Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 20 de 131
Filtrar
Más filtros










Base de datos
Intervalo de año de publicación
1.
Chem Commun (Camb) ; 52(11): 2405-7, 2016 Feb 07.
Artículo en Inglés | MEDLINE | ID: mdl-26735489

RESUMEN

Peptide nucleic acid bis-quinoline conjugates are reported as attractive far-red emitting probes that detect mutated mRNA in living cells at SNP resolution.


Asunto(s)
Neoplasias/genética , Mutación Puntual , Humanos , Microscopía Fluorescente , Sondas Moleculares , Ácidos Nucleicos de Péptidos/química , Polimorfismo de Nucleótido Simple , Espectrofotometría Ultravioleta
2.
Neuroscience ; 162(4): 1011-22, 2009 Sep 15.
Artículo en Inglés | MEDLINE | ID: mdl-19447164

RESUMEN

Diminished levels of docosahexaenoic acid (DHA, 22:6n-3), the major polyunsaturated fatty acid (FA) synthesized from alpha linolenic acid (ALA, 18:3n-3), have been implicated in changes in neurotransmitter production, ion channel disruption and impairments of a variety of cognitive, behavioral and motor functions in the perinatal and adult mammal. Neuronal migration in the cortex and hippocampus of newborn and postnatal rats after ALA-deficiency, beginning on the 2nd day after conception and continuing for three weeks, was investigated. A marked decrease in the migration of bromodeoxyuridine((+))/neuronal nuclei((+))/neurofilament((+)) and glia fibrillary acidic protein((-)) neuronal cells to the dense cortical plate was accompanied by a corresponding abundance of non-migrating cells in several regions such as cortical layers IV-VI, corpus callosum and the sub-ventricular zone of ALA-deficient newborns. Similarly, a delayed migration of cells to CA1 and dentate gyrus areas was noticed while most cells were retained in the subicular area adjacent to the hippocampus. The reversibility of delay in migration in the hippocampus and cortex, after one and two weeks respectively, may be attributed to a temporary reelin disorganization or partial deficiency. Transient obstruction of neuronal cell migration may have long-lasting consequences on the organization of neuronal assemblies, on the connection between neurons (lateral connections) and acquisition of function in the adult brain.


Asunto(s)
Encéfalo/citología , Intercambio Materno-Fetal , Neuronas/fisiología , Ácido alfa-Linolénico/deficiencia , Animales , Animales Recién Nacidos , Encéfalo/crecimiento & desarrollo , Movimiento Celular , Femenino , Hipocampo/citología , Hipocampo/crecimiento & desarrollo , Neocórtex/citología , Neocórtex/crecimiento & desarrollo , Embarazo , Ratas , Ratas Wistar , Proteína Reelina
4.
J Neurochem ; 95(6): 1550-62, 2005 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-16305626

RESUMEN

A combination of PCR-Select cDNA subtraction and gene array hybridization was used to identify differentially expressed genomic markers in brains of rats fed for 3 weeks in utero and 2 weeks after birth on an n-3 polyunsaturated fatty acid (PUFA)-deficient diet supplied to dams. Total RNA was isolated, switch mechanism at 5'-end of the RNA transcripts (SMART) applied and used for PCR-Select subtraction of PUFA-deficient and adequately-fed control preparations. Subtracted and amplified ds-cDNA end-products were fragmented, terminally labeled with biotin-ddUTP and hybridized with a RN-U34A gene array. A 10-fold increase in potential genes with log2(Tester/Driver) = 1.4 was found compared with traditional gene array technology when the same chip was tested using non-subtracted targets. Reverse transcription-real-time relative PCR confirmed 30% of the transcripts. Among the validated transcripts, D1 and D2 receptors for dopamine (DA), were most prominent among a number of over-expressed neurotransmitter receptors and retinoic acid receptor (RXR alpha-2 and alpha-1). Immunohistochemical staining of brain sections from 2-week-old pups revealed a substantial enrichment of the D2 receptor in discrete regions of the mesolimbic and mesocortical pathways as well as in a large number of brain areas from the n-3 PUFA-deficient pups. Punches of the same areas run on western blots showed similar results. The overwhelming expression of D1 and D2 receptors may be attributed to a behavioral hypersensitivity caused by the possible impairment of DA production during brain development, which may have implications in certain disorders of the nervous system.


Asunto(s)
Animales Recién Nacidos/fisiología , Química Encefálica/genética , Ácidos Grasos Omega-3/fisiología , Receptores Dopaminérgicos/biosíntesis , Receptores Dopaminérgicos/genética , Animales , Western Blotting , Corteza Cerebral/metabolismo , Corteza Cerebral/fisiología , ADN Complementario/biosíntesis , Dieta , Ácidos Grasos/administración & dosificación , Femenino , Expresión Génica/fisiología , Regulación de la Expresión Génica , Biblioteca de Genes , Inmunohistoquímica , Hibridación in Situ , Sistema Límbico/metabolismo , Sistema Límbico/fisiología , Proteínas del Tejido Nervioso/metabolismo , Análisis de Secuencia por Matrices de Oligonucleótidos , ARN/biosíntesis , Ratas , Ratas Sprague-Dawley , Receptores de Dopamina D1/fisiología , Receptores de Dopamina D2/fisiología , Reacción en Cadena de la Polimerasa de Transcriptasa Inversa
5.
Brain Res Mol Brain Res ; 137(1-2): 110-8, 2005 Jun 13.
Artículo en Inglés | MEDLINE | ID: mdl-15950768

RESUMEN

Despite the success and popularity of microarrays as a high-throughput technology for gene-expression studies, its sensitivity is as yet fairly limited. We have successfully combined the use of PCR-Select cDNA subtraction and Affymetrix GeneChips (AGC) to identify differentially expressed gene markers. Total RNA (totRNA) from combined hippocampus and cerebellum tissues of 2-week-old rat pups maintained for 5 weeks on an n-3 fatty acid (FA) deficient diet supplied to dams was isolated, SMART-amplified, and used for PCR-Select subtraction versus an adequately fed control litter preparation. Subtracted and amplified ds-cDNA end products were fragmented, terminally labeled with biotin-ddUTP and hybridized with RN-U34A AGC. At least 10-fold more potential gene markers with log2(T/D) > or = 1.4 were found versus the traditional AGC technology when the same chip was tested using nonsubtracted targets. Of this set of markers, 30% were robustly validated by real-time relative RT-PCR (rtrRT-PCR) and grouped as "confirmed" markers while the remaining were ascribed as "latent" markers. An improved and universal protocol to provide a rapid assessment for gene profiling in biological specimens is indicated.


Asunto(s)
ADN Complementario/análisis , Perfilación de la Expresión Génica/métodos , Marcadores Genéticos/genética , Análisis de Secuencia por Matrices de Oligonucleótidos/métodos , Reacción en Cadena de la Polimerasa/métodos , ARN Mensajero/análisis , Animales , Animales Recién Nacidos , Química Encefálica/genética , Cerebelo/metabolismo , ADN Complementario/genética , Ácidos Grasos Omega-3/metabolismo , Alimentos Formulados , Regulación de la Expresión Génica/genética , Hipocampo/metabolismo , Lípidos/deficiencia , Proteínas del Tejido Nervioso/genética , Proteínas del Tejido Nervioso/metabolismo , ARN Mensajero/genética , Ratas , Ratas Sprague-Dawley , Estrés Fisiológico/genética , Estrés Fisiológico/metabolismo , Estrés Fisiológico/fisiopatología
6.
Brain Res Mol Brain Res ; 127(1-2): 10-26, 2004 Aug 23.
Artículo en Inglés | MEDLINE | ID: mdl-15306117

RESUMEN

Ischemic stress is associated with marked changes in gene expression in the hippocampus--albeit little information exists on the activation of nonabundant genes. We have examined the expression of several known genes and identified novel ones in the adult rat hippocampus after a mild, transient, hypovolemic and hypotensive, global ischemic stress. An initial differential screening using a prototype array to assess gene expression after stress followed by a suppression subtractive hybridization protocol and cDNA microarray revealed 124 nonoverlapped transcripts predominantly expressed in the CA1 rat hippocampus region in response to ischemic stress. About 78% of these genes were not detected with nonsubtracted probes. Reverse transcription polymerase chain reaction (RT-PCR) and in situ hybridization on these 124 transcripts confirmed the differential expression of at least 83. Most robustly expressed were gene sequences NFI-B, ATP1B1, RHOGAP, PLA2G4A, BAX, CASP3, P53, MAO-A, FRA1, HSP70.2, and NR4A1 (NUR77), as well as sequence tags of unknown function. New stress-related genes of similar functional motifs were identified, reemphasizing the importance of functional grouping in the analysis of multiple gene expression profiles. These data indicate that ischemia elicits expression of an array of functional gene clusters that may be used as an index for stress severity and a template for target therapy design.


Asunto(s)
Expresión Génica/fisiología , Hipocampo/metabolismo , Ataque Isquémico Transitorio/metabolismo , Animales , Northern Blotting , Proteínas de Unión al ADN/genética , Proteínas de Unión al ADN/metabolismo , Perfilación de la Expresión Génica , Regulación de la Expresión Génica , Proteínas HSP70 de Choque Térmico/genética , Proteínas HSP70 de Choque Térmico/metabolismo , Hipocampo/anatomía & histología , Hibridación in Situ/métodos , Ataque Isquémico Transitorio/genética , Masculino , Miembro 1 del Grupo A de la Subfamilia 4 de Receptores Nucleares , Análisis de Secuencia por Matrices de Oligonucleótidos/métodos , ARN Mensajero/metabolismo , Ratas , Ratas Wistar , Receptores Citoplasmáticos y Nucleares , Receptores de Esteroides , Reacción en Cadena de la Polimerasa de Transcriptasa Inversa/métodos , Factores de Transcripción/genética , Factores de Transcripción/metabolismo , Transcripción Genética , Proteína p53 Supresora de Tumor/genética , Proteína p53 Supresora de Tumor/metabolismo
7.
J Neurochem ; 78(6): 1208-18, 2001 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-11579130

RESUMEN

The consequences of H(2)O(2)/Fe(2+)-induced oxidative stress on translocation of ethanolamine phosphoglyceride (EPG) and serine phosphoglyceride (SPG) were studied in an oligodendroglia-like cell line (OLN 93) following 3 days of supplementation with 0.1 mM docosahexaenoic acid (DHA) and a series of polar head group precursors, including N-monomethyl- and N,N-dimethylethanolamine at millimolar concentrations. Added DHA was predominantly esterified in EPG species and those cells enriched in DHA showed enhanced sensitivity to oxidative stress and eventually died by apoptosis. Co-supplements with ethanolamine and DHA resulted in a rapid, but transient, EPG translocation with a maximum at 30 min following stress, as characterized by a trinitrobenzenesulfonic acid reagent. There was no significant translocation of SPG as evidenced by annexin V binding. Unlike SPG, which is usually irreversibly translocated to subserve as a tag for phagocytosis, EPG acted as a signaling molecule with biphasic kinetic characteristics. N-Monomethyl- and N,N-dimethylethanolamine supplements reduced EPG synthesis, prevented its externalization and rescued cells from apoptotic death. Following stress, the fatty acid profile of the externalized EPG showed marked losses in polyunsaturated fatty acids and aldehydes compared with the remaining intracellular EPG. Prevention of EPG species selective translocation to the outer membrane leaflet by altering phospholipid asymmetry may be important in the mechanism of rescue from cell death.


Asunto(s)
Apoptosis/fisiología , Etanolamina/metabolismo , Oligodendroglía/fisiología , Fosfolípidos/metabolismo , Estrés Fisiológico/fisiopatología , Animales , Transporte Biológico/fisiología , Línea Celular , Supervivencia Celular/fisiología , Ácidos Docosahexaenoicos/farmacología , Ácidos Grasos Insaturados/metabolismo , Cinética , Metabolismo de los Lípidos , Oligodendroglía/metabolismo , Ratas , Factores de Tiempo
8.
J Mol Neurosci ; 16(2-3): 229-35; discussion 279-84, 2001.
Artículo en Inglés | MEDLINE | ID: mdl-11478378

RESUMEN

Docosahexaenoic acid (DHA; 22:6n-3) is the major polyunsaturated fatty acid (FA) in the adult rat brain and it accumulates significantly more than any other FA prior to birth. Under normal nutritional conditions, fetal-brain DHA accumulation is substantial, with a "DHA accretion spurt" being demonstrated in the last period of gestation. Under stress conditions, this spurt may be harmful owing to an increase in multiple double-bond targets for lipid peroxidation. The "DHA accretion spurt" is supported by the maternal supply of DHA or its precursor. Under maternal dietary n-3 FA deficiency, DHA content in the fetal brain can be restored by direct intraamniotic injection of mM concentrations of ethyl-DHA (Et-DHA). This approach may hold a potential advantage in the event of maternal-fetal insufficiency, a stress that may cause intrauterine growth retardation. It also revealed a potential beneficial effect after in utero ischemic stress; brain slices from Et-DHA-treated fetuses formed less oxidation products, as detected by thiobarbituric acid (TBA), compared to controls. Furthermore, brain-lipid extracts from Et-DHA but not ethyl-oleate treated fetuses, exhibited hydroxyl radical scavenging activity, as demonstrated by electron spin-resonance technique. Part of the beneficial effect of Et-DHA administration on the fetal brain may be attributed to enhanced free-radical scavenging capability, a phenomenon not directly related to vitamin E or lipid-soluble antioxidant levels.


Asunto(s)
Encéfalo/metabolismo , Ácidos Docosahexaenoicos/metabolismo , Animales , Encéfalo/embriología , Grasas de la Dieta/farmacocinética , Suplementos Dietéticos , Ácidos Docosahexaenoicos/farmacología , Espectroscopía de Resonancia por Spin del Electrón , Ácidos Grasos Insaturados/farmacocinética , Femenino , Retardo del Crecimiento Fetal/metabolismo , Depuradores de Radicales Libres/metabolismo , Isquemia/metabolismo , Peroxidación de Lípido , Intercambio Materno-Fetal , Ácido Oléico/farmacología , Oxidación-Reducción , Estrés Oxidativo , Fosfatidiletanolaminas/metabolismo , Fosfatidilserinas/metabolismo , Placenta/irrigación sanguínea , Aceites de Plantas/administración & dosificación , Aceites de Plantas/farmacocinética , Embarazo , Ratas , Sustancias Reactivas al Ácido Tiobarbitúrico/análisis
9.
Biochim Biophys Acta ; 1532(3): 203-12, 2001 Jun 29.
Artículo en Inglés | MEDLINE | ID: mdl-11470241

RESUMEN

In order to explore possible mechanisms to explain previously observed decreases in fetal brain lipid peroxidation (LPO) following intraamniotic administration of ethyl docosahexaenoate (Et-DHA) to near term fetuses, the hydroxyl radical trapping capacity of Et-DHA treated fetal brain preparations was compared to control ethyl oleate injected fetuses by electron spin resonance using 5,5'-dimethyl-1-pyrroline N-oxide (DMPO) probe. Lipid extracts from control brains showed little hydroxyl radical scavenging activity, whereas those from the Et-DHA injected animals exhibited an almost 70% decrease in the amount of DMPO-OH adducts. A marked decrease (58%) in LPO formation was noticed in the Et-DHA treated animals compared to controls. The Et-DHA treatment related trapping capacity resided in the phospholipid fraction of the lipid extract, which was enriched in both docosahexaenoic acid and aminophospholipid contents. The decreased LPO production, as well as increased production of prostaglandin E(2) and nitric oxide by the fetal brain following Et-DHA administration, could be mimicked by a synthetic quinone possessing both hydroxyl radical producing and LPO propagation inhibiting properties. The data are consistent with the possibility that the neuroprotective effect of Et-DHA might be due to possible free radical scavenging ability of the brain tissue and interference with LPO propagation.


Asunto(s)
Encéfalo/efectos de los fármacos , Ácidos Docosahexaenoicos/farmacología , Depuradores de Radicales Libres/metabolismo , Peroxidación de Lípido/efectos de los fármacos , Amnios , Animales , Antioxidantes/análisis , Encéfalo/metabolismo , Química Encefálica , Óxidos N-Cíclicos , Dinoprostona/análisis , Dinoprostona/metabolismo , Ácidos Docosahexaenoicos/administración & dosificación , Espectroscopía de Resonancia por Spin del Electrón , Femenino , Feto , Peróxidos Lipídicos/metabolismo , Lípidos/análisis , Óxido Nítrico/análisis , Óxido Nítrico/metabolismo , Fosfolípidos/metabolismo , Embarazo , Ratas , Ratas Wistar , Marcadores de Spin , Sustancias Reactivas al Ácido Tiobarbitúrico/análisis
10.
Biochim Biophys Acta ; 1531(1-2): 156-64, 2001 Mar 30.
Artículo en Inglés | MEDLINE | ID: mdl-11278180

RESUMEN

Previously we have shown that intraamniotic administration of ethyl docosahexaenoate (Et-DHA) to pregnant rats resulted in decreased lipid peroxidation in the fetal brain, under a variety of conditions (S. Glozman, P. Green, E. Yavin, J. Neurochem. 70 (1998) 2482-2491). In the present study we examine the potential mechanisms to explain this effect. This was done by a pharmacological approach, utilizing brain slice preparations from Et-DHA treated or control rats in the presence of various agents and examining the formation of products in the tissue slices or incubation medium. Et-DHA treated brains produced 2-3-fold more prostanoids (PN) than control brains, indicating cyclooxygenase (COX) activation. Indomethacin at 50 microM inhibited PN formation and also abolished Et-DHA induced decrease in lipid peroxides, as evident by the levels of thiobarbituric acid reactive substances (TBARS) released in the medium. The phospholipase A2 inhibitors quinacrine and p-bromophenacyl bromide added at 0.1 mM concentration each to either slices from controls or Et-DHA treated fetal brains, decreased TBARS production. Et-DHA treated brains released 2.2-fold more nitric oxide (NO) than control brains and NO synthase (NOS) inhibitors abolished this effect. Increasing the concentration of NO by the addition of an NO donor greatly decreased the concentration of the TBARS in the medium. These results suggest that at least some of the effect of Et-DHA on decreased lipid peroxidation may be explained by a shift of oxygen species utilization via enzymatically regulated, therefore metabolically controlled, COX and NOS activities.


Asunto(s)
Encéfalo/efectos de los fármacos , Ácidos Docosahexaenoicos/farmacología , Peróxidos Lipídicos/metabolismo , Prostaglandinas/metabolismo , Animales , Encéfalo/metabolismo , Dinoprostona/metabolismo , Femenino , Feto , Humanos , Óxido Nítrico/metabolismo , Embarazo , Ratas , Sustancias Reactivas al Ácido Tiobarbitúrico/metabolismo
11.
J Neurochem ; 76(3): 758-67, 2001 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-11158247

RESUMEN

A major feature of Alzheimer's disease is the deposition of the amyloid beta peptide (Abeta) in the brain by mechanisms which remain unclear. One hypothesis suggests that oxidative stress and Abeta aggregation are interrelated processes. Protein kinase C, a major neuronal regulatory protein is activated after oxidative stress and is also altered in the Alzheimer's disease brain. Therefore, we examined the effects of Abeta(1-40) peptide on the protein kinase C cascade and cell death in primary neuronal cultures following anoxic conditions. Treatment with Abeta(1-40) for 48 h caused a significant increase in the content and activity of Ca2+ dependent and Ca2+ independent protein kinase C isoforms. By 72 h various protein kinase C isoforms were down-regulated. Following 90 min anoxia and 6 h normoxia, a decrease in protein kinase C isoforms was noticed, independent of Abeta(1-40) treatment. A combination of Abeta(1-40) and 30-min anoxia enhanced cytotoxicity as noticed by a marked loss in the mitochondrial ability to convert 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl-tetrazolium bromide and by enhanced 4',6-diamidino-2-phenylindole nuclear staining. Phosphorylation of two downstream protein kinase C substrates of apparent molecular mass 80 and 43 kDa, tentatively identified as the myristoyl alanine-rich C-kinase substrate (MARCKS), were gradually elevated up to 72 h upon incubation with Abeta(1-40). Anoxia followed by 30 min normoxia enhanced MARCKS phosphorylation in the membrane but not in the cytosolic fraction. In the presence of Abeta(1-40), phosphorylation of MARCKS was reduced. After 6 h normoxia, MARCKS phosphorylatability was diminished possibly because of protein kinase C down-regulation. The data suggest that a biphasic modulation of protein kinase C and MARCKS by Abeta(1-40) combined with anoxic stress may play a role in Alzheimer's disease pathology.


Asunto(s)
Péptidos beta-Amiloides/envenenamiento , Hipoxia/fisiopatología , Péptidos y Proteínas de Señalización Intracelular , Proteínas de la Membrana , Neuronas/efectos de los fármacos , Neuronas/fisiología , Proteína Quinasa C/metabolismo , Péptidos beta-Amiloides/farmacología , Animales , Calcio/fisiología , Muerte Celular , Membrana Celular/metabolismo , Células Cultivadas , Regulación hacia Abajo , Activación Enzimática , Isoenzimas/metabolismo , Sustrato de la Proteína Quinasa C Rico en Alanina Miristoilada , Neuronas/metabolismo , Fragmentos de Péptidos/farmacología , Fosforilación , Proteína Quinasa C/fisiología , Proteínas/metabolismo , Ratas , Factores de Tiempo
12.
J Neurochem ; 76(3): 910-8, 2001 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-11158263

RESUMEN

The present work examines the effect of membrane lipid composition on activation of extracellular signal-regulated protein kinases (ERK) and cell death following oxidative stress. When subjected to 50 microM docosahexaenoic acid (DHA, 22 : 6 n-3), cellular phospholipids of OLN 93 cells, a clonal line of oligodendroglia origin low in DHA, were enriched with this polyunsaturated fatty acid. In the presence of 1 mM N,N-dimethylethanolamine (dEa) a new phospholipid species analog was formed in lieu of phosphatidylcholine. Exposure of DHA-enriched cells to 0.5 mM H2O2, caused sustained activation of ERK up to 24 h. At this time massive apoptotic cell death was demonstrated by ladder and TUNEL techniques. H2O2-induced stress applied to dEa or DHA/dEa co-supplemented cells showed only a transient ERK activation and no cell death after 24 h. Moreover, while ERK was rapidly translocated into the nucleus in DHA-enriched cells, dEa supplements completely blocked ERK nuclear translocation. This study suggests that H2O2-induced apoptotic cell death is associated with prolonged ERK activation and nuclear translocation in DHA-enriched OLN 93 cells, while both phenomena are prevented by dEa supplements. Thus, the membrane lipid composition ultimately modulates ERK activation and translocation and therefore can promote or prevent apoptotic cell death.


Asunto(s)
Apoptosis/fisiología , Peróxido de Hidrógeno/farmacología , Lípidos/fisiología , Proteínas Quinasas Activadas por Mitógenos/metabolismo , Oligodendroglía/efectos de los fármacos , Oligodendroglía/fisiología , Oxidantes/farmacología , Transporte Biológico/fisiología , Butadienos/farmacología , Muerte Celular/efectos de los fármacos , Línea Celular , Núcleo Celular/enzimología , Deanol/farmacología , Ácidos Docosahexaenoicos/farmacología , Resistencia a Medicamentos , Activación Enzimática/efectos de los fármacos , Activación Enzimática/fisiología , Inhibidores Enzimáticos/farmacología , Nitrilos/farmacología , Oligodendroglía/citología , Oligodendroglía/metabolismo , Estrés Oxidativo , Factores de Tiempo
13.
Nutr Health ; 15(3-4): 219-24, 2001.
Artículo en Inglés | MEDLINE | ID: mdl-12003088

RESUMEN

Docosahexaenoic acid (DHA, 22: 6n-3) and arachidonic acid (AA, 20: 4n-6) provision to the developing fetus, with emphasis towards brain and vascular system growth, is a subject of increasing concern particularly under pathological conditions associated with premature birth or in utero growth restriction following obstruction of the maternal-fetal blood flow. Most of DHA, but also AA accretion under physiological conditions, is maternally dependent and requires adequate maternal nutrition and normally functioning placental-fetal circulation. It has been demonstrated that unlike other fatty acids (FA), DHA is preferentially transported across the placenta into the fetal circulation. The selective transplacental DHA transfer is probably mediated by specific carrier proteins. While some of the latter may be acting in fetal organs, the mechanism(s) for the selective accumulation of DHA in brain is still unknown. The fetal brain and also the fetal liver are capable of producing DHA from linolenic (LnA, 18:3 n-3) acid. How effective this local elongation-desaturation mechanism for DHA provision is and to what degree this route is activated in premature births is not clear. Transfer of DHA via the fetal gastrointestinal tract is an additional route to provide DHA to other fetal organs. As indicated by animal model studies, it holds the potential for DHA supply when the maternal pathway is compromised.


Asunto(s)
Encéfalo/embriología , Encéfalo/metabolismo , Ácidos Docosahexaenoicos/metabolismo , Desarrollo Embrionario y Fetal/efectos de los fármacos , Desarrollo Embrionario y Fetal/fisiología , Animales , Ratas
14.
Biochim Biophys Acta ; 1499(1-2): 144-153, 2000 Dec 11.
Artículo en Inglés | MEDLINE | ID: mdl-11118647

RESUMEN

The reaction between allicin (diallylthiosulfinate), the active component of garlic and reduced glutathione was investigated. The product of this reaction, mixed disulfide S-allylmercaptoglutathione (GSSA) was separated by high performance liquid chromatography and identified by 1H and (13)C nuclear magnetic resonance and mass spectroscopy. The reaction is fast (with an apparent bimolecular reaction rate constant of 3.0 M(-1) s(-1)). It is pH-dependent, which reveals a direct correlation to the actual concentration of mercaptide ion (GS(-)). Both GSSA and S-allylmercaptocysteine (prepared from allicin and cysteine) reacted with SH-containing enzymes, papain and alcohol dehydrogenase from Thermoanaerobium brockii yielding the corresponding S-allylmercapto proteins, and caused inactivation of the enzymes. The activity was restored with dithiothreitol or 2-mercaptoethanol. In addition, GSSA also exhibited high antioxidant properties. It showed significant inhibition of the reaction between OH radicals and the spin trap 5,5'-dimethyl-1-pyroline N-oxide in the Fenton system as well as in the UV photolysis of H2O2. In ex vivo experiments done with fetal brain slices under iron-induced oxidative stress, GSSA significantly lowered the production levels of lipid peroxides. The similar activity of GSSA and allicin as SH-modifiers and antioxidants suggests that the thioallyl moiety has a key role in the biological activity of allicin and its derivatives.


Asunto(s)
Antioxidantes/química , Cisteína/análogos & derivados , Cisteína/síntesis química , Glutatión/química , Ácidos Sulfínicos/química , Alcohol Deshidrogenasa/antagonistas & inhibidores , Cromatografía Líquida de Alta Presión , Disulfuros , Inhibidores Enzimáticos/química , Ajo , Cinética , Espectroscopía de Resonancia Magnética , Papaína/antagonistas & inhibidores , Plantas Medicinales , Compuestos de Sulfhidrilo/química
15.
Biochim Biophys Acta ; 1487(2-3): 135-44, 2000 Sep 27.
Artículo en Inglés | MEDLINE | ID: mdl-11018466

RESUMEN

The over-expressed Cu/Zn-superoxide dismutase (Cu/Zn-SOD) gene has been found in some circumstances phenotypically deleterious and associated with oxidative injury-mediated aberrations while in other studies it was considered neuroprotective. In this work we examine a number of biochemical markers in fetal and adult brain from transgenic (tg) mice expressing the human Cu/Zn-SOD gene, which may determine this dual characteristic. These markers include the polyunsaturated fatty acid (PUFA) profile in discrete phospholipid species, the alpha-tocopherol levels, a marker for lipid anti-oxidant status, and thiobarbituric acid reactive substance (TBARS), a marker for the tissue oxidative status. The PUFA profile in choline- and ethanolamine-phosphoglycerides was similar in tg and nontransgenic (ntg) animals of either fetal or adult brain. Serine-phosphoglycerides, however, showed a marked decrease from 20. 07+/-0.53 to 14.92+/-0.87 wt% and 14.52+/-1.15 wt% in docosahexaenoic acid (DHA; 22:6 n3), in the tg 51 and tg 69 fetal brains, respectively, but not in the comparable adult tissues. The alpha-tocopherol levels were significantly higher in the fetal compared to the adult brain. There were no differences in the anti-oxidant levels between the ntg and tg fetal brains, but there were differences in the adult animals; the tg mice were higher by at least two-fold than the control animals. The basal TBARS in the tg 51 fetal brain was 35% lower than that of ntg mouse and in the presence of Fe(2+), brain slices from the former released less TBARS (57% reduction) into the medium than the latter. These results suggest that higher dosages of Cu/Zn-SOD gene are compatible with increased alpha-tocopherol levels, reduced basal TBARS levels and a DHA deficiency in the fetal, but not the adult, tg brain.


Asunto(s)
Antioxidantes/análisis , Encéfalo/metabolismo , Ácidos Docosahexaenoicos/análisis , Síndrome de Down/metabolismo , Fosfatidilserinas/química , Superóxido Dismutasa/biosíntesis , Vitamina E/análisis , Animales , Encéfalo/embriología , Humanos , Ratones , Ratones Transgénicos , Sustancias Reactivas al Ácido Tiobarbitúrico/análisis
16.
Neurochem Res ; 25(5): 653-60, 2000 May.
Artículo en Inglés | MEDLINE | ID: mdl-10905627

RESUMEN

The effect of amyloid beta (Abeta), the major constituent of the Alzheimer's (AD) brain on lipid metabolism was investigated in cultured nerve cells and in a fetal rat brain model. Differentiated (NGF) and undifferentiated PC12 cells or primary cerebral cell cultures were incubated with [14C]acetate in the absence or presence of Abeta1-40. Incorporation of label into lipid species was determined after lipid extraction and TLC separation. Phosphatidylcholine (PC) and phosphatidylserine (PS) synthesis was increased by Abeta1-40, in a dose dependent manner, an effect which was more pronounced in differentiated PC12 cells. A significant proportion of radioactivity (5-6%) was released into the medium with a radioactivity distribution similar to that of the cellular lipids. Cholesterol and PC were the highest labeled medium lipids. Increasing Abeta1-40 concentration up to 0.1 microg/ml in cerebral cells but not in PC12 cells, caused a relative increase (1.5 fold) in release of PS, while that of PE decreased. Stimulation of PS release may possibly be associated with apoptotic cell death. Abeta1-40 peptide (5 microg) was administered intraperitoneally into rat fetuses (18 days gestation) along with [14C]acetate (2 microCi/fetus). After 24 h, the maternal-fetal blood supply was occluded for 20 min (ischemia) followed by 15 min reperfusion. Fetuses were killed and liver and brain tissue subjected to lipid extraction and radioactivity determination after TLC. Abeta1-40 peptide increased synthesis of different classes of lipids up to 20-40% in brain tissue compared to controls. Labeling of liver lipids was decreased by Abeta1-40 by 20-30%. A general decrease in synthesis of lipids was observed after ischemia/reperfusion. Our data suggest that Abeta1-40 peptide regulates normal lipid biosynthesis but under ischemia it compromises it. The latter finding may confirm the oxidative stress etiology in AD and suggests that Abeta1-40 modulation of lipid metabolism may have Alzheimer's pathological relevance, particularly at high peptide concentrations.


Asunto(s)
Péptidos beta-Amiloides/farmacología , Corteza Cerebral/fisiología , Colesterol/biosíntesis , Neuronas/fisiología , Estrés Oxidativo/fisiología , Fragmentos de Péptidos/farmacología , Fosfolípidos/biosíntesis , Acetatos/metabolismo , Animales , Autorradiografía , Radioisótopos de Carbono , Células Cultivadas , Corteza Cerebral/efectos de los fármacos , Corteza Cerebral/embriología , Feto , Cinética , Neuronas/efectos de los fármacos , Células PC12 , Fosfatidilcolinas/biosíntesis , Fosfatidiletanolaminas/biosíntesis , Fosfatidilserinas/biosíntesis , Ratas
17.
FEBS Lett ; 472(2-3): 259-62, 2000 Apr 28.
Artículo en Inglés | MEDLINE | ID: mdl-10788622

RESUMEN

Serum amyloid A (SAA) is a major acute-phase protein whose biochemical functions remain largely obscure. Human rheumatic synovial fluids were screened by high performance liquid chromatography mass spectrometry for SAA-derived peptides, specifically the sequence AGLPEKY (SAA(98-104)) which was previously shown to modulate various leukocyte functions. Two such fluids were found to contain a truncated version of SAA(98-104). Synthetic SAA(98-104) and several of its analogs were shown capable of binding isolated human CD(4)(+) T-lymphocytes and stimulating them to produce interferon-gamma. Given the high acute-phase serum level of SAA and its massive proteolysis by inflammatory related enzymes, SAA-derived peptides may be involved in host defense mechanisms.


Asunto(s)
Apolipoproteínas/inmunología , Artritis Reumatoide/inmunología , Linfocitos T CD4-Positivos/inmunología , Interferón gamma/metabolismo , Péptidos/inmunología , Proteína Amiloide A Sérica/inmunología , Humanos , Péptidos/síntesis química , Líquido Sinovial/inmunología
18.
J Neurochem ; 74(4): 1596-604, 2000 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-10737617

RESUMEN

A major reason for brain tissue vulnerability to oxidative damage is the high content of polyunsaturated fatty acids (PUFAs). Oligodendroglia-like OLN 93 cells lack PUFAs and are relatively insensitive to oxidative stress. When grown in serum-free defined medium in the presence of 0.1 mM docosahexaenoic acid (DHA; 22:6 n-3) for 3 days, OLN 93 cells release in the medium 2.6-fold more thiobarbituric acid-reactive substances (TBARS) after a 30-min exposure to 0.1 mM H2O2 and 50 microM Fe2+. Release of TBARS was substantially decreased by approximately 20 and 30% on coincubation with either 1 mM N-monomethylethanolamine or N,N'-dimethylethanolamine (dEa), respectively. The protective effect of dEa was concentration- and time-dependent and was still visible after dEa removal, suggesting a long-lasting mechanism of protection. After 24 h following H2O2-induced stress, cell death monitored by cell sorting showed 16% of the cells in the sub-G1 area, indicative of apoptotic cell death. DHA-supplemented cultures showed 35% cell death, whereas cosupplements with dEa reduced cell death to 12%, indicating cell rescue. Although the exact mechanism for this protection is not known, the nature of the polar head group and the degree of unsaturation may determine the ultimate resistance of nerve cells to oxidative stress.


Asunto(s)
Apoptosis/efectos de los fármacos , Etanolamina/farmacología , Oligodendroglía/citología , Estrés Oxidativo/fisiología , Animales , Línea Celular , Supervivencia Celular/efectos de los fármacos , Etanolamina/química , Ácidos Grasos Insaturados/química , Ácidos Grasos Insaturados/metabolismo , Glucosa 1-Deshidrogenasa , Glucosa Deshidrogenasas/metabolismo , Peróxido de Hidrógeno/farmacología , Peroxidación de Lípido/efectos de los fármacos , Oligodendroglía/enzimología , Oxidantes/farmacología , Ratas , Sustancias Reactivas al Ácido Tiobarbitúrico/metabolismo
20.
J Neurosci Res ; 56(5): 447-56, 1999 Jun 01.
Artículo en Inglés | MEDLINE | ID: mdl-10369212

RESUMEN

When deprived of serum, oligodendroglialike (OLN 93) cells grown on poly-L-lysine-coated culture dishes cease to proliferate after 3 days and morphologically extend many fibers resembling morphologically differentiated, immature oligodendrocytes. At this time no cell death is apparent unless serum deprivation is extended for a period longer than 1 week. After 3 days in serum-deprived medium, treatment of cells with 1 mM H2O2 for 30 min facilitates apoptotic cell death, even when serum is added during the recovery period. Both serum-deprived, differentiated cells, and proliferating cells, respond to H2O2 by an initial growth arrest followed by growth resumption after 48 hr. However proliferating cells show resistance to the apoptotic effect of H2O2. This is correlated with growth arrest in the S phase at different stages of DNA replication, as well as with different timing of induced p21Waf1 expression. Thus, cells grown in serum, express elevated p21Waf1 protein levels after 4 hr, whereas serum-deprived, differentiated cells, only after 24 hr. The mRNA levels of p21Waf1 follow a similar timed pattern. Hence p21Waf1 may protect OLN 93 cells against the genotoxic effect of H2O2. The data suggest an intimate relationship between G1-arrest, morphological differentiation, and H2O2-mediated apoptosis.


Asunto(s)
Apoptosis/fisiología , Peróxido de Hidrógeno/farmacología , Oligodendroglía/citología , Animales , Apoptosis/efectos de los fármacos , Ciclo Celular/efectos de los fármacos , Diferenciación Celular/efectos de los fármacos , Diferenciación Celular/fisiología , División Celular/efectos de los fármacos , División Celular/fisiología , Supervivencia Celular/efectos de los fármacos , Supervivencia Celular/fisiología , Células Clonales , Medio de Cultivo Libre de Suero , Inhibidor p21 de las Quinasas Dependientes de la Ciclina , Ciclinas/biosíntesis , Ciclinas/genética , Fragmentación del ADN , Cinética , Oligodendroglía/efectos de los fármacos , Oligodendroglía/fisiología , Polilisina , ARN Mensajero/genética , Ratas , Transcripción Genética/efectos de los fármacos
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA
...