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1.
Sci Rep ; 12(1): 822, 2022 01 17.
Artigo em Inglês | MEDLINE | ID: mdl-35039558

RESUMO

Scoparone (6,7-dimethoxycoumarin) is a simple coumarin from botanical drugs of Artemisia species used in Traditional Chinese Medicine and Génépi liquor. However, its bioavailability to the brain and potential central effects remain unexplored. We profiled the neuropharmacological effects of scoparone upon acute and subchronic intraperitoneal administration (2.5-25 mg/kg) in Swiss mice and determined its brain concentrations and its effects on the endocannabinoid system (ECS) and related lipids using LC-ESI-MS/MS. Scoparone showed no effect in the forced swimming test (FST) but, administered acutely, led to a bell-shaped anxiogenic-like behavior in the elevated plus-maze test and bell-shaped procognitive effects in the passive avoidance test when given subchronically and acutely. Scoparone rapidly but moderately accumulated in the brain (Cmax < 15 min) with an apparent first-order elimination (95% eliminated at 1 h). Acute scoparone administration (5 mg/kg) significantly increased brain arachidonic acid, prostaglandins, and N-acylethanolamines (NAEs) in the FST. Conversely, subchronic scoparone treatment (2.5 mg/kg) decreased NAEs and increased 2-arachidonoylglycerol. Scoparone differentially impacted ECS lipid remodeling in the brain independent of serine hydrolase modulation. Overall, the unexpectedly potent central effects of scoparone observed in mice could have toxicopharmacological implications for humans.


Assuntos
Encéfalo/metabolismo , Cumarínicos/farmacologia , Animais , Ácido Araquidônico/metabolismo , Ácidos Araquidônicos/metabolismo , Aprendizagem da Esquiva/efeitos dos fármacos , Comportamento Animal/efeitos dos fármacos , Disponibilidade Biológica , Cognição/efeitos dos fármacos , Cumarínicos/administração & dosagem , Cumarínicos/farmacocinética , Endocanabinoides/metabolismo , Etanolaminas/metabolismo , Glicerídeos/metabolismo , Infusões Parenterais , Metabolismo dos Lipídeos , Masculino , Aprendizagem em Labirinto/efeitos dos fármacos , Camundongos , Prostaglandinas/metabolismo
2.
Behav Brain Res ; 399: 112985, 2021 02 05.
Artigo em Inglês | MEDLINE | ID: mdl-33144177

RESUMO

The present study aimed to evaluate xanthotoxin's influence on male and female Swiss mice's depression-like behaviors and investigate the potential mechanism of this effect. Naturally derived furanocoumarin (the Apiaceae family), xanthotoxin, administered acutely (12.5 mg/kg), diminished the immobility level in the forced swim test only in males. The immobility level was lower in females than males, which may be associated with a higher serotonin level in the female prefrontal cortex. A dose-dependent increase of serotonin and noradrenaline was reported in the reverse-phase ion-pair liquid chromatography in the female prefrontal cortex but not in the hippocampus. We suggest that xanthotoxin may exert antidepressant properties and affect males and females differently. The increasing level of serotonin in the male and female prefrontal cortex may underlie this effect.


Assuntos
Antidepressivos/farmacologia , Comportamento Animal/efeitos dos fármacos , Depressão/tratamento farmacológico , Hipocampo/efeitos dos fármacos , Metoxaleno/farmacologia , Norepinefrina/metabolismo , Córtex Pré-Frontal/efeitos dos fármacos , Serotonina/metabolismo , Animais , Antidepressivos/administração & dosagem , Feminino , Hipocampo/metabolismo , Masculino , Metoxaleno/administração & dosagem , Camundongos , Preparações de Plantas , Córtex Pré-Frontal/metabolismo , Caracteres Sexuais , Fatores Sexuais
3.
BMC Genomics ; 18(1): 900, 2017 Nov 23.
Artigo em Inglês | MEDLINE | ID: mdl-29169319

RESUMO

BACKGROUND: The Aspergillus niger genome contains a large repertoire of genes encoding carbohydrate active enzymes (CAZymes) that are targeted to plant polysaccharide degradation enabling A. niger to grow on a wide range of plant biomass substrates. Which genes need to be activated in certain environmental conditions depends on the composition of the available substrate. Previous studies have demonstrated the involvement of a number of transcriptional regulators in plant biomass degradation and have identified sets of target genes for each regulator. In this study, a broad transcriptional analysis was performed of the A. niger genes encoding (putative) plant polysaccharide degrading enzymes. Microarray data focusing on the initial response of A. niger to the presence of plant biomass related carbon sources were analyzed of a wild-type strain N402 that was grown on a large range of carbon sources and of the regulatory mutant strains ΔxlnR, ΔaraR, ΔamyR, ΔrhaR and ΔgalX that were grown on their specific inducing compounds. RESULTS: The cluster analysis of the expression data revealed several groups of co-regulated genes, which goes beyond the traditionally described co-regulated gene sets. Additional putative target genes of the selected regulators were identified, based on their expression profile. Notably, in several cases the expression profile puts questions on the function assignment of uncharacterized genes that was based on homology searches, highlighting the need for more extensive biochemical studies into the substrate specificity of enzymes encoded by these non-characterized genes. The data also revealed sets of genes that were upregulated in the regulatory mutants, suggesting interaction between the regulatory systems and a therefore even more complex overall regulatory network than has been reported so far. CONCLUSIONS: Expression profiling on a large number of substrates provides better insight in the complex regulatory systems that drive the conversion of plant biomass by fungi. In addition, the data provides additional evidence in favor of and against the similarity-based functions assigned to uncharacterized genes.


Assuntos
Aspergillus niger/genética , Regulação Fúngica da Expressão Gênica , Aspergillus niger/enzimologia , Aspergillus niger/metabolismo , Metabolismo dos Carboidratos/genética , Análise por Conglomerados , Proteínas Fúngicas/metabolismo , Perfilação da Expressão Gênica , Regulação Enzimológica da Expressão Gênica , Inulina/metabolismo , Mutação , Pectinas/metabolismo , Amido/metabolismo , Sacarose/metabolismo , Transativadores/metabolismo
4.
Sci Rep ; 7(1): 12356, 2017 09 27.
Artigo em Inglês | MEDLINE | ID: mdl-28955038

RESUMO

Aspergillus niger produces an arsenal of extracellular enzymes that allow synergistic degradation of plant biomass found in its environment. Pectin is a heteropolymer abundantly present in the primary cell wall of plants. The complex structure of pectin requires multiple enzymes to act together. Production of pectinolytic enzymes in A. niger is highly regulated, which allows flexible and efficient capture of nutrients. So far, three transcriptional activators have been linked to regulation of pectin degradation in A. niger. The L-rhamnose-responsive regulator RhaR controls the production of enzymes that degrade rhamnogalacturonan-I. The L-arabinose-responsive regulator AraR controls the production of enzymes that decompose the arabinan and arabinogalactan side chains of rhamnogalacturonan-II. The D-galacturonic acid-responsive regulator GaaR controls the production of enzymes that act on the polygalacturonic acid backbone of pectin. This project aims to better understand how RhaR, AraR and GaaR co-regulate pectin degradation. For that reason, we constructed single, double and triple disruptant strains of these regulators and analyzed their growth phenotype and pectinolytic gene expression in A. niger grown on sugar beet pectin.


Assuntos
Aspergillus niger/genética , Proteínas Fúngicas/metabolismo , Regulação Fúngica da Expressão Gênica , Pectinas/metabolismo , Transativadores/metabolismo , Arabinose/genética , Arabinose/metabolismo , Aspergillus niger/metabolismo , Beta vulgaris , Parede Celular/metabolismo , Proteínas Fúngicas/genética , Perfilação da Expressão Gênica , Ácidos Hexurônicos/metabolismo , Ramnose/genética , Ramnose/metabolismo
5.
FEBS Lett ; 590(12): 1804-15, 2016 06.
Artigo em Inglês | MEDLINE | ID: mdl-27174630

RESUMO

We identified the d-galacturonic acid (GA)-responsive transcriptional activator GaaR of the saprotrophic fungus, Aspergillus niger, which was found to be essential for growth on GA and polygalacturonic acid (PGA). Growth of the ΔgaaR strain was reduced on complex pectins. Genome-wide expression analysis showed that GaaR is required for the expression of genes necessary to release GA from PGA and more complex pectins, to transport GA into the cell, and to induce the GA catabolic pathway. Residual growth of ΔgaaR on complex pectins is likely due to the expression of pectinases acting on rhamnogalacturonan and subsequent metabolism of the monosaccharides other than GA.


Assuntos
Aspergillus niger/metabolismo , Proteínas Fúngicas/metabolismo , Ácidos Hexurônicos/metabolismo , Pectinas/metabolismo , Transativadores/metabolismo , Aspergillus niger/genética , Transporte Biológico Ativo/fisiologia , Proteínas Fúngicas/genética , Deleção de Genes , Estudo de Associação Genômica Ampla , Transativadores/genética
6.
J Gastrointest Surg ; 15(7): 1289-91, 2011 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-21404077

RESUMO

UNLABELLED: Giant colonic diverticulum is an extremely rare condition in colonic diverticular disease. More than 90% of giant colonic diverticula are found in the sigmoid colon. Inflammatory and pseudodiverticula are the most frequent. Only one case of a true diverticulum of the transverse colon has been reported in the literature. CASE REPORT: We report a case of a 22-year-old woman presenting with constipation and meteorism from childhood. A plain abdominal X-ray showed a round radiolucent air-filled cyst. Barium enema revealed a single, large diverticulum of the transverse colon. An extended right hemicolectomy with primary end-to-end anastomosis was performed. The postoperative course was uneventful, and she was discharged in 1 week without any complications. Histopathology showed a true diverticulum containing all layers of the colon.


Assuntos
Colonoscopia/métodos , Divertículo do Colo/diagnóstico , Radiografia Abdominal/métodos , Colectomia/métodos , Diagnóstico Diferencial , Divertículo do Colo/cirurgia , Feminino , Humanos , Laparotomia , Adulto Jovem
7.
Neurochem Int ; 55(1-3): 157-63, 2009.
Artigo em Inglês | MEDLINE | ID: mdl-19428821

RESUMO

Recent findings support the idea that mitochondrial integrity plays an important role in the propagation of excitotoxic ischemic signal and PKC is implicated in the regulation of mitochondrial membranes properties. One of the targets of PKC delta is phospholipid scramblase 3 (PLSCR3), an enzyme responsible for cardiolipin translocation from the inner to outer mitochondrial membrane. To get an insight into in vivo mechanism by which PKC delta mediates ischemia/reperfusion injury of hippocampal neurons, we examined the effects of transient brain ischemia in gerbil on association of PKC delta with mitochondria isolated from ischemia-vulnerable (CA1) and ischemia-resistant regions, and interactions between PKC delta and PLSCR3. Postischemic, biphasic and brain region-specific translocation of PKC delta to mitochondria was observed. First peak was at 30-60 min of reperfusion and the second was observed after 72-96 h following ischemia. PKC delta was translocated to mitochondria only in CA1 region. The PLSCR3 mRNA and protein was detected in brain by RT-PCR and sequence analysis, Western blotting and immunocytochemistry in electron microscopy (EM). Co-immunoprecipitation and double-labeled immuno-EM showed association of PKC delta and PLSCR3 in postischemic CA1 mitochondria. Additionally, the amount of tBid associated with mitochondria was elevated 96 h following ischemia. Our data suggest that in the postischemic brain PKC delta co-localizes with PLSCR3 in mitochondria and this event might influence the mitochondrial membranes architecture and delayed neurons degeneration.


Assuntos
Isquemia Encefálica/enzimologia , Hipocampo/enzimologia , Mitocôndrias/enzimologia , Neurônios/enzimologia , Proteínas de Transferência de Fosfolipídeos/metabolismo , Proteína Quinase C-delta/metabolismo , Animais , Western Blotting , DNA Complementar/biossíntese , DNA Complementar/genética , Eletroforese em Gel de Poliacrilamida , Gerbillinae , Imuno-Histoquímica , Imunoprecipitação , Isoenzimas/metabolismo , Masculino , Camundongos , Camundongos Endogâmicos C57BL , Microscopia Eletrônica de Transmissão , Degeneração Neural/enzimologia , Degeneração Neural/patologia , RNA/biossíntese , RNA/genética , Ratos , Ratos Wistar , Reação em Cadeia da Polimerase Via Transcriptase Reversa
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