Northwestern University, Department of Psychiatry, 446 East Ontario, Suite 7-100, Chicago, IL 60611, United States.
Behav Brain Res. 2011 Mar 17;218(1):106-13. doi: 10.1016/j.bbr.2010.11.025. Epub 2010 Nov 17.
Polydipsic hyponatremic schizophrenic (PHS) patients exhibit altered neuroendocrine activity that has been linked to their life-threatening water imbalance, as well as to impaired function and reduced volume of the anterior hippocampus. Polydipsic patients without hyponatremia (polydipsic normonatremic schizophrenics: PNS) exhibit similar, albeit less marked, changes in neuroendocrine activity and anterior hippocampal function, but not reduced anterior hippocampal volume. Indeed, reduced anterior hippocampal volume is seen in patients with normal water balance (nonpolydipsic normonatremic schizophrenics: NNS) whose neuroendocrine activity and anterior hippocampal function differ markedly from those with polydipsia. In an effort to reconcile these findings we measured hippocampal, amygdala and 3rd ventricle shapes in 26 schizophrenic patients (10 PNS, 7 PHS, 9 NNS) and 12 healthy controls matched for age and gender. Bilateral inward deformations were localized to the anterior lateral hippocampal surface (part of a neurocircuit which modulates neuroendocrine responses to psychological stimuli) in PHS and to a lesser extent in PNS, while deformations in NNS were restricted to the medial surface. Proportional deformations of the right medial amygdala, a key segment of this neurocircuit, were seen in both polydipsic groups, and correlated with the volume of the 3rd ventricle, which lies adjacent to the neuroendocrine nuclei. Finally, these structural findings were most marked in those with impaired hippocampal-mediated stress responses. These results reconcile previously conflicting data, and support the view that anterior lateral hippocampal pathology disrupts neuroendocrine function in polydipsic patients with and without hyponatremia. The relationship of these findings to the underlying mental illness remains to be established.
多饮性低钠血症精神分裂症(PHS)患者表现出改变的神经内分泌活动,这与他们危及生命的水失衡有关,以及与前海马功能受损和体积减小有关。没有低钠血症的多饮患者(多饮性正常钠血症精神分裂症患者:PNS)表现出类似的、尽管不太明显的神经内分泌活动和前海马功能变化,但前海马体积没有减小。事实上,在水平衡正常的患者(非多饮性正常钠血症精神分裂症患者:NNS)中可以看到前海马体积减小,他们的神经内分泌活动和前海马功能与多饮患者有明显差异。为了协调这些发现,我们测量了 26 名精神分裂症患者(10 名 PNS、7 名 PHS、9 名 NNS)和 12 名年龄和性别匹配的健康对照者的海马体、杏仁核和第三脑室的形状。双侧向内变形定位于 PHS 的前外侧海马表面(调节神经内分泌对心理刺激反应的神经回路的一部分),在 PNS 中则不太明显,而 NNS 的变形则局限于内侧表面。右侧内侧杏仁核的比例变形在两个多饮组中都可见,这是神经回路的一个关键部分,与位于神经内分泌核附近的第三脑室体积相关。最后,这些结构发现在前海马介导的应激反应受损的患者中最为明显。这些结果协调了以前相互矛盾的数据,并支持前外侧海马体病理学破坏了有或没有低钠血症的多饮患者的神经内分泌功能的观点。这些发现与潜在的精神疾病的关系仍有待确定。