脂质代谢中的过氧化物酶体。

U Seedorf
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引用次数: 0

摘要

遗传过氧化物酶体疾病的基因靶向和突变的阐明为体内过氧化物酶体脂质代谢提供了新的见解。这项工作鉴定了一种新的过氧化物酶体β氧化途径,并清楚地确定了脂肪酸高效过氧化物酶体氧化所需的基因同时也是体内PPAR α功能的关键调节因子。新的小鼠模型可能为寻找未知的天然PPAR α激动剂和筛选体内PPAR α拮抗剂提供有用的工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Peroxisomes in lipid metabolism.

Gene targeting and the elucidation of mutations underlying inherited peroxisomal diseases have provided new insights in peroxisomal lipid metabolism in vivo. The work led to the identification of a novel peroxisomal beta-oxidation pathway and established clearly that genes, which are required for efficient peroxisomal oxidation of fatty acids, at the same time are key regulators of PPAR alpha function in vivo. The new mouse models may provide helpful tools in the search for unknown natural PPAR alpha agonists and in screening for in vivo PPAR alpha antagonists.

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