Potent lipophilic substituted benzamide drugs are not selective D-1 dopamine receptor antagonists in the rat

作者：Simon Fleminger, H. Van De Waterbeemd, Nadia M.J. Rupniak, Charles A. Reavill, Bernard Testa, Peter G. Jenner, C. DAVID MARSDEN · 发表于：Journal of Pharmacy and Pharmacology · 年份：1983 · DOI：10.1111/j.2042-7158.1983.tb02957.x · 被引用次数：32 · 研究领域：Receptor Mechanisms and Signaling、Pharmacological Receptor Mechanisms and Effects、Neuroscience and Neuropharmacology Research

The substituted benzamide drugs YM 09151-2 and clebopride potently inhibited apomorphine-induced stereotyped behaviour in the rat and caused displacement of the specific binding of [3H]spiperone to D-2 binding sites on striatal membranes in low nanomolar concentrations. Other substituted benzamide drugs including metoclopramide, sultopride and flubepride also inhibited stereotyped behaviour to a greater or lesser degree, but were less potent in displacing [3H]spiperone from D-2 sites. YM 09151-2 and clebopride only weakly displaced specific binding of [3H]piflutixol to D-1 sites on rat striatal membranes, and only weakly inhibited striatal dopamine stimulated adenylate cyclase activity, when compared with cis-flupenthixol. The other substituted benzamide drugs did not displace [3H]piflutixol or inhibit dopamine stimulation of adenylate cyclase activity in the concentration range used. Clebopride and YM 09151-2 were highly lipophilic with apparent partition coefficient (log P') values equivalent to those of classical neuroleptic compounds, such as cis-flupenthixol. In contrast, the other substituted benzamide drugs were markedly less lipophilic. A log P' value of approximately 2 was required before inhibition of adenylate cyclase activity or displacement of [3H]piflutixol binding occurred. However, in excess of this value there was no correlation between either inhibition of adenylate cyclase activity or displacement of [3H]piflutixol binding and the lipophilicity of the vario...