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1.
Nat Prod Res ; : 1-6, 2023 Dec 20.
Artículo en Inglés | MEDLINE | ID: mdl-38124391

RESUMEN

A new lignan named (-)-ginkgool-9-O-ß-glucopyranoside (1) together with eight known lignans (2-9) were isolated from Urtica triangularis subsp. pinnatifida (Hand.-Mazz.) C.J.Chen. According to the mass spectrometry and spectroscopic analyses, the gross structure and absolute configuration of the new lignan were elucidated. The cytotoxic effects of compounds 1-9 on BPH-1 cells and the docking results on type II 5α-reductase were analysed to evaluate their anti-BPH activity. The results showed better anti-BPH activity that compound 4 displaying an IC50 of 79.75 ± 3.68 µM than finasteride presenting an IC50 of 91.8 ± 3.74 µM. Compounds 1, 2 and 5 had moderate anti-BPH activity compared with finasteride.

2.
Phytochemistry ; 208: 113609, 2023 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-36758886

RESUMEN

Nine tetrahydrofuran lignans, including three undescribed spiro-lignans, were isolated from Isatis indigotica Fortune (Brassicaceae). Extensive spectroscopic analyses achieved the structure elucidation of these tetrahydrofuran lignans, and quantum chemical calculation combined with the MAEΔΔδ parameter. Notably, isatispironeols A-B have a unique spiro[dienone-tetrahydrofuran] molecular core. These spiro[dienone-tetrahydrofuran] lignans showed comparable neuroprotective effects as the positive control in the H2O2-induced SH-SY5Y cells model. In addition, (-)-(7R,8S,1'R,7'R,8'R)-isatispironeol A possessed more significant AChE inhibitory activity, further interact sites were also predicted by the in silico assay.


Asunto(s)
Isatis , Lignanos , Neuroblastoma , Humanos , Lignanos/química , Isatis/química , Acetilcolinesterasa , Inhibidores de la Colinesterasa , Peróxido de Hidrógeno , Furanos/química , Estructura Molecular
3.
Genes (Basel) ; 14(1)2023 01 07.
Artículo en Inglés | MEDLINE | ID: mdl-36672909

RESUMEN

Intramuscular fat (IMF) is an essential trait closely related to meat quality. The IMF trait is a complex quantitative trait that is regulated by multiple genes. In order to better understand the process of IMF and explore the key factors affecting IMF deposition, we identified differentially expressed mRNA, miRNA, and lncRNA in the longissimus dorsi muscle (LD) between Songliao Black (SL) pigs and Landrace pigs. We obtained 606 differentially expressed genes (DEGs), 55 differentially expressed miRNAs (DEMs), and 30 differentially expressed lncRNAs (DELs) between the SL pig and Landrace pig. Enrichment results from GO and KEGG indicate that DEGs are involved in fatty acid metabolism and some pathways related to glycogen synthesis. We constructed an lncRNA-miRNA-mRNA interaction network with 18 DELs, 11 DEMs, and 42 DEGs. Finally, the research suggests that ARID5B, CPT1B, ACSL1, LPIN1, HSP90AA1, IRS1, IRS2, PIK3CA, PIK3CB, and PLIN2 may be the key genes affecting IMF deposition. The LncRNAs MSTRG.19948.1, MSTRG.13120.1, MSTRG.20210.1, and MSTRG.10023.1, and the miRNAs ssc-miRNA-429 and ssc-miRNA-7-1, may play a regulatory role in IMF deposition through their respective target genes. Our research provides a reference for further understanding the regulatory mechanism of IMF.


Asunto(s)
MicroARNs , ARN Largo no Codificante , Animales , Porcinos/genética , Perfilación de la Expresión Génica/métodos , ARN Largo no Codificante/genética , ARN Mensajero/genética , Metabolismo de los Lípidos/genética , MicroARNs/genética
4.
Fitoterapia ; 164: 105361, 2023 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-36435487

RESUMEN

Seven undescribed polyketide compounds (1-4, 9-11) and six known polyketide compounds (5-8,12, 13) were isolated from Rhodiola tibetica endophytic Penicillium sp. HJT-A-10. The structural of seven undescribed polyketides metabolites were established on the basis of spectroscopic methods. The results of anti-inflammatory activity showed that compounds 1-8,10-13 had significant inhibitory effects on LPS-induced NO production in RAW 264.7 cells.


Asunto(s)
Penicillium , Policétidos , Rhodiola , Penicillium/química , Estructura Molecular , Antiinflamatorios/química
5.
Bioorg Chem ; 119: 105521, 2022 02.
Artículo en Inglés | MEDLINE | ID: mdl-34871788

RESUMEN

UV-guided fractionation led to the isolation of thirteen new polyacetylenes (1-13) from the roots of Bupleurum scorzonerifolium Willd. All polyacetylenes were analyzed as racemates since the lack of optical activity and Cotton effects in the ECD spectra. The sequent chiral-phase HPLC resolution successfully gave twelve pairs of enantiomers 1a/1b and 3a/3b-13a/13b. Their structures were elucidated based on the HRESIMS and NMR data analyses. The absolute configurations were determined by the combination of Snatzke's method, electronic circular dichroism calculations, and single-crystal X-ray diffraction. Using Griess methods and MTT assays, polyacetylenes 1a, 3a, 4a/4b-12a/12b, and 13a displayed inhibitory activities against LPS-induced NO release in BV-2 microglial cells.


Asunto(s)
Bupleurum/química , Óxido Nítrico/antagonistas & inhibidores , Extractos Vegetales/farmacología , Polímero Poliacetilénico/farmacología , Animales , Células Cultivadas , Relación Dosis-Respuesta a Droga , Lipopolisacáridos/antagonistas & inhibidores , Lipopolisacáridos/farmacología , Ratones , Estructura Molecular , Óxido Nítrico/biosíntesis , Extractos Vegetales/química , Extractos Vegetales/aislamiento & purificación , Raíces de Plantas/química , Polímero Poliacetilénico/química , Polímero Poliacetilénico/aislamiento & purificación , Estereoisomerismo , Relación Estructura-Actividad , Rayos Ultravioleta
6.
Chin J Nat Med ; 19(9): 680-685, 2021 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-34561079

RESUMEN

Seven alkaloids including five undescribed ones (1a/1b, 2, 3 and 5) were obtained from the leaves of Isatis indigotica Fortune. Their structures were established by extensive spectroscopic analyses. The absolute configurations of compounds 1a, 1b, 3 and 5 were determined by comparison of the experimental and calculated electronic circular dichroism (ECD) spectra. Subsequently, the neuroprotective effects of all the isolates against H2O2-induced injury in SH-SY5Y cells were evaluated in vitro by MTT assay. Moreover, Annexin V-FITC/PI double staining was performed, while the activities of antioxidant enzymes (SOD, CAT and GSH-Px) for compounds 1a and 1b were measured.


Asunto(s)
Alcaloides , Isatis , Fármacos Neuroprotectores , Alcaloides/farmacología , Peróxido de Hidrógeno/toxicidad , Estructura Molecular , Fármacos Neuroprotectores/farmacología , Hojas de la Planta
7.
Bioorg Chem ; 96: 103650, 2020 03.
Artículo en Inglés | MEDLINE | ID: mdl-32044515

RESUMEN

In the current study, four pairs of new enantiomeric alkaloids (1a/1b-4a/4b) were obtained from the leaves of Isatis indigotica Fortune Ex Land. Their structures were elucidated through spectroscopic methods and quantum mechanical calculations. Biologically, all isolates were evaluated for their neuroprotective effects against H2O2-induced SH-SY5Y cell injury. As a result, 1a and 1b exhibited enantioselective neuroprotective effects, further Annexin V-FITC/PI analysis showed that apoptosis ratios of 1a and 1b were reduced to 20.93% and 17.87%, respectively.


Asunto(s)
Alcaloides/farmacología , Peróxido de Hidrógeno/metabolismo , Isatis/química , Neuronas/efectos de los fármacos , Fármacos Neuroprotectores/farmacología , Alcaloides/química , Apoptosis/efectos de los fármacos , Línea Celular , Humanos , Neuronas/citología , Neuronas/metabolismo , Fármacos Neuroprotectores/química , Hojas de la Planta/química , Estereoisomerismo
8.
Planta Med ; 85(17): 1374-1382, 2019 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-31801158

RESUMEN

Six pairs of alkaloid enantiomers including 11 new alkaloids (1A: /1B: -5A: /5B, 6A: ) were isolated from the leaves of Isatis tinctoria. Their structures were established by extensive spectroscopic analyses. Enantiomers were separated successfully by chiral chromatographic column and the absolute configurations of all isolates were determined by comparison of experimental and calculated electronic circular dichroism spectra. The isolated alkaloids were evaluated for their neuroprotective activities against H2O2-induced cell injury in human neuroblastoma SH-SY5Y cells. The results showed that 5A/5B: and 6A/6B: exhibited potent neuroprotective activities at 50 µM compared with the H2O2-treated group.


Asunto(s)
Isatis/química , Fármacos Neuroprotectores/farmacología , Extractos Vegetales/farmacología , Línea Celular Tumoral , Humanos , Peróxido de Hidrógeno , Isomerismo , Estructura Molecular , Neuroblastoma , Neuronas/efectos de los fármacos , Fármacos Neuroprotectores/química , Fármacos Neuroprotectores/aislamiento & purificación , Extractos Vegetales/química , Extractos Vegetales/aislamiento & purificación
9.
Fitoterapia ; 138: 104356, 2019 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-31520649

RESUMEN

Five pairs of enantiomeric compounds (1a/1b-5a/5b) including seven undescribed compounds (1a/1b-3a/3b, 4b) along with two known ones (. and .) have been isolated from corn silk (Stigma maydis). Racemic mixtures of these enantiomers were separated by HPLC with different types of chiral columns. Their structures were elucidated based on comprehensive spectroscopic analyses together with quantum chemical calculations of 13C NMR data and electronic circular dichroism (ECD) curves. All the isolates were evaluated for their inhibition ability of self-induced Aß1-42 aggregation. Among them, compounds 4a (88.36%), 4b (74.66%) and . (85.65%) showed stronger inhibitory activity than the positive control curcumin (61.90%). The different inhibition profiles of enantiomers 4a and 4b were explained by docking simulation studies.


Asunto(s)
Péptidos beta-Amiloides/antagonistas & inhibidores , Flores/química , Fragmentos de Péptidos/antagonistas & inhibidores , Fitoquímicos/farmacología , Agregación Patológica de Proteínas/prevención & control , Zea mays/química , China , Simulación del Acoplamiento Molecular , Estructura Molecular , Fitoquímicos/aislamiento & purificación
10.
Bioorg Chem ; 88: 102926, 2019 07.
Artículo en Inglés | MEDLINE | ID: mdl-31005021

RESUMEN

A pair of new cycloneolignan enantiomers (1a and 1b) were isolated from the leaves of Isatis indigotica Fortune. Their structures were elucidated by extensive spectroscopic data analysis, including 1D and 2D NMR, HRESIMS, MS/MS analysis, together with theoretical electronic circular dichroism (ECD) calculations. Compounds 1a and 1b were then evaluated for their neuroprotective effects against MPP+-induced SH-SY5Y cell injury. As a result, compounds 1a (77.64%) and 1b (78.62%) exhibited moderate neuroprotective activity at the concentration of 12.5 µM compared with that of MPP+ treated group (62.00% at 1 mM) by MTT assay. Furthermore, Annexin V-FITC/PI analysis showed that apoptosis ratios of 1a and 1b were reduced to 10.99% and 9.31%, respectively.


Asunto(s)
1-Metil-4-fenilpiridinio/antagonistas & inhibidores , Descubrimiento de Drogas , Isatis/química , Lignanos/farmacología , Fármacos Neuroprotectores/farmacología , 1-Metil-4-fenilpiridinio/farmacología , Supervivencia Celular/efectos de los fármacos , Relación Dosis-Respuesta a Droga , Humanos , Lignanos/química , Lignanos/aislamiento & purificación , Estructura Molecular , Fármacos Neuroprotectores/química , Fármacos Neuroprotectores/aislamiento & purificación , Hojas de la Planta/química , Estereoisomerismo , Relación Estructura-Actividad , Células Tumorales Cultivadas
11.
Org Biomol Chem ; 17(9): 2564, 2019 02 27.
Artículo en Inglés | MEDLINE | ID: mdl-30768080

RESUMEN

Correction for 'Bioactive spiropyrrolizidine oxindole alkaloid enantiomers from Isatis indigotica fortune' by Si-Fan Liu et al., Org. Biomol. Chem., 2018, 16, 9430-9439.

12.
Org Biomol Chem ; 16(48): 9430-9439, 2018 12 12.
Artículo en Inglés | MEDLINE | ID: mdl-30511067

RESUMEN

Four pairs of new spiropyrrolizidine oxindole enantiomers (1a/1b-4a/4b) were isolated from the leaves of Isatis indigotica Fortune. Their structures and absolute configurations were elucidated by a combination of NMR spectroscopic analyses, experimental and calculated electronic circular dichroism (ECD) and the assistance of quantum chemical predictions (QCP) of 13C NMR chemical shifts. Notably, all the isolated spiropyrrolizidine oxindoles are reported as natural products for the first time. The biosynthetic pathway of these unique structures was proposed to be formed by cycloaddition reaction. In addition, all the compounds were evaluated for their inhibitory effects on ß-amyloid aggregation by ThT assay, and the optically pure compounds 1a/1b and 2a/2b exhibited better Aß1-42 aggregation inhibition potency (85.8% and 73.6%, 71.5% and 75.8%, respectively) at a concentration of 20 µM, compared with the positive control curcumin (57.0%). The difference of the inhibitory pattern caused by chirality was also explained by molecular docking studies.


Asunto(s)
Isatis/química , Oxindoles/química , Alcaloides de Pirrolicidina/química , Compuestos de Espiro/química , Péptidos beta-Amiloides/metabolismo , Humanos , Simulación del Acoplamiento Molecular , Oxindoles/aislamiento & purificación , Oxindoles/farmacología , Fragmentos de Péptidos/metabolismo , Agregado de Proteínas/efectos de los fármacos , Alcaloides de Pirrolicidina/aislamiento & purificación , Alcaloides de Pirrolicidina/farmacología , Compuestos de Espiro/aislamiento & purificación , Compuestos de Espiro/farmacología , Estereoisomerismo
13.
Fitoterapia ; 128: 169-174, 2018 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-29787805

RESUMEN

Seven new N-acylanthranilic acid derivatives (1-3, 4a/4b, 5a/5b) including two pairs of enantiomers (4a/4b and 5a/5b) were isolated from the leaves of Isatis indigotica Fortune. Their chemical structures were elucidated by extensive spectroscopic data analyses. The absolute configurations of compounds 4a/4b and 5a/5b were determined by comparison of the experimental and calculated ECD spectra. All compounds were tested for their anti-Aß1-42 aggregation activity. As a result, compounds 1 (72.1%), 2 (79.8%) and 5a (81.8%) showed stronger inhibitory activity than the positive control curcumin (67.0%). By the comparison between 5a (81.8%) and 5b (63.1%), it was found that stereochemical configurations may affect Aß1-42 aggregation activity, which was discussed through the molecular docking results of compounds 5a and 5b.


Asunto(s)
Péptidos beta-Amiloides/antagonistas & inhibidores , Isatis/química , Fragmentos de Péptidos/antagonistas & inhibidores , Hojas de la Planta/química , ortoaminobenzoatos/aislamiento & purificación , Simulación del Acoplamiento Molecular , Estereoisomerismo
14.
Fitoterapia ; 127: 56-61, 2018 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-29371160

RESUMEN

Rubus ideaus L., a member of the Rosaceae family, is popular for its distinctive flavor and attractive red color. In order to explore the functional factors possibly presented in the fruit, seven new benzofuran neolignans (1a/1b-3a/3b and 4b), together with one known neolignan 4a, were isolated from the fruit of R. ideaus. Compounds 1a/1b-4a/4b as four pairs of enantiomers were separated on a chiral chromatographic column. Their structures including absolute configurations were elucidated by extensive spectroscopic data analyses, including UV, IR, HRESIMS, NMR, and comparing their experimental electronic circular dichroism (ECD) spectra with calculated ECD spectra. Additionally, all these enantiomeric compounds were evaluated for their antioxidant, neuroprotective, and anti-Aß1-42 aggregation activities.


Asunto(s)
Benzofuranos/química , Frutas/química , Lignanos/química , Rubus/química , Péptidos beta-Amiloides/química , Línea Celular Tumoral , Dicroismo Circular , Depuradores de Radicales Libres/química , Humanos , Espectroscopía de Resonancia Magnética , Estructura Molecular , Fragmentos de Péptidos/química , Estereoisomerismo
15.
Eur J Med Chem ; 133: 1-10, 2017 Jun 16.
Artículo en Inglés | MEDLINE | ID: mdl-28371676

RESUMEN

Enantiomers account for quite a large percentage of compounds in natural products. Our team is interested in the separation and biological activity of racemic compounds. In this report, four pairs of prenylated flavan enantiomers [(±)-1-(±)-4], including five new compounds, were isolated from the stem and root bark of Daphne giraldii, and separated successfully by using chiral chromatographic column. Their planar structures and absolute configurations were established by comprehensive spectroscopic analyses as well as circular dichroism (CD) spectroscopy. The isolates had a selective cytotoxicity towards hepatic carcinoma cell lines. Among them, new compound (+)-4 showed a more potent inhibitory effect on Hep3B cells with an IC50 value of 30.3 µM, compared with its racemic mixture 4. Therefore, the action mechanism of (+)-4in vitro was subsequently investigated. The morphological observation and Western blot analysis demonstrated that (+)-4 could markedly induce apoptosis through intrinsic and extrinsic pathways, and also cause autophagy by increasing the phosphorylation of AMP-activated protein kinase (AMPK) in Hep3B cells. After treatment with the autophagic inhibitor bafilomycin A1 (Baf A1), (+)-4-induced apoptosis increased significantly, suggesting that the autophagy induced by (+)-4 performed a protective effect on apoptotic cell death.


Asunto(s)
Antineoplásicos Fitogénicos/química , Antineoplásicos Fitogénicos/farmacología , Apoptosis/efectos de los fármacos , Autofagia/efectos de los fármacos , Daphne/química , Flavonoides/química , Flavonoides/farmacología , Neoplasias Hepáticas/tratamiento farmacológico , Proteínas Quinasas Activadas por AMP/metabolismo , Línea Celular Tumoral , Humanos , Hígado/efectos de los fármacos , Hígado/metabolismo , Hígado/patología , Neoplasias Hepáticas/metabolismo , Neoplasias Hepáticas/patología , Fosforilación/efectos de los fármacos , Prenilación , Estereoisomerismo
16.
Sci Rep ; 6: 33034, 2016 09 09.
Artículo en Inglés | MEDLINE | ID: mdl-27611737

RESUMEN

The Earth's engine is driven by unknown proportions of primordial energy and heat produced in radioactive decay. Unfortunately, competing models of Earth's composition reveal an order of magnitude uncertainty in the amount of radiogenic power driving mantle dynamics. Recent measurements of the Earth's flux of geoneutrinos, electron antineutrinos from terrestrial natural radioactivity, reveal the amount of uranium and thorium in the Earth and set limits on the residual proportion of primordial energy. Comparison of the flux measured at large underground neutrino experiments with geologically informed predictions of geoneutrino emission from the crust provide the critical test needed to define the mantle's radiogenic power. Measurement at an oceanic location, distant from nuclear reactors and continental crust, would best reveal the mantle flux, however, no such experiment is anticipated. We predict the geoneutrino flux at the site of the Jinping Neutrino Experiment (Sichuan, China). Within 8 years, the combination of existing data and measurements from soon to come experiments, including Jinping, will exclude end-member models at the 1σ level, define the mantle's radiogenic contribution to the surface heat loss, set limits on the composition of the silicate Earth, and provide significant parameter bounds for models defining the mode of mantle convection.

17.
Exp Ther Med ; 11(3): 731-736, 2016 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-26997986

RESUMEN

The present retrospective study aimed to investigate the antibiotic susceptibility of bacteria at Shanghai First People's Hospital (Shanghai, China) between 2009 and 2011. An increasing trend of antibiotic resistance was observed in this hospital between 2009 and 2011. Escherichia coli, Acinetobacter baumannii and Staphylococcus aureus were the most prevalent resistant strains. Antimicrobial susceptibility was detected using standard Kirby-Bauer disk diffusion and analyzed using World Health Organization software. E. coli was demonstrated to be the most prevalent bacterium in the present survey between 2009 and 2011 (16.2, 20.0 and 19.6%, respectively); followed by A. baumannii (13.5, 13.3 and 10.6%, respectively) and S. aureus. Notably, >70% of E. coli and 70% of S. aureus were resistant to common antibiotics; whereas 60% of A. baumannii and 20% of Pseudomonas aeruginosa were resistant to the majority of the antibiotics investigated. In 2011, Enterococcus faecalis exhibited a resistance rate of 55.6% against levofloxacin and E. faecium exhibited a 53.2% resistance rate. The present survey demonstrated an increasing trend in bacterial resistance against antibiotics; therefore, more stringent guidelines for antibiotics should be advocated.

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