As such, protective doses of a given SV2A ligand in one model could be easily predicted based on the data obtained in-another model. Taken together, these results support the concept that SV2A protein is an important target for both partial and generalized epilepsies and thereby relevant for the generation of new antiepileptic drugs with potential broad-spectrum efficacy. (c) 2007 Elsevier Ltd. All rights reserved.”
“Objective: In a previous study we showed that recellularization of a stentless bioprosthetic valve is stimulated 1 month after

implantation check details in the pulmonary position, when its matrix (acellular photo-oxidized bovine pericardium) was preseeded by intraperitoneal implantation during a 3-day period.

Methods: The PND-1186 present study reports on the functional and biomechanical properties

of such valves (n 5 19) in sheep up to 5 months after implantation. Similar valves (n 5 20) that were not intraperitoneally preseeded served as controls.

Results: Recellularization was partial in control valves and excessive in preseeded valves: 66% versus 223% of cellularity of native valves, respectively (P < .05). The valves were endothelialized and contained interstitial cells depositing new matrix (collagens and elastin). However, phenotyping revealed an increased proportion of cells with contractile properties (30% -40% alpha smooth muscle actin 1) in both groups. Intraperitoneally seeded valves had thicker and shorter leaflets that were associated with mildly increased peak gradients and regurgitation. Characterization of the matrix properties revealed a gradually degrading matrix (625% loss of collagen organization at 5 months) and a concomitant alteration of its biomechanical properties, that is, decreased strength, stiffness, and maximum force. However,

overall valve function remained intact, and the biomechanical properties of the whole valves were superior to that of the native valves.

Conclusion: The ectopic in vivo seeding paradigm provides full recellularization. However, the volume fraction of the cellular phenotypes is not optimal, resulting in inadequate remodeling Carnitine palmitoyltransferase II of the valves.”
“The invariant characteristic features associated with Alzheimer’s disease (AD) brain include the presence of extracellular neuritic plaques composed of amyloid beta (A beta) peptide, intracellular neurofibrillary tangles containing hyper-phosphorylated tau protein and the loss of basal forebrain cholinergic neurons. Studies of the pathological changes that characterize AD and several other lines of evidence indicate that in vivo accumulation of A beta(1-42) may initiate the process of neurodegeneration observed in AD brains. However, the cause of degeneration of the basal forebrain cholinergic neurons and their association to AD peptides or phosphorylated tau protein have not been clearly established.