9 research outputs found
Pigmentos lipossolúveis e hidrossolúveis em plantas de salvínia sob toxicidade por cromo
Devido à intensa utilização industrial, o cromo é considerado um importante poluente ambiental. O presente trabalho objetivou determinar os teores de pigmentos hidro e lipossolúveis em plantas de salvínia expostas a concentrações crescentes de Cr, visando estabelecer parâmetros bioquímicos para utilização dessa macrófita em programas de biomonitoramento e/ou fitorremediação da poluição causada por esse poluente metálico em ambientes aquáticos. As plantas foram submetidas a concentrações crescentes de Cr e avaliadas após quatro, seis e dez dias de tratamento. Os resultados dos ensaios permitiram concluir que plantas de salvínia sob condições de estresse por Cr apresentam reduções nas concentrações das clorofilas a, b e total e, em contraste, aumentos nas concentrações de antocianinas totais. Embora a concentração de carotenoides totais não tenha sido alterada em resposta ao Cr, as variações nas concentrações dos demais pigmentos lipossolúveis e dos pigmentos hidrossolúveis observadas nas folhas das plantas de salvínia podem ser utilizadas como parâmetros bioquímicos de biomonitoramento da poluição causada por esse elemento metálico em ambientes aquáticos.Due to widespread industrial use, chromium is considered a serious environmental pollutant. This study aimed to determine the content of hydrosoluble and liposoluble pigments in salvinia plants exposed to increasing concentrations of Cr, to establish biochemical parameters for the use of macrophyta in pollution bio-monitoring programs and/or phyto-remediation in aquatic environments by this pollutant metal. The plants were exposed to increasing concentrations of Cr and evaluated after four, six, and ten days of treatment. The test results showed that salvinia plants under stress conditions for Cr exhibit decreases in the concentrations of chlorophylls a, b, and total, and, in contrast, increases in anthocyanin concentrations. Although the concentration of carotenoids has not been altered in response to Cr, the variations in the concentrations of other liposoluble and hydrosoluble pigments found in salvinia plant leaves can be used as biochemical parameters for biomonitoring of pollution caused by this metallic element in aquatic environments
Ligamento suspensório da articulação metacarpo/metatarso falangianas nos eqüinos: aspectos evolutivos, anatômicos, histofisiológicos e das afecções
Isolated abdominal fat tissue inflammation and necrosis in a cat
This report describes a rare clinical case of a 4.5-month-old, female domestic shorthair, cat with isolated abdominal fat tissue inflammation and necrosis, resembling human omental panniculitis. Its possible relationship with pancreatitis or bile induced chemical peritonitis is also discussed. The overall clinical course was considered benign. Initial clinical signs were vomiting and anorexia, presumably due to inflammation, followed by mass development. It was speculated that, eventually, the kitten was vomiting because of mechanical pressure from the mass, and that this pressure subsided as the kitten grew. The mass was surgically resected and no relapse was evident during the next 4 years. (c) 2007 ESFM and AAFP. Published by Elsevier Ltd. All rights reserved
Influence of hilar deposition in the evaluation of the alveolar epithelial permeability on 99mTc-DTPA aerosol inhaled scintigraphy
Neuromuscular disease genetics in under-represented populations: increasing data diversity
Neuromuscular diseases (NMDs) affect similar to 15 million people globally. In high income settings DNA-based diagnosis has transformed care pathways and led to gene-specific therapies. However, most affected families are in low-to-middle income countries (LMICs) with limited access to DNA-based diagnosis. Most (86%) published genetic data is derived from European ancestry. This marked genetic data inequality hampers understanding of genetic diversity and hinders accurate genetic diagnosis in all income settings. We developed a cloud-based transcontinental partnership to build diverse, deeply-phenotyped and genetically characterized cohorts to improve genetic architecture knowledge, and potentially advance diagnosis and clinical management.We connected 18 centres in Brazil, India, South Africa, Turkey, Zambia, Netherlands and the UK. We co-developed a cloud-based data solution and trained 17 international neurology fellows in clinical genomic data interpretation. Single gene and whole exome data were analysed via a bespoke bioinformatics pipeline and reviewed alongside clinical and phenotypic data in global webinars to inform genetic outcome decisions.We recruited 6001 participants in the first 43 months. Initial genetic analyses 'solved' or 'possibly solved' similar to 56% probands overall. In-depth genetic data review of the four commonest clinical categories (limb girdle muscular dystrophy, inherited peripheral neuropathies, congenital myopathy/muscular dystrophies and Duchenne/Becker muscular dystrophy) delivered a similar to 59% 'solved' and similar to 13% 'possibly solved' outcome. Almost 29% of disease causing variants were novel, increasing diverse pathogenic variant knowledge. Unsolved participants represent a new discovery cohort. The dataset provides a large resource from under-represented populations for genetic and translational research.In conclusion, we established a remote transcontinental partnership to assess genetic architecture of NMDs across diverse populations. It supported DNA-based diagnosis, potentially enabling genetic counselling, care pathways and eligibility for gene-specific trials. Similar virtual partnerships could be adopted by other areas of global genomic neurological practice to reduce genetic data inequality and benefit patients globally.Wilson et al. present the findings of an international partnership established to study genetic causes of neuromuscular diseases in under-represented diverse populations from 12 low-middle income sites. A genetic cause was identified in similar to 55% of cases and similar to 30% of variants were novel, improving understanding of neuromuscular disease genetics.Functional Genomics of Muscle, Nerve and Brain Disorder