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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 ω-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-α 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;然而,目前的治疗选择是有限的。流行病学研究表明,高ω-3多不饱和脂肪酸(n-3)的饮食可以减缓晚期AMD患者的疾病进展。在这项研究中,我们评估了这种饮食对> Ccl2 -/- / > Cx3cr1 -/-< / sup>小鼠,一种发展为AMD样视网膜病变的模型,其中包括局灶性深部视网膜病变,异常的视网膜色素上皮,光感受器变性和A2E积累。摄入高n-3脂肪酸饮食的> Ccl2 -/- / > Cx3cr1 -/-小鼠显示与低n-3脂肪酸组相比,视网膜病变的进展较慢。被给予高水平的n-3脂肪酸的一些小鼠患有病变逆转。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E2和白三烯B4)减少和抗炎衍生物(前列腺素D2)增加。我们还测量了饲喂高n-3脂肪酸饮食的小鼠的较低眼部> TNF-α和> IL-6 转录水平。我们在这些小鼠中的发现与人类通过长链n-3脂肪酸降低AMD风险的研究一致。该鼠模型提供了一种有用的工具,可以评估可能会延迟AMD发展的疗法。

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