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A High Omega-3 Fatty Acid Diet Reduces Retinal Lesions in a Murine Model of Macular Degeneration

机译:高Omega-3脂肪酸饮食可减少黄斑变性的小鼠模型中的视网膜病变。

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摘要

Age-related macular degeneration (AMD) is one of the leading cause of blindness among the elderly; however, current therapy options are limited. Epidemiological studies have shown that a diet that is high in -3 polyunsaturated (n-3) fatty acids can slow disease progression in patients with advanced AMD. In this study, we evaluated the effect of such a diet on the retinas of Ccl2–/–/Cx3cr1–/– mice, a model that develops AMD-like retinal lesions that include focal deep retinal lesions, abnormal retinal pigment epithelium, photoreceptor degeneration, and A2E accumulation. Ccl2–/–/Cx3cr1–/– mice that ingested a high n-3 fatty acid diet showed a slower progression of retinal lesions compared with the low n-3 fatty acids group. Some mice that were given high levels of n-3 fatty acids had lesion reversion. We found a shunted arachidonic acid metabolism that resulted in decreased pro-inflammatory derivatives (prostaglandin E2 and leukotriene B4) and an increased anti-inflammatory derivative (prostaglandin D2). We also measured lower ocular TNF- and IL-6 transcript levels in the mice fed a diet of high n-3 fatty acids. Our findings in these mice are in line with human studies of AMD risk reduction by long-chain n-3 fatty acids. This murine model provides a useful tool to evaluate therapies that might delay the development of AMD.
机译:年龄相关性黄斑变性(AMD)是老年人失明的主要原因之一。但是,目前的疗法 选项是有限的。流行病学研究表明, 高饮食的-3多不饱和(n-3)脂肪酸 可以减缓晚期AMD患者的疾病进展。 在本研究中,我们评估了这种饮食对Ccl2 – / – / Cx3cr1 – / – 小鼠 视网膜的影响,一个 模型,其发展为AMD样视网膜病变,包括局灶性 深度视网膜病变,异常的视网膜色素上皮,感光器 变性和A2E积累。摄入高n-3脂肪酸饮食的小鼠的Ccl2 – / – / Cx3cr1 – / – 表现出较慢的 酸组相比,视网膜病变的进展。给予高水平n-3脂肪酸 酸的某些小鼠具有病变逆转。我们发现分流的花生四烯酸 代谢导致促炎衍生物 (前列腺素E 2 和白三烯B 4 )和增加的抗炎性 衍生物(前列腺素D 2 )。我们还测量了喂食高 n-3脂肪酸饮食的小鼠的较低眼sups TNF-α和IL-6转录水平。我们在这些小鼠中的发现与 人类研究有关通过长链n-3脂肪 酸降低AMD风险的研究一致。此鼠模型提供了一种有用的工具,用于评估可能延缓AMD发展的 疗法。

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  • 来源
    《American Journal of Pathology》 |2009年第2期|799-807|共9页
  • 作者单位

    From the Section of Immunopathology,Laboratory of Immunology, National Eye Institute;

    From the Section of Immunopathology,Laboratory of Immunology, National Eye Institute;

    From the Section of Immunopathology,Laboratory of Immunology, National Eye Institute;

    From the Section of Immunopathology,Laboratory of Immunology, National Eye Institute;

    From the Section of Immunopathology,Laboratory of Immunology, National Eye Institute;

    From the Section of Immunopathology,Laboratory of Immunology, National Eye Institute;

    the Section on Neuroendocrinology,National Institute of Child Health and Human Development;

    Laboratory of Membrane Biochemistry and Biophysics,and the National Institute on Alcohol Abuse and Alcoholism, National Institutes of Health, Bethesda, Maryland;

    Laboratory of Membrane Biochemistry and Biophysics,and the National Institute on Alcohol Abuse and Alcoholism, National Institutes of Health, Bethesda, Maryland;

    From the Section of Immunopathology,Laboratory of Immunology, National Eye Institute;

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