Imaging and Laser Revascularization in Hibernation
冬眠期间的成像和激光血运重建
基本信息
- 批准号:6537857
- 负责人:
- 金额:$ 30.66万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2001
- 资助国家:美国
- 起止时间:2001-08-01 至 2004-05-31
- 项目状态:已结题
- 来源:
- 关键词:angiogenesis autoradiography bioimaging /biomedical imaging blood flow measurement denervation echocardiography electrocardiography heart catheterization heart imaging /visualization /scanning heart innervation heart revascularization histopathology laser therapy myocardial ischemia /hypoxia noninvasive diagnosis swine
项目摘要
DESCRIPTION (Provided by Applicant): Identifying chronically ischemic
dysfunctional or hibernating myocardium is an important clinical endeavor.
Patients who are not candidates for CABG or PICA are now being considered for
new methods of revascularization such as direct myocardial revascularization
with laser channels using catheter based approach (DMR). Electromechanical
endocardial (UPV) mapping is used to guide DMR but is not fully validated.
Perfusion imaging and dobutamine echocardiography are being used clinically to
identify dysfunctional viable myocardium and assess results of novel
revascularization techniques. The accuracy of these imaging techniques for
these indications have never been fully validated in an animal model. Gold
standards for viability used in clinical studies are imperfect. A double
ameroid constrictor/swine model for hibernating myocardium shows promise as a
good model to compare these technologies against one another and against
histopathology and to investigate the efficacy and mechanisms of DMR. In the
first aim we propose to use swine models of extensive hibernation and of scar
to validate UPV mapping to identify viability vs scar and to compare thallium
imaging and dobutamine echocardiography against histopathology to identify
viability and sear. Under aims 2 and 3 the double vessel ameroid model will be
used to investigate mechanisms for DMR. The effect of laser therapy on
angiogenesis will be assessed using combined morphometric tissue analysis and
angiographic techniques. The efficacy of noninvasive imaging (adenosine Tc-99m
sestamibilrest Tl-201 and dobutamine echo) to detect neovascularization will be
assessed. In aim 4 radioiodinated MIBG autoradiography will be used to look at
the effects of DMR on regional innervation. The results of these experiments
should better define the accuracy of methods to image viability
and image angiogenesis, and lead to a better understanding of whether DMR
revascularizes the heart and whether or not it denervates the heart.
描述(由申请人提供):鉴别慢性缺血性
功能障碍或冬眠心肌是重要的临床奋进。
不适合CABG或PICA的患者现在正在考虑
新的血运重建方法,如直接心肌血运重建
使用基于导管的方法(DMR)的激光通道。机电
内分泌(UPV)映射用于指导DMR,但尚未完全验证。
灌注成像和多巴酚丁胺超声心动图正在临床上用于
识别功能障碍存活心肌并评估新的
血管重建技术。这些成像技术的准确性,
这些适应症从未在动物模型中得到充分验证。黄金
临床研究中使用的生存力标准是不完善的。双
冬眠心肌的Ameroid缩窄肌/猪模型显示出作为
一个很好的模型来比较这些技术,
组织病理学检查并研究DMR的疗效和机制。在
第一个目的,我们建议使用猪的广泛冬眠和疤痕模型,
验证UPV标测,以确定存活率与瘢痕,并比较铊
影像学和多巴酚丁胺超声心动图对组织病理学,以确定
活力和烧灼。在目标2和3下,双容器ameroid模型将被
用于研究DMR的机制。激光治疗的效果
将使用组合的形态测量组织分析来评估血管生成,
血管造影技术。无创显像(99 mTc-腺苷)
sestamibilrest Tl-201和多巴酚丁胺超声)检测新血管形成
评估。在aim 4中,将使用放射性碘标记的MIBG放射自显影来观察
DMR对局部神经支配的影响。这些实验的结果
应更好地定义方法的准确性,以图像的可行性
和图像血管生成,并导致更好地了解DMR是否
心脏血管的重建以及心脏的神经是否被切断。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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LYNNE L. JOHNSON其他文献
LYNNE L. JOHNSON的其他文献
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Novel Therapy for Diabetic PAD Monitored With Dual Isotope Multimodality Imaging
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- 批准号:
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8197198 - 财政年份:2008
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RAGE-directed imaging in diabetes-induced accelerated atherosclerosis
RAGE 定向成像治疗糖尿病引起的加速动脉粥样硬化
- 批准号:
7743062 - 财政年份:2008
- 资助金额:
$ 30.66万 - 项目类别:
RAGE-directed imaging in diabetes-induced accelerated atherosclerosis
RAGE 定向成像治疗糖尿病引起的加速动脉粥样硬化
- 批准号:
7996594 - 财政年份:2008
- 资助金额:
$ 30.66万 - 项目类别:
Imaging and Laser Revascularization in Hibernation
冬眠期间的成像和激光血运重建
- 批准号:
6638679 - 财政年份:2001
- 资助金额:
$ 30.66万 - 项目类别:
Imaging and Laser Revascularization in Hibernation
冬眠期间的成像和激光血运重建
- 批准号:
6332162 - 财政年份:2001
- 资助金额:
$ 30.66万 - 项目类别:
IMAGING INTIMAL HYPERPLASIA, MYOCYTE HYPOXIA, NECROSIS
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- 资助金额:
$ 30.66万 - 项目类别:
IMAGING INTIMAL HYPERPLASIA, MYOCYTE HYPOXIA, NECROSIS
内膜增生、心肌细胞缺氧、坏死的影像学检查
- 批准号:
6184656 - 财政年份:1998
- 资助金额:
$ 30.66万 - 项目类别:
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