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Quantitative autoradiography of 5-CT-sensitive (5-HT1D) and 5-CT-insensitive (5-HT1E) serotonin receptors in human brain

Neuroscience LettersPublished 1 March 1992
Keith J. Miller, Milt Teitler
Citations46
SJR quartileQ2
SJR score0.77
SNIP0.67

TL;DR

The differential distribution patterns of the high-affinity, 5- CT-sensitive and 5-CT-insensitive [3H]5-HT binding sites indicate that these sites are expressed independently in human brain tissues, and are supportive of and consistent with previous pharmacological data that led to the division of 5- HT1D receptors into 5-HT1D and 5 -HT1E receptors.

Abstract

Quantitative receptor autoradiography was used to determine the distribution patterns of 5-CT-sensitive and 5-CT-insensitive binding of [3H]5-HT to high-affinity sites in human cortex, putamen, and globus pallidus. The binding of 3H-5-HT was limited to 5-HT1D sites (5-CT-sensitive) by co-incubating pindolol and mesulergine with [3H]5-HT, and by using 10 microM 5-HT to determine non-specific binding. The difference in the levels of binding between tissues exposed to the 5-CT-containing incubation media and tissue exposed to [3H]5-HT in the presence of 100 nM 5-CT was defined as 5-CT-insensitive binding (5-HT1E). The 5-HT1D receptor density in the frontal cortex was 189 fmol/mg, 226 fmol/mg was present in the globus pallidus, while the density in the putamen was only 28 fmol/mg. The 5-HT1E receptor density was 146 fmol/mg in frontal cortex, 224 fmol/mg in putamen and 140 fmol/mg in globus pallidus. The differential distribution patterns of the high-affinity, 5-CT-sensitive and 5-CT-insensitive [3H]5-HT binding sites indicate that these sites are expressed independently in human brain tissues. These data are supportive of and consistent with previous pharmacological data that led to the division of 5-HT1D receptors into 5-HT1D and 5-HT1E receptors and do not support the division of 5-HT1D receptors into 5-CT-sensitive and 5-CT-insensitive states.

Keywords

NeuroscienceBiochemistry, Genetics and Molecular Biology