ABSTRACT
As aging and cognitive decline progresses, the impact of a sedentary lifestyle on the appearance of environment-dependent cellular morphologies in the brain becomes more apparent. Sedentary living is also associated with poor oral health, which is known to correlate with the rate of cognitive decline. Here, we will review the evidence for the interplay between mastication and environmental enrichment and assess the impact of each on the structure of the brain. In previous studies, we explored the relationship between behavior and the morphological features of dentate gyrus glial fibrillary acidic protein (GFAP)-positive astrocytes during aging in contrasting environments and in the context of induced masticatory dysfunction. Hierarchical cluster and discriminant analysis of GFAP-positive astrocytes from the dentate gyrus molecular layer revealed that the proportion of AST1 (astrocyte arbors with greater complexity phenotype) and AST2 (lower complexity) are differentially affected by environment, aging and masticatory dysfunction, but the relationship is not straightforward. Here we re-evaluated our previous reconstructions by comparing dorsal and ventral astrocyte morphologies in the dentate gyrus, and we found that morphological complexity was the variable that contributed most to cluster formation across the experimental groups. In general, reducing masticatory activity increases astrocyte morphological complexity, and the effect is most marked in the ventral dentate gyrus, whereas the effect of environment was more marked in the dorsal dentate gyrus. All morphotypes retained their basic structural organization in intact tissue, suggesting that they are subtypes with a non-proliferative astrocyte profile. In summary, the increased complexity of astrocytes in situations where neuronal loss and behavioral deficits are present is counterintuitive, but highlights the need to better understand the role of the astrocyte in these conditions.
Subject(s)
Astrocytes , Cognitive Dysfunction , Aging , Astrocytes/metabolism , Cognitive Dysfunction/metabolism , Dentate Gyrus/metabolism , Glial Fibrillary Acidic Protein/metabolism , Hippocampus/metabolism , Humans , Sedentary BehaviorABSTRACT
A cardiomiopatia não compactada é uma doença congênita, que resulta de falha da compactação do miocárdio na vida embrionária. Nesse processo, há a persistência de trabeculações e recessos profundos, que se comunicam com a cavidade ventricular e geram espessamento do miocárdio em duas camadas distintas. O aspecto clínico dessa doença tanto em crianças como em adultos é muito heterogêneo, variando desde a ausência de sintomas até a tríade composta por insuficiência cardíaca congestiva, arritmias e tromboembolismo sistêmico, porém bradicardias sintomáticas são muito raras. Relatamos o caso de uma paciente com doença do nó sinusal como manifestação inicial de cardiomiopatia não compactada
Noncompaction cardiomyopathy is a congenital disease that results frommyocardial compaction failure in embryonic life. In this process there is the persistence of deep trabeculations and recesses that communicate with the ventricular cavity, resulting in myocardial thickening in two distinct layers. The clinical aspect of this disease in both children and adults is very heterogeneous, ranging from absence of symptomatology to a triad including congestive heart failure, arrhythmias and systemic thromboembolism. However, symptomatic bradycardias are very rare. We report the case of a patient with sinus node disease as the initial manifestation of non-compaction cardiomyopathy
Subject(s)
Humans , Female , Adult , Pacemaker, Artificial , Sick Sinus Syndrome/diagnosis , Sick Sinus Syndrome/therapy , Isolated Noncompaction of the Ventricular Myocardium , Arrhythmias, Cardiac/complications , Sinoatrial Node , Bradycardia/diagnosis , Echocardiography/methods , Magnetic Resonance Spectroscopy/methods , Prevalence , Heart Defects, Congenital , Heart Failure/complications , Heart VentriclesABSTRACT
O acometimento de bifurcação na doença arterial coronária envolve aproximadamente 15-20% de todos os procedimentos de intervenção coronária percutânea. Sua abordagem ainda permanece como um dos maiores desafios na cardiologia intervencionista em termos de sucesso do procedimento, assim como desfechos cardiovasculares a longo prazo. Apesar do grande desenvolvimento técnico na abordagem desse tipo de lesão e a despeito das evidências científicas na literatura médica...
Subject(s)
Coronary Disease , Percutaneous Coronary InterventionABSTRACT
BACKGROUND: Chewing imbalances are associated with neurodegeneration and are risk factors for senile dementia in humans and memory deficits in experimental animals. We investigated the impact of long-term reduced mastication on spatial memory in young, mature and aged female albino Swiss mice by stereological analysis of the laminar distribution of CA1 astrocytes. A soft diet (SD) was used to reduce mastication in the experimental group, whereas the control group was fed a hard diet (HD). Assays were performed in 3-, 6- and 18-month-old SD and HD mice. RESULTS: Eating a SD variably affected the number of astrocytes in the CA1 hippocampal field, and SD mice performed worse on water maze memory tests than HD mice. Three-month-old mice in both groups could remember/find a hidden platform in the water maze. However, 6-month-old SD mice, but not HD mice, exhibited significant spatial memory dysfunction. Both SD and HD 18-month-old mice showed spatial memory decline. Older SD mice had astrocyte hyperplasia in the strata pyramidale and oriens compared to 6-month-old mice. Aging induced astrocyte hypoplasia at 18 months in the lacunosum-moleculare layer of HD mice. CONCLUSIONS: Taken together, these results suggest that the impaired spatial learning and memory induced by masticatory deprivation and aging may be associated with altered astrocyte laminar distribution and number in the CA1 hippocampal field. The underlying molecular mechanisms are unknown and merit further investigation.
