Januel Dominique, Massot Olivier, Poirier Marie-France, Olié Jean-Pierre, Fillion Gilles
Unité de Pharmacologie Neuro-Immuno-Endocrinienne, Institut Pasteur, Paris, France.
Psychiatry Res. 2002 Aug 30;111(2-3):117-24. doi: 10.1016/s0165-1781(02)00136-1.
Lithium is commonly used in combination with antidepressant drugs as a treatment for refractory depression; less often, it is used in non-resistant depression. The aim of this study was to examine the interaction of lithium with 5-HT(1B) receptors in 10 non-resistant unipolar depressed patients treated with clomipramine+lithium (C+L) vs. clomipramine+placebo (C+P). A mediation of the serotonergic system has been proposed in the literature to explain the clinical effect of lithium. Indeed, in a previous study of healthy human blood platelets, we demonstrated the interaction of lithium with adenylate cyclase activity coupled to 5-HT(1B) receptors. The functional activity of these receptors was measured by studying the inhibitory effect of L694,247, a 5-HT(1B) receptor agonist, on the adenylate cyclase activity determined by the production of cAMP. Using the same technique in the present study, we found that lithium significantly reduced the inhibition of adenylate cyclase activity induced by 5-HT(1B) receptor activation. This result confirms the specific interaction of lithium with 5-HT(1B) receptors. Moreover, a correlation between the percentage of 5-HT(1B) receptor-dependent adenylate cyclase inhibition and the clinical benefit of lithium was established, suggesting 5-HT(1B) receptors may be a target for the therapeutic effect of lithium.
锂通常与抗抑郁药物联合使用,用于治疗难治性抑郁症;较少用于治疗非难治性抑郁症。本研究的目的是检验锂与5-羟色胺(5-HT)1B受体在10例接受氯米帕明+锂盐(C+L)与氯米帕明+安慰剂(C+P)治疗的非难治性单相抑郁症患者中的相互作用。文献中已提出血清素能系统的介导作用来解释锂的临床疗效。事实上,在之前一项针对健康人血小板的研究中,我们证明了锂与与5-HT1B受体偶联的腺苷酸环化酶活性之间存在相互作用。通过研究5-HT1B受体激动剂L694,247对由环磷酸腺苷(cAMP)生成所测定的腺苷酸环化酶活性的抑制作用,来测量这些受体的功能活性。在本研究中使用相同技术,我们发现锂显著降低了由5-HT1B受体激活所诱导的腺苷酸环化酶活性的抑制作用。这一结果证实了锂与5-HT1B受体之间存在特异性相互作用。此外,还建立了5-HT1B受体依赖性腺苷酸环化酶抑制百分比与锂的临床疗效之间的相关性,表明5-HT1B受体可能是锂治疗作用的靶点。