Suzuki Hidenobu, Gen Keishi
Tanzawa Hospital, Hadano, Kanagawa, Japan.
Hum Psychopharmacol. 2010 Jun-Jul;25(4):342-6. doi: 10.1002/hup.1124.
Blonanserin (BNS) possesses anti-serotonin 5-HT(2A) activity in addition to anti-dopamine D(2) activity, which is characteristic of second-generation antipsychotics, little information is available on its pharmacologic profile in vivo. We investigated the BNS daily dose, plasma concentration, plasma anti-D(2) activity, and plasma anti-5-HT(2A) activity in schizophrenia in a total of 14 subjects.
Blood samples were taken 14 days after the BNS dose was fixed, and the plasma concentration was measured by means of high-performance liquid chromatographic (HPLC) method. In addition, the plasma anti-D(2) activity and anti-5-HT(2A) activity were measured by means of radioreceptor assays in which [(3)H]-spiperone and [(3)H]-ketanserin were used.
The results revealed a statistically significant correlation between the daily dose and the plasma concentration (p = 0.04). Statistically significant correlations were also observed between the plasma concentration and the anti-D(2) activity and between the plasma concentration and the anti-5-HT(2A) activity (p = 0.003 and 0.04).
It is therefore believed that both the anti-D(2) activity in plasma and the anti-5-HT(2A) activity in plasma are regulated almost solely by the unchanged principal. Moreover, the mean plasma serotonin/dopamine (S/D) ratio was 0.9 and BNS exhibited both anti-D(2) activity and also anti-5-HT(2A) activity in vivo, as well, so it was clear that the in vitro pharmacological profile was retained in vivo.
布南色林(BNS)除具有抗多巴胺D(2)活性外,还具有抗5-羟色胺5-HT(2A)活性,这是第二代抗精神病药物的特征,但其体内药理学特征的相关信息较少。我们对14名精神分裂症患者的BNS日剂量、血浆浓度、血浆抗D(2)活性和血浆抗5-HT(2A)活性进行了研究。
在确定BNS剂量14天后采集血样,采用高效液相色谱(HPLC)法测定血浆浓度。此外,采用以[(3)H]-螺哌隆和[(3)H]-酮色林为试剂的放射受体分析法测定血浆抗D(2)活性和抗5-HT(2A)活性。
结果显示日剂量与血浆浓度之间存在统计学显著相关性(p = 0.04)。在血浆浓度与抗D(2)活性之间以及血浆浓度与抗5-HT(2A)活性之间也观察到统计学显著相关性(p = 0.003和0.04)。
因此,可以认为血浆中的抗D(2)活性和抗5-HT(2A)活性几乎完全由未改变的母体调节。此外,血浆中5-羟色胺/多巴胺(S/D)的平均比值为0.9,BNS在体内也同时表现出抗D(2)活性和抗5-HT(2A)活性,所以很明显其体外药理学特征在体内得以保留。