Novel regulatory roles of omega-3 fatty acids in metabolic pathways: a proteomics approach

被引:31
作者
Ahmed, Abeer A. [1 ]
Balogun, Kayode A. [1 ]
Bykova, Natalia V. [2 ]
Cheema, Sukhinder K. [1 ]
机构
[1] Mem Univ Newfoundland, Dept Biochem, St John, NF A1B 3X9, Canada
[2] Mem Univ Newfoundland, Dept Biol, St John, NF A1B 3X9, Canada
基金
加拿大健康研究院; 加拿大创新基金会; 加拿大自然科学与工程研究理事会;
关键词
POLYUNSATURATED FATTY-ACIDS; ADVANCED GLYCATION ENDPRODUCTS; ISCHEMIA-REPERFUSION INJURY; ORNITHINE AMINOTRANSFERASE; ADENOSINE KINASE; CARDIOVASCULAR-DISEASE; INSULIN-RESISTANCE; HEPATIC STEATOSIS; GLYOXALASE I; RAT-LIVER;
D O I
10.1186/1743-7075-11-6
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 [营养与食品卫生学];
摘要
Background: Omega-3 polyunsaturated fatty acids (n-3 PUFA) have been shown to alleviate the symptoms of metabolic disorders, such as heart disease, diabetes, obesity and insulin resistance. Several putative mechanisms by which n-3 PUFA elicit beneficial health effects have been proposed; however, there is still a shortage of knowledge on the proteins and pathways that are regulated by n-3 PUFA. Methods: Using two dimensional polyacrylamide gel electrophoresis (2D-PAGE) and liquid chromatography-tandem mass spectrometry (LC-MS/MS) analysis, we investigated the effects of diets high or low in n-3 PUFA on hepatic proteomic profile of C57BL/6 mice. Results: The findings show for the first time that high dietary n-3 PUFA reduced the expression of regucalcin, adenosine kinase and aldehyde dehydrogenase. On the other hand, diets high in n-3 PUFA increased the expression of apolipoprotein A-I, S-adenosylmethionine synthase, fructose-1, 6-bisphosphatase, ketohexokinase, malate dehydrogenase, GTP-specific succinyl CoA synthase, ornithine aminotransferase and protein disulfide isomerase-A3. Conclusions: Our findings revealed for the first time that n-3 PUFA causes alterations in several novel functional proteins involved in regulating lipid, carbohydrate, one-carbon, citric acid cycle and protein metabolism, suggesting integrated regulation of metabolic pathways. These novel proteins are potential targets to develop therapeutic strategies against metabolic disorders.
引用
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页数:11
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