Department of Physiology, Faculty of Medicine, Universidad Autónoma de Madrid, C/ Arzobispo Morcillo, 2, 28029 Madrid, Spain.
Department of Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, 330 Brookline Avenue, Boston, MA 02215, USA.
Nutrients. 2020 Jan 1;12(1):122. doi: 10.3390/nu12010122.
After birth, preterm infants are deficient in arachidonic acid (ARA), docosahexaenoic acid (DHA), and antioxidants, increasing their risk of oxidative stress-related pathologies. The principal aim was to evaluate if supplementation with long-chain polyunsaturated fatty acids (LCPUFAs) improves antioxidant defenses. In total, 21 preterm infants were supplemented with ARA and DHA in a 2:1 ratio (ARA:DHA-S) or with medium-chain triglycerides (MCT-S). Plasma -3 and -6 LCPUFAs were measured at birth, postnatal day 28, and 36 weeks of postmenstrual age (36 WPA) by gas chromatography-mass spectroscopy. Plasma antioxidants (glutathione (GSH), catalase, and thiols) and oxidative damage biomarkers (malondialdehyde (MDA), carbonyls) were analyzed at the same time points by spectrophotometry, and scores of antioxidant status (Antiox-S) and oxidative damage (Proxy-S) were calculated. At 36 WPA, linoleic acid (LA) and dihomo--linolenic acid (DGLA) were decreased in ARA:DHA-S compared to the MCT-S group (LA: ARA:DHA-S = 18.54 1.68, MCT-S = 22.80 1.41; = 0.018; DGLA: ARA:DHA-S = 1.68 0.38, MCT-S = 2.32 0.58; = 0.018). Furthermore, α-linolenic acid (ALA) was increased in ARA:DHA-S (ARA:DHA-S = 0.52 0.33, MCT-S = 0.22 0.10; = 0.018). Additionally, LA:DHA ratio was decreased in the ARA:DHA-S compared to control group (ARA:DHA-S = 6.26 2.35, MCT-S = 8.21 2.65; = 0.045). By the end of supplementation (36 WPA), catalase, thiol groups, and Antiox-S were significantly higher in neonates receiving ARA:DHA-S compared to those receiving MCT-S, with no differences in oxidative stress biomarkers. In conclusion, ARA:DHA supplementation in preterm neonates resulted in an overall improvement in antioxidant to oxidant balance and a decrease in early fatty acid precursors of the n-6 relative to the n-3 pathway. These effects may reduce oxidative stress and inflammation.
出生后,早产儿体内的花生四烯酸(ARA)、二十二碳六烯酸(DHA)和抗氧化剂含量不足,增加了他们患氧化应激相关疾病的风险。本研究的主要目的是评估补充长链多不饱和脂肪酸(LCPUFAs)是否能改善抗氧化防御能力。共有 21 名早产儿接受了 ARA 和 DHA 以 2:1 比例(ARA:DHA-S)或中链甘油三酯(MCT-S)的补充。通过气相色谱-质谱法在出生时、出生后 28 天和 36 周的校正胎龄(36 WPA)时测量血浆中的 -3 和 -6 LCPUFAs。同时通过分光光度法分析血浆中的抗氧化剂(谷胱甘肽(GSH)、过氧化氢酶和硫醇)和氧化损伤生物标志物(丙二醛(MDA)、羰基),并计算抗氧化状态评分(Antiox-S)和氧化损伤评分(Proxy-S)。在 36 WPA 时,与 MCT-S 组相比,ARA:DHA-S 组的亚油酸(LA)和二高--亚麻酸(DGLA)减少(LA:ARA:DHA-S = 18.54 1.68,MCT-S = 22.80 1.41; = 0.018;DGLA:ARA:DHA-S = 1.68 0.38,MCT-S = 2.32 0.58; = 0.018)。此外,ARA:DHA-S 组的α-亚麻酸(ALA)增加(ARA:DHA-S = 0.52 0.33,MCT-S = 0.22 0.10; = 0.018)。此外,与对照组相比,ARA:DHA-S 组的 LA:DHA 比值降低(ARA:DHA-S = 6.26 2.35,MCT-S = 8.21 2.65; = 0.045)。在补充结束时(36 WPA),接受 ARA:DHA-S 补充的新生儿的过氧化氢酶、硫醇基团和 Antiox-S 明显高于接受 MCT-S 补充的新生儿,而氧化应激生物标志物没有差异。总之,早产儿补充 ARA:DHA 可改善抗氧化剂与氧化剂的平衡,并减少早期 n-6 脂肪酸前体相对于 n-3 途径。这些作用可能会降低氧化应激和炎症。