Connor Caroline M, Guo Yin, Akbarian Schahram
Program in Neurobiology, Graduate School of Biomedical Sciences, Department of Psychiatry, University of Massachusetts Medical School, Worcester, Massachusetts 01604, USA.
Biol Psychiatry. 2009 Sep 1;66(5):486-93. doi: 10.1016/j.biopsych.2009.04.032. Epub 2009 Jun 25.
Increased neuronal density in prefrontal, parietal, and temporal white matter of schizophrenia subjects is thought to reflect disordered neurodevelopment; however, it is not known if this cellular alteration affects the cingulate cortex and whether similar changes exist in bipolar disorder.
Eighty-two postmortem specimens (bipolar 15, schizophrenia 22, control 45) were included in this clinical study. Densities for two neuronal markers, neuron-specific nuclear protein (NeuN) and neuregulin 1 alpha (NRG), were determined in white matter up to 2.5 mm beneath the anterior cingulate cortex; density of NeuN immunopositive neurons (NeuN+) was also determined for a subset of cases in prefrontal cortex. Changes during normal development were monitored in a separate cohort of 14 brains.
Both the schizophrenia and bipolar cohorts demonstrated a twofold increase in NeuN+ density in cingulate white matter; this effect could be attributed to approximately 25% of cases that exceeded the second standard deviation from control subjects. Similar changes were observed in prefrontal cortex. In contrast density of NRG expressing neurons was unaltered. Cases with increased NeuN+ densities in two-dimensional (2-D) counts also showed a pronounced, > fivefold elevation in NeuN+ nuclei per cubic millimeter. Additionally, the developmental cohort demonstrated a 75% decline in NeuN+ neuronal density during the first postnatal year but was stable thereafter.
Increased neuronal density in white matter of cingulate cortex in schizophrenia provides further evidence that this alteration occurs in multiple cortical areas. Similar changes in some cases with bipolar illness suggest that the two disorders may share a common underlying defect in late prenatal or early postnatal neurodevelopment.
精神分裂症患者前额叶、顶叶和颞叶白质中神经元密度增加被认为反映了神经发育紊乱;然而,尚不清楚这种细胞改变是否会影响扣带回皮质,以及双相情感障碍是否存在类似变化。
本临床研究纳入了82个尸检标本(双相情感障碍15例、精神分裂症22例、对照45例)。在前扣带回皮质下方2.5毫米以内的白质中测定两种神经元标志物神经元特异性核蛋白(NeuN)和神经调节蛋白1α(NRG)的密度;还对前额叶皮质部分病例的NeuN免疫阳性神经元(NeuN+)密度进行了测定。在另一组14个大脑中监测正常发育过程中的变化。
精神分裂症和双相情感障碍队列的扣带回白质中NeuN+密度均增加了两倍;这种效应可归因于约25%的病例,其超出了对照组第二个标准差。在前额叶皮质也观察到了类似变化。相比之下,表达NRG的神经元密度未改变。二维计数中NeuN+密度增加的病例每立方毫米NeuN+细胞核也有明显的、超过五倍的升高。此外,发育队列显示出生后第一年NeuN+神经元密度下降了75%,但此后保持稳定。
精神分裂症患者扣带回皮质白质中神经元密度增加进一步证明这种改变发生在多个皮质区域。双相情感障碍部分病例的类似变化表明,这两种疾病可能在产前晚期或产后早期神经发育中存在共同的潜在缺陷。