Gygi S P, Joseph R E, Cone E J, Wilkins D G, Rollins D E
Department of Pharmacology and Toxicology, University of Utah, Salt Lake City 84112, USA.
Drug Metab Dispos. 1996 Apr;24(4):495-501.
Xenobiotics circulating in the blood may become incorporated into growing hair. Melanin has affinity for many pharmacologically unrelated drugs and is responsible for the pigmentation in hair. To assess the role of pigmentation in the incorporation of drugs into hair, the distribution of codeine and its metabolites was studied in Sprague-Dawley (SD; white nonpigmented hair), Dark Agouti (DA; brown pigmented hair), and hooded Long-Evans (LE; both black pigmented and white nonpigmented hair) rats. Codeine was administered at a dose of 40 mg/kg/day i.p. for 5 days. Fourteen days after beginning the dosing protocol, hair was collected and analyzed for codeine, and its metabolite, morphine, by positive-ion chemical ionization GC/ion-trap MS. The plasma pharmacokinetics for codeine and morphine were also determined after a single 40 mg/kg injection (equivalent to first dose in 5-day dosing protocol) in all three strains of rats. Hair and plasma codeine and morphine concentrations were also determined after acid hydrolysis to evaluate the presence of glucuronide metabolites. Codeine concentrations in the hair of SD, DA, and pigmented LE hair were 0.98 +/- 0.10, 5.99 +/- 1.24, and 111.93 +/- 18.69 ng/mg hair, respectively; morphine concentrations were 0.34 +/- 0.04, 0.51 +/- 0.11, and 14.46 +/- 1.81 ng/mg hair, respectively; morphine glucuronide concentrations were 0.67 +/- 0.08, 1.04 +/- 0.37, and 13.80 +/- 3.60 ng/mg hair, respectively. Studies examining the in vitro binding of [3H] codeine and [3H]morphine to hair demonstrated both specific and nonspecific binding sites for codeine and morphine. Pigmented hair from LE rats possessed the greatest number of binding sites, white hair from SD rats contained the least, and brown hair from DA rats was intermediate. A time course study of codeine and its metabolites showed pigment-mediated differences in incorporation of codeine and metabolites within a few hours of drug administration. These data indicate that pigmented hair possesses a greater capacity to bind and incorporate codeine and its metabolites than does nonpigmented hair. Interpretation of hair concentrations of drugs should involve consideration of hair pigmentation.
在血液中循环的外源性物质可能会掺入到生长的毛发中。黑色素对许多药理性质不相关的药物具有亲和力,并导致毛发色素沉着。为了评估色素沉着在药物掺入毛发中的作用,研究了可待因及其代谢产物在斯普拉格-道利大鼠(SD;白色无色素毛发)、深色刺豚鼠(DA;棕色有色素毛发)和带帽长-伊文斯大鼠(LE;既有黑色有色素毛发又有白色无色素毛发)中的分布情况。可待因以40mg/kg/天的剂量腹腔注射,持续5天。在开始给药方案14天后,收集毛发并通过正离子化学电离气相色谱/离子阱质谱分析可待因及其代谢产物吗啡。在所有三种品系的大鼠单次注射40mg/kg(相当于5天给药方案中的首剂量)后,还测定了可待因和吗啡的血浆药代动力学。在酸水解后还测定了毛发和血浆中的可待因和吗啡浓度,以评估葡萄糖醛酸代谢产物的存在情况。SD大鼠、DA大鼠和LE品系有色素毛发中的可待因浓度分别为0.98±0.10、5.99±1.24和111.93±18.69ng/mg毛发;吗啡浓度分别为0.34±0.04、0.51±0.11和14.46±1.81ng/mg毛发;吗啡葡萄糖醛酸浓度分别为0.67±0.08、1.04±0.37和13.80±3.60ng/mg毛发。研究[3H]可待因和[3H]吗啡与毛发的体外结合情况表明,可待因和吗啡既有特异性结合位点,也有非特异性结合位点。LE大鼠的有色素毛发具有最多的结合位点,SD大鼠的白色毛发含有的结合位点最少,DA大鼠的棕色毛发则介于两者之间。一项关于可待因及其代谢产物的时间进程研究表明,在给药后数小时内,色素介导了可待因及其代谢产物掺入的差异。这些数据表明,有色素毛发比无色素毛发具有更大的结合和掺入可待因及其代谢产物的能力。对毛发中药物浓度的解释应考虑毛发色素沉着情况。