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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.
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页码:263 / 269
页数:7
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