The progression of β-amyloid deposition in the frontal cortex of the aged canine

• Published in: Brain research Vol. 774; no. 1; pp. 35 - 43
• Main Authors: Satou, Takao, Cummings, Brian J, Head, Elizabeth, Nielson, Kristy A, Hahn, Fletcher F, Milgram, Norton W, Velazquez, Peter, Cribbs, David H, Tenner, Andrea J, Cotman, Carl W
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier B.V 07.11.1997
• Subjects: Aging; Aging - metabolism; Alzheimer Disease - metabolism; Alzheimer Disease - pathology; Alzheimer's; Amyloid beta-Peptides - metabolism; Animal model; Animals; Beagle dog lifespan; Diffuse plaque; Disease Models, Animal; Disease Progression; Dogs; Female; Frontal Lobe - metabolism; Frontal Lobe - pathology; Immunohistochemistry; Isoaspartate β-amyloid; Male; Nerve Degeneration - pathology; Plaque type; Tissue Distribution; Animal model; Diffuse plaque; Aging; Isoaspartate β-amyloid; Plaque type; Beagle dog lifespan; Alzheimer's
• ISSN: 0006-8993; 1872-6240
• DOI: 10.1016/S0006-8993(97)81684-8

Brains from 41 aged canines (≥10 years of age) were examined immunohistochemically to characterize the laminar distribution and age-related progression of β-amyloid (A β) in frontal cortex. We classified the A β patterns into four distinct types. Type I was characterized by small, faint deposits of A β in deep cortical layers. Type II consisted of diffuse deposits of A β mainly in layers V and VI. Type III had both dense plaques in superficial layers, and diffuse deposits in deep layers. Finally, Type IV had solely dense plaques throughout all layers of cortex. We compared the A β distribution pattern between the Old canines (10–15 years, n=22) and the Very Old canines (>15 years, n=19). The Old group primarily had negative staining, or Type I and Type II patterns of amyloid deposition (73%). Conversely, the Very Old group had predominantly Types II, III and IV deposits (89.5%), a difference that was significant ( P<0.05). We suggest that A β deposition in canine frontal cortex is a progressive age-related process beginning with diffuse deposits in the deep cortical layers followed by the development of deposits in outer layers. In support of this hypothesis, the deeper layer diffuse plaques in the Very Old group of dogs also contain the largest proportion of β-amyloid with an isomerized aspartic acid residue at position 7, indicating that these deposits had been present for some time. We also observed fiber-like A β immunoreactivity within regions of diffuse A β deposits. These fibers appeared to be degenerating neurites, which were negative for hyperphosphorylated tau. Therefore, these fibers may represent a very early form of neuritic change that precede tau hyperphosphorylation or develop by an alternative pathway.