Prospect of Neuroscience in China

This article depicted how a young Chinese scientist got her training in China, how her training had impact on her scientific career in the US, and how she felt the prospect of Neuroscience in China.     

Cognitive aging: new answers to old questions

The use of techniques for functional brain imaging is beginning to provide insights into the psychological and neural mechanisms that underlie age-related changes in cognitive performance.     

中国引进的栽培植物

中国国外植物引种取得非常显著的成就,在中国农业发展中起到相当大的作用,可以说没有国外植物引种就不会有中国发达的农业。然而,关于中国引进作物种类及数量总体情况的报道极少见,卜慕华曾汇总出从国外引进的作物113种。笔者参阅有关文献,按粮食作物,经济作物、蔬菜作物、果树作物、饲用及绿肥作物、花卉作物、药用作物和林木作物,分别汇集了中国从国外引进的作物共计254种,涉及栽培物种305个。     

Visual function: how spiders find the right rock to crawl under

Animals that go on hunting expeditions face the problem of finding the way home at the end of the day. A group of hunting spiders has now been added to the list of animals that use the celestial pattern of polarized light as a compass to navigate with, and explains an old conundrum of spider eye anatomy.     

Ketone bodies promote stroke recovery via GAT-1-dependent cortical network remodeling

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中国鹿类动物遗传相关试验分析研究简述

介绍了国内学者对中国鹿类动物与遗传相关的试验研究的基本情况,涉及血液蛋白等分析、性状相关分析、染色体和线粒体相关分析等方面,对各项内容的总体及各项所采用的技术和方法、部分研究成果进行概述,并对其发展趋势进行展望。     

名词和动词加工的认知神经机制

关于名词和动词加工的认知神经机制,神经心理学和脑功能成像研究得出两种不同的结果:前者主张名词和动词认知加工的神经机制专门化,两者的神经机制分离;后者认为名词和动词认知加工的神经机制不分离。对此,语言表征的神经生物学及语义联想学分别给出了不同的解释。     

中国水杉引种研究

水杉(Metasequoia glyptostrobodies Hu & Cheng)是国家一级保护植物。水杉的发现是中国近代植物学界最值得自豪的一件大事,为中国植物学走向世界开辟了道路,被公认为是我国乃至世界二十世纪植物界的重大发现,它不仅对于中国有重要价值,也具有世界意义。水杉引种过程可以说是新中国植物引种过程的一个缩影,在发现50年后成功引种至26个省、市、区和特别行政区以及世界50多个国家和地区,成为我国重要的用材林树种、沿海防护林树种、农田防护林树种、城市绿化树种以及世界上著名的风景景观树种。水杉既为新中国林业的发展提供了重要实证,又是科学技术在林业及社会发展中的重要体现,同时水杉的发展也是我国林学界最值得骄傲的一件大事,是我国科技工作者集体智慧的结晶。该文仅对我国水杉引种学进行系统的论述,对水杉的引种阶段进行了划分,简述26个省、市、区和特别行政区的引种现状,分析了水杉在中国引种区的适生状况和原因。有关在国外的引种及迁地保护情况将另文发表。     

基因芯片技术和蛋白质组技术在神经科学中的应用及其研究进展

基因芯片技术和蛋白质组技术是最近发展起来的高通量技术,二者的出现使同时分析神经系统的大量基因的表达和基因产物蛋白质及其相互作用网络成为可能。它们在神经科学中的应用为了解脑功能提供了前所未有的机会。一个典型的基因芯片实验包括：芯片的准备或购买、靶DNA和探针的准备或标记、标记探针与靶DNA的杂交、芯片扫描和影象信息的数据分析。蛋白质组技术较为复杂,包括蛋白质分离、鉴定和信息分析三方面的内容。其中,分离技术多种多样。若分离技术以二维电泳为基础,则该实验通常由以下步骤组成：蛋白质样品的准备、电泳分离、染胶、分离蛋白点的切除、蛋白质的酶解(常用胰蛋白酶)、质谱分析(鉴定)和数据的信息处理。本文综述这两项技术的内容和实验步骤,然后着重叙述它们在神经科学中的应用,讨论其优缺点和面临的挑战,展望其发展前景。     

Quantification of Filamentous Actin (F-actin) Puncta in Rat Cortical Neurons

Filamentous actin protein (F-actin) plays a major role in spinogenesis, synaptic plasticity, and synaptic stability. Changes in dendritic F-actin rich structures suggest alterations in synaptic integrity and connectivity. Here we provide a detailed protocol for culturing primary rat cortical neurons, Phalloidin staining for F-actin puncta, and subsequent quantification techniques. First, the frontal cortex of E18 rat embryos are dissociated into low-density cell culture, then the neurons grown in vitro for at least 12-14 days. Following experimental treatment, the cortical neurons are stained with AlexaFluor 488 Phalloidin (to label the dendritic F-actin puncta) and microtubule-associated protein 2 (MAP2; to validate the neuronal cells and dendritic integrity). Finally, specialized software is used to analyze and quantify randomly selected neuronal dendrites. F-actin rich structures are identified on second order dendritic branches (length range 25-75 µm) with continuous MAP2 immunofluorescence. The protocol presented here will be a useful method for investigating changes in dendritic synapse structures subsequent to experimental treatments.     

人类脑计划与神经信息学

了解脑及其功能是21世纪科学的重大挑战之一。神经信息学是神经科学与信息科学相结合的交叉学科。目前的“人类脑计划”旨在加强脑功能的基础研究,并开发用于分析、整合、合成、建模、模拟与提供各种数据的工具。中国应参与人类脑计划,为发展神经信息学作出贡献。     

Micropipette aspiration of the Pacinian corpuscle

The Pacinian corpuscle (PC) is a cutaneous mechanoreceptor sensitive to high-frequency vibrations (20–1000 Hz). The PC is of importance due to its integral role in somatosensation and the critical need to understand PC function for haptic feedback system development. Previous theoretical and computational studies have modeled the physiological response of the PC to sustained or vibrating mechanical stimuli, but they have used estimates of the receptor’s mechanical properties, which remain largely unmeasured. In this study, we used micropipette aspiration (MPA) to determine an apparent Young’s modulus for PCs isolated from a cadaveric human hand. MPA was applied in increments of 5 mm H₂O (49 Pa), and the change in protrusion length of the PC into the pipette was recorded. The protrusion length vs. suction pressure data were used to calculate the apparent Young’s modulus. Using 10 PCs with long-axis lengths of 2.99 ± 0.41 mm and short-axis lengths of 1.45 ± 0.22 mm, we calculated a Young’s modulus of 1.40 ± 0.86 kPa. Our measurement is on the same order of magnitude as those approximated in previous models, which estimated the PC to be on the same order of magnitude as skin or isolated cells, so we recommend that a modulus in the kPa range be used in future studies.     

Investigating Social Cognition in Infants and Adults Using Dense Array Electroencephalography (dEEG)

Dense array electroencephalography (_dEEG), which provides a non-invasive window for measuring brain activity and a temporal resolution unsurpassed by any other current brain imaging technology^1,2, is being used increasingly in the study of social cognitive functioning in infants and adults. While _dEEG is enabling researchers to examine brain activity patterns with unprecedented levels of sensitivity, conventional EEG recording systems continue to face certain limitations, including 1) poor spatial resolution and source localization^3,4,2) the physical discomfort for test subjects of enduring the individual application of numerous electrodes to the surface of the scalp, and 3) the complexity for researchers of learning to use multiple software packages to collect and process data. Here we present an overview of an established methodology that represents a significant improvement on conventional methodologies for studying EEG in infants and adults. Although several analytical software techniques can be used to establish indirect indices of source localization to improve the spatial resolution of _dEEG, the HydroCel Geodesic Sensor Net (HCGSN) by Electrical Geodesics, Inc. (EGI), a dense sensory array that maintains equal distances among adjacent recording electrodes on all surfaces of the scalp, further enhances spatial resolution^4,5,6 compared to standard _dEEG systems. The sponge-based HCGSN can be applied rapidly and without scalp abrasion, making it ideal for use with adults^7,8, children^9,10,11, and infants¹², in both research and clinical^{4,5,6,13,14,15} settings. This feature allows for considerable cost and time savings by decreasing the average net application time compared to other _dEEG systems. Moreover, the HCGSN includes unified, seamless software applications for all phases of data, greatly simplifying the collection, processing, and analysis of _dEEG data.The HCGSN features a low-profile electrode pedestal, which, when filled with electrolyte solution, creates a sealed microenvironment and an electrode-scalp interface. In all Geodesic _dEEG systems, EEG sensors detect changes in voltage originating from the participant''s scalp, along with a small amount of electrical noise originating from the room environment. Electrical signals from all sensors of the Geodesic sensor net are received simultaneously by the amplifier, where they are automatically processed, packaged, and sent to the data-acquisition computer (DAC). Once received by the DAC, scalp electrical activity can be isolated from artifacts for analysis using the filtering and artifact detection tools included in the EGI software. Typically, the HCGSN can be used continuously for only up to two hours because the electrolyte solution dries out over time, gradually decreasing the quality of the scalp-electrode interface.In the Parent-Infant Research Lab at the University of Toronto, we are using _dEEG to study social cognitive processes including memory, emotion, goals, intentionality, anticipation, and executive functioning in both adult and infant participants.     

LHPP-mediated inorganic pyrophosphate hydrolysis-driven lysosomal acidification in astrocytes regulates adult neurogenesis

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Development of motor behaviour

The development of motor behaviour depends on the differentiation of underlying circuitry. Recent work with the zebrafish brings the simple swimming behaviour of lower vertebrates and their embryos into focus as a suitable model to study the development of motor circuitry and its genetic control. Changes in connectivity and excitability contribute to the development of swimming in this simple system. In the chick embryo, limb motor circuitry is spontaneously active before motor axons reach their muscle targets, and it has properties in common with the spontaneously active networks in the retina. The early rhythmic activity responsible for embryonic movement is probably a generalised property of developing spinal networks that precedes, and may be required for, the completion of functional locomotor circuitry.     

Neuromodulation during motor development and behavior

Important recent advances have been made in understanding the role of aminergic modulation during the maturation of Xenopus larvae swimming rhythms, including effects on particular ion channel types of component neurons, and the role of peptidergic modulation during development of adult central patterns generators in the stomatogastric ganglion of crustaceans. By recording from octopaminergic neuromodulatory neurons during ongoing motor behavior in the locust, new insights into the role of this peripheral neuromodulatory mechanism have been gained. In particular, it is now clear that the octopaminergic neuromodulatory system is automatically activated in parallel to the motor systems, and that both excitation and inhibition play important functional roles.     

Modular features of motor control and learning

The study of complex motor behaviours has highlighted the role of modular representations both in the planning and in the execution of actions. Recent findings suggest the presence of functional modules within a variety of neural structures. Computational investigations are now addressing the issue of how these modules may act concurrently to generate a wide repertoire of behaviours.     

Afferent modulation of dopamine neuron firing patterns

In recent studies examining the modulation of dopamine (DA) cell firing patterns, particular emphasis has been placed on excitatory afferents from the prefrontal cortex and the subthalamic nucleus. A number of inconsistencies in recently published reports, however, do not support the contention that tonic activation of NMDA receptors is the sole determinate of DA neuronal firing patterns. The results of work on the basic mechanism of DA firing and the action of apamin suggest that excitatory projections to DA neurons from cholinergic and glutamatergic neurons in the tegmental pedunculopontine nucleus, and/or inhibitory GABAergic projections, are also involved in modulating DA neuron firing behavior.     

Imaging Serotonergic Fibers in the Mouse Spinal Cord Using the CLARITY/CUBIC Technique

Long descending fibers to the spinal cord are essential for locomotion, pain perception, and other behaviors. The fiber termination pattern in the spinal cord of the majority of these fiber systems have not been thoroughly investigated in any species. Serotonergic fibers, which project to the spinal cord, have been studied in rats and opossums on histological sections and their functional significance has been deduced based on their fiber termination pattern in the spinal cord. With the development of CLARITY and CUBIC techniques, it is possible to investigate this fiber system and its distribution in the spinal cord, which is likely to reveal previously unknown features of serotonergic supraspinal pathways. Here, we provide a detailed protocol for imaging the serotonergic fibers in the mouse spinal cord using the combined CLARITY and CUBIC techniques. The method involves perfusion of a mouse with a hydrogel solution and clarification of the tissue with a combination of clearing reagents. Spinal cord tissue was cleared in just under two weeks, and the subsequent immunofluorescent staining against serotonin was completed in less than ten days. With a multi-photon fluorescent microscope, the tissue was scanned and a 3D image was reconstructed using Osirix software.