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1.
J Acad Nutr Diet ; 114(3): 475-488.e24, 2014 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-24534371

RESUMO

Sustainability is the ability of a system to be maintained over the long term. Resilience is the ability of a system to withstand disturbances and continue to function in a sustainable manner. Issues of sustainability and resilience apply to all aspects of nutrition and dietetics practice, can be practiced at both the program and systems level, and are broader than any one specific practice setting or individual intervention. Given an increasing need to apply principles of sustainability and resilience to nutrition and dietetics practice, as well as growing interest among the public and by Registered Dietitian Nutritionists of health issues related to food and water systems, the Hunger and Environmental Nutrition Dietetic Practice Group, with guidance from the Academy of Nutrition and Dietetics Quality Management Committee, has developed the Standards of Professional Performance as a tool for Registered Dietitian Nutritionists working in sustainable, resilient, and healthy food and water systems to assess their current skill levels and to identify areas for further professional development in this emerging practice area. This Standards of Professional Performance document covers six standards of professional performance: quality in practice, competence and accountability, provision of services, application of research, communication and application of knowledge, and utilization and management of resources. Within each standard, specific indicators provide measurable action statements that illustrate how sustainable, resilient, and healthy food and water systems principles can be applied to practice. The indicators describe three skill levels (competent, proficient, and expert) for Registered Dietitian Nutritionists working in sustainable, resilient, and healthy food and water systems.


Assuntos
Competência Clínica/normas , Conservação dos Recursos Naturais , Dietética/normas , Alimentos , Nutricionistas/normas , Água , Academias e Institutos , Agricultura , Bem-Estar do Animal , Animais , Biodiversidade , Diversidade Cultural , Promoção da Saúde , Humanos , Abastecimento de Água
2.
Toxicol Pathol ; 32(5): 558-66, 2004.
Artigo em Inglês | MEDLINE | ID: mdl-15603540

RESUMO

Phentolamine is a reversible competitive alpha-adrenergic antagonist with similar affinities for alphal and alpha2 receptors. It has a long history of safe clinical use, and was developed as a potential therapy for male erectile dysfunction because of its capacity to increase the arteriolar blood flow to the corpora cavernosa. Phentolamine mesylate was administered to rats by oral gavage at daily doses of 10, 50, and 150 mg/kg for 24 months. A dose-related increase in mortality, ascribed to an exaggerated pharmacologic effect, was seen at high doses. Systemic exposure as measured by plasma drug concentration increased with dose and duration of dosing and slight drug accumulation occurred, particularly in high-dose males. In the treated groups, 10 males and 1 female were diagnosed with hibernomas, neoplasms of brown adipose tissue, which appeared in the thoracic cavity or retroperitoneal area as circumscribed, tan to reddish-brown lobulated masses. Histologically, the masses were well circumscribed with variably sized lobules defined by a rich capillary network and consisted of closely apposed oval to polygonal cells with large amounts of cytoplasm and a centrally located nucleus. The cytoplasm's appearance varied from multivacuolated to univacuolated to granular eosinophilic. In a few cases, neoplastic emboli were observed in capsular vessels. Ultrastructurally, the neoplastic cells contained numerous mitochondria with transverse parallel cristae that occupied over 60% of the cytoplasm and lipid droplets. This study documents the previously unreported development of hibernomas in rats treated with phentolamine mesylate.


Assuntos
Antagonistas Adrenérgicos alfa/toxicidade , Carcinógenos/toxicidade , Lipoma/induzido quimicamente , Fentolamina/toxicidade , Neoplasias Retroperitoneais/induzido quimicamente , Neoplasias Torácicas/induzido quimicamente , Administração Oral , Antagonistas Adrenérgicos alfa/administração & dosagem , Antagonistas Adrenérgicos alfa/sangue , Animais , Testes de Carcinogenicidade , Carcinógenos/administração & dosagem , Relação Dose-Resposta a Droga , Feminino , Lipoma/patologia , Masculino , Mitocôndrias/efeitos dos fármacos , Mitocôndrias/ultraestrutura , Fentolamina/administração & dosagem , Fentolamina/sangue , Ratos , Ratos Sprague-Dawley , Neoplasias Retroperitoneais/patologia , Neoplasias Torácicas/patologia
3.
Toxicol Pathol ; 32(2): 243-9, 2004.
Artigo em Inglês | MEDLINE | ID: mdl-15200163

RESUMO

Flutamide, a potent nonsteroidal antiandrogen, was administered orally to male beagle dogs for 2, 3, or 4 years at doses of 10, 20, or 40 mg/kg/day. At each study interval, the results of clinical pathology examinations, organ weight determinations, necropsy, and histopathologic examinations generally were similar and included atrophy of the prostate gland, testicular interstitial cell hyperplasia, and seminiferous tubular atrophy and degeneration. After 3 years of drug exposure, there were 3 dogs with testicular interstitial cell adenomas and a few dogs with 1 or more enlarged mammary gland nipples. Based upon the pharmacologic activity of flutamide, these findings were expected and considered the consequence of long-term blocking of testosterone receptors and an exaggerated compensatory response to increased secretion of luteinizing hormone. The findings of this study were consistent with other examples of dysregulated hormone stimulation of target tissues noted during the nonclinical safety assessment of flutamide. In consideration of the clinical indication of flutamide for advanced prostatic carcinoma and based upon reports of minimal flutamide-related adverse clinical responses, the findings of this study pose no concern for human risk assessment.


Assuntos
Antineoplásicos Hormonais/toxicidade , Flutamida/toxicidade , Testes de Toxicidade Crônica , Administração Oral , Animais , Antineoplásicos Hormonais/administração & dosagem , Atrofia/induzido quimicamente , Atrofia/patologia , Química Clínica , Citoplasma/efeitos dos fármacos , Citoplasma/ultraestrutura , Cães , Relação Dose-Resposta a Droga , Flutamida/administração & dosagem , Testes Hematológicos , Hepatócitos/efeitos dos fármacos , Hepatócitos/ultraestrutura , Masculino , Microscopia Eletrônica , Tamanho do Órgão/efeitos dos fármacos , Próstata/efeitos dos fármacos , Próstata/patologia
4.
Hum Gene Ther ; 13(14): 1687-96, 2002 Sep 20.
Artigo em Inglês | MEDLINE | ID: mdl-12396622

RESUMO

A field emission scanning electron microscopy (FESEM) method was developed to assess the stability of a recombinant adenovirus (rAd). This method was designed to simultaneously sort, count, and size the total number of rAd viral species observed within an image field. To test the method, a preparation of p53 transgene-expressing recombinant adenovirus (rAd/p53) was incubated at 37 degrees C and the viral particles were evaluated by number, structure, and degree of aggregation as a function of time. Transmission electron microscopy (TEM) was also used to obtain ultrastructural detail. In addition, the infectious activity of the incubated rAd/p53 samples was determined using flow cytometry. FESEM image-analysis revealed that incubation at 37 degrees C resulted in a time-dependent decrease in the total number of detectable single rAd/p53 virus particles and an increase in apparent aggregates composed of more than three adenovirus particles. There was also an observed decrease in both the diameter and perimeter of the single rAd/p53 viral particles. TEM further revealed the accumulation of damaged single particles with time at 37 degrees C. The results of this study demonstrate that FESEM, coupled with sophisticated image analysis, may be an important tool in quantifying the distribution of aggregated species and assessing the overall stability of rAd samples.


Assuntos
Adenovírus Humanos/ultraestrutura , Vírus Defeituosos/ultraestrutura , Vetores Genéticos/ultraestrutura , Microscopia Eletrônica de Varredura/métodos , Adenovírus Humanos/genética , Calibragem , Proteínas do Capsídeo/genética , Proteínas do Capsídeo/fisiologia , Vírus Defeituosos/genética , Citometria de Fluxo , Genes p53 , Processamento de Imagem Assistida por Computador , Microscopia Eletrônica , Coloração Negativa , Tamanho da Partícula , Temperatura , Vírion/ultraestrutura
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