Lipid abnormalities in the brain in adult Down’s syndrome and Alzheimer’s disease
- 1 December 1989
- journal article
- research article
- Published by Springer Nature in Molecular and Chemical Neuropathology
- Vol. 11 (3) , 157-185
- https://doi.org/10.1007/bf03160049
Abstract
Quantitative analysis by HPTLC of the major lipid classes and dilichol, and of fatty acyl groups of separated phosphoglycerides by capillary GLC, has been carried out on the gray matter of frontal cerebral cortex of brains from six Down’s syndrome (DS) and six Alzheimer’s disease (AD) adults, and six each of two corresponding sets of age-matched controls; specimens of DS and control cerebellum and corpus callosum were also analyzed. In DS frontal cortex, but not in AD frontal cortex, compared to their respective controls there was a decrease in the fraction of phosphatidylethanolamine (PE) and an increase in the fractions of sphingomyelin (SPM) and phosphatidylserine (PS). Abnormalities were not found in the proportions of major lipid classes in DS cerebellum or corpus callosum. The concentration of dolichol was elevated for age in the frontal cortex of DS and of AD. In the phosphoglycerides of DS frontal cortex, the fatty acyl composition showed small, but statistically significant, differences from those of age-matched controls, and some slight abnormalities were also detected in DS corpus callosum. The alterations in DS frontal cortex included decreases in (n-6) and increases in (n-3) groups in choline and ethanolamine phosphoglycerides (CPG and EPG), as had previously been found in EPG and serine phosphoglyceride (SPG) of the DS fetal brain. In DS frontal cortex, the proportion of 22∶4(n-6) groups was decreased in SPG, and in inositol phosphoglyceride (IPG) 18∶1(n-9) was increased. There were also small but significant alterations in DS frontal cortex in the fractions of shorter chain groups in CPG. In marked contrast, most of the fatty acyl abnormalities seen in DS were absent in the AD frontal cortex. It is therefore suggested that some abnormalities in the composition of cerebral membranes present prenatally in DS may persist into adulthood, and are not directly related to AD-type pathology.This publication has 72 references indexed in Scilit:
- Amino acids, glutathione, and glutathione transferase activity in the brains of patients with Alzheimer's diseaseAnnals of Neurology, 1987
- Dolichol in Human Brain: Regional and Developmental AspectsJournal of Neurochemistry, 1985
- Dolichol and phosphorylated dolichol content of tissues in ceroid‐lipofuscinosisJournal of Inherited Metabolic Disease, 1985
- Superoxide dismutase, glutathione peroxidase and lipoperoxidation in Oown's syndrome fetal brainDevelopmental Brain Research, 1984
- Alterations in the Fatty Acid Composition of Rat Brain Cells (Neurons, Astrocytes, and Oligodendrocytes) and of Subcellular Fractions (Myelin and Synaptosomes) Induced by a Diet Devoid of n‐3 Fatty AcidsJournal of Neurochemistry, 1984
- Dolichol deposition in developing mammalian brain: Content of free and fatty-acylated dolichol and proportion of specific isoprenologuesDevelopmental Brain Research, 1984
- Age-associated increase of free dolichol levels in miceBiochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism, 1984
- Neurobiology of Down's syndromeProgress in Neurobiology, 1983
- The Role of Phosphatidylserine Decarboxylase in Brain Phospholipid MetabolismJournal of Neurochemistry, 1983
- Cerebral Lipids in Down's SyndromeDevelopmental Medicine and Child Neurology, 1969