Altered plasma arginine metabolome precedes behavioural and brain arginine metabolomic profile changes in the APPswe/PS1ΔE9 mouse model of Alzheimer's disease

被引:41
作者
Bergin, D. H. [1 ,2 ,3 ]
Jing, Y. [1 ,3 ]
Mockett, B. G. [3 ,4 ]
Zhang, H. [2 ,3 ]
Abraham, W. C. [3 ,4 ]
Liu, P. [1 ,3 ]
机构
[1] Univ Otago, Dept Anat, Dunedin, New Zealand
[2] Univ Otago, Sch Pharm, Dunedin, New Zealand
[3] Univ Otago, Brain Res New Zealand & Brain Hlth Res Ctr, Dunedin, New Zealand
[4] Univ Otago, Dept Psychol, Dunedin, New Zealand
关键词
NITRIC-OXIDE SYNTHASE; AGE-RELATED-CHANGES; REGIONAL-VARIATIONS; AMYLOID DEPOSITION; RAT HIPPOCAMPUS; TRANSGENIC MICE; IN-VIVO; MEMORY; AGMATINE; ARGINASE;
D O I
10.1038/s41398-018-0149-z
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
While amyloid-beta (A beta) peptides play a central role in the development of Alzheimer's disease (AD), recent evidence also implicates altered metabolism of L-arginine in the pathogenesis of AD. The present study systematically investigated how behavioural function and the brain and plasma arginine metabolic profiles changed in a chronic A beta accumulation model using male APPswe/PS1 Delta E9 transgenic (Tg) mice at 7 and 13 months of age. As compared to their wild-type (WT) littermates, Tg mice displayed age-related deficits in spatial water maze tasks and alterations in brain arginine metabolism. Interestingly, the plasma arginine metabolic profile was markedly altered in 7-month Tg mice prior to major behavioural impairment. Receiver operating characteristic curve analysis revealed that plasma putrescine and spermine significantly differentiated between Tg and WT mice. These results demonstrate the parallel development of altered brain arginine metabolism and behavioural deficits in Tg mice. The altered plasma arginine metabolic profile that preceded the behavioural and brain profile changes suggests that there may be merit in an arginine-centric set of ante-mortem biomarkers for AD.
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页数:14
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