Eap Chin B, Buclin Thierry, Cucchia Gianni, Zullino Daniele, Hustert Elisabeth, Bleiber Gabriela, Golay Kerry Powell, Aubert Anne-Catherine, Baumann Pierre, Telenti Amalio, Kerb Reinhold
Unit of Biochemistry and Clinical Psychopharmacology, Centre of Psychiatric Neurosciences, University Department of Adult Psychiatry, Prilly-Lausanne, Switzerland.
Eur J Clin Pharmacol. 2004 Jun;60(4):237-46. doi: 10.1007/s00228-004-0762-z. Epub 2004 Apr 28.
We investigated whether the oral administration of a low dose (75 micro g) of midazolam, a CYP3A probe, can be used to measure the in vivo CYP3A activity.
Plasma concentrations of midazolam, 1'OH-midazolam and 4'OH-midazolam were measured after the oral administration of 7.5 mg and 75 micro g midazolam in 13 healthy subjects without medication, in four subjects pretreated for 2 days with ketoconazole (200 mg b.i.d.), a CYP3A inhibitor, and in four subjects pretreated for 4 days with rifampicin (450 mg q.d.), a CYP3A inducer.
After oral administration of 75 micro g midazolam, the 30-min total (unconjugated + conjugated) 1'OH-midazolam/midazolam ratios measured in the groups without co-medication, with ketoconazole and with rifampicin were (mean+/-SD): 6.23+/-2.61, 0.79+/-0.39 and 56.1+/-12.4, respectively. No side effects were reported by the subjects taking this low dose of midazolam. Good correlations were observed between the 30-min total 1'OH-midazolam/midazolam ratio and midazolam clearance in the group without co-medication (r(2)=0.64, P<0.001) and in the three groups taken together (r(2)=0.91, P<0.0001). Good correlations were also observed between midazolam plasma levels and midazolam clearance, measured between 1.5 h and 4 h.
A low oral dose of midazolam can be used to phenotype CYP3A, either by the determination of total 1'OH-midazolam/midazolam ratios at 30 min or by the determination of midazolam plasma levels between 1.5 h and 4 h after its administration.
我们研究了口服低剂量(75微克)的咪达唑仑(一种CYP3A探针)是否可用于测量体内CYP3A活性。
在13名未用药的健康受试者、4名用酮康唑(200毫克,每日两次)预处理2天的受试者(酮康唑为CYP3A抑制剂)以及4名用利福平(450毫克,每日一次)预处理4天的受试者(利福平为CYP3A诱导剂)中,口服7.5毫克和75微克咪达唑仑后,测量咪达唑仑、1'-羟基咪达唑仑和4'-羟基咪达唑仑的血浆浓度。
口服75微克咪达唑仑后,在未合用药物组、酮康唑组和利福平组中测得的30分钟时总的(未结合+结合)1'-羟基咪达唑仑/咪达唑仑比值(均值±标准差)分别为:6.23±2.61、0.79±0.39和56.1±12.4。服用该低剂量咪达唑仑的受试者未报告有副作用。在未合用药物组中,30分钟时总的1'-羟基咪达唑仑/咪达唑仑比值与咪达唑仑清除率之间观察到良好的相关性(r²=0.64,P<0.001),在三组受试者合并分析时也观察到良好的相关性(r²=0.91,P<0.0001)。在1.5小时至4小时之间测量的咪达唑仑血浆水平与咪达唑仑清除率之间也观察到良好的相关性。
口服低剂量的咪达唑仑可用于对CYP3A进行表型分析,方法是在30分钟时测定总的1'-羟基咪达唑仑/咪达唑仑比值,或在给药后1.5小时至4小时之间测定咪达唑仑血浆水平。