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1.
Radiography (Lond) ; 28(3): 766-771, 2022 08.
Artigo em Inglês | MEDLINE | ID: mdl-35428572

RESUMO

INTRODUCTION: The purpose of this study was to demonstrate that dose reduction does not compromise image quality when combining high helical pitch (HP) and the ECG-Edit function during low HP retrospectively gated computed tomography angiography (CTA). METHODS: This study made use of a pulsating cardiac phantom (ALPHA 1 VTPC). The heart rate (HR) of the cardiac phantom was changed in five intervals, every 5 beats per minute (bpm), from 40 to 60 bpm. Evaluation of a range of HR was important because data loss might occur when combining a low HR and high HP. We performed retrospectively gated CTA scans five times using a low HP (0.16) and high HP (0.24), for each of the five HR intervals, using a 64-detector row CT scanner. The CT volume dose index (CTDIvol) was recorded from the CT console of each scan. For the images with data loss, data were repaired using the ECG-Edit function. We compared the CTDIvol, estimated cardiac phantom volume, and the visualization of the coronary ladder phantom between HP 0.16, with or without repaired HP 0.24, using the ECG-Edit function. RESULTS: Data loss occurred with a HR of 40 bpm and 45 bpm when using HP 0.24. The CTDIvol was reduced by approximately 33% with HP 0.24 when compared with HP 0.16. There were no significant differences in the mean cardiac motion phantom volume and visualization scores between HP 0.16 and with and without repaired HP 0.24 using the ECG-Edit function (p < 0.05). CONCLUSION: The ECG-Edit function is potential useful for repairing the lost data in patients with a low HR, and when combined with a high HP, it is possible to reduce the radiation dose by approximately 33%. IMPLICATIONS FOR PRACTICE: The ECG-Edit function and high HP may be a viable option in pediatric CTA studies.


Assuntos
Angiografia por Tomografia Computadorizada , Eletrocardiografia , Criança , Angiografia Coronária/métodos , Redução da Medicação , Eletrocardiografia/métodos , Humanos , Doses de Radiação , Estudos Retrospectivos
2.
Pediatr Surg Int ; 16(7): 533-5, 2000.
Artigo em Inglês | MEDLINE | ID: mdl-11057563

RESUMO

Balloon digits were found in two neonates with congenital constriction ring syndrome. The affected digits were the right long finger and right great toe. They were surgically treated at the age of 10 and 9 days, respectively. Morphologic improvement was dramatic after surgery. In cases with extensive enlargement, severe cyanosis, redness, and no subsidence of edema within several days after birth, early operative treatment may be necessary to maintain digit viability and prevent autoamputation due to circulatory embarrassment. It can also be helpful to prevent fibrosis of the subcutaneous tissue. Pathologic examination revealed marked proliferation of fibrous tissue and lymphatic vessels.


Assuntos
Dedos/anormalidades , Dedos/cirurgia , Deformidades Congênitas do Pé/cirurgia , Deformidades Congênitas da Mão/cirurgia , Dedos do Pé/anormalidades , Dedos do Pé/cirurgia , Constrição Patológica/congênito , Constrição Patológica/cirurgia , Feminino , Fibrose/congênito , Deformidades Congênitas do Pé/patologia , Deformidades Congênitas da Mão/patologia , Humanos , Recém-Nascido , Linfedema/congênito , Resultado do Tratamento
3.
Immunopharmacology ; 48(2): 129-35, 2000 Jul 20.
Artigo em Inglês | MEDLINE | ID: mdl-10936510

RESUMO

Santonin-related compounds (SRCs) were synthesized from the starting material L-alpha-santonin and tested for the biological activity on the expression of intercellular adhesion molecule-1 (ICAM-1) in response to IL-1 stimulation on human adenocarcinoma cells. One of the bromoketone derivatives termed SRC2 [11S-2 alpha-bromo-3-oxoeudesmanno-13,6 alpha-lactone] strongly inhibited the ICAM-1 expression at an IC(50) value of 5.9 microM, whereas L-alpha-santonin itself was totally inactive up to 100 microM. The blockage of ICAM-1 expression by SRC2 was not due to the direct inhibition of de novo RNA and protein synthesis. The nuclear translocation of NF-kappaB subunit p65 was markedly prevented by SRC2. Moreover, I kappa B alpha degradation upon IL-1 stimulation was strongly inhibited by SRC2. These observations suggest that SRC2 blocks the IL-1 signaling pathway upstream of I kappa B degradation.


Assuntos
Proteínas I-kappa B/antagonistas & inibidores , Molécula 1 de Adesão Intercelular/biossíntese , Interleucina-1/fisiologia , Santonina/farmacologia , Transdução de Sinais/efeitos dos fármacos , Transporte Biológico/efeitos dos fármacos , Núcleo Celular/efeitos dos fármacos , Núcleo Celular/metabolismo , Humanos , Proteínas I-kappa B/metabolismo , Molécula 1 de Adesão Intercelular/genética , Interleucina-1/antagonistas & inibidores , NF-kappa B/metabolismo , RNA/antagonistas & inibidores , RNA/biossíntese , Santonina/análogos & derivados , Transdução de Sinais/imunologia , Fator de Transcrição RelA , Células Tumorais Cultivadas
4.
Nephron ; 79(1): 80-90, 1998.
Artigo em Inglês | MEDLINE | ID: mdl-9609467

RESUMO

We have recently reported the presence of a novel perchloric acid soluble protein in rat liver (PSP1) that inhibits cell-free protein synthesis in a rabbit reticulocyte system. While studying the perchloric acid soluble proteins from different tissues of rats, we found that the kidney protein cross-reacted with antibody against the PSP1. In this investigation, we have purified a perchloric acid soluble protein from the rat kidney and studied its characterization and expression. The protein extracted from the postmitochondrial supernatant fraction with 5% perchloric acid was purified by ammonium sulfate fractionation and CM-Sephadex chromatography. By immunoscreening with the rabbit antisera against the PSP1, we detected a cDNA that contained an open reading frame of 411 bp, encoding a 137 amino-acid protein with a molecular mass of 14,149 daltons. The deduced amino acid sequence was completely identical with that of PSP1 from rat liver. The perchloric acid soluble protein from rat kidney (K-PSP1) also inhibited cell-free protein synthesis in the rabbit reticulocyte lysate system in a different manner than RNase A. Immunohistochemistry showed that the expression of K-PSP1 increased from fetal 17th day to postnatal 4th week, and it remained almost the same until the 7th week of postnatal age. Furthermore, the expression of K-PSP1 in the kidney of the nephrotic rat model was shown to be differentiation dependent. On the other hand, the expression of K-PSP1 in renal tumor cells was downregulated as compared with intact tissue. These results suggest that the expression of K-PSP1 is regulated in a differentiation-dependent manner in the kidney.


Assuntos
Diferenciação Celular/fisiologia , Proteínas de Choque Térmico/química , Rim/química , Proteínas/química , Ribonucleases , Sequência de Aminoácidos , Animais , Clonagem Molecular , Regulação da Expressão Gênica no Desenvolvimento/genética , Regulação Neoplásica da Expressão Gênica/genética , Imuno-Histoquímica , Neoplasias Renais/fisiopatologia , Masculino , Dados de Sequência Molecular , Proteínas de Neoplasias/análise , Percloratos/metabolismo , Inibidores da Síntese de Proteínas/química , RNA Mensageiro/metabolismo , Ratos , Ratos Wistar , Análise de Sequência de DNA , Solubilidade
5.
Biosci Biotechnol Biochem ; 59(11): 2064-7, 1995 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-8541643

RESUMO

Costunolide and dehydrocostus lactone were isolated from an extract of mokko (Saussurea lappa Clarke) as inhibitors of killing activity of cytotoxic T lymphocytes (CTL). Mokko lactone was also isolated as an inactive compound from the extract. The structure-activity relationship indicated that alpha-methylene-gamma-butyrolactone is required for the inhibitory effect. Costunolide markedly inhibited the granule exocytosis and the production of inositol phosphates in response to anti-CD3 monoclonal antibody (mAb) stimulation at a concentration that did not affect the binding of anti-CD3 mAb. Tyrosine phosphorylation induced by crosslinking of CD3 molecules was significantly inhibited by costunolide in a dose-dependent manner. These results suggest that costunolide inhibits the killing activity of CTL through preventing the increase in tyrosine phosphorylation in response to the crosslinking of T-cell receptors.


Assuntos
Citotoxicidade Imunológica/efeitos dos fármacos , Lactonas/farmacologia , Sesquiterpenos/farmacologia , Linfócitos T Citotóxicos/imunologia , 4-Butirolactona/análogos & derivados , 4-Butirolactona/farmacologia , Fosforilação , Linfócitos T Citotóxicos/metabolismo , Tirosina/metabolismo
6.
J Spinal Disord ; 8(5): 363-7, 1995 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-8563156

RESUMO

Paraplegia or paraparesis is uncommon in patients with neurofibromatous scoliosis. The main causes of spinal cord compression in neurofibromatosis are vertebral angulation, vertebral subluxation, and tumorous lesions around the spinal cord. We report a rare case of paraparesis due to spinal cord compression by a rib penetrating the spinal canal in a patient with neurofibromatous scoliosis. There was complete recovery after laminectomy and proximal resection of the compressing rib along with combined anterior and posterior spinal fusion.


Assuntos
Neurofibromatoses/complicações , Paraplegia/etiologia , Costelas/patologia , Escoliose/complicações , Canal Medular/patologia , Criança , Feminino , Humanos , Laminectomia , Neurofibromatoses/terapia , Escoliose/diagnóstico por imagem , Escoliose/terapia , Compressão da Medula Espinal/complicações , Tomografia Computadorizada por Raios X
7.
Am J Med Genet ; 51(3): 187-90, 1994 Jul 01.
Artigo em Inglês | MEDLINE | ID: mdl-8074142

RESUMO

We report on a boy born to a mother with pseudoachondroplasia and a father with osteogenesis imperfecta (Sillence type III). At birth, the boy was found to have osteogenesis imperfecta type III. Although clinical findings of pseudoachondroplasia were not manifested at the age of 8 months, roentgenographic findings showed characteristics of pseudoachondroplasia in addition to those of osteogenesis imperfecta. He died of respiratory distress at age 15 months.


Assuntos
Osteocondrodisplasias/genética , Acondroplasia/complicações , Adulto , Saúde da Família , Evolução Fatal , Feminino , Doenças Genéticas Inatas , Humanos , Recém-Nascido , Masculino , Osteogênese Imperfeita/complicações
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