptyl-4'-demethylharringtonine (1f, n-heptyl derivative) showed the most potent cytotoxicity among the HT ester derivatives produced, with IC50 values of 9.4 nM and 0.4 µM for HL-60 and HeLa cells, respectively. Interestingly, the cytotoxicity of derivative 1f against HL-60 and HeLa cells respectively was â¼5 (IC50 = 50.5 nM) and â¼10 times (IC50 = 4.0 µM) those of HT and â¼2 (IC50 = 21.8 nM) and â¼4 times (IC50 = 1.7 µM) more than homoharringtonine (HHT). These results demonstrate the potential of the derivative 1f as a lead compound against leukemia.
Assuntos
Harringtoninas , Leucemia Promielocítica Aguda , Ésteres/farmacologia , Células HL-60 , Harringtoninas/farmacologia , Células HeLa , HumanosRESUMO
A new α-pyrone derivative, with a rare substitution pattern, was isolated from the solid rice media of the fungal endophyte Aspergillus versicolor associated with the fruit of the mangrove Avicennia marina. It was named allantopyrone E, after allantopyrones C and D. The aforementioned three are the only diaryl-substituted α-pyrones to be reported from nature. The unique structure was elucidated based on one- and two dimensional NMR data as well as high resolution mass spectroscopy. A biosynthetic scheme was proposed for the new compound. Furthermore, allantopyrone E showed cytotoxic effect on HeLa cells with IC50= 50.97 µM.
Assuntos
Fungos , Pironas , Aspergillus , Células HeLa , Humanos , Estrutura MolecularRESUMO
The polar fraction of the MeOH extract of the roots of Corrigiola litoralis subsp. telephiifolia (Pourr.) Briq. (Caryophyllaceae) was investigated for its constituents and two previously unreported monodesmosides triterpene saponins, telephiifoliosides A and B (1 and 2), along with the known bonushenricoside A (3) were isolated. Their structures were elucidated by combined spectroscopic and spectrometric techniques (1H NMR, 13C NMR, HSQC, 1H-1H COSY, HMBC, TOCSY, NOESY, HRESIMS) and chemical methods. The structures of the new saponins were established as; 3-O-α-L-arabinopyranosyljaligonic acid (1), and 3-O-α-L-arabinopyranosylphytolaccagenin ester (2). Upon evaluation of the antiproliferative activity on human malignant epithelial (HeLa) cells, none of the isolated compounds was efficient at the concentration of 33 µM. [Formula: see text]HighlightsThis is the first phytochemical study on Corrigiola litoralis subsp. telephiifolia.Two new saponins were isolated from the roots of Corrigiola litoralis subsp. telephiifolia.The isolated compounds were tested for their antiproliferative activity.
Assuntos
Caryophyllaceae , Saponinas , Triterpenos , Caryophyllaceae/química , Ésteres/análise , Humanos , Estrutura Molecular , Extratos Vegetais/química , Raízes de Plantas/química , Saponinas/química , Triterpenos/químicaRESUMO
Four oleanane-type glycosides were isolated from a horticultural cultivar "Green Elf" of the endemic Pittosporum tenuifolium (Pittosporaceae) from New Zealand: three acylated barringtogenol C glycosides from the leaves, with two previously undescribed 3-O-ß-d-glucopyranosyl-(1â2)-[α-l-arabinopyranosyl-(1â3)]-ß-d-glucuronopyranosyl-21-O-angeloyl-28-O-acetylbarringtogenol C, 3-O-ß-d-galactopyranosyl-(1â2)-[α-l-arabinopyranosyl-(1â3)]-ß-d-glucuronopyranosyl-21-O-angeloyl-28-O-acetylbarringtogenol C, and the known 3-O-ß-d-glucopyranosyl-(1â2)-[α-l-arabinopyranosyl-(1â3)]-ß-d-glucuronopyranosyl-21-O-angeloyl-28-O-acetylbarringtogenol C (Eryngioside L). From the roots, the known 3-O-ß-d-glucopyranosyl-(1â2)-ß-d-galactopyranosyl-(1â2)-ß-d-glucuronopyranosyloleanolic acid (Sandrosaponin X) was identified. Their structures were elucidated by spectroscopic methods including 1D- and 2D-NMR experiments and mass spectrometry (ESI-MS). According to their structural similarities with gymnemic acids, the inhibitory activities on the sweet taste TAS1R2/TAS1R3 receptor of an aqueous ethanolic extract of the leaves and roots, a crude saponin mixture, 3-O-ß-d-glucopyranosyl-(1â2)-[α-l-arabinopyranosyl-(1â3)]-ß-d-glucuronopyranosyl-21-O-angeloyl-28-O-acetylbarringtogenol C, and Eryngioside L were evaluated.
Assuntos
Rosales/química , Saponinas/isolamento & purificação , Triterpenos/isolamento & purificação , Subunidades alfa Gq-G11 de Proteínas de Ligação ao GTP/antagonistas & inibidores , Células HEK293 , Humanos , Espectroscopia de Ressonância Magnética , Estrutura Molecular , Nova Zelândia , Extratos Vegetais/química , Extratos Vegetais/isolamento & purificação , Extratos Vegetais/farmacologia , Folhas de Planta/química , Raízes de Plantas/química , Plantas Medicinais/química , Receptores Acoplados a Proteínas G/antagonistas & inibidores , Saponinas/química , Saponinas/farmacologia , Espectrometria de Massas por Ionização por Electrospray , Triterpenos/química , Triterpenos/farmacologiaRESUMO
A phytochemical study of Cordyline fruticosa "Fairchild red" (Asparagaceae) from Vietnam, led to the isolation of fourteen steroidal glycosides, including twelve previously undescribed along with two known ones. Ten compounds were obtained by successive solid/liquid chromatographic methods from an aqueous-ethanolic extract of the roots, and four from the aerial parts. Their structures were elucidated mainly by spectroscopic analysis 2D NMR and mass spectroscopy (ESI-MS), as spirostanol glycosides, 5α-spirost-25(27)-ene-1ß,3ß,4α-triol 1-O-ß-D-fucopyranoside, 5α-spirost-(25)27-ene-1ß,3ß,4α-triol 1-O-ß-D-xylopyranoside, 5α-spirost-(25)27-ene-1ß,3ß,4α-triol 1-O-α-L-rhamnopyranosyl-(1 â 2)-ß-D-fucopyranoside, 5α-spirost-(25)27-ene-1ß,3ß,4α-triol 1-O-α-L-rhamnopyranosyl-(1 â 2)-(4-O-sulfo)-ß-D-fucopyranoside, 5α-spirost-25(27)-ene-1ß,3ß-diol 1-O-α-L-rhamnopyranosyl-(1 â 2)-ß-D-fucopyranoside, and 5α-spirost-25(27)-ene-1ß,3ß-diol 1-O-α-L-rhamnopyranosyl-(1 â 2)-α-L-arabinopyranoside. Furostanol glycosides were also isolated as 26-O-ß-D-glucopyranosyl-5α-furost-(25)27-ene-1ß,3ß,4α,22α,26-pentol 1-O-ß-D-fucopyranoside, 26-O-ß-D-glucopyranosyl-22α-methoxy-5α-furost-(25)27-ene-1ß,3ß,4α,26-tetrol 1-O-ß-D-fucopyranoside, 26-O-ß-D-glucopyranosyl-5α-furost-(25)27-ene-1ß,3ß,22α,26-tetrol 1-O-ß-D-glucopyranoside, 26-O-ß-D-glucopyranosyl-5α-furost-(25)27-ene-1ß,3ß,22α,26-tetrol 1-O-α-L-rhamnopyranosyl-(1 â 2)-ß-D-glucopyranoside, 26-O-ß-D-glucopyranosyl-5α-furost-(25)27-ene-1ß,3ß,22α,26-tetrol 1-O-α-L-rhamnopyranosyl-(1 â 2)-ß-D-fucopyranoside, and 26-O-ß-D-glucopyranosyl-22α-methoxy-5α-furost-(25)27-ene-1ß,3ß,26-triol 1-O-α-L-rhamnopyranosyl-(1 â 2)-ß-D-fucopyranoside. All the isolated compounds were further evaluated for their cytotoxicity against 4T1 cell line, from a mouse mammary gland tissue, using MTS method.
Assuntos
Cordyline , Saponinas , Animais , Povo Asiático , Cromatografia Líquida , Glicosídeos , Humanos , CamundongosRESUMO
Thraustochytrids, unicellular marine protists, synthesize polyunsaturated fatty acids (PUFAs) and PUFA-containing phospholipids; however, little is known about their glycolipids and their associated metabolism. Here, we report two glycolipids (GL-A, B) and their synthases in Aurantiochytrium limacinum mh0186. Two glycolipids were purified from A. limacinum mh0186, and they were determined by gas chromatography, mass spectrometry and 2D nuclear magnetic resonance to be 3-O-ß-D-glucopyranosyl-stigmasta-5,7,22-triene (GL-A) and 3-O-ß-D-glucopyranosyl-4α-methyl-stigmasta-7,22-diene (GL-B), both of which are sterol ß-glucosides (ß-SGs); the structure of GL-B has not been reported thus far. Seven candidate genes responsible for the synthesis of these ß-SGs were extracted from the draft genome database of A. limacinum using the yeast sterol ß-glucosyltransferase (SGT; EC 2.4.1.173) sequence as a query. Expression analysis using Saccharomyces cerevisiae revealed that two gene products (AlSGT-1 and 2) catalyze the transfer of glucose from uridine diphosphate (UDP)-glucose to sterols, generating sterylglucosides (SGs). Compared to AlSGT-1, AlSGT-2 exhibited wide specificity for sterols and used C4-monomethylsterol to synthesize GL-B. The disruption of alsgt-2 but not alsgt-1 in strain mh0186 resulted in a decrease in the total SG and an almost complete loss of GL-B, indicating that AlSGT-2 is responsible for the synthesis of ß-SGs in A. limacinum mh0186, especially GL-B, which possesses a unique sterol structure.
Assuntos
Glucosiltransferases/metabolismo , Glicolipídeos/metabolismo , Microalgas/enzimologia , Glucosiltransferases/genética , Glicolipídeos/química , Conformação MolecularRESUMO
The aim of this study was to evaluate the effects of ingesting fucoidan derived from Okinawa mozuku (Cladosiphon okamuranus) on natural killer (NK) cell activity and to assess its safety in healthy adults via a randomized, double-blind, parallel-group, placebo-controlled pilot study. Subjects were randomly divided into two groups-a placebo group (ingesting citric acid, sucralose, and caramel beverages; n = 20; 45.5 ± 7.8 years (mean ± standard deviation)) and a fucoidan group (3.0 g/day from beverages; n = 20; 47.0 ± 7.6 years); after 12 weeks, blood, biochemical, and immunological tests were performed. Clinically adverse events were not observed in any of the tests during the study period. In addition, adverse events due to the test food were not observed. In the immunological tests, NK cell activity was significantly enhanced at 8 weeks in the fucoidan group, compared to before ingestion (0 weeks). In addition, a significantly enhanced NK cell activity was observed in male subjects at 8 weeks, compared with the placebo group. These results confirm that Okinawa mozuku-derived fucoidan enhances NK cell activity and suggest that it is a safe food material.
Assuntos
Produtos Biológicos/farmacologia , Agentes de Imunomodulação/farmacologia , Células Matadoras Naturais/efeitos dos fármacos , Phaeophyceae/química , Polissacarídeos/farmacologia , Adulto , Idoso , Produtos Biológicos/isolamento & purificação , Biomarcadores/sangue , Método Duplo-Cego , Feminino , Voluntários Saudáveis , Humanos , Agentes de Imunomodulação/isolamento & purificação , Células Matadoras Naturais/imunologia , Masculino , Pessoa de Meia-Idade , Projetos Piloto , Polissacarídeos/isolamento & purificaçãoRESUMO
Chytranthus macrobotrys and Radlkofera calodendron are two Sapindaceae characterized by a lack of phytochemical data. Both root barks from the two Sapindaceae species were processed by ethanol extraction followed by the isolation of their primary constituents by liquid chromatography. This process yielded four previously undescribed terpenoid glycosides together with eight known analogues. Extracts and isolated compounds from C. macrobotrys and R. calodendron were then screened for antimicrobial activity against fifteen phytopathogens. The biological screening also involved extracts and pure compounds from Blighia unijugata and Blighia welwitschii, two Sapindaceae previously studied by our group. Phytopathogens were chosen based on their economic impact on agriculture worldwide. The selection was composed primarily of fungal species including; Pyricularia oryzae, Gaeumannomyces graminis var. tritici, Zymoseptoria tritici, Fusarium oxysporum, Botrytis cinerea, Pythium spp., Trichoderma spp. and Rhizoctonia solani. Furthermore, pure terpenoid glycosides were tested for the first time against wood-inhabiting phytopathogens such as; Phaeomoniella chlamydospora, Phaeoacremonium minimum, Fomitiporia mediterranea, Eutype lata and Xylella fastidiosa. Raw extracts exhibited different levels of activity dependent on the organism. Some pure compounds, including 3-O-α-L-arabinopyranosyl-(1 â 4)-ß-D-xylopyranosyl-(1 â 3)-α-L-rhamnopyranosyl-(1 â 2)-α-L-arabinopyranosylhederagenin, 3-O-α-L-rhamnopyranosyl-(1 â 2)-α-L-arabinopyranosylhederagenin (α-hederin), 3-O-ß-D-glucopyranosyl-(1 â 3)-α-L-rhamnopyranosyl-(1 â 2)-α-L-arabinopyranosylhederagenin (macranthoside A) and 3-O-α-L-arabinopyranosyl-(1 â 3)-α-L-rhamnopyranosyl-(1 â 2)-α-L-arabinopyranosylhederagenin (clemontanoside C), exhibited significant growth inhibitions on Pyricularia oryzae, Gaeumannomyces graminis var. tritici, Fomitiporia mediterranea and Zymoseptoria tritici. Monodesmoside triterpene saponins, in particular, exhibited MIC (IC100) values as low as 25 µg/ml and IC50 values as low as 10 µg/ml against these phytopathogens. Structure-activity relationships, as well as plant-microbe interactions, were discussed.
Assuntos
Sapindaceae , Saponinas , Ascomicetos , Basidiomycota , Botrytis , Fusarium , Glicosídeos/farmacologia , Casca de Planta , Extratos Vegetais , Rhizoctonia , Terpenos/farmacologia , XylellaRESUMO
Fifteen triterpenoid saponins including five new compounds (Mannioside B: 3ß-[(ß-d-glucopyranosyl)oxy]urs-12-en-28-oic acid α-l-rhamnopyranosyl-(1 â 4)-ß-d-glucopyranosyl-(1 â 6)-ß-d-glucopyranosyl ester (1), mannioside C: 3ß-[(ß-d-glucopyranosyl)23-dioxy]urs-12-en-28-oic acid α-l-rhamnopyranosyl-(1 â 4)-ß-d-glucopyranosyl-(1 â 6)-ß-d-glucopyranosyl ester (2), mannioside D: 3ß,23-dihydroxyurs-12-en-28-oic acid ß-d-glucopyranosyl-(1 â 6)- ß-d-glucopyranosyl ester (3), mannioside E: 3ß-hydroxy-23-oxolup-20(29)-en-28-oic acid α-l-rhamnopyranosyl-(1 â 4)-ß-d-glucopyranosyl-(1 â 6)-ß-d-glucopyranosyl ester (4) and mannioside F: (22S)-27ß-[(ß-d-glucopyranosyl)oxy]-22-hydroxyprotosta-12,24-dien-3ß-yl ß-d-glucopyranoside (5)) were isolated from the leaves of Schefflera mannii (Hook.f.) Harms. Their structures were established on the basis of 1D and 2D NMR data, mass spectrometry and chemical methods. The major isolated compounds were tested for their antiproliferative activity on human malignant epithelial (HeLa) cells but were not efficient at the concentration of 33 mM.
Assuntos
Araliaceae/química , Folhas de Planta/química , Saponinas/isolamento & purificação , Triterpenos/isolamento & purificação , Espectroscopia de Ressonância Magnética , Conformação Molecular , Saponinas/química , Triterpenos/químicaRESUMO
Helicobacter pylori causes gastritis, which has been attributed to the development of H. pylori-specific T cells during infection. However, the mechanism underlying innate immune detection leading to the priming of T cells is not fully understood, as H. pylori evades TLR detection. Here, we report that H. pylori metabolites modified from host cholesterol exacerbate gastritis through the interaction with C-type lectin receptors. Cholesteryl acyl α-glucoside (αCAG) and cholesteryl phosphatidyl α-glucoside (αCPG) were identified as noncanonical ligands for Mincle (Clec4e) and DCAR (Clec4b1). During chronic infection, H. pylori-specific T cell responses and gastritis were ameliorated in Mincle-deficient mice, although bacterial burdens remained unchanged. Furthermore, a mutant H. pylori strain lacking αCAG and αCPG exhibited an impaired ability to cause gastritis. Thus H. pylori-specific modification of host cholesterol plays a pathophysiological role that exacerbates gastric inflammation by triggering C-type lectin receptors.
Assuntos
Colesterol/metabolismo , Gastrite/metabolismo , Infecções por Helicobacter/metabolismo , Helicobacter pylori/metabolismo , Lectinas Tipo C/metabolismo , Proteínas de Membrana/metabolismo , Receptores Imunológicos/metabolismo , Animais , Colesterol/genética , Doença Crônica , Gastrite/genética , Gastrite/microbiologia , Infecções por Helicobacter/genética , Lectinas Tipo C/genética , Proteínas de Membrana/genética , Camundongos , Camundongos Knockout , Receptores Imunológicos/genéticaRESUMO
Ten pentacyclic triterpenes (1-10) were isolated from Lavandula coronopifolia. We evaluated their α-glucosidase inhibitory activity, and found that the aglycones, 1, 2, 3, 4, 7 and 10 showed superior IC50 values to the positive control. In order to explain the structural requirements for α-glucosidase inhibitory activity, eleven derivatives were prepared, including one new compound, 2-formyl-(A)1-19α-hydroxy-1-norursane-2, 12-dien-28-oic acid 10c. The results demonstrated that a free hydroxyl at ring-A and a free carboxylic group at position 28 are key structural features for the α-glucosidase inhibitory activity, also that an ursane skeleton is optimum for the activity. Additionally, enzyme kinetic analysis of pomolic acid 2, the most potent compound, revealed that it inhibited α-glucosidase in a mixed-type manner. The molecular docking simulation validated this type of inhibition and highlighted the role of the C-3 hydroxyl and C-28 carboxylic groups in interaction with the enzyme in silico.
Assuntos
Inibidores de Glicosídeo Hidrolases/química , Inibidores de Glicosídeo Hidrolases/farmacologia , Lavandula/química , Triterpenos Pentacíclicos/química , Triterpenos Pentacíclicos/isolamento & purificação , Espectroscopia de Ressonância Magnética Nuclear de Carbono-13 , Ensaios Enzimáticos , Concentração Inibidora 50 , Cinética , Simulação de Acoplamento Molecular , Ácido Oleanólico/análogos & derivados , Ácido Oleanólico/química , Ácido Oleanólico/farmacologia , Triterpenos Pentacíclicos/farmacologia , Espectroscopia de Prótons por Ressonância Magnética , Relação Estrutura-Atividade , alfa-Glucosidases/metabolismoRESUMO
AIMS: Coronary arteritis is a life-threatening complication that may arise in the acute stage of Kawasaki disease (KD), the leading cause of systemic vasculitis in childhood. Various microorganisms and molecular pathogens have been reported to cause KD. However, little is known about the key molecules that contribute to the development of coronary arteritis in KD. METHODS AND RESULTS: To identify causative molecules for coronary arteritis in KD, we prospectively recruited 105 patients with KD and 65 disease controls in four different parts of Japan from 2015 to 2018. During this period, we conducted lipidomics analyses of their sera using liquid chromatography-mass spectrometry (LC-MS). The comprehensive LC-MS system detected a total of 27 776 molecules harbouring the unique retention time and m/z values. In the first cohort of 57 KD patients, we found that a fraction of these molecules showed enrichment patterns that varied with the sampling region and season. Among them, 28 molecules were recurrently identified in KD patients but not in controls. The second and third cohorts of 48 more patients with KD revealed that these molecules were correlated with inflammatory markers (leucocyte counts and C-reactive proteins) in the acute stage. Notably, two of these molecules (m/z values: 822.55 and 834.59) were significantly associated with the development of coronary arteritis in the acute stage of KD. Their fragmentation patterns in the tandem MS/MS analysis were consistent with those of oxidized phosphatidylcholines (PCs). Further LC-MS/MS analysis supported the concept that reactive oxygen species caused the non-selective oxidization of PCs in KD patients. In addition, the concentrations of LOX-1 ligand containing apolipoprotein B in the plasma of KD patients were significantly higher than in controls. CONCLUSION: These data suggest that inflammatory signals activated by oxidized phospholipids are involved in the pathogenesis of coronary arteritis in KD. Because the present study recruited only Japanese patients, further examinations are required to determine whether oxidized PCs might be useful biomarkers for the development of coronary arteritis in broad populations of KD.
Assuntos
Arterite/sangue , Doença da Artéria Coronariana/sangue , Lipidômica , Síndrome de Linfonodos Mucocutâneos/sangue , Fosfatidilcolinas/sangue , Proteínas Adaptadoras de Transdução de Sinal/sangue , Arterite/diagnóstico , Arterite/etiologia , Biomarcadores/sangue , Estudos de Casos e Controles , Criança , Pré-Escolar , Cromatografia Líquida , Doença da Artéria Coronariana/diagnóstico , Doença da Artéria Coronariana/etiologia , Feminino , Humanos , Japão , Lipoproteínas LDL/sangue , Masculino , Síndrome de Linfonodos Mucocutâneos/complicações , Síndrome de Linfonodos Mucocutâneos/diagnóstico , Oxirredução , Fenilalanina/sangue , Estudos Prospectivos , Receptores Depuradores Classe E/sangue , Espectrometria de Massas em TandemRESUMO
Two new polyhydroxylated steroids, 3ß-acetoxy-gorgost-5α,6ß,11α-triol (3) and (23 R) methylergosta-20-ene-3ß,5α,6ß,17α-tetrol (4), together with three known gorgosteroid compounds, gorgost-3ß, 5α,6ß,11α- tetrol (1), 11α-acetoxy-gorgost- 3ß,5α, 6ß- triol (2), and gorgost-5 (E) ene-3-ß-ol (5), as well as batyl alcohol (6), were isolated from the Egyptian soft coral Heteroxenia fuscescens. The structures of these compounds were elucidated based on NMR spectroscopic analyses, HR-FAB-MS, and comparisons with published data. The cytotoxic activities of the fractions and compounds were evaluated against MCF-7 cancer cell lines using MTT colorimetric assay. Compounds 2 and 4 showed moderate cytotoxic activity, with IC50 values equal to 33.2 and 25.1 µM, respectively, in comparison with the IC50 of 5-fluorouracil 18.7 µM.
Assuntos
Antozoários/química , Antineoplásicos/química , Antineoplásicos/farmacologia , Esteroides/química , Esteroides/farmacologia , Animais , Ensaios de Seleção de Medicamentos Antitumorais , Egito , Humanos , Hidroxilação , Células MCF-7 , Espectroscopia de Ressonância Magnética , Espectrometria de Massas , Estrutura MolecularRESUMO
Accumulating evidence indicates that cell death triggers sterile inflammation and that impaired clearance of dead cells causes nonresolving inflammation; however, the underlying mechanisms are still unclear. Here, we show that macrophage-inducible C-type lectin (Mincle) senses renal tubular cell death to induce sustained inflammation after acute kidney injury in mice. Mincle-deficient mice were protected against tissue damage and subsequent atrophy of the kidney after ischemia-reperfusion injury. Using lipophilic extract from the injured kidney, we identified ß-glucosylceramide as an endogenous Mincle ligand. Notably, free cholesterol markedly enhanced the agonistic effect of ß-glucosylceramide on Mincle. Moreover, ß-glucosylceramide and free cholesterol accumulated in dead renal tubules in proximity to Mincle-expressing macrophages, where Mincle was supposed to inhibit clearance of dead cells and increase proinflammatory cytokine production. This study demonstrates that ß-glucosylceramide in combination with free cholesterol acts on Mincle as an endogenous ligand to induce cell death-triggered, sustained inflammation after acute kidney injury.
Assuntos
Injúria Renal Aguda/metabolismo , Morte Celular/genética , Lectinas Tipo C/metabolismo , Proteínas de Membrana/metabolismo , Injúria Renal Aguda/imunologia , Animais , Citocinas/metabolismo , Modelos Animais de Doenças , Feminino , Glucosilceramidase/metabolismo , Proteínas de Fluorescência Verde/genética , Inflamação/metabolismo , Lectinas Tipo C/deficiência , Lectinas Tipo C/genética , Ligantes , Macrófagos/imunologia , Macrófagos/metabolismo , Masculino , Proteínas de Membrana/deficiência , Proteínas de Membrana/genética , Camundongos , Camundongos Endogâmicos C57BL , Camundongos Knockout , Transdução de Sinais/genética , Transdução de Sinais/imunologiaRESUMO
Multiple sclerosis (MS) in a multifactorial autoimmune disease in which reliable biomarkers are needed for therapeutic monitoring and diagnosis. Autoantibodies (autoAbs) are known biomarker candidates although their detection in biological fluids requires a thorough characterization of their associated antigens. Over the past twenty years, a reverse chemical-based approach aiming to screen putative autoantigens has underlined the role of glycans, in particular glucose, in MS. Despite the progress achieved, a lack of consensus regarding the nature of innate antigens as well as difficulties proposing new synthetic glucose-based structures have proved to be obstacles. Here is proposed a strategy to extend the current methodology to the field of natural glycosides, in order to dramatically increase the diversity of glycans that could be tested. Triterpene saponins from the Sapindaceace family represent an optimal starting material as their abundant description in the literature has revealed a prevalence of glucose-based oligosaccharides. Blighia welwitschii (Sapindaceae) was thus selected as a case study and twelve triterpene saponins were isolated and characterized. Their structures were elucidated on the basis of 1D and 2D NMR as well as mass spectrometry, revealing seven undescribed compounds. A selection of natural glycosides exhibiting various oligosaccharide moieties were then tested as antigens in enzyme-linked immunosorbent assay (ELISA) to recognize IgM antibodies (Abs) in MS patients' sera. Immunoassay results indicated a correlation between the glycan structures and their antibody recognition capacity, allowing the determination of structure-activity relationships that were coherent with previous studies. This approach might help to identify sugar epitopes putatively involved in MS pathogenesis, which remains poorly understood.