Kim Hyung-Wook, Rao Jagadeesh S, Rapoport Stanley I, Igarashi Miki
National Institute on Aging, National Institutes of Health, Bethesda, MD, USA.
Biochim Biophys Acta. 2011 Feb;1811(2):111-7. doi: 10.1016/j.bbalip.2010.10.005. Epub 2010 Nov 9.
Dietary n-3 polyunsaturated fatty acid (PUFA) deprivation increases expression of arachidonic acid (AA 20:4n-6)-selective cytosolic phospholipase A(2) (cPLA(2)) IVA and cyclooxygenase (COX)-2 in rat brain, while decreasing expression of docosahexaenoic acid (DHA 22:6n-3)-selective calcium-independent iPLA(2) VIA. Assuming that these enzyme changes represent brain homeostatic responses to deprivation, we hypothesized that dietary n-6 PUFA deprivation would produce changes in the opposite directions.
Brain expression of PUFA-metabolizing enzymes and their transcription factors was quantified in male rats fed an n-6 PUFA adequate or deficient diet for 15weeks post-weaning.
The deficient compared with adequate diet increased brain mRNA, protein and activity of iPLA(2) VIA and 15-lipoxygenase (LOX), but decreased cPLA(2) IVA and COX-2 expression. The brain protein level of the iPLA(2) transcription factor SREBP-1 was elevated, while protein levels were decreased for AP-2α and NF-κB p65, cPLA(2) and COX-2 transcription factors, respectively.
With dietary n-6 PUFA deprivation, rat brain PUFA metabolizing enzymes and some of their transcription factors change in a way that would homeostatically dampen reductions in brain n-6 PUFA concentrations and metabolism, while n-3 PUFA metabolizing enzyme expression is increased. The changes correspond to reported in vitro enzyme selectivities for AA compared with DHA.
膳食中n-3多不饱和脂肪酸(PUFA)缺乏会增加大鼠脑中花生四烯酸(AA 20:4n-6)选择性胞质磷脂酶A2(cPLA2)IVA和环氧化酶(COX)-2的表达,同时降低二十二碳六烯酸(DHA 22:6n-3)选择性钙非依赖性iPLA2 VIA的表达。假设这些酶的变化代表大脑对缺乏的稳态反应,我们推测膳食中n-6 PUFA缺乏会产生相反方向的变化。
在断奶后15周喂食n-6 PUFA充足或缺乏饮食的雄性大鼠中,对PUFA代谢酶及其转录因子的脑表达进行定量。
与充足饮食相比,缺乏饮食增加了脑中iPLA2 VIA和15-脂氧合酶(LOX)的mRNA、蛋白质和活性,但降低了cPLA2 IVA和COX-2的表达。iPLA2转录因子SREBP-1的脑蛋白水平升高,而AP-2α和NF-κB p65、cPLA2和COX-2转录因子的蛋白水平分别降低。
在膳食n-6 PUFA缺乏的情况下,大鼠脑PUFA代谢酶及其一些转录因子的变化方式会在稳态上抑制脑n-6 PUFA浓度和代谢的降低,同时n-3 PUFA代谢酶的表达增加。这些变化与报道的体外酶对AA与DHA的选择性一致。