A Morphologic Study of the Effects of LSD on Neurons in Cultures of Cerebellum
Journal of Neuropathology & Experimental Neurology – July 01, 1972
Source: OpenAlex
Summary
LSD-25, or lysergic acid diethylamide, significantly impacts neuron structure, specifically within the lysosomal system. In organotypic cultures of mouse cerebellum (n=30), exposure to LSD for up to 53 hours resulted in coarse granules appearing in the cytoplasm of mature neurons at a concentration of 10-3 M. Electron microscopy revealed the formation of heterogeneous dense bodies, indicating changes in lysosomes without altering synaptic junctions. These findings suggest that LSD may enhance endocytosis or shift cellular metabolism, potentially affecting neuronal excitability and behavior.
Abstract
This study was undertaken to examine the possible cytologic action of LSD-25, lysergic acid diethylamide, on nervous tissue. Organotypic cultures of mouse cerebellum were exposed to LSD in their nutrient medium for periods up to 53 hours. Light-microscopically, at a dose of 10-3 M, coarse granules developed in the cytoplasm of mature neurons and in the cytoplasm of cells in the outgrowth region. Electron microscopy of these LSD-induced changes in the neurons revealed that the major qualitative change was the development of dense bodies, i.e. lysosomes. After several hours of exposure, these became heterogeneous dense bodies, HDBs, complex and varied in composition. The synaptic junction and other cell organelles were not altered morphologically. It was concluded that the cytologic site of action of LSD is the lysosomal system. Since it is known that LSD enters the cell, the possible site of interaction between the drug and the lysosomal system of the cell was considered. Two hypotheses were advanced in an attempt to correlate the effects on the lysosomal system of neurons and the known alterations in behaviour produced in man and animals by LSD: (i) an increase of endocytosis, and/or (ii) a shift of the internal metabolism of the cell. Either situation could result in an alteration of the excitability characteristics of a neuron.