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1.
Neuroscience ; 319: 206-20, 2016 Apr 05.
Artículo en Inglés | MEDLINE | ID: mdl-26777891

RESUMEN

Exposure to blast overpressure (BOP) is associated with behavioral, cognitive, and neuroimaging abnormalities. We investigated the dynamic responses of cortical vasculature and its relation to microglia/macrophage activation in mice using intravital two-photon microscopy following mild blast exposure. We found that blast caused vascular dysfunction evidenced by microdomains of aberrant vascular permeability. Microglial/macrophage activation was specifically associated with these restricted microdomains, as evidenced by rapid microglial process retraction, increased ameboid morphology, and escape of blood-borne Q-dot tracers that were internalized in microglial/macrophage cell bodies and phagosome-like compartments. Microdomains of cortical vascular disruption and microglial/macrophage activation were also associated with aberrant tight junction morphology that was more prominent after repetitive (3×) blast exposure. Repetitive, but not single, BOPs also caused TNFα elevation two weeks post-blast. In addition, following a single BOP we found that aberrantly phosphorylated tau rapidly accumulated in perivascular domains, but cleared within four hours, suggesting it was removed from the perivascular area, degraded, and/or dephosphorylated. Taken together these findings argue that mild blast exposure causes an evolving CNS insult that is initiated by discrete disturbances of vascular function, thereby setting the stage for more protracted and more widespread neuroinflammatory responses.


Asunto(s)
Traumatismos por Explosión/patología , Lesiones Encefálicas/patología , Macrófagos/patología , Microglía/patología , Animales , Barrera Hematoencefálica/patología , Western Blotting , Encéfalo/irrigación sanguínea , Encéfalo/patología , Modelos Animales de Enfermedad , Técnica del Anticuerpo Fluorescente , Inmunohistoquímica , Microscopía Intravital , Masculino , Ratones , Ratones Endogámicos C57BL , Microvasos/patología
2.
Mol Endocrinol ; 15(3): 398-410, 2001 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-11222741

RESUMEN

Separate genes encode thyroid hormone receptor subtypes TRalpha (NR1A1) and TRbeta (NR1A2). Products from each of these contribute to hormone action, but the subtypes differ in tissue distribution and physiological response. Compounds that discriminate between these subtypes in vivo may be useful in treating important medical problems such as obesity and hypercholesterolemia. We previously determined the crystal structure of the rat (r) TRalpha ligand-binding domain (LBD). In the present study, we determined the crystal structure of the rTRalpha LBD in a complex with an additional ligand, Triac (3,5, 3'-triiodothyroacetic acid), and two crystal structures of the human (h) TRbeta receptor LBD in a complex with either Triac or a TRbeta-selective compound, GC-1 [3,5-dimethyl-4-(4'-hydroy-3'-isopropylbenzyl)-phenoxy acetic acid]. The rTRalpha and hTRbeta LBDs show close structural similarity. However, the hTRbeta structures extend into the DNA-binding domain and allow definition of a structural "hinge" region of only three amino acids. The two TR subtypes differ in the loop between helices 1 and 3, which could affect both ligand recognition and the effects of ligand in binding coactivators and corepressors. The two subtypes also differ in a single amino acid residue in the hormone-binding pocket, Asn (TRbeta) for Ser (TRalpha). Studies here with TRs in which the subtype-specific residue is exchanged suggest that most of the selectivity in binding derives from this amino acid difference. The flexibility of the polar region in the TRbeta receptor, combined with differential recognition of the chemical group at the 1-carbon position, seems to stabilize the complex with GC-1 and contribute to its beta-selectivity. These results suggest a strategy for development of subtype-specific compounds involving modifications of the ligand at the 1-position.


Asunto(s)
Receptores de Hormona Tiroidea/química , Receptores de Hormona Tiroidea/metabolismo , Triyodotironina/análogos & derivados , Acetatos/química , Acetatos/metabolismo , Secuencia de Aminoácidos , Asparagina , Sitios de Unión , Cristalografía por Rayos X , Humanos , Datos de Secuencia Molecular , Mutación , Fenoles/química , Fenoles/metabolismo , Conformación Proteica , Receptores de Hormona Tiroidea/genética , Homología de Secuencia de Aminoácido , Hormonas Tiroideas/metabolismo , Triyodotironina/química , Triyodotironina/metabolismo
3.
Med Anthropol ; 17(1): 23-38, 1996 May.
Artículo en Inglés | MEDLINE | ID: mdl-8757711

RESUMEN

In the indigenous Mexican village of Hueyapan, there is a clear contrast between the supernatural beliefs curers use to explain illness and the naturalistic assumptions made by this community's bonesetters. In addition to employing different conceptual models, the two types of healers differ with respect to their manner of recruitment, training, types of illnesses treated, social status, and gender. These differences add up to a seeming enigma: in a community where men largely control political, economic, and religious affairs, the higher status role of curer is undertaken most frequently by women and the lower status specialty of bonesetter by men. Hueyapan's health care system becomes less problematical, however, when it is recognized that recruitment to the bonesetter and curer roles is shaped by pragmatic considerations of role continuity and compatibility independent of the social status of these two occupations.


Asunto(s)
Fracturas Óseas/terapia , Luxaciones Articulares/terapia , Medicina Tradicional , Curación Mental , Rol del Médico , Femenino , Fracturas Óseas/diagnóstico , Fracturas Óseas/etiología , Conocimientos, Actitudes y Práctica en Salud , Humanos , Luxaciones Articulares/diagnóstico , Luxaciones Articulares/etiología , Masculino , México , Selección de Personal , Factores Sexuales , Clase Social
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