Hyperphosphorylated tau and amyloid precursor protein deposition is increased in the brains of young drug abusers

被引:74
作者
Ramage, SN
Anthony, IC
Carnie, FW
Busuttil, A
Robertson, R
Bell, JE
机构
[1] Univ Edinburgh, Western Gen Hosp, Dept Pathol Neuropathol, Neuropathol Unit, Edinburgh EH4 2XU, Midlothian, Scotland
[2] Univ Edinburgh, Forens Med Unit, Edinburgh EH8 9YL, Midlothian, Scotland
[3] Muirhouse Med Ctr, Edinburgh, Midlothian, Scotland
关键词
drug abuse; human brain; neuropathology; opiate; tau protein;
D O I
10.1111/j.1365-2990.2005.00670.x
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Drug abuse is a major problem worldwide. The incidence of drug-related deaths attributed to opiate abuse is increasing annually. Apart from routine examination. little is known of the neuropathology of drug abuse. We, and others, have shown previously that drug abuse is associated with microglial activation. We hypothesised that neuroinflammation might lead to premature neurodegeneration in drug abusers. We investigated the brains of Young opiate abusers (n = 3 4, all < 40 years) for the presence of proteins associated with neurodegenerative diseases and compared them with the brains of age-matched, non-drug users (n=16) all of whom died suddenly. Detailed immunohistochemical analysis of the hippocampus, brainstem and basal ganglia for hyperphosphorylated tau, beta-amyloid, beta-amyloid precursor protein (PAPP) and ubiquitin demonstrated an excess of AT8-positive neurofibrillary tangles (NFT) in the drug abusers. These were not only more prevalent in the drug abusers than in controls (44% vs. 191%) but also involved more brain areas. In controls NFT were confined to the entorhinal cortex whereas in drug users they were also found in the subiculum. temporal neocortex. nucleus basalis of Meynert and the locus coeruleus. Virtually no amyloid plaques were present but PAPP positivity was again much more common in drug abusers than controls (73%, vs. 20%, in the brainstem and 59%, vs. 23% in the temporal lobe). There is no suggestion that these drug abusers had displayed major cognitive impairment although detailed neuropsychological assessment is difficult in this subject group. Likely causes of hyperphosphorylated tau deposition in drug abuse include hypoxic-ischaemic injury, microglial-associated cytokine release and possibly drug-associated neurotoxicity or hepatitis. Head injury. which is another major risk factor, does not appear to have contributed to our findings. Genetic factors also merit consideration. It is unclear at present how much of the hyperphosphorylated tau detected in these young drug abusers represents a transitory phenomenon.
引用
收藏
页码:439 / 448
页数:10
相关论文
共 49 条
[1]   Oxidative stress in neurodegeneration: cause or consequence? [J].
Andersen, JK .
NATURE MEDICINE, 2004, 10 (07) :S18-S25
[2]   Hypoxic ischaemic brain damage, especially pallidal lesions, in heroin addicts [J].
Andersen, SN ;
Skullerud, K .
FORENSIC SCIENCE INTERNATIONAL, 1999, 102 (01) :51-59
[3]  
Arango JC, 2004, AIDS, V18, pS69, DOI 10.1097/00002030-200401001-00010
[4]   Inflammation, apoptosis, and Alzheimer's disease [J].
Bamberger, ME ;
Landreth, GE .
NEUROSCIENTIST, 2002, 8 (03) :276-283
[5]   Influence of risk group and zidovudine therapy on the development of HIV encephalitis and cognitive impairment in AIDS patients [J].
Bell, JE ;
Donaldson, YK ;
Lowrie, S ;
McKenzie, CA ;
Elton, RA ;
Chiswick, A ;
Brettle, RP ;
Ironside, JW ;
Simmonds, P .
AIDS, 1996, 10 (05) :493-499
[6]   HUMAN-IMMUNODEFICIENCY-VIRUS AND THE BRAIN - INVESTIGATION OF VIRUS LOAD AND NEUROPATHOLOGIC CHANGES IN PRE-AIDS SUBJECTS [J].
BELL, JE ;
BUSUTTIL, A ;
IRONSIDE, JW ;
REBUS, S ;
DONALDSON, YK ;
SIMMONDS, P ;
PEUTHERER, JF .
JOURNAL OF INFECTIOUS DISEASES, 1993, 168 (04) :818-824
[7]   HIV and drug misuse in the Edinburgh cohort [J].
Bell, JE ;
Arango, JC ;
Robertson, T ;
Brettle, TP ;
Leen, T ;
Simmonds, P .
JAIDS-JOURNAL OF ACQUIRED IMMUNE DEFICIENCY SYNDROMES, 2002, 31 :S35-S42
[8]   Immunological aspects of microglia: relevance to Alzheimer's disease [J].
Benveniste, EN ;
Nguyen, VT ;
O'Keefe, GM .
NEUROCHEMISTRY INTERNATIONAL, 2001, 39 (5-6) :381-391
[9]   How chronic inflammation can affect the brain and support the development of Alzheimer's disease in old age: the role of microglia and astrocytes [J].
Blasko, I ;
Stampfer-Kountchev, M ;
Robatscher, P ;
Veerhuis, R ;
Eikelenboom, P ;
Grubeck-Loebenstein, B .
AGING CELL, 2004, 3 (04) :169-176
[10]   Alzheimer's disease:: intraneuronal alterations precede insoluble amyloid-β formation [J].
Braak, H ;
Del Tredici, K .
NEUROBIOLOGY OF AGING, 2004, 25 (06) :713-718