Pfau W, Skog K
Umweltmedizin Hamburg eV and Institute of Experimental and Clinical Toxicology, Hamburg University, Vogt-Kölln-Strasse 30, 22527 Hamburg, Germany.
J Chromatogr B Analyt Technol Biomed Life Sci. 2004 Mar 25;802(1):115-26. doi: 10.1016/j.jchromb.2003.10.044.
The aromatic beta-carbolines norharman and harman have been implicated in a number of human diseases including Parkinson's disease, tremor, addiction and cancer. It has been shown that these compounds are normal body constituents formed endogenously but external sources have been identified. Here, we summarise literature data on levels of norharman and harman in fried meat and fish, meat extracts, alcoholic drinks, and coffee brews. Other sources include edible and medicinal plants but tobacco smoke has been identified as a major source. Exposure levels from these different dietary sources are estimated to a maximum of 4 microg norharman per kg body weight (bw) per day and 1 microg harman per kg bw per day. Exposure via tobacco smoke depends on smoking habits and type of cigarettes but can be estimated to 1.1 microg/kg bw for norharman and 0.6 microg/kg bw for harman per package of cigarettes smoked. Studies on toxicokinetics indicate that inhalative exposure leads to a rapid increase in plasma levels and high bioavailability of norharman and harman. Oral bioavailability is lower but there are indications that sublingual absorption may increase dietary uptake of beta-carbolines. Endogenous formation can be estimated to be 50-100 ng/kg bw per day for norharman and about 20 ng/kg bw per day for harman but these rates may increase with high intake of precursors. Biomarker studies on plasma levels of beta-carbolines reported on elevated levels of norharman, harman or both in diseased patients, alcoholics and following tobacco smoking or consumption of beta-carboline-containing food. Cigarette smoking has been identified as major influence but dietary exposure may contribute to exposure.
芳香β-咔啉类化合物去甲哈尔满和哈尔满与包括帕金森病、震颤、成瘾和癌症在内的多种人类疾病有关。已表明这些化合物是内源性形成的正常身体成分,但也已确定了其外部来源。在此,我们总结了关于油炸肉类和鱼类、肉类提取物、酒精饮料及咖啡冲泡液中去甲哈尔满和哈尔满含量的文献数据。其他来源包括可食用和药用植物,但烟草烟雾已被确定为主要来源。据估计,来自这些不同饮食来源的暴露水平最高为每天每千克体重(bw)4微克去甲哈尔满和每天每千克bw 1微克哈尔满。通过烟草烟雾的暴露取决于吸烟习惯和香烟类型,但每吸一包烟,去甲哈尔满的暴露量估计为1.1微克/千克bw,哈尔满为0.6微克/千克bw。毒代动力学研究表明,吸入暴露会导致血浆水平迅速升高,且去甲哈尔满和哈尔满具有高生物利用度。口服生物利用度较低,但有迹象表明舌下吸收可能会增加β-咔啉类化合物的饮食摄入量。据估计,去甲哈尔满的内源性形成量为每天每千克bw 50 - 100纳克,哈尔满约为每天每千克bw 20纳克,但这些速率可能会随着前体摄入量的增加而升高。关于β-咔啉类化合物血浆水平的生物标志物研究报告称,患病患者、酗酒者以及吸烟或食用含β-咔啉类食物后,去甲哈尔满、哈尔满或两者的水平都会升高。吸烟已被确定为主要影响因素,但饮食暴露也可能导致暴露。