The general objective of this program project is to examine behavioral, anatomical and biochemical changes that occur during normal aging of the nervous system of mammals, and the potential of the aging nervous system to compensate for these changes. To accomplish these goals, a number of systems are being examined. In the auditory system the effect of age on the ability of rats to acquire and maintain auditory discrimination are being studied, and this ability is being correlated with morphological age changes in the cochleas, cochlear nuclei and spiral ganglion. The morphological changes include examination of the loss of receptor cells, changes in synapses between neurons, and accumulation of pigment. More centrally, the ability of neurons in the auditory cortex to respond to deafferentation at varying ages are being examined to determine if loss of the callosal input results in compensatory growth of afferents entering the cortex from the thalamus. In the olfactory system changes in the receptor cells, the morphology of neurons and their synaptic input are being studied as rats age. These studies will also indicate if the aging nervous system still exhibits plasticity, and collateral sprouting of axons is being further studied in the dentate gyrus. A possible important factor in the aging of neurons is the state of the microvascular network, and this is being examined both biochemically and anatomically. Additional biochemical studies are being carried out on nuclear chromatin, with which the effects of age are being assessed by determining the susceptibility of chromatin to cleavage by bacterial nuclease.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Research Program Projects (P01)
Project #
5P01AG000001-15
Application #
3090481
Study Section
Aging Review Committee (AGE)
Project Start
1975-06-01
Project End
1988-11-30
Budget Start
1986-12-01
Budget End
1987-11-30
Support Year
15
Fiscal Year
1987
Total Cost
Indirect Cost
Name
Boston University
Department
Type
Schools of Medicine
DUNS #
604483045
City
Boston
State
MA
Country
United States
Zip Code
02118
Robinson, Amy A; Abraham, Carmela R; Rosene, Douglas L (2018) Candidate molecular pathways of white matter vulnerability in the brain of normal aging rhesus monkeys. Geroscience 40:31-47
Ragan, I K; Davis, A S; McVey, D S et al. (2018) Evaluation of Fluorescence Microsphere Immunoassay for Detection of Antibodies to Rift Valley Fever Virus Nucleocapsid Protein and Glycoproteins. J Clin Microbiol 56:
Moore, Tara L; Bowley, Bethany G E; Shultz, Penny L et al. (2018) Oral curcumin supplementation improves fine motor function in the middle-aged rhesus monkey. Somatosens Mot Res 35:1-10
Hsu, Alexander; Luebke, Jennifer I; Medalla, Maria (2017) Comparative ultrastructural features of excitatory synapses in the visual and frontal cortices of the adult mouse and monkey. J Comp Neurol 525:2175-2191
Shobin, Eli; Bowley, Michael P; Estrada, Larissa I et al. (2017) Microglia activation and phagocytosis: relationship with aging and cognitive impairment in the rhesus monkey. Geroscience 39:199-220
Estrada, Larissa I; Robinson, Amy A; Amaral, Ana C et al. (2017) Evaluation of Long-Term Cryostorage of Brain Tissue Sections for Quantitative Histochemistry. J Histochem Cytochem 65:153-171
Medalla, Maria; Gilman, Joshua P; Wang, Jing-Yi et al. (2017) Strength and Diversity of Inhibitory Signaling Differentiates Primate Anterior Cingulate from Lateral Prefrontal Cortex. J Neurosci 37:4717-4734
Rumbell, Timothy H; Dragulji?, Danel; Yadav, Aniruddha et al. (2016) Automated evolutionary optimization of ion channel conductances and kinetics in models of young and aged rhesus monkey pyramidal neurons. J Comput Neurosci 41:65-90
Wilson, William C; Davis, A Sally; Gaudreault, Natasha N et al. (2016) Experimental Infection of Calves by Two Genetically-Distinct Strains of Rift Valley Fever Virus. Viruses 8:
Shivanna, Vinay; McDowell, Chester; Wilson, William C et al. (2016) Complete Genome Sequence of Two Rift Valley Fever Virus Strains Isolated from Outbreaks in Saudi Arabia (2000) and Kenya (2006 to 2007). Genome Announc 4:

Showing the most recent 10 out of 151 publications