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GABA‐Mimetic Activity and Effects on Diazepam Binding of Aminosulphonic Acids Structurally Related to Piperidine‐4‐Sulphonic Acid
Author(s) -
Falch Erik,
Jacobsen Poul,
KrogsgaardLarsen Povl,
Curtis David R.
Publication year - 1985
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.1471-4159.1985.tb07114.x
Subject(s) - chemistry , agonist , stereochemistry , piperidine , gabaa receptor , in vivo , bicuculline , in vitro , gaba receptor antagonist , binding site , butyric acid , biochemistry , receptor , biology , microbiology and biotechnology
The relationship between structure, in vivo activity, and in vitro activity of some analogues of the γ‐aminobutyric acid (GABA) agonist piperidine‐4‐sulphonic acid (P4S) was studied. The syntheses of 1,2,3,6‐tetrahydropyridine‐4‐sulphonic acid (DH‐P4S) and ( RS )‐pyrrolidin‐3‐yl‐methanesulphonamide (PMSA‐amide) are described. Like P4S, its unsaturated analogue DH‐P4S and the five‐ring isomer ( RS )‐pyrrolidin‐3‐yl‐methanesulphonic acid (PMSA) were bicuculline methochloride (BMC)‐sensitive inhibitors of the firing of neurones in the cat spinal cord. Whereas isonipecotic acid was less potent than its unsaturated analogue isoguvacine as a GABA‐mimetic and as an inhibitor of GABA binding, the opposite relative potencies of P4S and DH‐P4S were observed, P4S being proportionally more potent than DH‐P4S. In contrast with P4S and DH‐P4S, PMSA, which is an analogue of the potent GABA uptake inhibitor and BMC‐sensitive GABA‐mimetic homo‐β‐proline, was a relatively weak inhibitor of GABA uptake in vitro. PMSA‐amide was more than two orders of magnitude weaker than PMSA as an inhibitor of GABA binding and did not significantly affect GABA uptake in vitro. The effects of 3‐aminopropanesulphonic acid (3‐APS), PMSA, P4S, and DH‐P4S on the binding of [ 3 H]diazepam in vitro at 30°C, in the presence or absence of chloride ions, were studied and compared with those of the structurally related amino acids GABA, homo‐β‐proline, isonipecotic acid, and isoguvacine. Under these conditions the aminosulphonic acids were weaker than the respective amino acids in enhancing [ 3 H]diazepam binding, the difference being more pronounced in the absence of chloride.