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1.
Planta Med ; 85(1): 56-61, 2019 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-30086557

RESUMEN

In this study, the biocatalysis of 18ß-glycyrrhetinic acid by two strains of filamentous fungi, namely Rhizopus arrhizus AS 3.2893 and Circinella muscae AS 3.2695, was investigated. Scaled-up biotransformation reactions yielded 14 metabolites. Their structures were established based on extensive nuclear magnetic resonance and high-resolution electrospray ionization mass spectrometry data analyses, and seven of them are new compounds. The two fungal strains exhibited distinct biocatalytic features. R. arrhizus could catalyze hydroxylation and carbonylation reactions, whereas C. muscae preferred to catalyze hydroxylation and glycosidation reactions. These highly specific reactions are difficult to achieve by chemical synthesis, particularly under mild conditions. Furthermore, we found that most of the metabolites exhibited pronounced inhibitory activities on lipopolysaccharides-induced nitric oxide production in RAW264.7 cells. These biotransformed derivatives of 18ß-glycyrrhetinic acid could be potential anti-inflammatory agents.


Asunto(s)
Antiinflamatorios/farmacología , Ácido Glicirretínico/análogos & derivados , Animales , Antiinflamatorios/química , Antiinflamatorios/metabolismo , Biotransformación , Catálisis , Ácido Glicirretínico/química , Ácido Glicirretínico/metabolismo , Ácido Glicirretínico/farmacología , Hidroxilación , Ratones , Mucorales/metabolismo , Células RAW 264.7 , Rhizopus/metabolismo
2.
J Asian Nat Prod Res ; 20(8): 719-726, 2018 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-28944684

RESUMEN

The microbial transformation of 20(R)-panaxadiol (PD) by the fungus Absidia coerulea AS 3.3382 afforded three new and three known metabolites. The structures of the metabolites were characterized as 3-oxo-20(R)-panaxadiol (1), 3-oxo-7ß- hydroxyl-20(R)-panaxadiol (2), 3-oxo-22ß-hydroxyl-20(R)-panaxadiol (3), 3-oxo- 7ß,22ß-dihydroxyl-20(R)-panaxadiol (4), 3-oxo-7ß,24ß-dihydroxyl-20(R)-panaxadiol (5), and 3-oxo-7ß,24α-dihydroxyl-20(R)-panaxadiol (6). Among them, 2-4 were new compounds. In addition, compounds 3 and 4 exhibited significant anti-hepatic fibrosis activity.


Asunto(s)
Absidia/metabolismo , Ginsenósidos/metabolismo , Ginsenósidos/uso terapéutico , Línea Celular , Humanos , Cirrosis Hepática/tratamiento farmacológico , Estructura Molecular , FN-kappa B/metabolismo , Panax notoginseng/química , Espectrometría de Masa por Ionización de Electrospray
3.
Artículo en Inglés | MEDLINE | ID: mdl-38062726

RESUMEN

Aims: In addition to reducing the respiratory function, crystalline silica (SiO2) disturbs the immune response by affecting immune cells during the progression of silicosis. Regulatory T cell (Treg) differentiation may play a key role in the abnormal polarization of T helper cell (Th)1 and Th2 cells in the development of silicosis-induced fibrosis. Alpha-lipoic acid (ALA) has immunomodulatory effects by promoting Tregs differentiation. Thus, ALA may have a therapeutic potential for treating autoimmune disorders in patients with silicosis. However, little is known regarding whether ALA regulates the immune system during silicosis development. Results: We found that the expression levels of collagen increased, and the antioxidant capacity was lower in the Lias-/-+SiO2 group than in the Lias+/++SiO2 group. The proportion of Tregs decreased in the peripheral blood and spleen tissue in mice exposed to SiO2. The proportion of Tregs in the Lias-/-+SiO2 group was significantly lower than that in the Lias+/++SiO2 group. Supplementary exogenous ALA attenuates the accumulation of inflammatory cells and extracellular matrix in lung tissues. ALA promotes the immunological balance between Th17 and Treg responses during the development of silicosis-induced fibrosis. Innovation and Conclusion: Our findings confirmed that low expression of lipoic acid synthase aggravates SiO2-induced silicosis, and that supplementary exogenous ALA has therapeutic potential by improving Tregs in silicosis fibrosis.

4.
Genes (Basel) ; 15(1)2023 12 26.
Artículo en Inglés | MEDLINE | ID: mdl-38254930

RESUMEN

Improving the efficiency of hens and extending the egg-laying cycle require maintaining high egg production in the later stages. The ovarian follicles, as the primary functional units for ovarian development and oocyte maturation, play a crucial role in regulating the continuous ovulation of hens. The egg production rate of laying hens is mostly affected by proper follicle growth and ovulation in the ovaries. The objective of this study was to identify the key genes and signaling pathways involved in the development of ovarian follicles in Taihang hens through transcriptome screening. In this study, RNA sequencing was used to compare and analyze the transcriptomes of ovarian follicles at four developmental stages: small white follicles (SWF), small yellow follicles (SYF), F5 follicles, and F2 follicles, from two groups: the high continual production group (H-Group) and the low continual production group (L-Group). A total of 24 cDNA libraries were constructed, and significant differential expression of 96, 199, 591, and 314 mRNAs was detected in the SWF, SYF, F5, and F2 follicles of the H and L groups, respectively. Based on the results of GO and KEGG enrichment analyses, each stage of follicle growth possesses distinct molecular genetic features, which have important effects on follicle development and significantly promote the formation of continuous production traits through the biosynthesis of steroid hormones, cytokine-cytokine receptor interaction, and neuroactive ligand-receptor interaction. Additionally, through STEM analysis, we identified 59 DEGs, including ZP4, KCNH1, IGFs, HMGA2, and CDH1, potentially associated with follicular development within four significant modules. This study represents the first transcriptome investigation of follicles in hens with high and low egg-producing characteristics at four crucial developmental stages. These findings provide important molecular evidence for understanding the regulation of follicular development and its variations.


Asunto(s)
Pollos , Folículo Ovárico , Animales , Femenino , Pollos/genética , Ovario , Ovulación/genética , Citocinas
5.
Toxicol Lett ; 350: 121-132, 2021 Oct 10.
Artículo en Inglés | MEDLINE | ID: mdl-34252510

RESUMEN

Silicosis is characterized by pulmonary interstitial fibrosis that arises as a result of chronic exposure to silica. The few available treatments only delay its progression. As α-lipoic acid (ALA) has been shown to have various beneficial effects, including mitoprotective, antioxidant, and anti-inflammatory effects, we hypothesized that it may exhibit therapeutic effects in pulmonary fibrosis. Therefore, in the present study, we used a murine model of silicosis to investigate whether supplementation with exogenous ALA could attenuate silica-induced pulmonary fibrosis by improving mitochondrial function. ALA was administered to the model mice via continuous intragastric administration for 28 days, and then the antioxidant and mitoprotective effects of ALA were evaluated. The results showed that ALA decreased the production of reactive oxygen species, protected mitochondria from silica-induced dysfunction, and inhibited extracellular matrix deposition. ALA also decreased hyperglycemia and hyperlipidemia. Activation of the mitochondrial AMPK/PGC1α pathway might be responsible for these ALA-mediated anti-fibrotic effects. Exogenous ALA blocked oxidative stress by activating NRF2. Taken together, these findings demonstrate that exogenous ALA effectively prevents the progression of silicosis in a murine model, likely by stimulating mitochondrial biogenesis and endogenous antioxidant responses. Therefore, ALA can potentially delay the progression of silica-induced pulmonary fibrosis.


Asunto(s)
Proteínas Quinasas Activadas por AMP/metabolismo , Mitocondrias/metabolismo , Coactivador 1-alfa del Receptor Activado por Proliferadores de Peroxisomas gamma/metabolismo , Fibrosis Pulmonar/inducido químicamente , Fibrosis Pulmonar/tratamiento farmacológico , Dióxido de Silicio/efectos adversos , Silicosis/tratamiento farmacológico , Ácido Tióctico/uso terapéutico , Proteínas Quinasas Activadas por AMP/efectos de los fármacos , Animales , Antioxidantes/metabolismo , Antioxidantes/uso terapéutico , Humanos , Masculino , Redes y Vías Metabólicas , Ratones , Ratones Endogámicos C57BL , Mitocondrias/efectos de los fármacos , Modelos Animales , Coactivador 1-alfa del Receptor Activado por Proliferadores de Peroxisomas gamma/efectos de los fármacos , Fibrosis Pulmonar/metabolismo , Silicosis/metabolismo , Silicosis/fisiopatología , Ácido Tióctico/metabolismo
6.
Nat Prod Res ; 33(13): 1849-1855, 2019 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-29842789

RESUMEN

Biotransformation of oleanolic acid (OA) by Circinella muscae AS 3.2695 was investigated. Nine hydroxylated and glycosylated metabolites (1-9) were obtained. Their structures were elucidated as 3ß,7ß-dihydroxyolean-12-en-28-oic acid (1), 3ß,7ß,21ß-trihydroxyolean-12-en-28-oic acid (2), 3ß,7α,21ß-trihydroxyolean-12-en- 28-oic acid (3), 3ß,7ß,15α-trihydroxyolean-12-en-28-oic acid (4), 7ß,15α-dihydroxy- 3-oxo-olean-12-en-28-oic acid (5), 7ß-hydroxy-3-oxo-olean-12-en-28-oic acid (6), oleanolic acid-28-O-ß-D-glucopyranosyl ester (7), 3ß,21ß-dihydroxyolean-12-en-28- oic acid-28-O-ß-D-glucopyranosyl ester (8), and 3ß,7ß,15α-trihydroxyolean-12-en- 28-oic acid-28-O-ß-D-glucopyranosyl ester (9) by spectroscopic analysis. Among them, compounds 4 and 9 were new compounds. In addition, anti-inflammatory activities were assayed and evaluated for the isolated metabolites. Most of the metabolites exhibited significant inhibitory activities on lipopolysaccharides-induced NO production in RAW 264.7 cells.


Asunto(s)
Antiinflamatorios/farmacología , Biotransformación , Mucorales/metabolismo , Ácido Oleanólico/metabolismo , Animales , Glicosilación , Hidroxilación , Lipopolisacáridos/farmacología , Ratones , Estructura Molecular , Óxido Nítrico/biosíntesis , Ácido Oleanólico/química , Células RAW 264.7 , Análisis Espectral
7.
Nat Prod Res ; 31(16): 1880-1885, 2017 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-28004587

RESUMEN

Biocatalysis of 20(R)-panaxatriol (PT) was performed by the fungus Mucor racemosus. Six metabolites (1-6) including five new compounds were obtained, and their structures were elucidated as 20(R),25-epoxy-12ß,24ß-dihydroxydammaran-3,6-dione (2), 20(R),25-epoxy-12ß,22ß-dihydroxydammaran-3,6-dione (3), 20(R),25-epoxy-23ß-hydroxydammaran-3,6,12-trione (4), 20(R),25-epoxy-12ß,23α- dihydroxydammaran-3,6-dione (5), and 20(R),25-epoxy-12ß-hydroxydammaran-3,6,23-trione (6) by spectroscopic analysis. Pharmacological studies revealed that compounds 2, 3 and 5 exhibited significant antihepatic fibrosis activity, while 4 and 6 showed cytotoxicity against HSC-T6 cells.


Asunto(s)
Ginsenósidos/farmacocinética , Cirrosis Hepática/tratamiento farmacológico , Mucor/metabolismo , Triterpenos/farmacología , Biotransformación , Línea Celular , Evaluación Preclínica de Medicamentos/métodos , Células Estrelladas Hepáticas/efectos de los fármacos , Células Estrelladas Hepáticas/patología , Humanos , Espectroscopía de Resonancia Magnética , Estructura Molecular , Triterpenos/química
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