TY - JOUR
T1 - Detection of age-dependent brain injury in a mouse model of brain amyloidosis associated with Alzheimer's disease using magnetic resonance diffusion tensor imaging
AU - Sun, Shu Wei
AU - Song, Sheng Kwei
AU - Harms, Michael P.
AU - Lin, Shiow Jiuan
AU - Holtzman, David M.
AU - Merchant, Kalpana M.
AU - Kotyk, John J.
N1 - Funding Information:
This study was supported in part by NIA grant P50AG05681 and the National Cancer Institute Small Animal Imaging Resource Program at Washington University (1 R24 CA83060-01). The authors acknowledge the technical assistance of Maia Parsadanian. Helpful discussions with Drs. Joseph J. H. Ackerman, Jeffrey J. Neil, and members of the Washington University Biomedical Magnetic Resonance Laboratory are gratefully acknowledged.
PY - 2005/1
Y1 - 2005/1
N2 - Using magnetic resonance diffusion tensor imaging (DTI), the present study investigates changes in both gray and white matter in the APPsw transgenic mouse (Tg2576), a model of β-amyloid plaque deposition associated with Alzheimer's disease (AD). DTI analyses were performed in cross-sectional groups of transgene-positive and -negative mice at 8, 12, 16, and 18 months of age to assess the magnitude of water diffusion in gray matter (i.e., Tr(D)) and changes in diffusion in white matter that may be indicative of axonal degeneration (i.e., reduced water diffusion parallel to axonal tracts, λ ||) and myelin degradation (i.e., increased water diffusion perpendicular to axonal tracts, λ ⊥). No appreciable changes in gray or white matter were observed between the APPsw and the age-matched control mice at 8 months of age. Reduced Tr(D) and λ || were observed in gray and white matter, respectively, for the APPsw mice at ages greater than 8 months, which coincides with the time period when appreciable amyloid plaque accumulation was confirmed by ex vivo histopathological studies. The decreases in λ || suggest the presence of axonal injury in multiple white matter tracts of APPsw mice. Unlike λ ||, λ ⊥was unaltered between control and APPsw mice in most white matter tracts. However, in the corpus collosum (CC), λ ⊥ increased at 16 and 18 months of age, suggesting the possibility of myelin damage in the CC at these later ages. This work demonstrates the potential for DTI as a noninvasive modality to detect evolving pathology associated with changes in tissue water diffusion properties in brain tissues.
AB - Using magnetic resonance diffusion tensor imaging (DTI), the present study investigates changes in both gray and white matter in the APPsw transgenic mouse (Tg2576), a model of β-amyloid plaque deposition associated with Alzheimer's disease (AD). DTI analyses were performed in cross-sectional groups of transgene-positive and -negative mice at 8, 12, 16, and 18 months of age to assess the magnitude of water diffusion in gray matter (i.e., Tr(D)) and changes in diffusion in white matter that may be indicative of axonal degeneration (i.e., reduced water diffusion parallel to axonal tracts, λ ||) and myelin degradation (i.e., increased water diffusion perpendicular to axonal tracts, λ ⊥). No appreciable changes in gray or white matter were observed between the APPsw and the age-matched control mice at 8 months of age. Reduced Tr(D) and λ || were observed in gray and white matter, respectively, for the APPsw mice at ages greater than 8 months, which coincides with the time period when appreciable amyloid plaque accumulation was confirmed by ex vivo histopathological studies. The decreases in λ || suggest the presence of axonal injury in multiple white matter tracts of APPsw mice. Unlike λ ||, λ ⊥was unaltered between control and APPsw mice in most white matter tracts. However, in the corpus collosum (CC), λ ⊥ increased at 16 and 18 months of age, suggesting the possibility of myelin damage in the CC at these later ages. This work demonstrates the potential for DTI as a noninvasive modality to detect evolving pathology associated with changes in tissue water diffusion properties in brain tissues.
KW - APPsw
KW - Alzheimer's disease (AD)
KW - Axial diffusivity
KW - Diffusion tensor imaging (DTI)
KW - Radial diffusivity
KW - Tg2576
KW - White matter
UR - http://www.scopus.com/inward/record.url?scp=10044290352&partnerID=8YFLogxK
U2 - 10.1016/j.expneurol.2004.09.006
DO - 10.1016/j.expneurol.2004.09.006
M3 - Article
C2 - 15589514
AN - SCOPUS:10044290352
SN - 0014-4886
VL - 191
SP - 77
EP - 85
JO - Experimental Neurology
JF - Experimental Neurology
IS - 1
ER -