Semi-quantitative analysis of LRRK2 immunohistochemical staining demonstrated regional variation in staining intensity, with weak LRRK2 immunoreactivity consistently recorded in the striatum and substantia nigra. No clear differences were identified in LRRK2 immunoreactivity between control, IPD and G2019S positive PD cases. LRRK2 protein was identified in a small proportion of Lewy bodies. Conclusions: Our data suggest that

widespread dysregulation of LRRK2 mRNA expression may contribute to the pathogenesis of IPD. “
“Epilepsy is a nervous system disorder characterized by recurrent seizures. Among several types of epilepsy, which accounts for a significant portion of the disease worldwide, temporal lobe epilepsy (TLE) is one of the most common types of intractable epilepsy in adulthood. It has been suggested that complex febrile seizures in early life are associated with the development of TLE Epacadostat concentration selleck chemicals llc later in life; however, cellular and molecular links between febrile seizures and TLE remain unclear because of the lack of an appropriate in vitro system. Using rat hippocampal slice cultures, in which many features of native organotypic organization are retained, we found that the dentate granule cells exhibit aberrant migration in the dentate hilus via enhanced excitatory GABAA

receptor (GABAA-R) signaling, which results in granule cell ectopia that persists into adulthood. We further found that the granule cell ectopia PLEK2 is associated with spontaneous limbic seizures in adulthood. Importantly, both of these phenomena were prevented by inhibiting Na+K+2Cl− co-transporter (NKCC1) which mediates the excitatory action of GABA. The hippocampi of individuals with mesial temporal lobe epilepsy (TLE) and corresponding animal models are accompanied by several pathological changes, such as the dispersion of dentate granule cells,[1-3] the emergence of ectopic granule cells,[4-7] the sprouting of hippocampal mossy fibers,[8-10] and hippocampal sclerosis, including selective neuronal loss and reactive gliosis in Ammon’s horn.[11] Each of these features has been suggested to play a role in the initiation and

propagation of epileptic activity in the hippocampus. These pathological changes may be triggered by early-life seizures considering that retrospective studies have suggested a correlation between a history of early-life seizures and hippocampal sclerosis;[12-16] however, direct evidence is lacking. Febrile seizures, which are associated with fevers (typically greater than 38.5°C), are the most common convulsive events in infancy and childhood between 6 months and 5 years of age with a prevalence of 2–14%[17] of the population. Although febrile seizures are benign in most instances, 30–40% of them are “complex”,[18, 19] with a prolonged seizure duration of >15 min, and are subsequently associated with 30–70% of the cases of adult TLE.