Liang Bingqing, Zhan Yunyun, Huang Xiangxin, Gu Ermin, Dai Dapeng, Cai Jianping, Hu Guoxin
School of Pharmacy, Wenzhou Medical University, Wenzhou, 325035, Zhejiang, People's Republic of China.
The Key Laboratory of Geriatrics, Beijing Hospital and Beijing Institute of Geriatrics, Ministry of Health, Beijing, 100730, People's Republic of China.
Eur J Drug Metab Pharmacokinet. 2016 Dec;41(6):759-765. doi: 10.1007/s13318-015-0307-0.
Hemangeol, approved for the treatment of proliferative infantile hemangiomas requiring systemic therapy, is metabolized by cytochrome P450 2D6 (CYP2D6), which is a highly polymorphic enzyme that metabolizes a large number of drugs. More than 100 CYP2D6 allelic variants have been reported so far, including 22 novel variants that discovered in our lab in the Chinese population. Our study aimed to probe the enzymatic activity of these variants toward hemangeol in vitro with recombinant microsomes that expressed in sf21 insect cells using a baculovirus-mediated expression system.
The wild-type CYP2D6.1 and other variants (CYP2D6.2, CYP2D6.10 and 22 novel CYP2D6 variants) were incubated with 1-200 μM hemangeol for 50 min at 37 °C. Then the products were extracted, and signal detection was performed by high-performance liquid chromatography with fluorescence detector.
All of the variants exhibited changed apparent Michaelis-Menten constant (Km) or maximum velocity of the reaction (V ) values compared with that of wild-type protein. The intrinsic clearances (V /Km) were significantly decreased by 0.37 to 42.74 %. However, CYP2D6.92 and CYP2D6.96 showed no or minimal enzymatic activity as no concentration of 4'-hydroxypropranolol was detected.
The comprehensive in vitro assessment of CYP2D6 variants provides significant insights into allele-specific activity towards hemangeol in vivo.
Hemangeol已被批准用于治疗需要全身治疗的增殖性婴儿血管瘤,它由细胞色素P450 2D6(CYP2D6)代谢,CYP2D6是一种高度多态性的酶,可代谢大量药物。迄今为止,已报道了100多种CYP2D6等位基因变体,其中包括我们实验室在中国人群中发现的22种新变体。我们的研究旨在使用杆状病毒介导的表达系统,在sf21昆虫细胞中表达的重组微粒体,体外探究这些变体对Hemangeol的酶活性。
将野生型CYP2D6.1和其他变体(CYP2D6.2、CYP2D6.10和22种新的CYP2D6变体)与1-200μM的Hemangeol在37℃下孵育50分钟。然后提取产物,并用带荧光检测器的高效液相色谱进行信号检测。
与野生型蛋白相比,所有变体的表观米氏常数(Km)或反应最大速度(V)值均发生了变化。内在清除率(V/Km)显著降低了0.37%至42.74%。然而,CYP2D6.92和CYP2D6.96未显示酶活性或酶活性极小,因为未检测到4'-羟基普萘洛尔的浓度。
对CYP2D6变体的全面体外评估为体内对Hemangeol的等位基因特异性活性提供了重要见解。