André A, Juanéda P, Sébédio J L, Chardigny J M
Unité Mixte de Recherche Institut National de la Recherche Agronomique-Etablissement National d'Enseignement Superieur Agronomique de Dijon Flaveur, Vision et Comportement du consommateur, France.
Lipids. 2005 Aug;40(8):799-806. doi: 10.1007/s11745-005-1441-x.
The aging brain undergoes modifications in the lipid composition of cell membranes and especially in plasmalogens. These phospholipids represent between one-half and two-thirds of the ethanolamine phospholipids in the brain. They are known to facilitate membrane fusion and act as endogenous antioxidants. During normal aging and in some pathological conditions, plasmalogen and DHA levels fall. In this context, we aimed to evaluate the influence of n-3 FA intake on plasmalogens in the brain during aging. Littermates from two generations of n-3-deficient rats were fed an n-3-deficient diet or an equilibrated diet containing either alpha-linolenic acid alone (alpha-LNA) or with two doses of DHA (0.3 or 0.6% w/w). After weaning, 9 mon of diet, or 21 mon of diet, plasmalogen levels were assessed, and the sn-2 substitutions of plasmenylethanolamines were analyzed in the cortex, striatum, and hippocampus. Our results showed that plasmalogen contents were not influenced by the diet. Plasmalogen levels were significantly decreased in aged rats compared with adults, whereas DHA levels increased in the hippocampus and remained stable in the cortex and striatum. DHA levels were significantly and similarly increased in total phospholipids and especially in plasmenylethanolamines after 9 mon of diet containing alpha-LNA alone or combined with DHA. This study showed that each structure sustained specific age-induced modifications. Dietary n-3 FA may not oppose the physiological decrease in brain plasmalogen levels during aging. Moreover, alpha-LNA appears to be equally as potent as preformed DHA at replacing DHA in the brain of our rat model.
衰老的大脑在细胞膜的脂质组成,尤其是缩醛磷脂方面会发生改变。这些磷脂占大脑中乙醇胺磷脂的二分之一到三分之二。已知它们有助于膜融合并作为内源性抗氧化剂发挥作用。在正常衰老过程以及某些病理状况下,缩醛磷脂和二十二碳六烯酸(DHA)水平会下降。在此背景下,我们旨在评估n-3脂肪酸摄入对衰老过程中大脑缩醛磷脂的影响。两代n-3缺乏大鼠的同窝仔鼠被喂食n-3缺乏饮食或平衡饮食,后者单独含有α-亚麻酸(α-LNA)或添加两剂DHA(0.3%或0.6% w/w)。断奶后、饮食9个月或21个月后,评估缩醛磷脂水平,并分析皮质、纹状体和海马体中缩醛乙醇胺的sn-2取代情况。我们的结果表明,缩醛磷脂含量不受饮食影响。与成年大鼠相比,老年大鼠的缩醛磷脂水平显著降低,而海马体中的DHA水平升高,皮质和纹状体中的DHA水平保持稳定。在单独含有α-LNA或与DHA组合的饮食9个月后,总磷脂尤其是缩醛乙醇胺中的DHA水平显著且相似地升高。这项研究表明,每个结构都经历了特定的年龄诱导变化。饮食中的n-3脂肪酸可能无法对抗衰老过程中大脑缩醛磷脂水平的生理性下降。此外,在我们的大鼠模型大脑中,α-LNA在替代DHA方面似乎与预先形成的DHA同样有效。