Analytical subcellular fractionation of rat cortex: resolution of serotonergic nerve endings and receptors

• Published in: Journal of neurochemistry Vol. 41; no. 1; p. 84
• Main Authors: Laduron, P M, Janssen, P F, Ilien, B
• Format: Journal Article
• Language: English
• Published: England 01.01.1983
• Subjects: Animals; Cell Fractionation - methods; Centrifugation, Density Gradient; Cerebral Cortex - metabolism; Cerebral Cortex - ultrastructure; Corpus Striatum - metabolism; Male; Neurons - metabolism; Neurons - ultrastructure; Rats; Rats, Inbred Strains; Receptors, Serotonin - isolation & purification; Receptors, Serotonin - metabolism; Serotonin - physiology; Subcellular Fractions - metabolism
• ISSN: 0022-3042
• DOI: 10.1111/j.1471-4159.1983.tb11817.x

An analytical procedure for the subcellular fractionation of rat brain cortex is presented; it consists of a two-step procedure involving a differential centrifugation using the five-fraction scheme and an isopycnic centrifugation in continuous sucrose gradients. All fractions obtained were analyzed for their content of various constituents, such as receptor binding, uptake, and several marker enzymes. Special attention was paid to the subcellular distribution of the serotonin S2 receptors; they were mainly recovered in the microsomal P fraction, but a significant amount was also associated with the mitochondrial (M and L) fractions. After equilibration in density gradients, serotonin S2 receptors revealed two peaks, which were similarly affected after treatment with amitriptyline and/or yohimbine. There is no evidence to suggest that serotonin S2 receptors are associated with nerve endings containing the neurotransmitter serotonin. Although three main profiles, a microsomal, a mitochondrial, and a mixed one, clearly appear from the differential centrifugation, subgroups of these main profiles were also found. For instance, the microsomal distribution patterns of serotonin S2 receptors and 5'-nucleotidase are very similar, but differ from that of UDP-galactosyltransferase. Similarly, the mitochondrial profiles of cytochrome oxidase and 5-HT (serotonin) uptake are different. An analytical approach for brain fractionation, when performed with appropriate measurements (cytochrome oxidase, amine uptake, 5'-nucleotidase, and receptor binding), is rapid and clearly differentiates pre- and postsynaptic constituents.