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1.
J Neurosci ; 41(2): 354-365, 2021 01 13.
Artículo en Inglés | MEDLINE | ID: mdl-33219004

RESUMEN

Drug addiction is a chronic disorder characterized by compulsive drug seeking, and involves repetitive cycles of compulsive drug use, abstinence, and relapse. In both human and animal models of addiction, chronic food restriction increases rates of relapse. Our laboratory has reported a robust increase in drug seeking following a period of withdrawal in chronically food-restricted rats compared with sated controls. Recently, we reported that activation of the paraventricular nucleus of the thalamus (PVT) abolished heroin seeking in chronically food-restricted rats. However, the precise inputs and outputs of the PVT that mediate this effect remain elusive. The goal of the current study was to determine the role of corticothalamic and thalamo-accumbens projections in the augmentation of heroin seeking induced by chronic food restriction. Male Long-Evans rats were trained to self-administer heroin for 10 d. Next, rats were removed from the self-administration chambers and were subjected to a 14 d withdrawal period while sated (unlimited access to food) or mildly food-restricted (FDR). On day 14, rats were returned to the self-administration context for a 3 h heroin-seeking test under extinction conditions during which corticothalamic and thalamo-accumbens neural activity was altered using chemogenetics. Surprisingly, chemogenetic activation or inhibition of corticothalamic projections did not alter heroin-seeking behavior. Chemogenetic activation of thalamo-accumbens shell, but not core, projectors attenuated heroin seeking in FDR rats. The results indicate an important role for the PVT to nucleus accumbens shell projections in the augmentation of heroin seeking induced by chronic food restriction.SIGNIFICANCE STATEMENT Relapse to heroin use is one of the major obstacles in the treatment of opiate addiction. Triggers for relapse are modulated by environmental challenges such as caloric restriction. Elucidating the brain mechanisms that underlie relapse is critical for evidence-based treatment development. Here we demonstrate a critical role for the input from the paraventricular thalamus (PVT), a hub for cortical, sensory, and limbic information, to the nucleus accumbens shell (an area known to be important for reward and motivation) in the augmentation of heroin seeking in food-restricted rats. Our findings highlight a previously unknown role for the PVT in heroin seeking following a period of abstinence.


Asunto(s)
Corteza Cerebral/fisiología , Comportamiento de Búsqueda de Drogas/efectos de los fármacos , Privación de Alimentos , Dependencia de Heroína/psicología , Vías Nerviosas/fisiología , Núcleo Accumbens/fisiología , Tálamo/fisiología , Animales , Conducta Adictiva/fisiopatología , Clozapina/farmacología , Heroína/farmacología , Masculino , Actividad Motora/efectos de los fármacos , Narcóticos/farmacología , Ratas , Ratas Long-Evans , Recurrencia , Autoadministración , Síndrome de Abstinencia a Sustancias/psicología
2.
Clin Chim Acta ; 365(1-2): 188-93, 2006 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-16183048

RESUMEN

BACKGROUND: Analbuminemia is a rare autosomal recessive disorder manifested by the absence, or severe reduction, of circulating serum albumin. Here we report three new cases of hereditary analbuminemia, fortuitously detected in three Slovak Romany children, members of the same family, and define the molecular defect that causes the analbuminemic trait. METHODS: Total DNA, extracted from peripheral blood samples from six members of the family, was PCR-amplified using oligonucleotide primers designed to amplify the 14 exons of the human albumin gene and the flanking intron regions. The products were screened for mutations by single-strand conformation polymorphism (SSCP) and heteroduplex analyses (HA). HA allowed the identification of the abnormal fragment, which was then sequenced. RESULTS: In the 3 patients the analbuminemic trait was caused by the same mutation, an AT deletion at nucleotides 2430-31, the 91 th and 92 th bases of exon 3. This defect, previously identified as Kayseri mutation, produces a frameshift leading to a premature stop, two codons downstream. The predicted translation product would consist of 54 amino acid residues. The parents were found to be heterozygous for the mutation. CONCLUSIONS: Our results confirm that the combination of SSCP and HA represents a powerful tool to study the molecular defects causing analbuminemia in humans.


Asunto(s)
Análisis Mutacional de ADN , Albúmina Sérica/análisis , Secuencia de Aminoácidos , Secuencia de Bases , Preescolar , Cartilla de ADN , Electroforesis en Gel Bidimensional , Humanos , Masculino , Datos de Secuencia Molecular , Ácidos Nucleicos Heterodúplex , Polimorfismo Conformacional Retorcido-Simple , Albúmina Sérica/química , Albúmina Sérica/genética , Eslovaquia
3.
Clin Biochem ; 36(8): 597-605, 2003 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-14636873

RESUMEN

OBJECTIVES: To purify and structurally identify two albumin variants found in the Canadian population of native Amerindian origin. To assess the ability of variant albumins to bind lauric acid and L-thyroxine. METHODS: The structural characterization of the alloalbumins was performed by conventional protein chemistry methods and by mass spectrometric analysis. Lauric acid and L-thyroxine affinities to variant albumins were assessed by kinetic dialysis and equilibrium dialysis techniques, respectively. RESULTS: The sequence investigations proved the two variants to be albumin Naskapi [372Lys --> Glu] and albumin Vancouver [501Glu --> Lys], respectively. Among the carriers of albumin Naskapi, we found a rare case of homozygosity. Furthermore, this is the first reported case of the 501Glu-->Lys mutation in the native North American population. Scatchard plot analysis revealed that the association constants for lauric acid and L-thyroxine to the two variants were indistinguishable from the endogenous form of albumin. CONCLUSION: We show that albumin variants Vancouver and Naskapi have normal fatty acid and L-thyroxine binding capabilities. These findings support the assumption that bisalbuminemias associated with these albumin variants are benign conditions.


Asunto(s)
Ácidos Grasos/metabolismo , Variación Genética/genética , Albúmina Sérica/química , Albúmina Sérica/genética , Albúmina Sérica/metabolismo , Tiroxina/metabolismo , Colombia Británica , Electroforesis en Gel de Agar , Humanos , Indígenas Norteamericanos/genética , Mutación , Unión Proteica/fisiología , Saskatchewan , Albúmina Sérica Humana
4.
Hum Mol Genet ; 14(6): 859-71, 2005 Mar 15.
Artículo en Inglés | MEDLINE | ID: mdl-15703192

RESUMEN

Mutations in the diastrophic dysplasia sulfate transporter (DTDST or SLC26A2) cause a family of recessively inherited chondrodysplasias including, in order of decreasing severity, achondrogenesis 1B, atelosteogenesis 2, diastrophic dysplasia (DTD) and recessive multiple epiphyseal dysplasia. The gene encodes a widely distributed sulfate/chloride antiporter of the cell membrane whose function is crucial for the uptake of inorganic sulfate, which is needed for proteoglycan sulfation. To provide new insights in the pathogenetic mechanisms leading to skeletal and connective tissue dysplasia and to obtain an in vivo model for therapeutic approaches to DTD, we generated a Dtdst knock-in mouse with a partial loss of function of the sulfate transporter. In addition, the intronic neomycine cassette in the mutant allele contributed to the hypomorphic phenotype by inducing abnormal splicing. Homozygous mutant mice were characterized by growth retardation, skeletal dysplasia and joint contractures, thereby recapitulating essential aspects of the DTD phenotype in man. The skeletal phenotype included reduced toluidine blue staining of cartilage, chondrocytes of irregular size, delay in the formation of the secondary ossification center and osteoporosis of long bones. Impaired sulfate uptake was demonstrated in chondrocytes, osteoblasts and fibroblasts. In spite of the generalized nature of the sulfate uptake defect, significant proteoglycan undersulfation was detected only in cartilage. Chondrocyte proliferation and apoptosis studies suggested that reduced proliferation and/or lack of terminal chondrocyte differentiation might contribute to reduced bone growth. The similarity with human DTD makes this mouse strain a useful model to explore pathogenetic and therapeutic aspects of DTDST-related disorders.


Asunto(s)
Proteínas Portadoras/genética , Osteocondrodisplasias/genética , Osteocondrodisplasias/patología , Fenotipo , Animales , Proteínas de Transporte de Anión , Proteínas Portadoras/metabolismo , Modelos Animales de Enfermedad , Humanos , Proteínas de Transporte de Membrana , Ratones , Ratones Transgénicos , Osteocondrodisplasias/metabolismo , Transportadores de Sulfato
5.
J Biol Chem ; 280(33): 29812-9, 2005 Aug 19.
Artículo en Inglés | MEDLINE | ID: mdl-15972819

RESUMEN

Insulin-like growth factor (IGF)-binding protein-1 (IGFBP-1) regulates the activity of the insulin-like growth factors in early pregnancy and is, thus, thought to play a key role at the fetal-maternal interface. The C-terminal domain of IGFBP-1 and three isoforms of the intact protein were isolated from human amniotic fluid, and sequencing of the four N-terminal polypeptide chains showed them to be highly pure. The addition of both intact IGFBP-1 and its C-terminal fragment to cultured fibroblasts has a similar stimulating effect on cell migration, and therefore, the domain has a biological activity on its own. The three-dimensional structure of the C-terminal domain was determined by x-ray crystallography to 1.8 Angstroms resolution. The fragment folds as a thyroglobulin type I domain and was found to bind the Fe(2+) ion in the crystals through the only histidine residue present in the polypeptide chain. Iron (II) decreases the binding of intact IGFBP-1 and the C-terminal domain to IGF-II, suggesting that the metal binding site is close to or part of the surface of interaction of the two molecules.


Asunto(s)
Líquido Amniótico/química , Proteína 1 de Unión a Factor de Crecimiento Similar a la Insulina/química , Secuencia de Aminoácidos , Movimiento Celular , Cristalografía por Rayos X , Humanos , Hierro/metabolismo , Datos de Secuencia Molecular , Pliegue de Proteína , Estructura Secundaria de Proteína , Estructura Terciaria de Proteína
6.
J Biol Chem ; 279(49): 51033-41, 2004 Dec 03.
Artículo en Inglés | MEDLINE | ID: mdl-15452109

RESUMEN

Alpha-1-microglobulin carries a set of covalently linked chromophores that give it a peculiar yellow-brown color, fluorescence properties, and both charge and size heterogeneity. In this report it is shown that these features are due to the adducts with the tryptophan metabolite, 3-hydroxykynurenine, and its autoxidation products and that the modification is more pronounced in the protein isolated from urine of hemodialyzed patients. The light yellow amniotic fluid alpha-1-microglobulin acquires the optical properties and charge heterogeneity of the urinary counterpart following incubation with kynurenines. The colored amino acid adducts of urinary and amniotic fluid alpha-1-microglobulins were separated by chromatography after acid hydrolysis and analyzed by mass spectrometry. Human serum albumin samples, native and treated with 3-hydroxykynurenine in the presence of oxygen, were used as a control. The retention times and mass fragmentation products were compared, and a lysyl adduct with hydroxantommathin was identified in the urinary alpha-1-microglobulin and in the modified albumin samples. The more extensive modification of the urinary protein appears to be correlated with uremia, a condition in which the catabolism of tryptophan via the kynurenine pathway is increased, and the consequent rise in the concentration of its derivatives is accompanied by the oxidative processes due to the hemodialysis treatment. The oxidative derivatives of 3-hydroxykynurenine, which are known to act as protein cross-linking agents, are the likely cause of the propensity of urinary alpha-1-microglobulin to form dimers and oligomers. This process, as well as the redox properties of these metabolites, may contribute to the toxic effects of the kynurenine species.


Asunto(s)
alfa-Globulinas/química , Quinurenina/análogos & derivados , Quinurenina/química , alfa-Globulinas/metabolismo , alfa-Globulinas/orina , Líquido Amniótico/metabolismo , Proteínas Portadoras/química , Cromatografía Líquida de Alta Presión , Aductos de ADN , Dimerización , Electroforesis en Gel de Poliacrilamida , Humanos , Concentración de Iones de Hidrógeno , Hidrólisis , Focalización Isoeléctrica , Lipocalina 1 , Espectrometría de Masas , Modelos Químicos , Oxidación-Reducción , Oxígeno/química , Oxígeno/metabolismo , Unión Proteica , Espectrometría de Fluorescencia , Espectrometría de Masa por Ionización de Electrospray , Espectrofotometría , Factores de Tiempo , Triptófano/química , Rayos Ultravioleta
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