Development of the vestibular system

This review mainly focuses on the development of the vestibular system in humans and other mammals, but reference is made to anurans and other species where applicable. In the first section, the steps involved in the development of undifferentiated cells into mature vestibular receptors are analysed. Available data indicate that in humans, maturation of the vestibular receptor and its afferent innervations involves a similar sequence of events as in other mammalian species. In the second section, morphological and physiological aspects of the maturation of the central vestibular system are presented. Undifferentiated neuron precursors have been identified in specific segregrated domains of the hindbrain neural tube, and these can develop into secondary vestibular neurons with unique properties. Several neuronal populations in the vestibulospinal and vestibulo-ocular pathways have been found to correlate with rhombomeric domains at early embryonic stages. In rodents, the vestibular system continues to develop postnatally in terms of morphology and function until it achieves its final form. The postnatal changes in the properties of vestibular nuclear neurons are chronologically matched with structural changes and serve to prime the development of vestibular-induced reflexes. Copyright © 2002 S. Karger AG, Basel.published_or_final_versio

海浪發電

由於全球人口不斷增長，所以能源需求日益增加。地球上大部份的能源主要來自化石燃料。不過，燃燒化石燃料發電會釋出大量二氧化碳和污染物，造成溫室效應從而導致環境破壞；而且，化石燃料是有限的能源。雖然可用核原料發電，但是核能的安全問題與風險管理不斷受人們爭論。故此，對再生能源的研究及開發是刻不容緩的。本章主要討論其中一種再生能源，海浪發電的好處及近期一些研究成果。published_or_final_versio

A chromatic transient visual evoked potential based encoding/decoding approach for brain-computer interface

This paper presents a new encoding/decoding approach to brain-computer interface (BCI) based on chromatic transient visual evoked potential (CTVEP). The proposed CTVEP-based encoding/decoding approach is designed to provide a safer and more comfortable stimulation method than the conventional VEP-based stimulation methods for BCI without loss of efficiency. For this purpose, low-frequency isoluminant chromatic stimuli are time-encoded to serve as different input commands for BCI control, and the superior comfortableness of the proposed stimulation method is validated by a survey. A combination of diversified signal processing techniques are further employed to decode the information from CTVEP. Based on experimental results, a properly designed configuration of the CTVEP-based stimulation method and a tailored signal processing framework are developed. It is demonstrated that high performance (at information transfer rate: 58.0 bits/min, accuracy: 94.9%, false alarm rate: 1.3%) for BCI can be achieved by means of the CTVEP-based encoding/decoding approach. It turns out that to achieve such good performance, only simple signal processing algorithms with very low computational complexity are required, which makes the method suitable for the development of a practical BCI system. A preliminary prototype of such a system has been implemented with demonstrated applicability. © 2011 IEEE.published_or_final_versio

The role of proheparanase in synaptic plasticity at the hippocampus

Abstract no. P-110Perineuronal heparan sulfate (HS) moieties are implicated in the modulation of neurotransmission by controlling the functional properties of AMPA-type glutamate receptors. We hypothesize that neuronal mechanisms modulate peri-synaptic HS level, thereby regulating synaptic strength and plasticity. To address this, basal synaptic strength and long-term changes in synaptic efficacy in the Schaffer collateral pathway of the rat hippocampus were assessed in relation to strategies that perturb peri-synaptic HS. In hippocampal slices, heparitinase treatment led to dose-dependent attenuation of long-term potentiation (LTP) in correlation with loss of perineuronal HS …postprin

Primary biliary cirrhosis and scleroderma complicated by Barrett's oesophagus A case report

Oesophageal problems are common in patients with scleroderma. but the association of primary biliary cirrhosis and scleroderma is uncommon. A Barrett's oesophagus identified in a patient with primary biliary cirrhosis and scleroderma is described. The Barrett's oesophagus was probably a complication of scleroderma and resulted from low lower-oesophageal sphincter pressure and severe gastro-oesophageal reflux

Development of an RFID-based traceability system : experiences and lessons learned from an aircraft engineering company

Author name used in this publication: E. W. T. NgaiAuthor name used in this publication: T. C. E. ChengAuthor name used in this publication: Kee-hung Lai2007-2008 > Academic research: refereed > Publication in refereed journalVersion of RecordPublishe

Neuroprotective effects of minocycline on double-stranded RNA-induced neurotoxicity in cultured cortical neurons

1. Minocycline, memantine,and glycoconjugate were assessed for their ability to protect cultured primary cortical neurons against double-stranded RNA-induced neurotoxicity. 2. Minocycline but not memantine or glycoconjugate protected cultured cells and warrants further investigation.published_or_final_versio

The Nucleosome Assembly Protein TSPYL2 Regulates the Expression of NMDA Receptor Subunits GluN2A and GluN2B

published_or_final_versio

A pro-drug of the green tea polyphenol (-)-epigallocatechin-3-gallate (EGCG) prevents differentiated SH-SY5Y cells from toxicity induced by 6-hydroxydopamine

Regular consumption of green tea benefits people in prevention from cardiovascular disorders, obesity as well as neurodegenerative diseases. (-)-Epigallocatechin-3-gallate (EGCG) is regarded as the most biologically active catechin in green tea. However, the stability and bioavailability of EGCG are restricted. The purpose of the present study was to investigate whether a pro-drug, a fully acetylated EGCG (pEGCG), could be more effective in neuroprotection in Parkinsonism mimic cellular model. Retinoic acid (RA)-differentiated neuroblastoma SH-SY5Y cells were pre-treated with different concentrations of EGCG and pEGCG for 30 min and followed by incubation of 25 μM 6-hydroxydopamine (6-OHDA) for 24 h. We found that a broad dosage range of pEGCG (from 0.1 to 10 μM) could significantly reduce lactate dehydrogenase release. Likewise, 10 μM of pEGCG was effective in reducing caspase-3 activity, while EGCG at all concentrations tested in the model failed to attenuate caspase-3 activity induced by 6-OHDA. Furthermore, Western-blot analysis showed that Akt could be one of the specific signaling pathways stimulated by pEGCG in neuroprotection. It was demonstrated that 25 μM of 6-OHDA significantly suppressed the phosphorylation level of Akt. Only pEGCG at 10 μM markedly increased its phosphorylation level compared to 6-OHDA alone. Taken together, as pEGCG has higher stability and bioavailbility for further investigation, it could be a potential neuroprotective agent and our current findings may offer certain clues for optimizing its application in future. © 2009 Elsevier Ireland Ltd. All rights reserved.postprin