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BIOCHEMISTRY AND PHARMACOLOGY OF THE MACULAR CAROTENOIDS

BIOCHEMISTRY AND PHARMACOLOGY OF THE MACULAR CAROTENOIDS
黄斑类胡萝卜素的生物化学和药理学
批准号:
2711202
负责人:
PAUL STEVEN BERNSTEIN
金额:
$16.92万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
1997
资助国家:
美国
项目状态:
已结题
起止时间:
1997-08-01 至 2002-07-31

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中文摘要
翻译
人类的黄斑,视网膜的专门区域, 对于高分辨率视觉敏锐度,选择性地积累两个 叶黄素11类胡萝卜素来源于饮食,叶黄素和 玉米黄质 最近的一些流行病学研究表明, 显示了饮食摄入量与 叶黄素和玉米黄质与疾病进展风险相关 黄斑变性(AMD)是导致失明的主要原因, 美国的老年人。 人们认为黄斑 类胡萝卜素保护视网膜免受最小的损伤, 过滤掉有害波长的光, 抗氧化剂 介导选择性摄取的生化机制, 浓度和稳定的黄斑类胡萝卜素是 未知 在低等动物中,如龙虾和蓝藻, 专门的类胡萝卜素结合蛋白执行这些任务。 是 假设类似的类胡萝卜素结合蛋白可能具有 在人类黄斑中也有类似的作用。 该项目的一个主要目标是 去理解那些负责特定的 叶黄素和玉米黄质沉积的黄斑,具有特殊的 重点是寻找潜在的类胡萝卜素结合蛋白。 该项目还将研究类胡萝卜素的性质- 通过定量结合的蛋白质和类胡萝卜素-脂质相互作用 研究和各种光谱方法,包括共振 拉曼光谱,在模型系统和完整的视网膜组织。 这一建议的实验可能会提供新的见解 叶黄素和玉米黄质特异性摄取的生化基础 黄斑摄取机制紊乱, 黄斑类胡萝卜素的稳定可能会产生深远的影响 AMD和遗传性视网膜营养不良的进展。 预期的干预性临床研究可能会采取 具体吸收系统的优势,以提高水平, 黄斑类胡萝卜素色素,可能延缓或阻止 由这些疾病引起的渐进性失明。
英文摘要
The human macula, the specialized region of the retina responsible for high resolution visual acuity, selectively accumulates two xanthophy11 carotenoids derived from the diet, lutein and zeaxanthin. Several recent epidemiological studies have demonstrated a strong inverse correlation between dietary intake of lutein and zeaxanthin and the risk of progression Age-Related Macular Degeneration (AMD) the leading cause of blindness among the elderly in the United States. It is thought that the macular carotenoids protect against least-induced damage to the retina by filtering out damaging wavelengths of light and by acting as antioxidants. The biochemical mechanisms that mediate the selective uptake, concentration, and stabilization of the macular carotenoids are unknown. In lower animals, such as lobsters and cyanobacteria, specialized carotenoid-binding proteins perform these tasks. It is hypothesized that comparable carotenoid-binding proteins may have a similar role in the human macula. A major goal of this project is to understand the biochemical processes responsible for the specific deposition of lutein and zeaxanthin the macula, with special emphasis on the search for potential carotenoid-binding proteins. This project will also investigate the properties of carotenoid- protein and carotenoid-lipid interactions through quantitative binding studies and various spectroscopic methods, including resonance Raman spectroscopy, in model systems and in intact retinal tissue. The experiments of this proposal may provide new insights into the biochemical basis of the specific uptake lutein and zeaxanthin into the macula. Derangements of the mechanisms of uptake and stabilization of the macular carotenoids could have profound impact on the progression of AMD and inherited retinal dystrophies. Anticipated interventional clinical studies may be able to take advantage of the specific uptake systems to increase the level of macular carotenoid pigment and perhaps retard or prevent the progressive blindness produced by these diseases.
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海外基金