Contrasting effects of fish oil and safflower oil on hepatic peroxisomal and tissue lipid content

被引:122
作者
Neschen, S
Moore, I
Regittnig, W
Yu, CL
Wang, YL
Pypaert, M
Petersen, KF
Shulman, GI
机构
[1] Yale Univ, Sch Med, Howard Hughes Med Inst, New Haven, CT 06520 USA
[2] Yale Univ, Sch Med, Dept Internal Med Cellular & Mol Physiol, New Haven, CT 06520 USA
[3] Yale Univ, Sch Med, Dept Cell Biol, New Haven, CT 06520 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM | 2002年 / 282卷 / 02期
关键词
peroxisome proliferator-activating receptor-alpha; beta-oxidation; diacylglycerol; acyl-CoA oxidase; 3-ketoacyl-CoA thiolase;
D O I
10.1152/ajpendo.00414.2001
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
To examine the mechanism by which fish oil protects against fat-induced insulin resistance, we studied the effects of control, fish oil, and safflower oil diets on peroxisomal content, fatty acyl-CoA, diacylglycerol, and ceramide content in rat liver and muscle. We found that, in contrast to control and safflower oil-fed rats, fish oil feeding induced a 150% increase in the abundance of peroxisomal acyl-CoA oxidase and 3-ketoacyl-CoA thiolase in liver but lacked similar effects in muscle. This was paralleled by an almost twofold increase in hepatic peroxisome content (both P < 0.002 vs. control and safflower). These changes in the fish oil-fed rats were associated with a more than twofold lower hepatic triglyceride/diacylglycerol, as well as intramuscular triglyceride/fatty acyl-CoA, content. In conclusion, these data strongly support the hypothesis that n-3 fatty acids protect against fat-induced insulin resistance by serving as peroxisome proliferator-activated receptor-alpha ligands and thereby induce hepatic, but not intramuscular, peroxisome proliferation. In turn, an increased hepatic beta-oxidative capacity results in lower hepatic triglyceride/diacylglycerol and intramyocellular triglyceride/fatty acyl-CoA content.
引用
收藏
页码:E395 / E401
页数:7
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