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Métodos Terapéuticos y Terapias MTCI
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1.
J Surg Res ; 235: 440-446, 2019 03.
Artículo en Inglés | MEDLINE | ID: mdl-30691827

RESUMEN

BACKGROUND: Surgery, steroids, and/or observations alone have been proposed for patients with nonlactational mastitis (NLM), but most of these studies were retrospective. The optimal treatment for these patients remains unclear. This prospective, single-arm, proof-of-concept trial aimed to evaluate the feasibility and safety of ductal lavage as a novel treatment for patients with NLM. METHODS: Eligible patients with NLM received an intraductal infusion of corticosteroids and antimicrobial agents and returned the next day for a breast massage. This cycle was repeated for 2 wk, and we followed up these patients for 1 y. Patients did not receive surgery or steroids after ductal lavage. The primary endpoint was the time to complete response (CR). RESULTS: This trial included 32 patients with a median (range) age of 32 (20-53). Skin erythema and tenderness were the major symptoms. The median (range) visual analog score was 5 (0-9). There were 21 (65.6%), 4 (12.5%), and 7 (21.9%) patients diagnosed as idiopathic granulomatous mastitis, periductal mastitis, and unspecific NLM, respectively. During the ductal lavage, the median (range) number of cannulated ducts at first attempt was 5 (3-8). Ductal lavage significantly reduced the visual analog score and mastitis score (M-score) (P < 0.01). Within a median follow-up of 15.6 mo, 93.8% (30/32) of patients achieved CR. The median (range) time to CR was 6 (0.5-21) mo. Three patients (10.0%) relapsed. No adverse events associated with ductal lavage were observed. CONCLUSIONS: Ductal lavage for patients with NLM is feasible and safe, and a definitive randomized controlled trial for further investigation is warranted. TRIAL REGISTRATION: ClinicalTrials.gov, NCT02794688.


Asunto(s)
Mastitis/terapia , Irrigación Terapéutica/métodos , Adulto , Femenino , Humanos , Masaje , Mastitis/sangre , Persona de Mediana Edad , Prueba de Estudio Conceptual , Estudios Prospectivos , Adulto Joven
2.
Anim Sci J ; 85(4): 411-9, 2014 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-24450936

RESUMEN

This study was conducted to estimate different levels of protein supplementary diet on gene expressions related to intramuscular deposition in early-weaned yaks. Results showed that supplementary dietary protein significantly increased final weight, average daily gain (ADG), intramuscular fat (IMF), serum free fatty acid (FFA), total triglycerides, total cholesterol (Ch), low-density lipoprotein cholesterol (LDL) and high-density lipoprotein cholesterol (HDL) content. There was a quadratic response of ADG, IMF, FFA, Ch, HDL and LDL to dietary crude protein (CP) level. Lipoprotein lipase (LPL), fatty acid synthase (FAS) and acetyl-CoA carboxylase (ACC) enzyme activities were significantly increased by supplementary dietary CP, while hormone-sensitive lipase (HSL) and carnitine palmitoyltransferase-1 (CPT-1) activities were significantly decreased. LPL, ACC and FAS enzyme activities showed quadratic increase as dietary CP increased. Peroxisome proliferator-activated receptor γ (PPARγ), LPL, FAS, sterol regulatory element binding protein 1 (SREBP-1), ACC, stearoyl-CoA desaturase (SCD) and heart fatty-acid binding protein (H-FABP) gene expression were significantly increased by supplementary dietary CP, while HSL and CPT-1 gene expression were significantly decreased. PPARγ, LPL, SREBP-1, ACC and H-FABP gene expression showed quadratic increase as dietary CP increased. These results indicated that supplementary dietary protein increased IMF accumulation mainly to increased intramuscular lipogenic gene expression and decreased lipolytic gene expression.


Asunto(s)
Tejido Adiposo/metabolismo , Alimentación Animal , Fenómenos Fisiológicos Nutricionales de los Animales/genética , Bovinos/genética , Bovinos/metabolismo , Proteínas en la Dieta/administración & dosificación , Suplementos Dietéticos , Regulación del Desarrollo de la Expresión Génica/genética , Expresión Génica , Metabolismo de los Lípidos/genética , Lipogénesis/genética , Músculos/metabolismo , Acetil-CoA Carboxilasa/genética , Acetil-CoA Carboxilasa/metabolismo , Fenómenos Fisiológicos Nutricionales de los Animales/fisiología , Animales , Ácido Graso Sintasas/genética , Ácido Graso Sintasas/metabolismo , Lipólisis/genética , Lipoproteína Lipasa/genética , Lipoproteína Lipasa/metabolismo , PPAR gamma/genética , PPAR gamma/metabolismo , Proteína 1 de Unión a los Elementos Reguladores de Esteroles/genética , Proteína 1 de Unión a los Elementos Reguladores de Esteroles/metabolismo
3.
Nucleic Acids Res ; 33(2): e17, 2005 Jan 31.
Artículo en Inglés | MEDLINE | ID: mdl-15684409

RESUMEN

MicroRNAs (miRNAs) play important regulatory roles in animals and plants by targeting mRNAs for cleavage or translational repression. They have diverse expression patterns and might regulate various developmental and physiological processes. Profiling miRNA expression is very helpful for studying biological functions of miRNAs. We report a novel miRNA profiling microarray, in which miRNAs were directly labeled at the 3' terminus with biotin and hybridized with complementary oligo-DNA probes immobilized on glass slides, and subsequently detected by measuring fluorescence of quantum dots labeled with streptavidin bound to miRNAs through streptavidin-biotin interaction. The detection limit of this microarray for miRNA was approximately 0.4 fmol, and the detection dynamic range spanned about 2 orders of magnitude. We made a model microarray to profile 11 miRNAs from leaf and root of rice (Oryza sativa L. ssp. indica) seedlings. The analysis results of the miRNAs had a good reproducibility and were consistent with the northern blot result. To avoid using high-cost detection equipment, colorimetric detection, a method based on nanogold probe coupled with silver enhancement, was also successfully introduced into miRNA profiling microarray detection.


Asunto(s)
Perfilación de la Expresión Génica/métodos , Oro/química , MicroARNs/genética , Sondas Moleculares/química , Análisis de Secuencia por Matrices de Oligonucleótidos/métodos , Biotinilación , Colorimetría , MicroARNs/biosíntesis , MicroARNs/química , Nanoestructuras , Oryza/genética , Puntos Cuánticos , ARN de Planta/biosíntesis , ARN de Planta/química , ARN de Planta/genética , Plata/química
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