Premium
Effect of Homo‐β‐Proline and Other Heterocyclic GAB A Analogues on GABA Uptake in Neurons and Astroglial Cells and on GABA Receptor Binding
Author(s) -
Larsson O. M.,
Thorbek P.,
KrogsgaardLarsen P.,
Schousboe A.
Publication year - 1981
Publication title -
journal of neurochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.75
H-Index - 229
eISSN - 1471-4159
pISSN - 0022-3042
DOI - 10.1111/j.1471-4159.1981.tb06320.x
Subject(s) - nipecotic acid , proline , biochemistry , gamma aminobutyric acid , neuroglia , receptor , gabaa receptor , chemistry , inhibitory postsynaptic potential , stereochemistry , amino acid , biology , neurotransmitter , neuroscience , central nervous system
Two groups of GABA (γ‐aminobutyric acid) analogues, one comprising derivatives of β‐proline and the other compounds structurally related to nipecotic acid, were investigated as potential inhibitors of high‐affinity GABA transport in neurons and glial cells, as well as displacers of GABA receptor binding. In addition to cis ‐4‐hydroxynipecotic acid, which is known as a potent inhibitor of GABA uptake, homo‐β‐proline was the only compound which proved to be a potent inhibitor of glial as well as neuronal GABA uptake. IC 50 values for GABA uptake into glial cells and brain cortex “prisms” were 20 and 75 μM, respectively, and the IC 50 value obtained for GABA uptake into cultured neurons was 10 μM. A kinetic analysis of the action of homo‐β‐proline on GABA uptake into cultured astrocytes and neurons showed that this compound acts as a competitive inhibitor of GABA uptake in both cell types. From the apparent K m values, K i values for homo‐β‐proline of 16 and 6 μM could be calculated for glial and neuronal uptake, respectively. This mechanism of action strongly suggests that homo‐β‐proline interacts with the GABA carriers. Furthermore, homo‐β‐proline also displaced GABA from its receptor with an IC 50 value of 0.3 μM. The cis ‐4‐hydroxynipecotic acid analogues, cis‐ and trans‐4‐mercaptonipecotic acid, had no inhibitory effect on glial or neuronal GABA uptake. Other SH reagents, PCMB, NEM and DTNB, were shown to be relatively weak inhibitors of GABA uptake into cultured astrocytes, suggesting that SH groups are not directly involved in the interaction between GABA and its transport carrier.