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1.
Shinrigaku Kenkyu ; 72(3): 234-9, 2001 Aug.
Artículo en Japonés | MEDLINE | ID: mdl-11697278

RESUMEN

The authors proposed "mental image manipulation of expression" as processing strategy for faces, and investigated whether this strategy facilitates memory for faces or not. In the Experiment, four groups of subjects were assigned to a combination of a task (mental image manipulation of expression or distinctive feature scan) and a retention interval (short-term latency or long-term latency). Each task was followed by an unexpected yes-no recognition test in which identical pictures of the target faces or the same person's expression-changed faces were randomly presented with distractor faces. The mental image manipulation group was better than distinctive feature scan group in long-term storage. This result is considered as a long-term effect of imagery encoding and a configurational encoding by mental image manipulation.


Asunto(s)
Cara/fisiología , Expresión Facial , Maquiavelismo , Memoria/fisiología , Reconocimiento en Psicología/fisiología , Adolescente , Adulto , Femenino , Humanos , Masculino , Estimulación Luminosa
2.
Cancer ; 91(8): 1429-36, 2001 Apr 15.
Artículo en Inglés | MEDLINE | ID: mdl-11301389

RESUMEN

BACKGROUND: Endothelial PAS domain protein 1 (EPAS1) is a basic helix-loop-helix/PAS domain transcription factor that expressed most abundantly in highly vascularized organs. The authors examined the effect of transfection of EPAS1 cDNA on the endogenous expression of vascular endothelial growth factor (VEGF) in the 293 Tet-Off cell line and the possible involvement of EPAS1 in the angiogenesis of renal cell carcinoma (RCC). METHODS: Complete cDNA of EPAS1 was cloned and transfected to cells from the 293 Tet-Off fetal kidney cell line, in which the expression of EPAS1 can be inhibited by doxycycline. The subsequent changes in expression pattern of VEGF and transferrin receptor (TfR), a target gene of hypoxia-inducible factor 1alpha (HIF-1alpha), were examined by semiquantitative reverse transcription-polymerase chain reaction (RT-PCR) and enzyme-linked immunosorbent assay. In addition, expression of EPAS1, HIF-1alpha, and VEGF were analyzed by semiquantitative RT-PCR in five RCC cell lines and in 13 RCC tissue samples. In situ hybridization was performed on 7 of the 13 RCC tissue samples. RESULTS: Endogenous VEGF was increased significantly by the introduction of EPAS1 cDNA at both the mRNA level and the protein level. With the inhibition of EPAS1 by doxycycline treatment, the expression of VEGF was significantly decreased accordingly, whereas the expression of TfR was not affected. EPAS1 was detected in all of the RCC cell lines examined. In RCC tissue samples, EPAS1 mRNA and VEGF mRNA were increased significantly in tumor tissues compared with normal adjacent kidney tissues. In situ hybridization showed that EPAS1 and VEGF were coexpressed topographically in tumor tissues. CONCLUSIONS: These results suggest that endogenous VEGF can be up-regulated transcriptionally by EPAS1, and EPAS1 may be involved in the angiogenesis of RCC.


Asunto(s)
Carcinoma de Células Renales/fisiopatología , Factores de Crecimiento Endotelial/biosíntesis , Regulación Neoplásica de la Expresión Génica , Neoplasias Renales/fisiopatología , Linfocinas/biosíntesis , Neovascularización Patológica/fisiopatología , Transactivadores/farmacología , Antibacterianos/farmacología , Factores de Transcripción con Motivo Hélice-Asa-Hélice Básico , Carcinoma de Células Renales/genética , ADN Complementario/genética , Doxiciclina/farmacología , Humanos , Neoplasias Renales/genética , Reacción en Cadena de la Polimerasa de Transcriptasa Inversa , Transfección , Células Tumorales Cultivadas , Factor A de Crecimiento Endotelial Vascular , Factores de Crecimiento Endotelial Vascular
3.
Eur J Neurol ; 7(3): 337-40, 2000 May.
Artículo en Inglés | MEDLINE | ID: mdl-10886319

RESUMEN

Apraxia of lid opening (ALO) is a syndrome characterized by a non-paralytic inability to open the eyes at will in the absence of visible contraction of the orbicularis oculi muscle. Here we report that globus pallidus internus deep brain stimulation on the right side markedly alleviates ALO as well as gait freezing in a patient with Parkinson's disease.


Asunto(s)
Apraxia Ideomotora/terapia , Terapia por Estimulación Eléctrica , Enfermedades de los Párpados/terapia , Globo Pálido/fisiopatología , Enfermedad de Parkinson/complicaciones , Anciano , Apraxia Ideomotora/etiología , Apraxia Ideomotora/fisiopatología , Enfermedades de los Párpados/etiología , Enfermedades de los Párpados/fisiopatología , Femenino , Apraxia de la Marcha/etiología , Apraxia de la Marcha/fisiopatología , Apraxia de la Marcha/terapia , Humanos , Enfermedad de Parkinson/fisiopatología , Enfermedad de Parkinson/terapia
4.
Hepatogastroenterology ; 46(27): 1798-9, 1999.
Artículo en Inglés | MEDLINE | ID: mdl-10430348

RESUMEN

BACKGROUND/AIMS: To investigate the effect of acute hyperbaric oxygen therapy (HBOT) on post-operative sinusoidal endothelial cell (SEC) damage caused by activated neutrophils. METHODOLOGY: 12 non-cirrhotic patients (Group H), who underwent elective hepatectomy for liver cancer, were given 2 courses of HBOT: 2.0 atm with inhalation of 100% oxygen, for 60 min, at 3 hours and 24 hours after hepatectomy; they were then compared with the 12 patients (Group C) who had been treated to maintain normal hemodynamic values. RESULTS: In group H, peak levels of polymorphonuclear leukocyte elastase (PMNE) and thrombomodulin (TM) were clearly diminished and delayed compared to Group C. All subjects in Group C showed more than a 10% increase in CD18 12 hours after surgery; however, in Group H, the elevation of CD18 expression was clearly suppressed compared to Group C. No patient in Group H had post-operative hyperbilirubinemia or hepatic failure; however, 3 had post-operative hyperbilirubinemia and 1 had intraperitoneal infection in Group C. CONCLUSIONS: Our results provide direct evidence that HBOT, especially at 3 hours after hepatectomy, has favorable effects on the activation of neutrophiles decreasing SEC injury.


Asunto(s)
Hepatectomía , Oxigenoterapia Hiperbárica , Cirrosis Hepática/cirugía , Neoplasias Hepáticas/cirugía , Activación Neutrófila/inmunología , Complicaciones Posoperatorias/inmunología , Antígenos CD18/sangre , Endotelio Vascular/inmunología , Humanos , Elastasa de Leucocito/sangre , Hígado/irrigación sanguínea , Cuidados Posoperatorios , Pronóstico , Estudios Prospectivos , Trombomodulina/sangre
5.
J Androl ; 15(5): 479-83, 1994.
Artículo en Inglés | MEDLINE | ID: mdl-7860429

RESUMEN

Seminal emission from the ejaculatory duct (SEED) by direct electrical stimulation of the vas deferens was investigated in the dog, and the technique was applied to men. The stimulus parameters used were 2 msec, 10 Hz, and 8 V for dogs or 15-20 V for humans. In vitro studies using tetrodotoxin demonstrated that the major portion of the muscle contraction under the above stimulation was neurogenic. The stimulation of the pars epididymica, the middle vas, or the ampulla of the vas caused SEED in all dogs having intact hypogastric nerves (HNs) and receiving transection of bilateral HNs 1, 6, and 12 months before electrical stimulation. The dye instilled into the canine cauda epididymis was transported to the ampulla and emitted into the posterior urethra by electrical stimulation of the vas regardless of the site stimulated. The electrical stimulation of eight vasa deferentia (pars epididymica) of five prostatic carcinoma patients generated emission from the severed proximal end of all vasa examined at orchidectomy. All of the stimulations of 13 middle vasa of seven patients with emission loss caused SEED. The above results indicate that direct electrical stimulation of the canine and human vas deferens causes SEED regardless of the site stimulated or the absence of HNs, which are the major pathway of the efferent signal for SEED.


Asunto(s)
Eyaculación/fisiología , Terapia por Estimulación Eléctrica , Conducto Deferente , Animales , Perros , Humanos , Plexo Hipogástrico/fisiología , Carmin de Índigo , Masculino , Semen , Transmisión Sináptica/fisiología
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