Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1993 Feb;18(2):139-45.
doi: 10.1007/BF01474676.

Transmembrane signaling through phospholipase C in human cortical membranes

Affiliations

Transmembrane signaling through phospholipase C in human cortical membranes

M A Wallace et al. Neurochem Res. 1993 Feb.

Abstract

Stimulation of phosphoinositide-specific phospholipase C (PLC) by carbachol, dopamine and serotonin was measured by supplying exogenous [3H]phosphatidylinositol 4,5-bisphosphate to membranes prepared from human cortex dissected and frozen at autopsy. Subjects with Alzheimer's disease, Parkinson's disease or schizophrenia were compared to age-matched controls with no known neurological disorders. Stimulation of PLC by the neurotransmitters was dependent on the presence of GTP gamma S. Carbachol elicited the greatest stimulations of PLC followed by serotonin and then dopamine. The maximal stimulations of PLC evoked by a neurotransmitter were similar for the various categories of subjects except in Parkinson's patients, where dopamine failed to stimulate PLC beyond the activity attained with carbachol. In the presence of carbachol, the sensitivity of PLC to GTP gamma S was significantly increased in Alzheimer's membranes, but not in age-matched controls or Parkinson's. Overall, the experiments demonstrate the feasibility for using the exogenous substrate assay to study the functionality of the phosphoinositide transmembrane signaling system in human brain.

PubMed Disclaimer

Similar articles

Cited by

References

    1. J Neurochem. 1987 Oct;49(4):1075-83 - PubMed
    1. Trends Pharmacol Sci. 1990 Jun;11(6):231-6 - PubMed
    1. J Biol Chem. 1989 Nov 5;264(31):18288-95 - PubMed
    1. Trends Pharmacol Sci. 1990 May;11(5):183-4 - PubMed
    1. J Pharmacol Exp Ther. 1990 Dec;255(3):1296-300 - PubMed

Publication types

MeSH terms

Substances