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Exposure to stressful events early in life may have permanent deleterious consequences on nervous system function and increase the susceptibility to psychiatric conditions later in life. Maternal deprivation, commonly used as a source of neonatal stress, impairs memory in adult rats and reduces hippocampal brain-derived neurotrophic factor (BDNF) levels. Inflammatory cytokines, such as interleukins (IL) and tumor necrosis factor-α (TNF-α) have been shown to be increased in the peripheral blood of patients with psychiatric disorders. The aim of the present study was to investigate the effects of maternal separation on the levels of IL-10 and TNF-α, and BDNF in the hippocampus and prefrontal cortex of adult rats. We also evaluated the potential ameliorating properties of topiramate and valproic acid on memory deficits and cytokine and BDNF changes associated with maternal deprivation. The results indicated that, in addition to inducing memory deficits, maternal deprivation increased the levels of IL-10 in the hippocampus, and TNF-α in the hippocampus and in the cortex, and decreased hippocampal levels of BDNF, in adult life. Neither valproic acid nor topiramate were able to ameliorate memory deficits or the reduction in BDNF induced by maternal separation. The highest dose of topiramate was able to reduce IL-10 in the hippocampus and TNF-α in the prefrontal cortex, while valproate only reduced IL-10 levels in the hippocampus. These findings may have implications for a better understanding of the mechanisms associated with alterations observed in adult life induced by early stressful events, and for the proposal of novel therapeutic strategies.

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Background: Although much progress has been made in the acute ischemic stroke care in low- and middle-income countries (LMIC), there is a paucity of specific data on the early management of TIA patients. Patients with TIA present a substantial risk of stroke during the first few hours of symptom onset, when secondary prevention therapies should be urgently initiated. Therefore, hospital admission may offer some advantages for early management. Our aim was to evaluate the benefit of hospital admission of TIA patients in a LMIC. Methods: All TIA patients who arrived at our emergency room (ER) between March 2015 to March 2016 were admitted to the hospital. All patients were submitted to the following diagnostic protocol: brain imaging, intra and extracranial vascular imaging, echocardiography (TT and or TEE) and ECG. Baseline, imaging characteristics and early outcome were analyzed. Results: Among 845 consecutive stroke patients evaluated at our ER, 12.8% were diagnosed as TIA. Although vascular risk factors and presentation with weakness or speech disturbances were frequent findings among our TIA patients, only 1 in 5 patients (17.4%) required specific treatment (anticoagulation or carotid revascularization). In addition, half of our patients were classified as cryptogenic TIA. The average length of stay was 7.03 and there were no in-hospital stroke or death. We did not detect significant differences in demographics, risk factors and imaging features between patients that received standard vs. specific treatment. Conclusions: Many TIA patients with mild symptoms may not have reached our ER and among those who were evaluated some may not have required hospital admission. Clustering of risk factors among TIA patients may not be a variable helpful to identify high-risk patients in LMIC. A 24/7 emergency TIA clinic may be an option to improve urgent treatment and reduce acute care cost.