An immunohistochemical study of GABAA receptor gamma subunits in Alzheimer's disease hippocampus: Relationship to neurofibrillary tangle progression

被引:37
|
作者
Iwakiri, Masahiko [2 ]
Mizukami, Katsuyoshi [1 ]
Ikonomovic, Milos D. [4 ,5 ]
Ishikawa, Masanori [3 ]
Abrahamson, Eric E. [4 ]
DeKosky, Steven T. [4 ,5 ]
Asada, Takashi [1 ]
机构
[1] Univ Tsukuba, Inst Clin Med, Dept Psychiat, Tsukuba, Ibaraki 3058575, Japan
[2] Ishizaki Hosipital, Dept Psychiat, Ibaraki, Japan
[3] Natl Ctr Neurol & Psychiat, Dept Psychiat, Kodaira, Tokyo, Japan
[4] Univ Pittsburgh, Dept Neurol, Pittsburgh, PA 15260 USA
[5] Univ Pittsburgh, Dept Psychiat, Pittsburgh, PA USA
关键词
Alzheimer's disease; excitotoxicity; GABA; neurodegeneration; tau; AGED BRAINS; BENZODIAZEPINE; DEMENTIA;
D O I
10.1111/j.1440-1789.2008.00978.x
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Immunohistochemical characterization of the distribution of GABA(A) receptor subunits gamma 1/3 and 2 in the hippocampus relative to neurofibrillary tangle (NFT) pathology staging was performed in cognitively normal subjects (Braak stage I/II, n = 4) and two groups of Alzheimer's disease (AD) patients (Braak stage III/IV, n = 4; Braak stage V/VI, n = 8). In both Braak groups of AD patients, neuronal gamma 1/3 and gamma 2 immunoreactivity was preserved in all hippocampal subfields. However, compared to normal controls neuronal gamma 1/3 immunoreactivity was more intense in several end-stage AD subjects. Despite increased NFT pathology in the Braak V/VI AD group, GABA(A) gamma 1/3 and gamma 2 immunoreactivity did not co-localize with markers of NFT. These results suggest that upregulating or preserving GABA(A) gamma 1/3 and gamma 2 receptors may protect neurons against neurofibrillary pathology in AD.
引用
收藏
页码:263 / 269
页数:7
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