Slow and fast rhythms generated in the cerebral cortex of the anesthetized mouse

A characterization of the oscillatory activity in the cerebral cortex of the mouse was realized under ketamine anesthesia. Bilateral recordings were obtained from deep layers of primary visual, somatosensory, motor, and medial prefrontal cortex. A slow oscillatory activity consisting of up and down states was detected, the average frequency being 0.97 Hz in all areas. Different parameters of the oscillation were estimated across cortical areas, including duration of up and down states and their variability, speed of state transitions, and population firing rate. Similar values were obtained for all areas except for prefrontal cortex, which showed significant faster down-to-up state transitions, higher firing rate during up states, and more regular cycles. The wave propagation patterns in the anteroposterior axis in motor cortex and the mediolateral axis in visual cortex were studied with multielectrode recordings, yielding speed values between 8 and 93 mm/s. The firing of single units was analyzed with respect to the population activity. The most common pattern was that of neurons firing in >90% of the up states with 1-6 spikes. Finally, fast rhythms (beta, low gamma, and high gamma) were analyzed, all of them showing significantly larger power during up states than in down states. Prefrontal cortex exhibited significantly larger power in both beta and gamma bands (up to 1 order of magnitude larger in the case of high gamma) than the rest of the cortical areas. This study allows us to carry out interareal comparisons and provides a baseline to compare against cortical emerging activity from genetically altered animals.     

Cystogenic potential of CD133+ progenitor cells of human polycystic kidneys

In autosomal dominant polycystic kidney disease, cysts arise focally and disrupt normal renal tissue leading to renal failure. In the present study, we show that cyst-lining cells express the stem cell marker CD133. CD133+ progenitor cells isolated from polycystic kidney, carrying mutations of PKD genes, showed a dedifferentiated phenotype similar to CD133+ progenitor cells from normal kidney. However, these cells were more proliferative and presented a defective epithelial differentiation phenotype with respect to normal renal CD133+ cells as they were not able to express all tubular epithelial cell markers when cultured in epithelial differentiation medium. Polycystic CD133+ cells, in contrast to normal renal CD133+ cells, formed cysts in vitro in a three-dimensional culture system and in vivo when injected subcutaneously within Matrigel in SCID mice. Rapamycin treatment reduced in vitro proliferation of polycystic CD133+ cells and decreased cystogenesis both in vitro and in vivo. The in vitro epithelial differentiation was only partially improved by rapamycin. These results indicate that polycystic CD133+ cells retain a dedifferentiated phenotype and the ability to generate cysts.     

Why is TOF PET reconstruction a more robust method in the presence of inconsistent data?

In order to obtain an accurate and quantitative positron emission tomography (PET) image, emission data need to be corrected for random coincidences, photon attenuation and Compton scattering of photons in the tissue, and detector efficiency response or normalization. The accuracy of these corrections strongly affects the quality of the PET image. There is evidence that time-of-flight (TOF) PET reconstruction is less sensitive than non-TOF reconstruction to inconsistencies between emission data and corrections. The purpose of this study is to analyze and discuss such experimental evidence. In this work, inconsistent correction data (inconsistent normalization, absence of scatter correction and mismatched attenuation correction) are introduced in experimental phantom data. Both TOF and non-TOF reconstructed images are analyzed to examine the effect of flawed data. The behavior of TOF reconstruction in respiratory artifacts, a very common example of inconsistency in the data, is studied in patient images. TOF reconstruction is less sensitive to mismatched attenuation correction, erroneous normalization and poorly estimated scatter correction. Such robustness depends strongly on the time resolution of the TOF PET scanner. In particular, the robustness of TOF in the presence of attenuation correction inconsistencies is discussed, using a simulation of a simple model of respiratory artifacts. We expect new generations of PET scanners, with improved time resolution, to be less and less sensitive to poor quality normalization, scatter and attenuation corrections. This not only reduces artifacts in the PET image, but also opens the way to less stringent requirements for the quality of the CT image (reducing either the equipment cost or the dose to the patient), and for the normalization protocols (simplifying or shortening the normalization procedures). Moreover, TOF reconstruction can be beneficial in multimodalities such as PET/MR, where a direct attenuation measurement is not available and attenuation correction can only be approximated.     

Amyotrophic lateral sclerosis,enteral nutrition and the risk of iron overload

Journal of Neurology -     

Cerebrospinal fluid biomarkers in human genetic transmissible spongiform encephalopathies

The 14-3-3 protein test has been shown to support the clinical diagnosis of sporadic Creutzfeldt-Jakob disease (CJD) when associated with an adequate clinical context, and a high differential potential for the diagnosis of sporadic CJD has been attributed to other cerebrospinal fluid (CSF) proteins such as tau protein, S100b and neuron specific enolase (NSE). So far there has been only limited information available about biochemical markers in genetic transmissible spongiform encephalopathies (gTSE), although they represent 10–15% of human TSEs. In this study, we analyzed CSF of 174 patients with gTSEs for 14-3-3 (n = 166), tau protein (n = 78), S100b (n = 46) and NSE (n = 50). Levels of brain-derived proteins in CSF varied in different forms of gTSE. Biomarkers were found positive in the majority of gCJD (81%) and insert gTSE (69%), while they were negative in most cases of fatal familial insomnia (13%) and Gerstmann-Sträussler-Scheinker syndrome (10%). Disease duration and codon 129 genotype influence the findings in a different way than in sporadic CJD.     

Restless legs syndrome in multiple sclerosis: A case‐control study

The aim of our study was to explore restless legs syndrome (RLS) frequency in multiple sclerosis (MS)‐patients and establish whether RLS could be a symptom of MS. Over a period of 1 year, we consecutively enrolled 202 MS‐patients and 212 healthy controls, matched for sex and age, in a case‐control study. All of them filled in a structured questionnaire according to IRLSSG criteria. Those patients who fit the diagnostic criteria were subsequently examined by a neurologist to verify the effective presence of RLS. A total of 91 MS‐patients (45%) responded positively to the questionnaires. The diagnosis of RLS was carried out in 29subjects (14.4%). Among the healthy controls, a definite diagnosis of RLS was achieved only in 6 subjects (2.8%). The risk of MS patients to present RLS was significantly higher (OR.5.76 P:0.00002) than the general population. None of them was affected by other medical conditions related to RLS developing. The 62 remaining patients presented numbness and weakness of the legs not suggestive of RLS. Our findings confirm a significant correlation between MS and RLS. In our opinion, MS must be definitively included among RLS causes. © 2008 Movement Disorder Society