Matsuki Y, Yamada H, Oguri K
Faculty of Pharmaceutical Sciences, Kyushu University, Fukuoka, Japan.
Biol Pharm Bull. 1998 Nov;21(11):1160-2. doi: 10.1248/bpb.21.1160.
Our previous study indicated that picrotoxin competes with phenobarbital (PB) for the binding to liver microsomes, although the target of binding and the physiological role were not determined (unpublished observation). To seek information on the target site of PB, reflecting the induction of hepatic enzymes, we examined here the effect of picrotoxin on PB-mediated induction of hepatic cytochrome P450 and UDP-glucuronosyltransferase in vivo in rats. The induction of the CYP2B1/2 was estimated by immunoblot analysis and by measuring the activity of testosterone 16beta-hydroxylation. Intraperitoneal injection of picrotoxin alone slightly increased CYP2B1/2 protein. An experiment on co-treatment of picrotoxin and PB showed that picrotoxin enhanced rather than antagonized the inducing effect of PB. The results suggest two possibilities: that 1) picrotoxin increases the CYP2B subfamily by binding to the same site as PB; or 2) the site in microsomes for the competition between PB and picrotoxin does not reflect the induction of P450.
我们之前的研究表明,印防己毒素与苯巴比妥(PB)竞争结合肝微粒体,尽管结合靶点和生理作用尚未确定(未发表的观察结果)。为了探寻反映肝酶诱导作用的PB靶点位点信息,我们在此研究了印防己毒素对大鼠体内PB介导的肝细胞色素P450和UDP-葡萄糖醛酸转移酶诱导作用的影响。通过免疫印迹分析和测量睾酮16β-羟化活性来评估CYP2B1/2的诱导情况。单独腹腔注射印防己毒素会使CYP2B1/2蛋白略有增加。印防己毒素与PB联合处理的实验表明,印防己毒素增强而非拮抗PB的诱导作用。结果提示两种可能性:1)印防己毒素通过与PB结合于同一位点来增加CYP2B亚家族;或2)PB与印防己毒素竞争的微粒体位点并不反映P450的诱导情况。