Levant Beth, Ozias Marlies K, Davis Paul F, Winter Michelle, Russell Kristin L, Carlson Susan E, Reed Gregory A, McCarson Kenneth E
Department of Pharmacology, Toxicology, and Therapeutics, University of Kansas Medical Center, Kansas City, KS 66160, USA.
Psychoneuroendocrinology. 2008 Oct;33(9):1279-92. doi: 10.1016/j.psyneuen.2008.06.012. Epub 2008 Aug 15.
Decreased tissue levels of docosahexaenoic acid (DHA; 22:6n-3) are implicated in the etiologies of non-puerperal and postpartum depression. With the aim of determining neurobiological sequelae of decreased brain DHA content, this study examined the effects of a loss of brain DHA content and concurrent reproductive status in adult female Long-Evans rats. An alpha-linolenic acid-deficient diet and breeding protocols were used to produce virgin and parous female rats with cortical phospholipid DHA levels 23-26% lower than virgin and parous rats fed a control diet containing adequate alpha-linolenic acid. Parous dams were tested/euthanized at weaning (postnatal day 20) of the second litter; virgin females, during diestrus. Decreased brain DHA was associated with decreased hippocampal BDNF gene expression and increased relative corticosterone response to an intense stressor, regardless of reproductive status. In virgin females with decreased brain DHA, serotonin content and turnover in frontal cortex were decreased compared to virgin females with normal brain DHA. In parous dams with decreased brain DHA, the density of 5-HT(1A) receptors in the hippocampus was increased, corticosterone response to an intense stressor was increased, and the latency to immobility in the forced swim test was decreased compared to parous dams with normal DHA. These findings demonstrate neurobiological alterations attributable to decreased brain DHA or an interaction of parous status and brain DHA level. Furthermore, the data are consistent with findings in depressed humans, and thus support a role for DHA as a factor in the etiologies of depressive illnesses, particularly postpartum depression.
二十二碳六烯酸(DHA;22:6n-3)组织水平降低与非产褥期及产后抑郁症的病因有关。为了确定脑内DHA含量降低的神经生物学后遗症,本研究检测了成年雌性Long-Evans大鼠脑内DHA含量降低及同时存在的生殖状态的影响。采用α-亚麻酸缺乏饮食和繁殖方案,以产生皮质磷脂DHA水平比喂食含充足α-亚麻酸对照饮食的未生育和已生育大鼠低23-26%的未生育和已生育雌性大鼠。已生育的母鼠在第二窝仔鼠断奶时(出生后第20天)进行测试/安乐死;未生育雌性大鼠在动情间期进行测试。无论生殖状态如何,脑内DHA降低均与海马脑源性神经营养因子(BDNF)基因表达降低及对应激源的皮质酮反应增加有关。与脑内DHA正常的未生育雌性大鼠相比,脑内DHA降低的未生育雌性大鼠额叶皮质中血清素含量和周转率降低。与脑内DHA正常的已生育母鼠相比,脑内DHA降低的已生育母鼠海马中5-HT(1A)受体密度增加,对应激源的皮质酮反应增加,强迫游泳试验中不动潜伏期缩短。这些发现表明了脑内DHA降低或已生育状态与脑内DHA水平相互作用所致的神经生物学改变。此外,这些数据与抑郁症患者的研究结果一致,因此支持DHA在抑郁症病因中起作用,尤其是产后抑郁症。