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过氧化物酶体增殖物激活受体α作为转录调控因子,参与植物源性不良化合物的解毒。

PPARα as a Transcriptional Regulator for Detoxification of Plant Diet-Derived Unfavorable Compounds.

机构信息

Department of Biochemistry, Meiji Pharmaceutical University, 2-522-1 Kiyose, Tokyo 204-8588, Japan.

出版信息

PPAR Res. 2012;2012:814945. doi: 10.1155/2012/814945. Epub 2012 Apr 19.

DOI:10.1155/2012/814945
PMID:22577367
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3345252/
Abstract

Plants contain potentially toxic compounds for animals and animals have developed physiological strategies to detoxify the ingested toxins during evolution. Feeding mice with various plant seeds and grains showed unexpected result that only sesame killed PPARα-null mice but not wild-type mice at all. A detailed analysis of this observation revealed that PPARα is involved in the metabolism of toxic compounds from plants as well as endobiotic substrates by inducing phase I and phase II detoxification enzymes. PPARα plays a vital role in direct or indirect activation of the relevant genes via the complex network among other xenobiotic nuclear receptors. Thus, PPARα plays its wider and more extensive role in energy metabolism from natural food intake to fat storage than previously thought.

摘要

植物中含有对动物有毒的化合物,而动物在进化过程中已经发展出了生理策略来解毒摄入的毒素。用各种植物种子和谷物喂养老鼠,结果出人意料,只有芝麻会杀死 PPARα 基因敲除的老鼠,而对野生型老鼠完全没有影响。对这一观察结果的详细分析表明,PPARα 参与了植物和内源性底物有毒化合物的代谢,通过诱导 I 相和 II 相解毒酶。PPARα 通过其他外来核受体之间的复杂网络,在直接或间接激活相关基因方面发挥着至关重要的作用。因此,PPARα 在从天然食物摄入到脂肪储存的能量代谢中发挥的作用比之前认为的更广泛、更深远。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebfe/3345252/f3574a57bf4a/PPAR2012-814945.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebfe/3345252/06af3ab38b6d/PPAR2012-814945.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebfe/3345252/03c22048adae/PPAR2012-814945.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebfe/3345252/f3574a57bf4a/PPAR2012-814945.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebfe/3345252/06af3ab38b6d/PPAR2012-814945.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebfe/3345252/03c22048adae/PPAR2012-814945.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebfe/3345252/f3574a57bf4a/PPAR2012-814945.003.jpg

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本文引用的文献

1
Physiologic roles of hepatic lipid droplets and involvement of peroxisome proliferator-activated receptor alpha in their dynamism.肝脂滴的生理作用及过氧化物酶体增殖物激活受体α在其动态变化中的作用。
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Fatty aldehyde dehydrogenase is up-regulated by polyunsaturated fatty acid via peroxisome proliferator-activated receptor alpha and suppresses polyunsaturated fatty acid-induced endoplasmic reticulum stress.脂酰辅酶 A 脱氢酶通过过氧化物酶体增殖物激活受体α被多不饱和脂肪酸上调,并抑制多不饱和脂肪酸诱导的内质网应激。
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11型17β-羟基类固醇脱氢酶中内质网/脂滴靶向序列的鉴定与表征
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Regulated expression by PPARalpha and unique localization of 17beta-hydroxysteroid dehydrogenase type 11 protein in mouse intestine and liver.过氧化物酶体增殖物激活受体α(PPARα)对11型17β-羟类固醇脱氢酶蛋白在小鼠肠道和肝脏中的表达调控及独特定位
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Dual subcellular localization in the endoplasmic reticulum and peroxisomes and a vital role in protecting against oxidative stress of fatty aldehyde dehydrogenase are achieved by alternative splicing.通过可变剪接实现脂肪醛脱氢酶在内质网和过氧化物酶体中的双亚细胞定位以及在抵御氧化应激方面的重要作用。
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Peroxisome proliferator-activated receptor alpha plays a vital role in inducing a detoxification system against plant compounds with crosstalk with other xenobiotic nuclear receptors.
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8
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