Lyons D M, Yang C, Sawyer-Glover A M, Moseley M E, Schatzberg A F
Department of Psychiatry and Behavioral Science, 1201 Welch Rd, Medical School Laboratory Surge Bldg, Room P104-Mail Code 5485, Stanford University School of Medicine, Stanford, CA 94305-5485, USA.
Arch Gen Psychiatry. 2001 Dec;58(12):1145-51. doi: 10.1001/archpsyc.58.12.1145.
Opportunities for research on the causes and consequences of stress-related hippocampal atrophy are limited in human psychiatric disorders. Therefore, this longitudinal study investigated early life stress and inherited variation in monkey hippocampal volumes.
Paternal half-siblings raised apart from one another by different mothers in the absence of fathers were randomized to 1 of 3 postnatal conditions that disrupted diverse aspects of early maternal care (n = 13 monkeys per condition). These conditions were previously shown to produce differences in social behavior, emotional reactivity, and neuroendocrine stress physiology. Hippocampal volumes were subsequently determined in adulthood by high-resolution magnetic resonance imaging.
Adult hippocampal volumes did not differ with respect to the stressful postnatal conditions. Based on paternal half-sibling effects, the estimated proportion of genetic variance, ie, heritability, was 54% for hippocampal size. Paternal half-siblings with small adult hippocampal volumes responded to the removal of all mothers after weaning with initially larger relative increases in cortisol levels. Plasma cortisol levels 3 and 7 days later, and measures of cortisol-negative feedback in adulthood were not, however, correlated with hippocampal size.
In humans with mood and anxiety disorders, small hippocampal volumes have been taken as evidence that excessive stress levels of cortisol induce hippocampal volume loss. Results from this study of monkeys suggest that small hippocampi also reflect an inherited characteristic of the brain. Genetically informed clinical studies should assess whether inherited variation in hippocampal morphology contributes to excessive stress levels of cortisol through diminished neuroendocrine regulation.
在人类精神疾病中,研究与应激相关的海马萎缩的原因及后果的机会有限。因此,这项纵向研究调查了幼年应激和猕猴海马体积的遗传变异。
在没有父亲的情况下由不同母亲分别抚养长大的同父异母的猕猴被随机分配到3种产后条件中的一种,这些条件破坏了早期母性照料的不同方面(每种条件下n = 13只猴子)。先前已表明这些条件会导致社交行为、情绪反应性和神经内分泌应激生理学方面的差异。随后在成年期通过高分辨率磁共振成像确定海马体积。
成年海马体积在应激性产后条件方面没有差异。基于同父异母效应,海马大小的遗传方差估计比例,即遗传率为54%。成年海马体积小的同父异母猕猴在断奶后所有母亲被移除时,最初皮质醇水平的相对升高幅度更大。然而,3天和7天后的血浆皮质醇水平以及成年期皮质醇负反馈指标与海马大小无关。
在患有情绪和焦虑障碍的人类中,海马体积小被视为皮质醇应激水平过高导致海马体积缩小的证据。这项对猕猴的研究结果表明,小海马也反映了大脑的一种遗传特征。有遗传学依据的临床研究应评估海马形态的遗传变异是否通过神经内分泌调节减弱导致皮质醇应激水平过高。