Monitoring Disease Progression in Transgenic Mouse Models of Alzheimer's Disease with Proton Magnetic Resonance Spectroscopy
Currently no definitive biomarker of Alzheimer's disease (AD) is available, and this impedes both clinical diagnosis in humans and drug discovery in transgenic animal models. Proton magnetic resonance spectroscopy (1H MRS) provides a noninvasive way to investigate in vivo neurochemical abnormal...
Saved in:
Published in | Proceedings of the National Academy of Sciences - PNAS Vol. 102; no. 33; pp. 11906 - 11910 |
---|---|
Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
National Academy of Sciences
16.08.2005
National Acad Sciences |
Subjects | |
Online Access | Get full text |
Cover
Loading…
Summary: | Currently no definitive biomarker of Alzheimer's disease (AD) is available, and this impedes both clinical diagnosis in humans and drug discovery in transgenic animal models. Proton magnetic resonance spectroscopy (1H MRS) provides a noninvasive way to investigate in vivo neurochemical abnormalities. Each observable metabolite can potentially provide information about unique in vivo pathological processes at the molecular or cellular level. In this study, the age-dependent1H MRS profile of transfenic AD mice was compared to that of wild-type mice. Twenty-seven APP-PS1 mice (which coexpress mutated human presenilin 1 and amyloid-β precursor protein) and 30 wild-type mice age 66-904 days were examined, some repeatedly. A reduction in the levels of N-acetylaspartate and glutamate, compared with total creatine levels, was found in APP-PS1 mice with advancing age. The most striking finding was a dramatic increase in the concentration of myo-inositol with age in APP-PS1 mice, which was not observed in wild-type mice. The age-dependent neurochemical changes observed in APP-PS1 mice agree with results obtained from in vivo human MRS studies. Among the different transgenic mouse models of AD that have been studied with1H MRS, APP-PS1 mice seem to best match the neurochemical profile exhibited in human AD.1H MRS could serve as a sensitive in vivo surrogate indicator of therapeutic efficacy in trials of agents designed to reduce neurotoxicity due to microglial activation. Because of its noninvasive and repeatable nature, MRS in transgenic models of AD could substantially accelerate drug discovery for this disease. |
---|---|
Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 Author contributions: M.M., J.F.P., C.R.J., K.U., and M.G. designed research; M.M., G.L.C., and T.M.W. performed research; P.-G.H. contributed new reagents/analytic tools; M.M. and R.L.B. analyzed data; and M.M. wrote the paper. Abbreviations: 1H MRS, proton magnetic resonance spectroscopy; NAA, N-acetylaspartate; Glu, glutamate; mIns, myo-inositol; AD, Alzheimer's disease; APP, amyloid-β precursor protein; PS1, presenilin 1; PS2, presenilin 2; tCr, total creatine. Communicated by Alexander Pines, University of California, Berkeley, CA, June 30, 2005 To whom correspondence should be addressed. E-mail: gosia@cmrr.umn.edu. |
ISSN: | 0027-8424 1091-6490 |
DOI: | 10.1073/pnas.0505513102 |