Spreux-Varoquaux O, Gailledreau J, Vanier B, Bothua D, Plas J, Chevalier J F, Advenier C, Pays M, Brion S
Centre Hospitalier de Versailles, Département de Biochimie-Pharmacologie-Toxicologie, Hopital A. Mignot, Le Chesnay France.
Biol Psychiatry. 1996 Sep 15;40(6):465-73. doi: 10.1016/0006-3223(95)00449-1.
Hypofunction of the serotonin (5-HT) system might be involved in depression. Initial effects of the 5-HT reuptake inhibitor clomipramine (CMI) on plasma 5-HT have never been assessed. On Day 1, 27 depressed patients received either a 25-mg CMI slow infusion or a 25-mg CMI tablet in a randomized, double-blind, double-dummy design. The daily dose was subsequently titrated up to 75 mg i.v. or 150 mg orally. The Montgomery-Asberg Depression Rating Scale (MADRS) was rated on Days 1, 4, 7 and 14. High-performance liquid chromatography (HPLC-EC) assays of plasma 5-HT, platelet 5-HT, and CMI were performed on Day 1 before and after the infusion. On Day 1, both groups experienced a mean (nonsignificant) plasma 5-HT increase; in the i.v. group this initial increase correlated with MADRS decrease over 14 days (r = 0.76, p = .0025). Correlations between platelet 5-HT and MADRS decrease were not significant. These preliminary data show that: i) CMI administration results in initial changes in plasma 5-HT; and ii) i.v. CMI-induced initial plasma 5-HT increase is consistent with the CMI 5-HT profile, and might predict the clinical response to CMI.
血清素(5-羟色胺,5-HT)系统功能减退可能与抑郁症有关。5-HT再摄取抑制剂氯米帕明(CMI)对血浆5-HT的初始作用从未得到评估。在第1天,27名抑郁症患者采用随机、双盲、双模拟设计,接受25毫克CMI缓慢静脉输注或25毫克CMI片剂治疗。随后将每日剂量滴定至静脉注射75毫克或口服150毫克。在第1、4、7和14天使用蒙哥马利-阿斯伯格抑郁评定量表(MADRS)进行评分。在第1天输液前后,对血浆5-HT、血小板5-HT和CMI进行高效液相色谱(HPLC-EC)测定。在第1天,两组患者的血浆5-HT均出现平均(无显著意义)升高;在静脉注射组中,这种初始升高与14天内MADRS评分降低相关(r = 0.76,p = 0.0025)。血小板5-HT与MADRS评分降低之间的相关性不显著。这些初步数据表明:i)给予CMI会导致血浆5-HT的初始变化;ii)静脉注射CMI引起的血浆5-HT初始升高与CMI的5-HT特征一致,并且可能预测对CMI的临床反应。