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1.
J Enzyme Inhib Med Chem ; 28(6): 1199-204, 2013 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-23009604

RESUMEN

A series of 5,7-dihydroxyflavanone derivatives were synthesized and identified as reversible and competitive protein tyrosine phosphatase (PTP) 1B inhibitors with IC50 values in the micromolar range. Compound 4k had the most potent in vitro inhibition activity against PTP1B (IC50 = 2.37 ± 0.37 µM) and the greatest selectivity (3.7-fold) for PTP1B relative to T-cell protein tyrosine phosphatase. Cell-based studies revealed that 4k was membrane-permeable and enhanced insulin receptor tyrosine phosphorylation in CHO/hIR cells.


Asunto(s)
Inhibidores Enzimáticos/síntesis química , Inhibidores Enzimáticos/farmacología , Flavanonas/química , Flavanonas/farmacología , Proteína Tirosina Fosfatasa no Receptora Tipo 1/antagonistas & inhibidores , Animales , Células CHO , Cricetulus , Relación Dosis-Respuesta a Droga , Inhibidores Enzimáticos/química , Flavanonas/síntesis química , Humanos , Modelos Moleculares , Estructura Molecular , Proteína Tirosina Fosfatasa no Receptora Tipo 1/metabolismo , Relación Estructura-Actividad
2.
Yi Chuan Xue Bao ; 33(10): 908-16, 2006 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-17046591

RESUMEN

In this article, population variations and genetic structures of two populations of northern sheatfish (Silurus soldatovi) were analyzed using 24 microsatellite loci enriched from southern catfish (S. meriaionalis Chen) by magnetic beads. Gene frequency (P), observed heterozygosity (Ho), expected heterozygosity (He), polymorphism information contents (PIC), and number of effective alleles (Ne) were determined. One population was wild, ripe individuals collected from Heilongjiang River (HNS); the other was cultured fry collected from Songhuajiang River (SNS). The Hardy-Weinberg equilibrium (HWE) was tested by the genetic departure index (d). The coefficient of gene differentiation G(ST) and Phi(ST) by AMOVA (Analysis of Molecular Variety) was imputed using Arlequin software in this study. In addition, a phylogenetic tree was constructed by UPGMA method based on the pairwise Nei's standard distances using PHYLIP. A total of 1,357 fragments with sizes ranging between 102 bp and 385 bp were acquired by PCR amplifications. The average number of alleles of the two populations was 8.875. Results indicated that these microsatellite loci were highly polymorphic and could be used as genetic markers. The mean values of the parameters P, Ho, He, PIC, and Ne were 0.165, 0.435, 0.758, 0.742, and 5.019 for HNS and 0.147, 0.299, 0.847, 0.764, and 5.944 for SNS, respectively. Although there were differences, there were no significant differentiations except for the locus HLJcf37. These populations to a certain extent deviated from HWE, such as excessive and deficient heterozygote numbers. The value of G(ST) was 0.078 and above 98% of the variation were differences among individuals within the population, so the variation between populations was insignificant. Cluster analysis also showed that the relationships among individuals were very close. In conclusion, the microsatellite markers that were developed through this study are useful for genetic analysis and the genetic culture that was proposed in this study has no significant impact on S. soldatovi.


Asunto(s)
Alelos , Repeticiones de Microsatélite/genética , Polimorfismo Genético , Animales , ADN/análisis , Filogenia
3.
Yi Chuan ; 28(12): 1541-8, 2006 Dec.
Artículo en Zh | MEDLINE | ID: mdl-17138540

RESUMEN

In this paper, population genetic variability and genetic structure of five populations of an important cultivation species, mirror carp (Cyprinus carpio L.) were analyzed using 30 microsatellite loci. The observed (Ho) and expected (He) heterozygosity values, polymorphic information content (PIC) and number of effective alleles (Ae) were all determined. The genetic similarity coefficient and Nei's standard genetic distance were computed based on the allele frequencies. The Hardy-Weinberg equilibrium was checked by chi2 test. Genetic differentiation and hierarchical partition of genetic diversity were evaluated by FST and Nm. A dendrogram was constructed based on UPGMA methods using PHYLIP software package supported by a bootstrap value of 91.0%. Totally 7,083 fragments were procured. Their lengths were from 102 bp to 446 bp. For each locus, 1-16 alleles were amplified, adding up to 356 alleles in all the 5 populations. We found the genetic variability level was relatively high in all five populations, as shown by Ae = 1.07-2.30, He= 0.70-0.78 and PIC=0.69-0.75, respectively. The genetic similarity coefficients were all above 0.52, indicating their close genetic relationships. The UPGMA phylogenetic tree showed mirror carps sampled from Donggang, Fengcheng and Liaozhong were clustered into one group and the other two populations, both collected from Songpu, were grouped together. There were obvious relations between genetic distances and geographical distributions of the five populations. No fragments were amplified from some loci of EST-SSRs, which may suggest the loss of these loci in mirror carp genome or sequence divergence at the primer binding sites. These null alleles may result from selection because functional genes are under more selection pressure than non-encoding loci. Overall, population genetic variation is high for each of the five mirror carp, and the differentiations are also significant among populations.


Asunto(s)
Carpas/genética , Variación Genética , Repeticiones de Microsatélite/genética , Alelos , Animales , Carpas/clasificación , Análisis por Conglomerados , Conservación de los Recursos Naturales , Genotipo , Heterocigoto , Desequilibrio de Ligamiento , Reacción en Cadena de la Polimerasa
4.
Chem Biol Drug Des ; 87(6): 858-66, 2016 06.
Artículo en Inglés | MEDLINE | ID: mdl-26705885

RESUMEN

A series of 7-prenyloxy-2, 3-dihydroflavanone derivatives were synthesized and screened for their antidepressant-like activity. Among them, it was observed that compounds 5j and 5k were found to be the most antidepressant-like activity. In addition, it was found that compounds 5j and 5k significantly increased the concentrations of the main neurotransmitters 5-HT and NE in the hippocampus, hypothalamus, and cortex. Compounds 5j and 5k also significantly increased the contents of 5-HIAA in the hippocampus and cortex, shut down 5-HT metabolism compared with mice treated with stress vehicle. These results suggested that compounds 5j and 5k displayed potent antidepressant-like properties that were mediated via neurochemical systems.


Asunto(s)
Antidepresivos , Encéfalo/metabolismo , Diseño de Fármacos , Flavanonas , Serotonina/metabolismo , Animales , Antidepresivos/síntesis química , Antidepresivos/química , Antidepresivos/farmacología , Química Encefálica/efectos de los fármacos , Femenino , Flavanonas/síntesis química , Flavanonas/química , Flavanonas/farmacología , Masculino , Ratones
5.
Chem Biol Drug Des ; 87(3): 342-51, 2016 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-26390915

RESUMEN

Herein, a series of 3-phenyliminoindolin-2-one derivatives were designed, synthesized, and screened for their antidepressant and anticonvulsant activities. The IR spectra of the compounds afforded NH stretching (3340-3346 cm(-1)) bands and C=O stretching (1731-1746 cm(-1)). In the (1)H-NMR spectra of the compounds, N-H protons of indoline ring were observed at 10.65-10.89 ppm generally as broad bands, and (13)C-NMR spectra of the compounds C=O were seen at 161.72-169.27 ppm. Interestingly, compounds 3o, 3p and 3r significantly shortened immobility time in the The forced swimming test (FST) and The tail suspension test (TST) at 50 mg/kg dose levels. In addition, compound 3r exhibited higher levels of efficacy than the reference standard fluoxetine but had no effect on locomotor activity in the open-field test. Compound 3r significantly increased serotonin and norepinephrine and the metabolite 5-hydroxyindoleacetic acid in mouse brain, suggesting that the effects of compound 3r may be mediated through these neurotransmitters. In the seizure screen, 15 compounds showed some degree against PTZ-induced seizure at a dose of 100 mg/kg, and the tested compounds did not show any neurotoxicity at a dose of 300 mg/kg in the rotarod test.


Asunto(s)
Anticonvulsivantes/síntesis química , Anticonvulsivantes/farmacología , Antidepresivos/síntesis química , Antidepresivos/farmacología , Indoles/síntesis química , Indoles/farmacología , Animales , Ratones , Espectroscopía de Protones por Resonancia Magnética , Espectrometría de Masa por Ionización de Electrospray
6.
Med Chem ; 12(8): 786-794, 2016.
Artículo en Inglés | MEDLINE | ID: mdl-26833072

RESUMEN

BACKGROUND: To discover a novel antidepressant-like effect and anticonvulsant compound, seventeen new 2-oxo-3-phenyliminoindolin-1-Nphenylacetamide compounds were synthesized and screened for the antidepressant activity and anticonvulsant effects. METHOD: 2-oxo-3-phenyliminoindolin-1-N-phenylacetamide derivatives were synthesized with indoline-2, 3-dione as the starting material, through a nucleophilic substitution reaction and a nucleophilic addition-elimination reaction. The target derivatives 2a-2q were evaluated the antidepressant-like activity using the FST, TST, and evaluated anticonvulsant effect by MES test. The main monoamine neurotransmitters and their metabolites in mouse brain regions were also simultaneously determined by HPLC-ECD. RESULTS: It was observed that 13 compounds showed significant reductions in the immobility time in the FST at a concentration of 50 mg/kg. Compound 2b was found to have the most potent antidepressant activity in the FST and the TST for 30 min after treatment. Compound 2b significantly increased the concentrations of the main neurotransmitters 5-HT, NE and the metabolite (5-HIAA, suggesting that the effects of compound 2b may be mediated through these neurotransmitters. As assessed using maximal electroshock, 13 compounds showed the anticonvulsant effects administered at the concentration levels of 100 or 300 mg/kg. Compound 2b showed anticonvulsant effect. Compound 2b could potentially be used as adjuncts of the antidepressants to treat depression in patients with epilepsy. CONCLUSION: In conclusion, compound 2b produced significant antidepressant-like activity and the mechanism of action may be due to increased 5-HT and NE in the mouse. Compound 2b showed more anticonvulsant effect. Compound 2b could potentially be used as adjuncts of the antidepressants to treat depression in patients with epilepsy.


Asunto(s)
Acetanilidas/farmacología , Anticonvulsivantes/farmacología , Antidepresivos/farmacología , Indoles/farmacología , Acetanilidas/administración & dosificación , Acetanilidas/síntesis química , Animales , Anticonvulsivantes/administración & dosificación , Anticonvulsivantes/síntesis química , Antidepresivos/administración & dosificación , Antidepresivos/síntesis química , Dopamina/sangre , Electrochoque , Fluoxetina/farmacología , Ácido Hidroxiindolacético/sangre , Indoles/administración & dosificación , Indoles/síntesis química , Masculino , Ratones , Norepinefrina/sangre , Convulsiones/sangre , Convulsiones/tratamiento farmacológico , Serotonina/sangre , Ácido Valproico/farmacología
7.
Eur J Pharmacol ; 768: 131-8, 2015 Dec 05.
Artículo en Inglés | MEDLINE | ID: mdl-26515446

RESUMEN

We previously showed that extracts of Sargassum fusiforme significantly reduce immobility time in the forced swim test and tail suspension test, suggesting that these extracts possess antidepressant-like effects. Here, fucosterol extracted from S. fusiforme was evaluated for antidepressant and anticonvulsant activities in mice. Fucosterol (10, 20, 30 and 40mg/kg) significantly shortened immobility time in the forced swim test and tail suspension test for30min after treatment but had no effect on locomotor activity in the open field test. Fucosterol significantly increased serotonin, norepinephrine and the metabolite 5-hydroxyindoleacetic acid in mouse brain, suggesting that the effects of fucosterol may be mediated through these neurotransmitters. As assessed using maximal electroshock, fucosterol (20, 40, 100mg/kg) possessed anticonvulsant activity, whereas rotarod toxicity test results indicated that fucosterol did not induce neurotoxicity at the same dose levels in mice. Thus, fucosterol may be a useful antidepressant adjunct candidate for treating depression in patients with epilepsy. A significant increase in hippocampal brain-derived neurotrophic factor (BDNF) levels was found in the fucosterol 20mg/kg group (P<0.05). Our findings suggested that fucosterol may possess an antidepressant-like effect, which may be mediated by increasing central BDNF levels.


Asunto(s)
Anticonvulsivantes/farmacología , Antidepresivos/farmacología , Depresión/tratamiento farmacológico , Sargassum/química , Convulsiones/tratamiento farmacológico , Estigmasterol/análogos & derivados , Animales , Anticonvulsivantes/aislamiento & purificación , Anticonvulsivantes/uso terapéutico , Antidepresivos/aislamiento & purificación , Antidepresivos/uso terapéutico , Monoaminas Biogénicas/metabolismo , Encéfalo/efectos de los fármacos , Encéfalo/metabolismo , Masculino , Ratones , Ratones Endogámicos BALB C , Actividad Motora/efectos de los fármacos , Neurotransmisores/metabolismo , Estigmasterol/aislamiento & purificación , Estigmasterol/farmacología , Estigmasterol/uso terapéutico , Natación
8.
Zhong Yao Cai ; 27(10): 751-3, 2004 Oct.
Artículo en Zh | MEDLINE | ID: mdl-15850357

RESUMEN

OBJECTIVE: To study the effects of Sorbaria sorbifolia extract (SSE) on DMN-induced chronic liver damage in rats. METHODS: Seventy-two rats were divided into four groups, normal, model, SSE and colchicin group. Serum hyaluronic (HA) and type precollagen (PCIII) were detected by radioimmunoassay. Degrees of fibrosis and alpha-smooth muscle actin (alpha-SMA) were determined by histopathology under microscope. Hydroxyproline (Hyp) and the markers of liver function were examined also. RESULTS: The levels of serum ALT, AST, ALb, AKP in SSE groups were notably improved as compared with the model group. Serum HA, PCIII and Hyp of hepatic tissue in SSE groups were obviously lower than those of model group. The markers of oxidative stress( SOD, MDA, GSH-Px) were strikingly improved also in SSE groups. HE stains and alpha-SMA expression showed that the degrees of liver fibrosis in SSE groups was slighter than that of model group. There was significant difference between the model group and SSE groups (P < 0.05 or P < 0.01). The rats in SSE groups were better than those of colchinicines group. CONCLUSION: SSE is able to protect against DMN-induced chronic liver damage, which may act through oxidative stress.


Asunto(s)
Medicamentos Herbarios Chinos/uso terapéutico , Cirrosis Hepática Experimental/tratamiento farmacológico , Fitoterapia , Plantas Medicinales/química , Rosaceae/química , Animales , Cirrosis Hepática Experimental/inducido químicamente , Ratas , Ratas Wistar
9.
Zhong Yao Cai ; 27(1): 36-8, 2004 Jan.
Artículo en Zh | MEDLINE | ID: mdl-15179788

RESUMEN

OBJECTIVE: To study the constituents from Sorbaria sorbifolia and their antitumor activities. METHODS: The constituents were isolated with silia gel column chromatography and identified by physicochemical properties and spectroscopic analysis. Thirty six mice were inoculated with sarcocarcinoma 180 according to the standard method, Sorbaria sorbifolia ethyl acetate etract was administrated for 10 days, tumor and body weight, the activities of NK cell and the contents of TNF-alpha, IL-2 in serum were detected. RESULTS: Three compounds were isolated from the ethyl acetate extract and identified as 5,2',4'-trihydroxy-6,7,5'-trimethoxyflavone(I), succinic acid(II) and p-hydroxybenzoic acid(III). The tumor of the test groups were lighter than that of control group(P < 0.05). There was no remarkable difference between the control and test groups in body weight (P > 0.05). The activity of NK cell and the contents of TNF-alpha, IL-2 in serum were higher than that of control group (P < 0.05). CONCLUSION: Compounds I and II were isolated from Sorbaria sorbifolia ethyl acetate extract for the first time. The ethyl acetate extract could improve immune function and strengthen antitumor effect in sarcocarcinoma 180.


Asunto(s)
Medicamentos Herbarios Chinos/farmacología , Rosaceae/química , Sarcoma 180/patología , Ácido Succínico/farmacología , Animales , Antineoplásicos Fitogénicos/farmacología , Flavonas/análisis , Flavonas/aislamiento & purificación , Flavonas/farmacología , Interleucina-2/sangre , Ratones , Parabenos/análisis , Parabenos/farmacología , Plantas Medicinales/química , Ácido Succínico/análisis , Factor de Necrosis Tumoral alfa/análisis
10.
J Aquat Anim Health ; 25(3): 197-204, 2013 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-23915177

RESUMEN

In April 2011, 40% mortality of Largemouth Bass Micropterus salmoides juveniles occurred at a farm of Zhongshan City, Guangdong Province, China. Infected fish became lethargic, exhibited corkscrew and irregular swimming, and developed a distended abdomen and crooked body. Fish began to die within 2 d after the appearance of clinical signs. In order to analyze the pathogeny and diagnose the disease earlier, observation of clinical signs, cell infection, titer calculation, electron microscopy, immersion infection assay for fish, and nucleotide sequence analysis were carried out. Fathead minnow (FHM) cell cultures, inoculated with filtrate of liver and spleen homogenates from the diseased fish, developed the obvious cytopathic effect 46 h after inoculation in the primary culture and 24 h at the first passage. Typical rhabdovirus particles, 115-143 nm in length and 62-78 nm in diameter, were observed in infected FHM cells by direct transmission electron microscopy. The isolated virus produced a titer of 10(7.15) TCID50/mL. Immersion-Fish infected with the virus had similar clinical signs and 80% mortality with 10(2.5) LD50/mL. The data indicated that the rhabdovirus was the lethal pathogeny of the current disease. Based on nucleoprotein-gene nucleotide sequence multiple alignment analysis, the newly isolated virus is a strain of Siniperca chuatsi rhabdovirus (SCRV) under family Rhabdoviridae, which was initially isolated from Mandarin Fish Siniperca chuatsi. Up to the present, at least four virus strains have been isolated from diseased Largemouth Bass, which have had different clinical signs. Comparison of the clinical signs can help in an early diagnosis of the disease.


Asunto(s)
Lubina , Enfermedades de los Peces/virología , Infecciones por Rhabdoviridae/veterinaria , Rhabdoviridae/clasificación , Animales , Acuicultura , China/epidemiología , Enfermedades de los Peces/epidemiología , Enfermedades de los Peces/mortalidad , Filogenia , Reacción en Cadena de la Polimerasa/veterinaria , Rhabdoviridae/genética , Infecciones por Rhabdoviridae/epidemiología , Infecciones por Rhabdoviridae/mortalidad , Infecciones por Rhabdoviridae/virología
11.
Eur J Med Chem ; 45(5): 1746-52, 2010 May.
Artículo en Inglés | MEDLINE | ID: mdl-20116141

RESUMEN

A series of 6-alkoxy-[1,2,4]triazolo[4,3-b]pyridazine derivatives were synthesized. In initial screening and quantitative evaluation, compound 2r was among the most active agents, exhibiting in the same time the lowest toxicity. In the anti-maximal electroshock test, it showed median effective dose (ED50) of 17.3 mg/kg and median toxicity dose (TD50) of 380.3 mg/kg, and the protective index (PI) of 22.0, which is much better than PI of the reference drugs. In a subsequent test, compound 2r had median hypnotic dose (HD50) of 746.6 mg/kg, thus demonstrating much better margin of safety compared to reference drugs. Compound 2r also showed oral activity against MES-induced seizures and lower oral neurotoxicity. For explanation of the putative mechanism of action, compound 2r was tested in chemical induced models.


Asunto(s)
Anticonvulsivantes/farmacología , Actividad Motora/efectos de los fármacos , Piridazinas/farmacología , Convulsiones/tratamiento farmacológico , Triazoles/farmacología , Animales , Anticonvulsivantes/síntesis química , Anticonvulsivantes/química , Modelos Animales de Enfermedad , Relación Dosis-Respuesta a Droga , Evaluación Preclínica de Medicamentos , Ratones , Estructura Molecular , Piridazinas/síntesis química , Piridazinas/química , Prueba de Desempeño de Rotación con Aceleración Constante , Convulsiones/inducido químicamente , Estereoisomerismo , Relación Estructura-Actividad , Triazoles/síntesis química , Triazoles/química
12.
Mitochondrial DNA ; 20(4): 72-7, 2009 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-19575330

RESUMEN

BACKGROUND AND AIMS: The swordtail (Xiphophorus helleri) has been used in studies of behavior, phylogenetics, genetics, physiology, cell biology, cancer research, and biomedicine. Mitochondrial DNA (mtDNA) studies are of pressing need in order to assess the population history of the species. MATERIALS AND METHOD: In this study, we present the complete mtDNA genome sequence of two specimens: one from a RR-B strain, a 27-generation inbred line; and one non-selective swordtail with red eyes and red body color from the Guangzhou market, measuring 16,638 and 16,635 bp, respectively. RESULTS: The genome comprises 13 protein-coding genes, 22 tRNAs, two rRNAs and a major non-coding region. The comparison of the two specimens' mitogenomes revealed a relatively low number (57) of single nucleotide polymorphisms-29 located in protein-coding genes, 11 in rRNA genes, six in tRNA genes, and six in the non-coding region. CONCLUSION: We present an important genetic resource for the RR-B strain of swordtails and swordtail species in general.


Asunto(s)
Ciprinodontiformes/genética , Genoma Mitocondrial/genética , Animales , Animales Endogámicos , Genes Mitocondriales/genética , Proteínas Mitocondriales/genética , ARN Ribosómico/genética , ARN de Transferencia/genética , ARN no Traducido/genética , Análisis de Secuencia de ADN
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