Compounds that show their pharmacological actions via specific receptors are considered potential candidates for new drugs. Recently, several compounds that have specific binding sites and show certain pharmacological actions have been identified, but neither their binding sites, their endogenous substances, nor the functional role of the binding sites have been clarified. Regardless of the exact role of the binding sites of the compounds, research into the sites has opened up new areas of receptor investigation, and also new strategies for developing drugs. The sigma-ligand is one such kind of compound, and the existence of a binding site for the ligand was first postulated to account for the psychotomimetic effects of N-allylnormetazocine and related racemic benzomorphans. The binding site of the sigma-ligand is widely distributed in the central nervous system and peripheral systems. However, it still remain to be established whether sigma-ligand binding sites are to be referred to as "receptors". The classification of the ligands as agonists or antagonists at the sites and the heterogeneity and the functional role of the binding sites have not yet been clarified. Furthermore, the therapeutic targets have not been clearly determined. However, the sigma-ligands have high potential for developing new drugs. One of the possible targets of the sigma-ligands as new forms of drugs is schizophrenia. Recently, we identified two potent and highly selective sigma-ligands, FH-510 and NE-100. Together with the data on the binding properties and pharmacological actions of these compounds, the possibilities of the sigma-ligand as a new therapeutic drug were discussed.

01 Nov 1993·European Journal of PharmacologyQ3 · MEDICINE

Discrimination of (+)-3-PPP sites from DTG sites by FH-510, a novel potent σ ligand, in rat brain

Q3 · MEDICINE

Article

Author: Susumu Otomo ; Makoto Tanaka ; Makoto Muramatsu ; Shigeyuki Chaki

The effect of 5,8-dimethyl-4-(2-di-n-propylaminoethyl)carbazol monohydrochloride (FH-510) on the binding of sigma ligands such as [3H](+)-3-(3-hydroxyphenyl)-N-(1-propyl)piperidine ([3H](+)-3-PPP) and [3H]1,3-di-o-tolylguanidine ([3H]DTG) to rat brain membranes was studied. The inhibitory effect of FH-510 on [3H](+)-3-PPP binding to membranes of rat brain was 260 times more potent than that on [3H]DTG binding. Scatchard plot analysis showed that FH-510 inhibited [3H](+)-3-PPP binding in a competitive manner, while the inhibitory effect of FH-510 on [3H]DTG binding was noncompetitive. These results suggest that (+)-3-PPP sites could be discriminated from DTG sites, and that FH-510 binds preferentially to (+)-3-PPP recognition sites in rat brain.

01 Jul 1993·European Journal of PharmacologyQ3 · MEDICINE

Binding of [3H]FH-510 to σ ligand recognition sites in guinea-pig brain membranes

Q3 · MEDICINE

Article

Author: Otomo, Susumu ; Kaku, Shinsuke ; Tanaka, Makoto ; Muramatsu, Makoto

We examined the characteristics of the binding of radiolabeled 5,8-dimethyl-4-(2-di-n-propylaminoethyl)carbazol monohydrochloride ([3H]FH-510), a highly potent and selective sigma ligand, to guinea-pig brain membranes. [3H]FH-510 showed saturable and reversible binding to sigma binding sites. The association rate constant (k+1) and dissociation rate constant (k-1) of [3H]FH-510 were 0.023 min-1.nM-1 and 0.081 min-1, respectively. Scatchard plot analysis showed a dissociation constant (Kd) and maximal number of binding sites (Bmax) of 6.0 +/- 0.63 nM and 1763.3 +/- 177.4 fmol/mg protein (n = 7), respectively. The rank order of potency (Ki) of several structurally dissimilar sigma ligands obtained for the displacement of [3H]FH-510 binding was highly correlated with that determined for [3H](+)-3-(3-hydroxyphenyl)-N-(1-propyl)piperidine ([3H](+)-3-PPP) binding. The binding of [3H]FH-510 was not influenced by histaminergic, dopaminergic, adrenergic, serotonergic or cholinergic agents at 10(-7) M. Higher [3H]FH-510 binding to brain regions was observed in the cerebellum and pons-plus-medulla. Except for the nuclear fraction, the highest level of [3H]FH-510 and [3H](+)-3-PPP binding to subcellular fractions was observed in the microsomal fraction. From these results, it is suggested that FH-510 selectively binds with high affinity to sigma binding sites in guinea-pig membranes.

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Indication	Highest Phase	Country/Location	Organization	Date
Behavioural disorders	Preclinical	-	Taisho Pharmaceutical Holdings Co., Ltd.	-

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