[3H]vesamicol binding in human brain cholinergic deficiency disorders.

Abstract

We measured the binding of the vesicular acetylcholine transport blocker [3H]vesamicol (2-[4-phenylpiperidino] cyclohexanol; AH-5183) to autopsied frontal cortex and amygdala of patients from 4 disorders having a marked brain cholinergic reduction, namely Alzheimer's disease, Parkinson's disease with dementia, dominantly inherited olivopontocerebellar atrophy and Down's syndrome. Although mean activity of the specific cholinergic marker enzyme choline acetyltransferase (ChAT) was markedly reduced by about 60% in frontal cortex in the 4 patient groups and by 80% or greater in amygdala of the Alzheimer's and Down's syndrome patients, [3H]vesamicol binding density was, on average, either normal or only slightly reduced as compared with the controls. This discrepancy suggests that in human brain [3H]vesamicol binding is either not preferentially localized to cholinergic nerve endings or, in these cholinergic deficiency syndromes, a substantial proportion of the vesamicol binding sites persist on cholinergic nerve terminals despite loss of ChAT activity.

• Authors: S J Kish, L M Distefano, S Dozic, Y Robitaille, A Rajput, J H Deck, O Hornykiewicz
• Journal: Neuroscience letters (Neurosci Lett) Vol. 117 Issue 3 Pg. 347-52 (Sep 18 1990) ISSN: 0304-3940 [Print] Ireland
• PMID: 2151294 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.)

Chemical References

• Neuromuscular Depolarizing Agents
• Piperidines
• vesamicol
• Choline O-Acetyltransferase
• Acetylcholine

Topics

• Acetylcholine (metabolism)
• Adult
• Aged
• Alzheimer Disease (metabolism)
• Amygdala (metabolism)
• Autonomic Nervous System Diseases (metabolism)
• Brain Chemistry
• Cerebral Cortex (metabolism)
• Choline O-Acetyltransferase (metabolism)
• Down Syndrome (metabolism)
• Humans
• Middle Aged
• Neuromuscular Depolarizing Agents (metabolism)
• Olivopontocerebellar Atrophies (metabolism)
• Parasympathetic Nervous System (metabolism)
• Parkinson Disease (metabolism)
• Piperidines (metabolism)