Gefvert Ola, Eriksson Bo, Persson Per, Helldin Lars, Björner Annika, Mannaert Erik, Remmerie Bart, Eerdekens Mariëlle, Nyberg Svante
Centre for Clinical Research, University of Uppsala, Central Hospital Västerås, Sweden.
Int J Neuropsychopharmacol. 2005 Mar;8(1):27-36. doi: 10.1017/S1461145704004924.
Thirteen patients with schizophrenia received injections of 25, 50, or 75 mg of long-acting risperidone every 2 wk. Brain D2 receptor occupancy was assessed with [11C]raclopride 2 wk after the last (fifth) injection (day 71) in seven subjects and 2 wk after the third injection (day 44) in one subject. Stable plasma concentrations were reached after the third injection and steady-state concentrations of the active moiety (risperidone + 9-hydroxyrisperidone) after the fourth injection. Steady-state plasma concentrations were maintained for 4-5 wk after the last injection and then declined rapidly. After injections of 25, 50 and 75 mg on day 44 or day 71, D2 receptor occupancy ranged from 25-48%, 59-83% and 62-72% respectively, while plasma active-moiety levels ranged from 4.4-8.8, 15.0-31.1 and 22.5-26.3 ng/ml respectively. The results indicate that brain D2 receptor occupancy at steady state after injections of long-acting risperidone was in the range found in patients effectively treated with 2-6 mg of oral risperidone.
13名精神分裂症患者每2周接受一次25毫克、50毫克或75毫克长效利培酮注射。在最后一次(第五次)注射后2周(第71天),对7名受试者用[11C]雷氯必利评估脑D2受体占有率;对1名受试者在第三次注射后2周(第44天)评估。第三次注射后达到稳定的血浆浓度,第四次注射后达到活性部分(利培酮+9-羟基利培酮)的稳态浓度。最后一次注射后,稳态血浆浓度维持4-5周,然后迅速下降。在第44天或第71天注射25毫克、50毫克和75毫克后,D2受体占有率分别为25%-48%、59%-83%和62%-72%,而血浆活性部分水平分别为4.4-8.8、15.0-31.1和22.5-26.3纳克/毫升。结果表明,长效利培酮注射后稳态时脑D2受体占有率处于口服2-6毫克利培酮有效治疗的患者中所发现的范围内。