基于内源信息的脑光学成像系统的研制

基于内源信号的脑光学成像技术是近年出现的研究脑功能的新技术。它因具有高空间分辨率,可连续长时间记录,使用简便,费用较低等特点,成为在视觉,听觉以及其他各种脑功能研究的有力工具。本文介绍了国内第一套脑光学成像系统的和研制,以及用于视觉研究皮层功能方位柱研究的初步结果。     

应用基于内源信号的光学成像技术的视觉脑研究现状

基于脑内源信号的光学成像技术是近来国际上出现的一种脑功能成像方法。该技术既无毒,又具有较高的空间分辨率,因而被迅速应用于动物的视觉、听觉、体感皮层功能构筑的研究中。本文综述了这种光学脑功能成像在视觉脑研究方面所取得的重要进展,并分析了该方法与其他脑成像技术、微电极单细胞技术的关系。报道了国内自行研制第、套脑功能光学成像系统的研究工作,该系统已在猫初级视觉皮层不同深度获得了清晰的方位功能图,并已经和     

高时空分辨的脑功能光学成像研究进展

脑功能成像技术对深入分析脑的信息加工过程,揭示脑的高级功能至关重要,是目前国际研究热点,已经在神经科学研究和神经系统疾病的临床诊断方面取得了很大的进展.已有脑功能成像技术如:功能磁共振成像(fMRI)、正电子断层成像(PET)、脑电图(EEG)、脑磁图(MEG)等等,虽然已被成功用于脑功能研究,但是目前这些方法也存在着时间或空间分辨率不够的局限.比较而言,光学成像方法表现出其独特魅力.激光散斑衬比成像和内源信号光学成像由于能提供空间取样、时间分辨率及空间分辨率三者的最佳组合和不需加入外源性标记物等特点,与其他脑功能成像技术相比其优势可能更为突出.具有较高的时间和空间分辨率的这两种脑功能光学成像技术及其应用都取得了重大发展,成为研究脑皮层功能构筑和脑病理生理的有力工具.但是目前这两种成像方法也面临着一些挑战.     

光学神经成像研究进展

大脑功能的成像检测在认知神经科学领域具有极其重要的意义。现代光子学技术的发展为认知脑成像提供了新的研究手段,在神经系统信息处理机制研究中发挥重要作用。文章介绍了在神经元、神经元网络、特定脑皮层功能构筑以及系统与行为等不同层次开展神经系统信息处理机制研究的各种光学成像技术,包括多光子激发荧光显微成像、内源信号光学成像、激光散斑成像和近红外光学成像等,并评述了这些有特色的光学成像技术在多层次获取和分析神经信息中的研究进展。     

脑科学和脑功能MR成像

目的：在对大脑认知功能进行脑功能成像研究之中,随着磁共振成像技术的发展,人们现在可以对脑的认知功能,如视觉、运动、语言和记忆等功能中枢进行成像。本文首先介绍了脑科学的发展历程,并从脑功能MR成像的方法出发,分析了其成像机理,探讨了用脑功能MR成像为手段对脑科学—认知科学进行的方法研究,最后对脑功能MR成像应用于脑科学的研究作了展望。     

脑光学成像技术揭示的猫初级视皮层方位倾斜效应

方位倾斜效应（ｏｂｌｉｑｕｅ ｅｆｆｅｃｔ）是人类普遍存在的视觉心理效应。为了检测其神经基础,我们采用脑光学成像方法,对猫初级视觉皮层较大范围内的水平－垂直方位光栅刺激敏感区和倾斜方位光栅刺激敏感区的大小及其反应强度进行了定量分析。结果表明：水平－垂直敏感区比倾斜角敏感区面积大,平均差异为４．７％;水平－垂直方位刺激引起的反应强度整体上比倾斜角方位刺激大。以上结果澄清了以往一些电生理研究结果的不同     

国际生物光子及生物光子学会议将于2003年10月在北京召开

00 3年 10月 12～ 16日将在北京召开国际生物光子及生物光子学会议 (ＩＣＢＢ) ,议题包括 :生物光子的物理、化学和生物学性质 ;生物光子在医学、农业和环境中的应用 ;生物系统中光子传播、散射、反射的物理学 ;生物大分子荧光标记的新方法 ;肿瘤非损伤诊断、定位和治疗的光学新进展 ;光成像和内窥镜 ;亚细胞水平的光学成像 ;功能分子成像和分子化学成像 ;测量及可视化的新光学技术等等。感兴趣者 ,可与中国生物物理学会魏舜仪女士联系。Ｅ＿ｍａｉｌ:<ｓｂ @ｓｕｎ5 .ｉｂｐ .ａｃ .ｃｎ >.国际生物光子及生物光子学会议将于2003年10月在北…     

视皮层分区及其fMRI 研究进展

血氧水平依赖功能磁共振成像（BOLD—fMRI）作为一种无创、可精确定位的脑功能研究技术,已广泛应用于视觉系统的研究中,并取得了许多重要成果,本文就fMRI研究进展及其在大脑视觉皮层功能分区中的应用做一综述。     

具有选择注意机制的视觉系统模型

文章提出了一种新的具有选择注意机制的视觉系统模型,这种模型包含一个从视觉皮层级到丘脑中外侧膝状体神经（ＬＧＮ）的反馈联结。分析了该模型反映视觉信息处理中注意机制的能力,网丘脑核（ＮｕｃｌｅｕｓＲｅｔｉｃｕｌａｒｉｓＴｈａｌａｍｉ,简作ＮＲＴ）的功能作用可用于建立注意模型。阐明了被称为ＣＴＡＮＮ（Ｃｏｒｔｉｃａｌ－ＴｈａｌａｍｉＡｒａｙＮｅｕｒａｌＮｅｔｗｏｒｋｓ）模型的生物学背景及意义,采用全局Ｌｉａｐｕｎｏｖ泛函方法分析了系统的稳定性,并给出了处理图象信息的实验。该研究旨在探索发展新型的视觉信息处理理论与方法。     

医学上的磁共振成像与激光成像

医学上的磁共振成像与激光成像张新明（华侨大学医院泉州市３６２０１１）关键词磁共振成像激光成像对比分辨率临床应用ＭｅｄｉｃａｌＭａｇｎｅｔｉｃＲｅｓｏｎｃｍｃｅａｎｄＬａｓｅｒＩｍａｇｉｎｇｓＺｈａｎｇＸｉｎｍｉｎｇ（ＨｏｓｐｉｔａｌｏｆＨｕａＱｉａｏ...     

Neuroanatomical phenotyping of the mouse brain with three-dimensional autofluorescence imaging

The structural organization of the brain is important for normal brain function and is critical to understand in order to evaluate changes that occur during disease processes. Three-dimensional (3D) imaging of the mouse brain is necessary to appreciate the spatial context of structures within the brain. In addition, the small scale of many brain structures necessitates resolution at the ～10 μm scale. 3D optical imaging techniques, such as optical projection tomography (OPT), have the ability to image intact large specimens (1 cm(3)) with ～5 μm resolution. In this work we assessed the potential of autofluorescence optical imaging methods, and specifically OPT, for phenotyping the mouse brain. We found that both specimen size and fixation methods affected the quality of the OPT image. Based on these findings we developed a specimen preparation method to improve the images. Using this method we assessed the potential of optical imaging for phenotyping. Phenotypic differences between wild-type male and female mice were quantified using computer-automated methods. We found that optical imaging of the endogenous autofluorescence in the mouse brain allows for 3D characterization of neuroanatomy and detailed analysis of brain phenotypes. This will be a powerful tool for understanding mouse models of disease and development and is a technology that fits easily within the workflow of biology and neuroscience labs.     

Fiber optic in vivo imaging in the mammalian nervous system

The compact size, mechanical flexibility, and growing functionality of optical fiber and fiber optic devices are enabling several new modalities for imaging the mammalian nervous system in vivo. Fluorescence microendoscopy is a minimally invasive fiber modality that provides cellular resolution in deep brain areas. Diffuse optical tomography is a non-invasive modality that uses assemblies of fiber optic emitters and detectors on the cranium for volumetric imaging of brain activation. Optical coherence tomography is a sensitive interferometric imaging technique that can be implemented in a variety of fiber based formats and that might allow intrinsic optical detection of brain activity at a high resolution. Miniaturized fiber optic microscopy permits cellular level imaging in the brains of behaving animals. Together, these modalities will enable new uses of imaging in the intact nervous system for both research and clinical applications.     

Genetically expressed cameleon in Drosophila melanogaster is used to visualize olfactory information in projection neurons

Complex external stimuli such as odorants are believed to be internally represented in the brain by spatiotemporal activity patterns of extensive neuronal ensembles. These activity patterns can be recorded by optical imaging techniques. However, optical imaging with conventional fluorescence dyes usually does not allow for resolving the activity of biologically defined groups of neurons. Therefore, specifically targeting reporter molecules to neuron populations of common genetic identity is an important goal. We report the use of the genetically encoded calcium-sensitive fluorescence protein cameleon 2.1 in the Drosophila brain. We visualized odorant-evoked intracellular calcium concentration changes in selectively labeled olfactory projection neurons both postsynaptically in the antennal lobe, the primary olfactory neuropil, and presynaptically in the mushroom body calyx, a structure involved in olfactory learning and memory. As a technical achievement, we show that calcium imaging with a genetically encoded fluorescence probe is feasible in a brain in vivo. This will allow one to combine Drosophila's advanced genetic tools with the physiological analysis of brain function. Moreover, we report for the first time optical imaging recordings in synaptic regions of the Drosophila mushroom body calyx and antennal lobe. This provides an important step for the use of Drosophila as a model system in olfaction.     

体内光量子点可视化图像在脑肿瘤中的应用

恶性胶质瘤年发病率约为5/100,000。美国每年有超过14,000例的新发恶性脑胶质瘤患者。治疗主要以手术治疗为主,手术肿瘤的切除程度影响患者的预后。外科手术治疗脑肿瘤需要精确定位脑肿瘤组织在正常脑组织中的位置以便能够获得精确的组织活检和肿瘤的完全切除。量子点是稳定存在的,产生荧光的可视化半导体纳米晶体。静脉注射量子点伴随着网状内皮系统和巨噬细胞的隔离。巨噬细胞可渗入到肿瘤组织并且能够吞噬通过静脉注射的光量子来产生可视化的肿瘤标记。通过巨噬细胞介导,将光量子运输至肿瘤组织展现了一种新兴技术来标记术前肿瘤组织。由于肿瘤组织中的光量子可以被光学成像和光谱学工具来探测,因此在脑肿瘤组织活检和切除中可以为外科医生提供可视化得实时反馈。     

Noninvasive laser-induced photoacoustic tomography for structural and functional in vivo imaging of the brain

Imaging techniques based on optical contrast analysis can be used to visualize dynamic and functional properties of the nervous system via optical signals resulting from changes in blood volume, oxygen consumption and cellular swelling associated with brain physiology and pathology. Here we report in vivo noninvasive transdermal and transcranial imaging of the structure and function of rat brains by means of laser-induced photoacoustic tomography (PAT). The advantage of PAT over pure optical imaging is that it retains intrinsic optical contrast characteristics while taking advantage of the diffraction-limited high spatial resolution of ultrasound. We accurately mapped rat brain structures, with and without lesions, and functional cerebral hemodynamic changes in cortical blood vessels around the whisker-barrel cortex in response to whisker stimulation. We also imaged hyperoxia- and hypoxia-induced cerebral hemodynamic changes. This neuroimaging modality holds promise for applications in neurophysiology, neuropathology and neurotherapy.     

Imaging of molecular dynamics regulated by electrical activities in neural circuits and in synapses

One of the major challenges in brain research is to unravel a network of molecules, neurons, circuits and systems that are responsible for dynamic and hierarchical brain functions. To understand molecular events that occur in synapses could be an important key to exploring the mechanism of information processing. A spatiotemporal recording method is required to observe neuronal activities in a particular local circuit and to resolve single synaptic potential with high resolution. As alternative methods, real-time imaging using fluorescent probes and optical recording methods are also a powerful approach for investigating the molecular dynamics of biological events in neurons in vitro and in vivo. Recently, optical imaging techniques have become of great importance to visualize the molecular dynamics in a micron-sized compartment of a single neuron such as neuronal synapse. In general, the presynaptic axon forms synapses at the postsynaptic site on the dendritic spines in the mammalian central nervous system. Subsets of the synapses undergo a series of enduring changes in spine shape and density as well as alterations in electrophysiological functions. Here we describe recent optical imaging studies conducted by elaborate methods and techniques that provide evidence for the link between neural activity and molecular dynamics.     

Comparison of optically‐derived biomarkers in healthy and brain tumor tissue under one‐ and two‐photon excitation

The surgical outcome of brain tumor resection and needle biopsy is significantly correlated to the patient's prognosis. Brain tumor surgery is limited to resecting the solid portion of the tumor as current intraoperative imaging modalities are incapable of delineating infiltrative regions. For accurate delineation, in situ tissue interrogation at the submicron scale is warranted. Additionally, multimodal detection is required to remediate the genetically and molecularly heterogeneous nature of brain tumors, notably, that of gliomas, meningioma and brain metastasis. Multimodal detection, such as spectrally‐ and temporally‐resolved fluorescence under one‐ and two‐photon excitation, enables characterizing tissue based on several endogenous optical contrasts. In order to assign the optically‐derived parameters to different tissue types, construction of an optical database obtained from biopsied tissue is warranted. This report showcases the different quantitative and semi‐quantitative optical markers that may comprise the tissue discrimination database. These include: the optical index ratio, the optical redox ratio, the relative collagen density, spectrally‐resolved fluorescence lifetime parameters, two‐photon fluorescence imaging and second harmonic generation imaging.     

Optical calcium imaging in the nervous system of Drosophila melanogaster

BACKGROUND: Drosophila melanogaster is one of the best-studied model organisms in biology, mainly because of the versatility of methods by which heredity and specific expression of genes can be traced and manipulated. Sophisticated genetic tools have been developed to express transgenes in selected cell types, and these techniques can be utilized to target DNA-encoded fluorescence probes to genetically defined subsets of neurons. Neuroscientists make use of this approach to monitor the activity of restricted types or subsets of neurons in the brain and the peripheral nervous system. Since membrane depolarization is typically accompanied by an increase in intracellular calcium ions, calcium-sensitive fluorescence proteins provide favorable tools to monitor the spatio-temporal activity across groups of neurons. SCOPE OF REVIEW: Here we describe approaches to perform optical calcium imaging in Drosophila in consideration of various calcium sensors and expression systems. In addition, we outline by way of examples for which particular neuronal systems in Drosophila optical calcium imaging have been used. Finally, we exemplify briefly how optical calcium imaging in the brain of Drosophila can be carried out in practice. MAJOR CONCLUSIONS AND GENERAL SIGNIFICANCE: Drosophila provides an excellent model organism to combine genetic expression systems with optical calcium imaging in order to investigate principles of sensory coding, neuronal plasticity, and processing of neuronal information underlying behavior. This article is part of a Special Issue entitled Biochemical, Biophysical and Genetic Approaches to Intracellular Calcium Signaling.