Dysregulation of dynorphins in Alzheimer disease

被引:45
|
作者
Yakovleva, T.
Marinova, Z.
Kumin, A.
Seidah, N. G.
Haroutunian, V.
Terenius, L.
Bakalkin, G.
机构
[1] Karolinska Inst & Hosp, Dept Clin Neurosci, SE-17176 Stockholm, Sweden
[2] Clin Res Inst Montreal, Biochem Neuroendocrinol Lab, Montreal, PQ H2W 1R7, Canada
[3] Mt Sinai Sch Med, Dept Psychiat, New York, NY 10029 USA
基金
加拿大健康研究院;
关键词
dynorphin; Alzheimer disease; neurodegeneration; excitotoxicity; pro-hormone convertase 2; 7B2; prodynorphin; cognition;
D O I
10.1016/j.neurobiolaging.2006.07.002
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
The opioid peptides dynorphins may be involved in pathogenesis of Alzheimer disease (AD) by inducing neurodegeneration or cognitive impairment. To test this hypothesis, the dynorphin system was analyzed in postmortem samples from AD and control subjects, and subjects with Parkinson or cerebro-vascular diseases for comparison. Dynorphin A, dynorphin B and related neuropeptide nociceptin were deter-mined in the Brodmann area 7 by radioimmunoassay. The precursor protein prodynorphin, processing convertase PC2 and the neuroendocrine pro7B2 and 7132 proteins required for PC2 maturation were analyzed by Western blot. AD subjects displayed robustly elevated levels of dynorphin A and no differences in dynorphin B and nociceptin compared to controls. Subjects with Parkinson or cerebro-vascular diseases did not differ from controls with respect to any of the three peptides. PC2 levels were also increased, whereas, those of prodynorphin and pro7B2/7B2 were not changed in AD. Dynorphin A levels correlated with the neuritic plaque density. These results along with the known non-opioid ability of dynorphin A to induce neurodegeneration suggest a role for this neuropeptide in AD neuropathology. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:1700 / 1708
页数:9
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