Desempenho motor de idosos do Nordeste brasileiro: diferenças entre idade e sexo

O objetivo deste estudo foi identificar o desempenho motor, de acordo com o sexo e o grupo etário, em idosos residentes em comunidade do Nordeste brasileiro. Trata-se de estudo transversal que analisou dados de 316 idosos de uma pesquisa epidemiológica de base domiciliar e populacional realizada em janeiro de 2011. Participaram do estudo 173 mulheres (54,7%) e 143 homens com idade média de 74,2 (± 9,8 anos). As mulheres apresentaram maior declínio funcional com o avanço da idade e mais limitação funcional em testes de força/resistência de membros inferiores e locomoção. Em ambos os sexos, a prevalência de limitação funcional foi mais elevada nos grupos etários de 70-79 anos e > 80 anos, com as mulheres apresentando mais limitação a partir dos 70 anos e os homens, a partir dos 80 anos. Os dados desta pesquisa podem subsidiar o planejamento de medidas para prevenção, manutenção ou melhora da limitação funcional em idosos, proporcionando maiores cuidados integrados.

Motor Vehicle Accident Fatalities for the Week Ending, July 14, 2006

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CO-EXPRESSION OF GCDH AND OAT1 IN NEURONS AND PROXIMAL TUBULE CELLS

Tissue-specific expression studies of Glutaryl-CoA dehydrogenase (Gcdh) in adult rats revealed expression in the whole rat brain, almost exclusively in neurons, and surprisingly high expression in the juxtamedullar cortex of the kidney. The organic anion transporter 1 (OAT1) mediates basolateral uptake of glutarate derivatives from proximal tubule cells and contributes to their renal clearance. In brain, OAT1 is expressed at the choroid plexus, in neurons of cortex and hippocampus. We hypothesized that Gcdh and Oat1 are co-expressed in the same cells in kidney and brain and analyzed their mRNA expression by in situ hybridization on cryosections of adult rat brain, kidney and liver. In brain, Gcdh and Oat1 were found co-expressed in most neurons. Only the Purkinje neurons of the cerebellum were found to be Oat1 negative. In the kidney Gcdh and Oat1 are widely co-expressed with a specific high expression in proximal tubule cells. In conclusion there seems to be a functional coupling of Gcdh and Oat1 on a renal and neuronal level. Further studies are ongoing to confirm these findings in human tissues.

Motor Vehicle Accident Fatalities for the Week Ending, July 28, 2006

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Motor Vehicle Accident Fatalities for the Week Ending, July 21, 2006

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Motor Vehicle Accident Fatalities for the Week Ending, August 4, 2006

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Selective toxicity of the general anesthetic propofol for GABAergic neurons in rat brain cell cultures.

The intravenous, short-acting general anesthetic propofol was applied to three-dimensional (aggregating) cell cultures of fetal rat telencephalon. Both the clinically used formulation (Disoprivan, ICI Pharmaceuticals, Cheshire, England) and the pure form (2,6-diisopropylphenol) were tested at two different periods of brain development: immature brain cell cultures prior to synaptogenesis and at the time of intense synapses and myelin formation. At both time periods and for clinically relevant concentrations and time of exposure (i.e., concentrations > or = 2.0 micrograms/ml for 8 hr), propofol caused a significant decrease of glutamic acid decarboxylase activity. This effect persisted after removal of the drug, suggesting irreversible structural changes in GABAergic neurons. The gamma-aminobutyric acid type A (GABAA) blocking agents bicuculline and picrotoxin partially attenuated the neurotoxic effect of propofol in cultures treated at the more mature phase of development. This protective effect was not observed in the immature brain cells. The present data suggest that propofol may cause irreversible lesions to GABAergic neurons when given at a critical phase of brain development. In contrast, glial cells and myelin appeared resistant even to high doses of propofol.

Motor Vehicle Accident Fatalities for the Week Ending, August 11, 2006

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Occipitoaxial spinal interarticular stabilization with vertebral artery preservation for atlantal lateral mass failure.

The treatment of craniocervical instability caused by diverse conditions remains challenging. Different techniques have been described to stabilize the craniocervical junction. The authors present 2 cases in which tumoral destruction of the C-1 lateral mass caused craniocervical instability. A one-stage occipitoaxial spinal interarticular stabilization (OASIS) technique with titanium cages and posterior occipitocervical instrumentation was used to reconstruct the C-1 lateral mass and stabilize the craniocervical junction. The ipsilateral vertebral artery was preserved. The OASIS technique offers single-stage tumor resection, C-1 lateral mass reconstruction, and stabilization with a loadsharing construct. It could be an option in the treatment of select cases of C-1 lateral mass failure.

Motor Vehicle Accident Fatalities for the Week Ending, August 25, 2006

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Motor Vehicle Accident Fatalities for the Week Ending, August 18, 2006

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Motor Vehicle Accident Fatalities for the Week Ending, September 1, 2006

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Motor Vehicle Accident Fatalities for the Week Ending, September 8, 2006

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Motor Vehicle Accident Fatalities for the Week Ending, September 15, 2006

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Motor Vehicle Accident Fatalities for the Week Ending, September 29, 2006

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