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Suppression of rat hepatic fatty acid synthase and S14 gene transcription by dietary polyunsaturated fat.

作者信息

Blake W L, Clarke S D

机构信息

Unit of Reproduction and Growth Physiology, Upjohn Company, Kalamazoo, MI 49001.

出版信息

J Nutr. 1990 Dec;120(12):1727-9. doi: 10.1093/jn/120.12.1727.

DOI:10.1093/jn/120.12.1727
PMID:2175783
Abstract

The objective of this research was to determine whether dietary polyunsaturated fatty acids suppress hepatic fatty acid synthase (FAS) mRNA levels by altering FAS gene transcription. Male Sprague-Dawley rats were meal-fed for 10 d a high glucose diet supplemented with 20% digestible energy as menhaden oil or tripalmitin. The transcription rate for FAS was determined by nuclear run-on analysis in hepatic nuclei isolated from rats 2 h postmeal. The values for transcription rates of FAS and S14 (a putative lipogenic protein) in rats fed menhaden oil were only 6 and 21%, respectively, of the rates in rats fed the tripalmitin diet (p less than 0.02). Gene transcription for beta-actin and phosphoenolpyruvate carboxykinase did not differ between treatments. The reduction in hepatic FAS mRNA levels caused by dietary polyunsaturated fats appears to be caused primarily by an inhibition of FAS transcription. The control of transcription by polyunsaturated fats appears not to be mediated by cAMP because the transcription rate for phosphoenolpyruvate carboxykinase (whose gene is very sensitive to cAMP stimulation) was unaffected by the source of dietary fat.

摘要

相似文献

1
Suppression of rat hepatic fatty acid synthase and S14 gene transcription by dietary polyunsaturated fat.
J Nutr. 1990 Dec;120(12):1727-9. doi: 10.1093/jn/120.12.1727.
2
Dietary polyunsaturated fats uniquely suppress rat liver fatty acid synthase and S14 mRNA content.膳食多不饱和脂肪能独特地抑制大鼠肝脏脂肪酸合酶及S14 mRNA含量。
J Nutr. 1990 Feb;120(2):225-31. doi: 10.1093/jn/120.2.225.
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Dietary polyunsaturated fats regulate rat liver sterol regulatory element binding proteins-1 and -2 in three distinct stages and by different mechanisms.膳食多不饱和脂肪通过三种不同阶段和不同机制调节大鼠肝脏固醇调节元件结合蛋白-1和-2。
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Polyunsaturated fatty acid suppression of hepatic fatty acid synthase and S14 gene expression does not require peroxisome proliferator-activated receptor alpha.多不饱和脂肪酸对肝脏脂肪酸合酶和S14基因表达的抑制作用并不需要过氧化物酶体增殖物激活受体α。
J Biol Chem. 1997 Oct 24;272(43):26827-32. doi: 10.1074/jbc.272.43.26827.
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Nutritional control of rat liver fatty acid synthase and S14 mRNA abundance.大鼠肝脏脂肪酸合酶和S14 mRNA丰度的营养调控。
J Nutr. 1990 Feb;120(2):218-24. doi: 10.1093/jn/120.2.218.
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Suppression of fatty acid synthase by dietary polyunsaturated fatty acids is mediated by fat itself, not by peroxidative mechanism.膳食多不饱和脂肪酸对脂肪酸合酶的抑制作用是由脂肪本身介导的,而非通过过氧化机制。
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