Regulation of rat brain polyunsaturated fatty acid (PUFA) metabolism during graded dietary n-3 PUFA deprivation

被引:41
作者
Kim, Hyung-Wook [1 ]
Rao, Jagadeesh S. [1 ]
Rapoport, Stanley I. [1 ]
Igarashi, Miki [1 ]
机构
[1] NIA, Brain Physiol & Metab Sect, NIH, Bethesda, MD 20892 USA
来源
PROSTAGLANDINS LEUKOTRIENES AND ESSENTIAL FATTY ACIDS | 2011年 / 85卷 / 06期
基金
美国国家卫生研究院;
关键词
n-3 PUFA deprivation; Rat brain; Phospholipase A(2); Docosapentaenoic acid; ALPHA-LINOLENIC ACID; CA2+-INDEPENDENT PHOSPHOLIPASE A(2); AIN-93 PURIFIED DIETS; DOCOSAHEXAENOIC ACID; NUTRITIONAL DEPRIVATION; EXPRESSION; LIVER; PURIFICATION; DEPRESSION; MECHANISMS;
D O I
10.1016/j.plefa.2011.08.002
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Knowing threshold changes in brain lipids and lipid enzymes during dietary n-3 polyunsaturated fatty acid deprivation may elucidate dietary regulation of brain lipid metabolism. To determine thresholds, rats were fed for 15 weeks DHA-free diets having graded reductions of alpha-linolenic: acid (alpha-LNA). Compared with control diet (4.6% alpha-LNA), plasma DHA fell significantly at 1.7% dietary alpha-LNA while brain DHA remained unchanged down to 0.8% alpha-LNA, when plasma and brain docosapentaenoic acid (DPAn-6) were increased and DHA-selective iPLA(2) and COX-1 activities were downregulated. Brain AA was unchanged by deprivation, but AA selective-cPLA(2), sPLA(2) and COX-2 activities were increased at or below 0.8% dietary alpha-LNA, possibly in response to elevated brain DPAn-6. In summary, homeostatic mechanisms appear to maintain a control brain DHA concentration down to 0.8% dietary DHA despite reduced plasma DHA, when DPAn-6 replaces DHA. At extreme deprivation, decreased brain iPLA(2) and COX-1 activities may reduce brain DHA loss. Published by Elsevier Ltd.
引用
收藏
页码:361 / 368
页数:8
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