International Journal of Psychiatry and Neurology
Vol.06 No.03(2017), Article ID:21802,6 pages
10.12677/IJPN.2017.63009

DHA, Eat or Not Eat?

Wenfang Zhang1*, Haijing Yan2, Zhi Yang2, Dong Wang3#

1Binzhou Medical University, Yantai Shandong

2Institute for Metabolic and Neuropsychiatric Disorders, Binzhou Medical University, Yantai Shandong

3Yantai Affiliated Hospital of Binzhou Medical University, Yantai Shandong

Received: Aug. 4th, 2017; accepted: Aug. 18th, 2017; published: Aug. 24th, 2017

ABSTRACT

Various health products are sold on the market at present. How can we choose a health product which has no side effects and a wholesome product on disease? DHA (omega-3:7, 10, 13, 16, 19-docosahexaenoic acid) as a kind of polyunsaturated fatty acids, can across the blood-brain barrier, which are the important raw material for the formation of cerebral cortex neuron membrane and could improve human cognitive function and reduce the occurrence of Alzheimer's disease and depression. Method: This paper summarizes the research of DHA in foreign countries in recent years. Result and Conclusion: The development and utilization of DHA has been paid attention and concerned by all countries in the world. DHA can prevent and improve mental illnesses and neurodegenerative diseases. Choosing DHA as a health supplement is a wise choice.

Keywords:DHA, Fatty Acids, Health Products, Nervous System, Alzheimer’s Disease, Depression

DHA,吃还是不吃?

张文芳1*,闫海静2,杨志2,王东3#

1滨州医学院,山东 烟台

2滨州医学院代谢与神经精神疾病研究所,山东 烟台

3滨州医学院烟台附院,山东 烟台

收稿日期:2017年8月4日;录用日期:2017年8月18日;发布日期:2017年8月24日

摘 要

目的:目前市场上出售的保健品种类繁多,我们如何选择一种无副作用还能对疾病起到预防作用的保健品呢?DHA (ω-3:7,10,13,16,19-二十二碳六烯酸)作为一种多不饱和脂肪酸,能够通过血脑屏障,是大脑皮层神经元细胞膜的形成的重要原料;改善人类认知功能,减轻阿尔茨海默病和抑郁症的发生;方法:本文把近年来国外对DHA的研究情况作了系统综述。结果与结论:DHA的开发利用己受到世界各国的关注和重视。DHA能够预防和改善精神疾病和神经退行性病变。选择DHA作为一种保健品,不失为一种明智的选择。

关键词 :DHA,脂肪酸,保健品,神经系统,阿尔茨海默病,抑郁症

Copyright © 2017 by authors and Hans Publishers Inc.

This work is licensed under the Creative Commons Attribution International License (CC BY).

http://creativecommons.org/licenses/by/4.0/

1. 引言

中枢神经系统接受着全身各处的传入信息,经过大脑的整合加工后协调输出运动、感觉等信息,或者把信息储存在中枢神经系统内成为学习、记忆的神经基础 [1] [2] 。脑,作为中枢神经系统的重要组成部分,吸收了丰富的ω-3脂肪酸。以前大量研究结果表明 [3] [4] , DHA (ω-3:7,10,13,16,19-二十二碳六烯酸)作为一种多不饱和脂肪酸,对人体大有脾益。鉴于目前市面上所售的保健品琳琅满目,我们如何选择一种无副作用、还能对疾病起到预防作用的保健品呢?称为“脑黄金”的DHA是不是最好的选择?在这里,我们对DHA在中枢神经系统的作用作一下综述,特别是对阿尔茨海默病及抑郁症的预防和治疗提供新的方向。

2. 脂质与DHA

脂质种类繁多且结构复杂,它与生命活动和疾病的关系远比我们想象的要复杂 [5] 。脂质是脂肪和类脂的总称,脂肪即甘油三酯,也称三脂酰甘油。类脂包括固醇及其酯、磷脂、糖脂等。脂肪酸是脂肪烃的羧酸,脂肪酸的结构通式为CH3 (CH2)nCOOH [6] [7] 。高等动植物的脂肪酸碳链长度一般在14~20之间,为偶数碳。ω编码体系从甲基碳起计双键位置不含双键的脂肪酸为饱和脂肪酸,不饱和脂肪酸含一个或以上双键。含一个双键的脂肪酸称为单不饱和脂肪酸;含两个及以上双键的脂肪酸为多不饱和脂肪酸。根据双键的位置,多不饱和脂肪酸分为ω-3、ω-6、ω-7、ω-9四簇。高等动物体内的多不饱和脂肪酸多由相应的母体脂肪酸衍生而来,ω-3、ω-6和ω-9簇不能在体内相互转化 [8] [9] 。DHA (二十二碳六烯酸)是有六个双键的多不饱和脂肪酸,是一种ω-3必需脂肪酸它是由亚麻酸衍生而来。

3. DHA的代谢(合成与分解)

不饱和脂肪酸根据分子结构中双键数目的不同,分为单不饱和脂肪酸和多不饱和脂肪酸 [10] [11] 。在食物脂肪中,单不饱和脂肪酸主要有油酸,多不饱和脂肪酸主要有亚油酸、亚麻酸、花生四烯酸。人体不能合成油酸、亚油酸和亚麻酸,必须从日常膳食中补充,被称为必需脂肪酸。

DHA的体内来源是前体脂肪酸。亚麻酸、亚油酸进入人体后,经2次碳链延长酶和去饱和酶的作用衍生为DHA。DHA主要存在于海洋生物和植物油中。海洋生物如鱼类、虾类、海藻等 [12] [13] 。种籽油中富含丰富的亚麻酸,比如玫瑰籽油、印加果油、紫苏籽油、沙棘籽油等。葵花籽油富含多1%的亚麻酸、芥花籽油富含10%、玫瑰果油富含33%、美藤果油富含49%、奇亚籽油富含64%;亚麻酸的大量供给增加了多不饱和脂肪酸的抗氧化活性及脂肪酸的氧化。目前,市面上所售的DHA大多是由海洋生物或者植物籽油中提取或者纯化培养,经抽提和精炼得来。

人体摄入的脂质不溶于水,不能与消化酶充分接触 [14] 。胆汁酸有较强的乳化作用,能够降低脂-水相间的表面张力,将脂质乳化成小颗粒,极易进入小肠粘膜表面的水屏障,促进了脂质消化。胆汁和胰液分泌后进入十二指肠,所以小肠上段是消化脂质的主要场所。

4. DHA与脑

DHA大量存在于人脑细胞中 [15] ,占大脑脂肪酸的25%~33%,占细胞膜脂肪的50%,它与胆碱、磷脂等构成大脑皮层皮质的神经细胞膜,是脑神经元储存和处理信息的重要物质,对脑细胞的分裂、神经传导等有着极为重要的作用 [16] [17] 。DHA是细胞膜磷脂(磷脂酰胆碱、磷脂酰乙醇胺和磷脂酰丝氨酸)的重要组成部分,由于其特殊的3D结构,能够减轻细胞膜脂质双分子层的厚度、增加细胞膜的流动性、提高细胞膜的渗透性。DHA能够调节许多膜蛋白的活性,包括离子通道、受体和酶 [18] ,DHA还能够与许多脂质、胆固醇、神经鞘磷脂相互作用 [19] 。DHA比EPA更能增加细胞膜的流动性 [20] [21] 。PUFA对于神经元的发育也是很关键的,比如神经突触、神经轴突、视锥细胞、视杆细胞,神经髓鞘的生成。DHA还能调节突出功能和视觉的准确性。DHA通过激活PI3-K/Akt通路提高神经突触的可塑性。此外,EPA和DHA还能够通过n-6PUFAs抑制神经免疫 [22] 。

5. DHA与阿尔茨海默病

阿尔茨海默病(Alzheimer’s Disease, AD)是发生于老年和老年前期,以进行性认知功能障碍和行为损害为特征的中枢神经系统退行性疾病,是老年期痴呆最常见的类型。我国每年新发病例30万,且每20年翻一翻。AD可分为家族性AD和散发性AD,家族性AD呈常染色体显性遗传,多于年老起病,其病因是位于21染色体的淀粉样前体蛋白基因(Amyloid precursor protein, APP)、位于14号染色体的早老素1基因(Presenilin1, PS1)及位于1号染色体的早老素2基因(Presenilin2, PS2)突变。而大多数散发性AD与载脂蛋白E基因有关 [23] 。目前关于AD的发病机制有许多假说,β淀粉样蛋白(p-amyloid β)组成的斑块和由过度磷酸化的tau蛋白组成的纤维缠结是影响较为广泛地假说 [24] [25] [26] 。此外,还有细胞周期调节蛋白障碍、氧化应激、炎性机制、线粒体功能障碍等多种假说。

最近流行病学研究表明 [27] ,DHA由于其降低胆固醇的作用能够降低AD的发生。高胆固醇血症影响了β-淀粉样蛋白前体蛋白酶的处理,使Aβ-淀粉样蛋白沉积。而DHA通过调节胆固醇通路影响胆固醇的代谢,降低Aβ-淀粉样蛋白沉积。

DHA能够改善人类的认知功能。然而,其最佳摄入量是多少?没有一个确切的定义 [28] 。有研究者收录了具有轻度认知功能障碍、认知功能下降、痴呆、阿尔茨海默病、帕金森疾病的21个研究小组,181,580位参与者,并对4438例作了长期随访研究。得到的结论是:每周摄入一次鱼,能够降低得痴呆和帕金森的风险;相应的每天摄入8 g多不饱和脂肪酸,能够降低得认知功能障碍和痴呆的风险;DHA作为多不饱和脂肪酸的重要来源,每天摄入0.1 g的DHA,就能够降低得痴呆和帕金森的风险,但是两者之间没有线性相关关系。

DHA能够改善轻度记忆障碍成年患者的情景记忆功能 [29] 。载脂蛋白E (ApoE)主要是在脑内中枢神经系统中合成,载脂蛋白E对脂质的合成和转运起到了关键作用 [30] 。特别是ApoE及其受体通路在胆固醇转运中起关键作用。脑中的胆固醇含量是非常多的 [31] 。胆固醇在维持神经细胞的正常功能起关键作用,能促进突触形成及其发展。在细胞实验中,多不饱和脂肪酸能够促进神经轴突的生长、胞体的形成 [32] [33] [34] 。在AD动物模型中,脑组织中高表达的多不饱和脂肪酸能够降低tau蛋白的沉积 [35] 增加突触传递 [36] 、提高认知功能 [37] 、减轻AD症状。在得AD之前尽早进行干预及早预防,DHA比其他多数药物要健康,可以作为预防药物。随着年龄的增长,记忆力下降也需要提早进行干预。与其他营养保健品相比较,DHA是非常受欢迎的。

6. DHA与抑郁症

抑郁症是一种常见的心境障碍,可由各种原因引起,以显著而持久的心境低落为主要临床特征,心境低落与其处境不相称。严重者可出现自杀念头和行为。据世界卫生组织统计,抑郁症成为全球第四大疾病,预计2020年可能成为仅次于冠心病的大二大疾病 [19] 。目前,抑郁症的病因尚不明确,有两大假说,神经递质学说和神经回路学说。下丘脑–垂体–肾上腺轴功能紊乱和皮质–纹状体–丘脑–皮质回路出现信息传导不畅,最终导致神经退化、海马神经功能减退,而损害认知功能。

全球大约有10%重度抑郁的患者 [38] [39] ,根据第五版国际精神疾病的诊断和统计分析得出,重度抑郁表现为丧失兴趣、自卑、睡眠功能紊乱、食欲减退或、精力不能集中或者不能思考,这些症状会一直持续,变得越来越重,甚至会出现自杀倾向 [19] [37] 。据流行病学调查研究显示,大约20,000多篇报道证实多摄入多不饱和脂肪酸能够减轻抑郁的发生、改善抑郁症状 [40] [41] 。每天摄入1 g的DHA能够提高汉密顿抑郁量表的评分。

7. 结论

DHA大量存在于人脑细胞中,占大脑脂肪酸的25%~33%,占细胞膜脂肪的50%,它与胆碱、磷脂等构成大脑皮层皮质神经细胞膜,是脑细胞储存和处理信息的重要物质结构。DHA具有神经保护作用,能够稳定和修复神经细胞膜、增加细胞膜的流动性;营养修复神经细胞和突触小泡、增加神经细胞突触的可塑性。目前研究认为,DHA这种不饱和脂肪酸是神经系统细胞生长及维持的一种主要元素,是大脑和视网膜的重要构成成分,是对人体非常重要的多不饱和脂肪酸,尤其对婴幼儿及孕妇,是早产儿智力和视力发育关键因子。目前,DHA的开发利用己受到世界各国的关注和重视。DHA能够预防和改善精神疾病和神经退行性病变。特别是为阿尔茨海默病的预防和治疗提供了新的方向。综上所述,我们可以考虑选择DHA作为一种保健品。

基金项目

山东省自然科学基金(ZR2014HM026)。

致谢

感谢山东省自然科学基金(ZR2014HM026)、滨州医学院代谢与神经精神疾病研究所路新云教授泰山学者团队、滨州医学院医药研究中心的支持。

文章引用

张文芳,闫海静,杨 志,王 东. DHA,吃还是不吃?
DHA, Eat or Not Eat?[J]. 国际神经精神科学杂志, 2017, 06(03): 50-55. http://dx.doi.org/10.12677/IJPN.2017.63009

参考文献 (References)

  1. 1. Cruciani-Guglielmacci, C. and Magnan, C. (2017) Brain Lipoprotein Lipase as a Regulator of Energy Balance. Biochimie. https://doi.org/10.1016/j.biochi.2017.07.012

  2. 2. Sun, G.Y., Simonyi, A., Fritsche, K.L., et al. (2017) Docosahexaenoic acid (DHA): An Essential Nutrient and a Nutraceutical for Brain Health and Diseases. Prostaglandins, Leukotrienes, and Essential Fatty Acids. https://doi.org/10.1016/j.plefa.2017.03.006

  3. 3. Cardoso, C., Afonso, C. and Bandarra, N.M. (2016) Dietary DHA and Health: Cognitive Function Ageing. Nutrition Research Reviews, 29, 281-294. https://doi.org/10.1017/S0954422416000184

  4. 4. Lo Van, A., Sakayori, N., Hachem, M., et al. (2016) Mechanisms of DHA Transport to the Brain and Potential Therapy to Neurodegenerative Diseases. Biochimie, 130, 163-167. https://doi.org/10.1016/j.biochi.2016.07.011

  5. 5. Skjevik, A.A., Madej, B.D., Dickson, C.J., et al. (2016) Simulation of Lipid Bilayer Self-Assembly Using All-Atom Lipid Force Fields. Physical Chemistry Chemical Physics: PCCP, 18, 10573-10584. https://doi.org/10.1039/C5CP07379K

  6. 6. Soussi, J. and Chalopin, Y. (2015) Electric Polarizability of Lipid Bilayers: The Influence of the Structure. The Journal of Chemical Physics, 143, 144904. https://doi.org/10.1063/1.4932340

  7. 7. Kong, X., Lu, D., Wu, J. and Liu, Z. (2016) Spreading of a Unilamellar Liposome on Charged Substrates: A Coarse-Grained Molecular Simulation. Langmuir: The ACS Journal of Surfaces and Colloids, 32, 3785-3793. https://doi.org/10.1021/acs.langmuir.6b00043

  8. 8. Pomponi, M.F., Gambassi, G., Pomponi, M. and Masullo, C. (2010) Alzheimer’s Disease: Fatty Acids We Eat May Be Linked to a Specific Protection via Low-Dose Aspirin. Aging and Disease, 1, 37-59.

  9. 9. Yang, X., Sheng, W., Sun, G.Y. and Lee, J.C. (2011) Effects of Fatty Acid Unsaturation Numbers on Membrane Fluidity and Alpha-Secretase-Dependent Amyloid Precursor Protein Processing. Neurochemistry International, 58, 321-329. https://doi.org/10.1016/j.neuint.2010.12.004

  10. 10. Amiri-Jami, M., Abdelhamid, A.G., Hazaa, M., Kakuda, Y. and Griffths, M.W. (2015) Recombinant Production of Omega-3 Fatty Acids by Probiotic Escherichia coli Nissle 1917. FEMS Microbiology Letters, 362. https://doi.org/10.1093/femsle/fnv166

  11. 11. Ghasemifard, S., Hermon, K., Turchini, G.M. and Sinclair, A.J. (2015) Metabolic Fate (Absorption, Beta-Oxidation and Deposition) of Long-Chain n-3 Fatty Acids Is Affected by Sex and by the Oil Source (Krill Oil or Fish Oil) in the Rat. The British Journal of Nutrition, 114, 684-692. https://doi.org/10.1017/S0007114515002457

  12. 12. Rincon-Cervera, M.A., Valenzuela, R., Hernandez-Rodas, M.C., et al. (2016) Vegetable Oils Rich in Alpha Linolenic Acid Increment Hepatic n-3 LCPUFA, Modulating the Fatty Acid Metabolism and Antioxidant Response in Rats. Prostaglandins, Leukotrienes, and Essential Fatty Acids, 111, 25-35.

  13. 13. Kuda, O. (2017) Bioactive Metabolites of Docosahexaenoic Acid. Biochimie, 136, 12-20.

  14. 14. Petrie, J.R., Shrestha, P., Belide, S., et al. (2014) Metabolic Engineering Camelina sativa with Fish Oil-Like Levels of DHA. PLoS ONE, 9, e85061. https://doi.org/10.1371/journal.pone.0085061

  15. 15. Cansev, M., Wurtman, R.J., Sakamoto, T. and Ulus, I.H. (2008) Oral Administration of Circulating Precursors for Membrane Phosphatides Can Promote the Synthesis of New Brain Synapses. Alzheimer’s & Dementia: The Journal of the Alzheimer’s Association, 4, S153-S168.

  16. 16. Schwanke, R.C., Marcon, R., Bento, A.F. and Calixto, J.B. (2016) EPA- and DHA-Derived Resolvins’ Actions in Inflammatory Bowel Disease. European Journal of Pharmacology, 785, 156-164.

  17. 17. Song, C., Shieh, C.H., Wu, Y.S., Kalueff, A., Gaikwad, S. and Su, K.P. (2016) The Role of Omega-3 Polyunsaturated Fatty Acids Eicosapentaenoic and Docosahexaenoic Acids in the Treatment of Major Depression and Alzheimer’s Disease: Acting Separately or Synergistically? Progress in Lipid Research, 62, 41-54.

  18. 18. Wang, Y., Botelho, A.V., Martinez, G.V. and Brown, M.F. (2002) Electrostatic Properties of Membrane Lipids Coupled to Metarhodopsin II Formation in Visual Transduction. Journal of the American Chemical Society, 124, 7690-7701. https://doi.org/10.1021/ja0200488

  19. 19. Grimm, M.O., Zimmer, V.C., Lehmann, J., Grimm, H.S. and Hartmann, T. (2013) The Impact of Cholesterol, DHA, and Sphingolipids on Alzheimer’s Disease. BioMed Research International, 2013, Article ID: 814390. https://doi.org/10.1155/2013/814390

  20. 20. Treen, M., Uauy, R.D., Jameson, D.M., et al. (1992) Effect of Docosahexaenoic Acid on Membrane Fluidity and Function in Intact Cultured Y-79 Retinoblastoma Cells. Archives of Biochemistry and Biophysics, 294, 564-570.

  21. 21. Hashimoto, M., Hossain, S. and Shido, O. (2006) Docosahexaenoic Acid but Not Eicosapentaenoic Acid Withstands Dietary Cholesterol-Induced Decreases in Platelet Membrane Fluidity. Molecular and Cellular Biochemistry, 293, 1-8. https://doi.org/10.1007/s11010-006-0164-x

  22. 22. Czlonkowska, A. and Kurkowska-Jastrzebska, I. (2011) Inflammation and Gliosis in Neurological Diseases—Clinical Implications. Journal of Neuroimmunology, 231, 78-85.

  23. 23. Salem, N., Vandal, M. and Calon, F. (2015) The Benefit of Docosahexaenoic Acid for the Adult Brain in Aging and Dementia. Prostaglandins, Leukotrienes, and Essential Fatty Acids, 92, 15-22.

  24. 24. Yamashita, S., Kiko, T., Fujiwara, H., et al. (2016) Alterations in the Levels of Amyloid-Beta, Phospholipid Hydroperoxide, and Plasmalogen in the Blood of Patients with Alzheimer’s Disease: Possible Interactions between Amyloid-Beta and These Lipids. Journal of Alzheimer’s Disease, 50, 527-537. https://doi.org/10.3233/JAD-150640

  25. 25. Yassine, H.N., Feng, Q., Azizkhanian, I., et al. (2016) Association of Serum Docosahexaenoic Acid with Cerebral Amyloidosis. JAMA Neurology, 73, 1208-1216. https://doi.org/10.1001/jamaneurol.2016.1924

  26. 26. Yassine, H.N., Rawat, V., Mack, W.J., et al. (2016) The Effect of APOE Genotype on the Delivery of DHA to Cerebrospinal Fluid in Alzheimer’s Disease. Alzheimer’s Research & Therapy, 8, 25. https://doi.org/10.1186/s13195-016-0194-x

  27. 27. Bahety, P., Van Nguyen, T.H., Hong, Y., Zhang, L., Chan, E.C. and Ee, P.L. (2017) Understanding the Cholesterol Metabolism-Perturbing Effects of Docosahexaenoic Acid by Gas Chromatography-Mass Spectrometry Targeted Metabonomic Profiling. European Journal of Nutrition, 56, 29-43. https://doi.org/10.1007/s00394-015-1053-4

  28. 28. Zhang, Y., Chen, J., Qiu, J., Li, Y., Wang, J. and Jiao, J. (2016) Intakes of Fish and Polyunsaturated Fatty Acids and Mild-to-Severe Cognitive Impairment Risks: A Dose-Response Me-ta-Analysis of 21 Cohort Studies. The American Journal of Clinical Nutrition, 103, 330-340. https://doi.org/10.3945/ajcn.115.124081

  29. 29. De Souza Fernandes, D.P., Canaan Rezende, F.A., Pereira Rocha, G., De Santis Filgueiras, M., Silva Moreira, P.R. and Goncalves Alfenas Rde, C. (2015) Effect of Eicosapentaenoic Acid and Docosahexaenoic Acid Supplementations to Control Cognitive Decline in Dementia and Alzheimer’s Disease: A Systematic Review. Nutricion Hospitalaria, 32, 528-533.

  30. 30. Leduc, V., Jasmin-Belanger, S. and Poirier, J. (2010) APOE and Cholesterol Homeostasis in Alzheimer’s Disease. Trends in Molecular Medicine, 16, 469-477.

  31. 31. Sastry, P.S. (1985) Lipids of Nervous Tissue: Composition and Metabolism. Progress in Lipid Research, 24, 69-176.

  32. 32. Calderon, F. (2007) Role of RXR in Neurite Outgrowth Induced by Docosahexaenoic Acid. Prostaglandins, Leukotrienes, and Essential Fatty Acids, 77, 227-232.

  33. 33. Darios, F. and Davletov, B. (2006) Omega-3 and Omega-6 Fatty Acids Stimulate Cell Membrane Expansion by Acting on Syntaxin 3. Nature, 440, 813-817. https://doi.org/10.1038/nature04598

  34. 34. Calderon, F. and Kim, H.Y. (2007) Role of RXR in Neurite Outgrowth Induced by Docosahexaenoic Acid. Prostaglandins, Leukotrienes, and Essential Fatty Acids, 77, 227-232.

  35. 35. Perez, S.E., Berg, B.M., Moore, K.A., et al. (2010) DHA Diet Reduces AD Pathology in Young APPswe/PS1 Delta E9 Transgenic Mice: Possible Gender Effects. Journal of Neuroscience Research, 88, 1026-1040.

  36. 36. Hooijmans, C.R., Van der Zee, C.E., Dederen, P.J., et al. (2009) DHA and Cholesterol Containing Diets Influence Alzheimer-Like Pathology, Cognition and Cerebral Vasculature in APPswe/PS1dE9 Mice. Neurobiology of Disease, 33, 482-498.

  37. 37. Kim, H.Y. (2014) Neuroprotection by Docosahexaenoic Acid in Brain Injury. Military Medicine, 179, 106-111. https://doi.org/10.7205/MILMED-D-14-00162

  38. 38. Collaborators GBDEMRMH and Mokdad, A.H. (2017) The Burden of Mental Disorders in the Eastern Mediterranean Region, 1990-2015: Findings from the Global Burden of Disease 2015 Study. International Journal of Public Health, 1-13.

  39. 39. Kratz, T. (2017) The Diagnosis and Treatment of Behavioral Disorders in Dementia. Deutsches Arzteblatt International, 114, 447-454.

  40. 40. Chung, W.L., Chen, J.J. and Su, H.M. (2008) Fish Oil Supplementation of Control and (n-3) Fatty Acid-Deficient Male Rats Enhances Reference and Working Memory Performance and Increases Brain Regional Docosahexaenoic Acid Levels 1-3. The Journal of Nutrition, 138, 1165-1171.

  41. 41. Yuki, D., Sugiura, Y., Zaima, N., et al. (2014) DHA-PC and PSD-95 Decrease after Loss of Synaptophysin and before Neuronal Loss in Patients with Alzheimer’s Disease. Scientific Reports, 4, 7130. https://doi.org/10.1038/srep07130

期刊菜单