In another set of rats, HR and AP responses to L-glutamate (L-Glu) microinjections (10 mM, 20 nl) BAY 73-4506 chemical structure into the left NA and electrical stimulation of the left cervical vagus nerve at 1-30 Hz (0.5 mA, 1 ms) for 20 s were measured. Brainstem slices at the level of -800, -400, 0, +400, +800 mu m relative to the obex were processed in additional rats using Nissl staining. The NA was identified by retrogradely labeling vagal motoneurons using the tracer tetra-methylrhodamine
dextran (TMR-D) which was injected into the ipsilateral nodose ganglion. We found that CIH significantly 1) reduced the baro-reflex control of HR (slope RA: -1.2 +/- 0.2 bpm/ mmHg; CIH -0.5 +/- 0.1 bpm/mmHg; P < 0.05); 2) attenuated the HR responses to L-Glu injections into the NA [HR: -280 +/- 15 (RA) vs. -235 +/- 16 (CIH) beats/min; P < 0.05]; 3) augmented the HR responses to electrical stimulation of the vagus (P < 0.05); 4) induced a significant cellular loss in the NA region (P < 0.05). Thus, CIH induces a cell loss in the NA Selleckchem Elafibranor region which may contribute to attenuation of baroreflex sensitivity and NA control of HR following CIH. (c) 2008 IBRO. Published by Elsevier Ltd. All rights reserved.”
“The mammalian cerebellar cortex is highly compartmentalized. First, it is subdivided into four transverse expression domains: the anterior zone (AZ), the central zone (CZ), the posterior zone (PZ), and the nodular
zone (NZ). Within each zone, the cortex is further subdivided into a symmetrical array of parasagittal stripes. The most extensively
studied compartmentation antigen is zebrin II/aldolase c, which is expressed by a subset of Purkinje cells forming parasagittal stripes. Stripe phenotypes are specified early in cerebellar development, in part through the action of early B-cell factor 2 (Ebf2), a member of the atypical helix-loop-helix transcription factor family Collier/Olf1/EBF. In the murine cerebellum, PND-1186 research buy Ebf2 expression is restricted to the zebrin II-immunonegative (zebrin II-) Purkinje cell population. We have identified multiple cerebellar defects in the Ebf2 null mouse involving a combination of selective Purkinje cell death and ectopic expression of multiple genes normally restricted to the zebrin II- subset. The nature of the cerebellar defect in the Ebf2 null is different in each transverse zone. In contrast to the ectopic expression of genes characteristic of the zebrin II+ Purkinje cell phenotype, phospholipase C beta 4 expression, restricted to zebrin II- Purkinje cells in control mice, is well maintained, and the normal number of stripes is present. Taken together, these data suggest that Ebf2 regulates the expression of genes associated with the zebrin II+ Purkinje cell phenotype and that the zebrin II- Purkinje cell subtype is specified independently. (c) 2008 IBRO. Published by Elsevier Ltd. All rights reserved.”
“The protein alpha-synuclein is implicated in the development of Parkinson’s disease.