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Biomedical subjects

J Tigges

Publications and source records attributed to J Tigges.

77 records · Page 5Linked to original sources

beta-Amyloid (A beta) deposition in the brains of aged orangutans.

While aged monkeys of several species show cerebral amyloid deposition in senile plaques and blood vessels similar to that seen in human aging and Alzheimer's disease (AD), studies of great apes have been limited. Using histological and immunohistochemical methods, we examined the brains of four orangutans aged 10, 28, 31, and 36 years. We encountered sparse beta-amyloid (A beta)-immunoreactive, silver-negative plaque-like structures in the brains of the three older apes. The 36-year-old orangutan also evidenced small A beta-positive deposits in subcortical white matter and sparse vascular amyloid deposition, primarily in meningeal vessels. Neurofibrillary tangles were not detected on silver stains or on tau or ubiquitin immunohistochemistry. Many of the A beta-positive plaque-like deposits in the orangutans were apolipoprotein E-immunoreactive, as we have previously reported in aged rhesus monkeys and an aged chimpanzee. Also, paralleling our earlier findings in these nonhuman primates, A beta 40 in plaques was more prominent in the orangutan than is typically seen in human aging, AD, and Down syndrome. These intriguing species differences may provide clues to the mechanisms of amyloid deposition and the development of neuropathologic changes in AD.

Aging↗

Brain weight does not decrease with age in adult rhesus monkeys.

Cross-sectional studies on adult human autopsy material have shown that younger cohorts have heavier brains than older groups. We sought to determine whether a similar pattern is present in the rhesus monkey, a species that serves as a useful model of human brain and cognitive aging. Data were obtained from necropsies of 399 rhesus monkeys (180 females; 219 males), of ages covering the entire adult lifespan of this species. In addition to fresh brain weight, variables considered were age, sex, body weight, heart weight, identity of the prosector, and circumstance of death. Initial bivariate analyses revealed a significant sex difference in brain weight (mean for males: 96.1 g; for females: 86.1 g; p < 0.001), as well as significant correlations of brain weight with body weight (r = 0.20, p < 0.01 for females; r = 0.27, p < 0.001 for males), and heart weight (r = 0.27, p < 0.001 for females; r = 0.38, p < 0.001 for males). Identity of prosector, circumstance of death, and age were not significantly related to brain weight in bivariate analyses. Multiple linear regression, controlling for possible confounding effects of body weight and sex, also suggested that brain weight is stable throughout adulthood in the rhesus monkey.

Aging↗

Parvalbumin immunoreactivity in the lateral geniculate nucleus of rhesus monkeys raised under monocular and binocular deprivation conditions.

Newborn rhesus monkeys were raised under monocular (lid suture, aphakia, aphakia corrected optically with contact lenses, and occlusion with opaque occluder lenses) and under binocular visual deprivation conditions (aphakia combined with occlusion or optical undercorrection of the fellow eye). Routine immunohistochemical methods with an antibody to the calcium-binding protein paravalbumin (PV) were used to examine the distribution of PV+ neurons and PV+ processes in the LGN of these monkeys. Under all rearing conditions, we found no obvious difference in PV density in neurons in any lamina, although in all monocularly deprived and in two of the three binocularly deprived monkeys neurons connected to the deprived eye were of reduced size. Furthermore, PV-immunoreactive processes in the neuropil of deprived laminae were as numerous and of the same morphologies as those in nondeprived laminae or as in normal controls. Thus, in the LGN of rhesus monkeys, the calcium-binding protein paravalbumin is resistant to monocular as well as binocular visual deprivation during the postnatal maturation process of the visual system.

Animals↗