课题基金 / 基金详情

项目摘要

项目成果

Hiroshi Nakamura的其他基金

相似基金

相关文献

中文摘要
翻译
描述(由申请人提供):众所周知,原发性开角型青光眼的眼压升高与房水流出阻力增加有关。然而,阻力的确切位置和房水流出受损的机制仍不清楚。即使在正常的眼睛中,房水流出阻力的位置也没有被确定。为了解决这些问题,需要新的成像技术。双光子激光扫描显微镜是一种很有前途的成像技术,它具有扫描速率高、光毒性小等优点。此外,双光子激光扫描显微镜具有显著的优势,能够成像组织深处的结构,而不会引起失焦漂白。这种显微技术的分析适用于观察器官的三维组织。然而,它的应用仅限于那些可以很容易地固定在普通显微镜台上的覆盖玻璃上的对象。最近有人试图研制一种微型内窥镜。一种带有微型探针的双光子内窥镜系统能够实时成像各种组织,例如位于体腔内和/或难以在常规显微镜上放置的大脑。使用这种内窥镜系统对眼睛流出通道进行实时活细胞/结构成像还需要进一步的改进。特别是,微探针/扫描系统应该是水密的,特别是对于离体(ab interno)实验,探针应该以水密的方式安装到灌注前段培养中。我们建议建立一种新的双光子内窥镜,该内窥镜专为眼睛而设计,能够研究流出通道的活细胞/结构。该系统将由包括飞秒激发激光器、激光传输单元、荧光探测单元、成像采集单元和新的内探针/扫描系统在内的组件组成。由于了解流出通道需要对活细胞/结构进行实时成像,因此双光子内窥镜系统将用于体外灌注的人类前段培养以及猴子眼睛的体内研究。为了观察人体流出通道ab interno(从前房侧)的活细胞/结构,将双光子内镜系统安装在离体灌注人体前段培养系统上,建立实时活细胞/结构成像。对于水流出通道的体内成像,将观察猴子的眼睛,并从眼外观察水流出通道,在不干扰前房的情况下对其成像。这将在巩膜瓣被移除后进行尝试,有或没有移除施勒姆管的外壁。活体组织的荧光素染色将是实验设计的一部分。这些研究努力的发现可能会导致新的实时成像方法来研究流出通道,并将有助于说明水流出路径和事件。
英文摘要
DESCRIPTION (provided by applicant): It is well known that the elevated intraocular pressure of primary open angle glaucoma is related to an increased resistance to the outflow of aqueous humor. The precise location of the resistance and the mechanisms by which aqueous humor outflow is impaired, however, are still not clear. Even in normal eyes, the locus of aqueous humor outflow resistance has not been pinpointed. In order to resolve these questions, novel imaging techniques are needed. Two-photon laser scanning microscopy is a promising imaging technique that has many advantages over conventional techniques, including higher scanning rate and lower phototoxicity. In addition, two-photon laser scanning microscopy has the significant advantage of being able to image structures deep within a tissue without incurring out-of-focus bleaching. Analyses from this microscopic technique are appropriate for observing the three-dimensional organization of organs. Its application, however, is limited to subjects that can be easily immobilized and apposed to a coverglass on the stage of a regular microscope. Attempts have recently been made to develop a miniaturized microendoscope. A two-photon endoscope system with a miniaturized probe has enabled real time imaging of various tissues, such as the brain, that sit inside a body cavity and/or are difficult to place on a regular microscope stage. Further improvements are required to use such endoscope systems for real time live cell/structure imaging of the outflow pathway in the eye. In particular, the microprobe/scanning system should be watertight, and, especially for ex vivo (ab interno) experiments, the probe should be mounted into the perfusion anterior segment culture in a watertight fashion. We propose to build a new two-photon endoscope that is specific for the eye and capable of studying live cell/structure of the outflow pathway. The system will be built with components including a femtosecond excitation laser, a laser delivery unit, a fluorescence detection unit, an imaging acquisition unit, and a new endoprobe/scanning system. Because understanding the outflow pathway necessitates real time imaging of live cell/structure, the two-photon endoscopy system will be used in an ex vivo perfusion human anterior segment culture as well as in in vivo studies of monkey eyes. To observe the live cell/structure of the human outflow pathway ab interno (from anterior chamber side), the two-photon endoscopic system will be mounted on an ex vivo perfusion human anterior segment culture system, and real time live cell/structure imaging will be established. For in vivo imaging of the aqueous outflow pathway, monkey eyes will be observed, and the aqueous outflow pathway will be observed ab externo (from outside of the eye) to image it without disturbing the anterior chamber. This will be attempted after scleral flaps have been removed, with and without removal of the outer wall of Schlemm's canal. Fluorescein staining for live tissue will be part of the experimental design. The findings of these research endeavors may lead to novel real time imaging methods for investigating the outflow pathway and will help illustrate the aqueous outflow route and events. PUBLIC HEALTH RELEVANCE: The elevation of intraocular pressure often associated with glaucoma is related to reduced drainage of the aqueous humor fluid from the eye. The drainage pathway of the aqueous outflow is difficult to view with current technology; therefore, a new imaging system, such as two-photon laser scanning microscopy, would provide a better understanding of this system which may lead to newer treatments for glaucoma. The goal of the project is to develop a new endoscope system that is specifically designed for the study of the eye with excellent resolution and scanning speed so that two-photon imaging of the living outflow pathway can be achieved.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
Suppression of Ocular Scarring - Controlled Delivery of an ALK-5 Inhibitor
  • 批准号:
    8187958
  • 项目类别:
  • 资助金额:
    $31.05万
  • 财政年份:
    2011
  • 负责人:
    Hiroshi Nakamura
  • 依托单位:
Suppression of Ocular Scarring - Controlled Delivery of an ALK-5 Inhibitor
  • 批准号:
    8323428
  • 项目类别:
  • 资助金额:
    $31.05万
  • 财政年份:
    2011
  • 负责人:
    Hiroshi Nakamura
  • 依托单位:
Suppression of Ocular Scarring - Controlled Delivery of an ALK-5 Inhibitor
  • 批准号:
    8537461
  • 项目类别:
  • 资助金额:
    $29.5万
  • 财政年份:
    2011
  • 负责人:
    Hiroshi Nakamura
  • 依托单位:
Real time imaging of the aqueous outflow pathway by two-photon endoscopy
  • 批准号:
    7469304
  • 项目类别:
  • 资助金额:
    $24.17万
  • 财政年份:
    2008
  • 负责人:
    Hiroshi Nakamura
  • 依托单位:
海外基金