Erythropoietin:: a candidate compound for neuroprotection in schizophrenia

被引:154
作者
Ehrenreich, H
Degner, D
Meller, J
Brines, M
Béhé, M
Hasselblatt, M
Woldt, H
Falkai, P
Knerlich, F
Jacob, S
von Ahsen, N
Maier, W
Brück, W
Rüther, E
Cerami, A
Becker, W
Sirén, AL
机构
[1] Univ Gottingen, Max Planck Inst Expt Med, D-37075 Gottingen, Germany
[2] Univ Gottingen, Dept Psychiat, D-37075 Gottingen, Germany
[3] Univ Gottingen, Dept Nucl Med, D-3400 Gottingen, Germany
[4] Kenneth S Warren Inst, Kitchawan, NY USA
[5] Univ Bonn, Dept Psychiat, D-5300 Bonn, Germany
[6] Univ Gottingen, Dept Clin Chem, D-3400 Gottingen, Germany
[7] Univ Gottingen, Dept Neuropathol, D-3400 Gottingen, Germany
关键词
recombinant human erythropoietin; EPO; schizophrenia; clinical; rodent; SPECT;
D O I
10.1038/sj.mp.4001442
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Erythropoietin (EPO) is a candidate compound for neuroprotection in human brain disease capable of combating a spectrum of pathophysiological processes operational during the progression of schizophrenic psychosis. The purpose of the present study was to prepare the ground for its application in a first neuroprotective add-on strategy in schizophrenia, aiming at improvement of cognitive brain function as well as prevention/slowing of degenerative processes. Using rodent studies, primary hippocampal neurons in culture, immunohistochemical analysis of human post-mortem brain tissue and nuclear imaging technology in man, we demonstrate that: (1) peripherally applied recombinant human (rh) EPO penetrates into the brain efficiently both in rat and humans, (2) rhEPO is enriched intracranially in healthy men and more distinctly in schizophrenic patients, (3) EPO receptors are densely expressed in hippocampus and cortex of schizophrenic subjects but distinctly less in controls, (4) rhEPO attenuates the haloperidol-induced neuronal death in vitro, and (4) peripherally administered rhEPO enhances cognitive functioning in mice in the context of an aversion task involving cortical and subcortical pathways presumably affected in schizophrenia. These observations, together with the known safety of rhEPO, render it an interesting compound for neuroprotective add-on strategies in schizophrenia and other human diseases characterized by a progressive decline in cognitive performance.
引用
收藏
页码:42 / 54
页数:13
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