Effects of postmortem interval, age, and Alzheimer's disease on G-proteins in human brain

X Li, AF Greenwood, R Powers, RS Jope - Neurobiology of aging, 1996 - Elsevier
X Li, AF Greenwood, R Powers, RS Jope
Neurobiology of aging, 1996Elsevier
Heterotrimeric G-proteins are critical components in many receptor-coupled signal
transduction systems, and altered levels and functions of G-proteins have been implicated in
several neurological disorders, including Alzheimer's disease. Investigations in postmortem
human brain provide a direct approach to study G-protein involvement in neurological
disorders. Therefore, the effects of postmortem interval, aging, and Alzheimer's disease on G-
protein levels were determined in postmortem human brain and an assay to measure …
Heterotrimeric G-proteins are critical components in many receptor-coupled signal transduction systems, and altered levels and functions of G-proteins have been implicated in several neurological disorders, including Alzheimer's disease. Investigations in postmortem human brain provide a direct approach to study G-protein involvement in neurological disorders. Therefore, the effects of postmortem interval, aging, and Alzheimer's disease on G-protein levels were determined in postmortem human brain and an assay to measure activation of G-proteins was developed. Within the postmortem interval range of 5 to 21 h, the levels of Gαi1, Gαi2, Gas, and Gβ were stable, whereas Gαq and Gαo decreased slightly, in human prefrontal cortex. In subjects aged 19 to 100 y, decreased levels of Gαq and Gαo were significantly correlated with increased age, but levels of the other G-protein subunits did not vary. In Alzheimer's disease prefrontal cortex, superior temporal gyrus, and occipital cortex, all G-protein subunit levels were equivalent to those in matched controls except for a slight deficit in Gail. An ELISA assay using selective antibodies was used to measure [35S]GTPγS binding to Gαo and Gαi1. Binding was proportional to the concentration of GTP-γS and was concentration-dependently stimulated by mastoparan equivalently in control and Alzheimer's disease prefrontal cortical membranes.
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