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Trazodone and its active metabolite m-chlorophenylpiperazine as partial agonists at 5-HT1A receptors assessed by [35S]GTPS binding

Ryoichi Toyoshima

Toshio Yamauchi

Department of Psychiatry, Saitama Medical School, Moroyama-machi, Iruma-gun, Saitama, Japan

Trazodone is an effective antidepressant drug with a broad therapeutic spectrum, including anxiolytic efficacy. Although trazodone is usually referred to as a serotonin (5-HT) reuptake inhibitor, this pharmacological effect appears to be too weak to fully account for its clinical effectiveness. The present study aimed to elucidate the agonist properties of trazodone and its active metabolite, m-chlorophenylpiperazine (m-CPP), at 5-HT_1A receptors by means of the guanosine-5'-O-(3-[³⁵S]thio)-triphosphate ([³⁵S]GTPS) binding assay. In membranes prepared from Chinese hamster ovary cells expressing human 5-HT_1A receptors (CHO/h5-HT_1A), trazodone behaved as an almost full agonist and m-CPP was also a highly efficacious partial agonist at 5-HT_1A receptors. The intrinsic activities of both compounds were higher than those of tandospirone and buspirone, which are clinically effective anxiolytics with well-known 5-HT_1A partial agonist properties. These effects were replicated in the 5-HT_1A receptor-mediated [³⁵S]GTP^S binding assay in native rat brain membranes (at least in hippocampal membranes), although the intrinsic activities of the compounds were low and differently ranked compared to those in CHO/h5-HT_1A cell membranes. When considering the implications of 5-HT_1A receptors in anxiety and/or depression, as well as the clinical effectiveness of azapirone anxiolytics with partial 5-HT_1A receptor agonist properties such as buspirone, it is possible that the agonist effects on 5-HT_1A receptors of trazodone and its active metabolite m-CPP presented in this study contribute, at least in part, to the clinical efficacy of the atypical antidepressant trazodone.

Key Words: buspirone • m-chlorophenylpiperazine (m-CPP) • 5-HT1A receptor • partial agonist • tandospirone • trazodone

Journal of Psychopharmacology, Vol. 19, No. 3, 235-241 (2005)
DOI: 10.1177/0269881105051526


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