Woods J S, Martin M D, Naleway C A, Echeverria D
Department of Environmental Health, School of Public Health and Community Medicine, University of Washington, Seattle.
J Toxicol Environ Health. 1993 Oct-Nov;40(2-3):235-46. doi: 10.1080/15287399309531791.
Porphyrins are formed as intermediates in the biosynthesis of heme. In humans and other mammals, porphyrins with eight, seven, six, five, and four carboxyl groups are excreted in the urine in a well-established pattern. Mercury selectively alters porphyrin metabolism in kidney proximal tubule cells, leading to an altered urinary porphyrin excretion pattern. Previous studies in rats have shown that changes in the urinary porphyrin profile during exposure to mercury as methylmercury hydroxide are uniquely characterized by highly elevated (20- to 30-fold) levels of four- and five-carboxyl porphyrins and by the excretion of an atypical porphyrin ("precoproporphyrin"), which elutes on high performance liquid chromatography (HPLC) approximately midway between penta- and coproporphyrins. Changes in the urinary porphyrin profile are highly correlated with the dose and duration of mercury exposure and persist for up to 20 wk following cessation of mercury treatment. In the present studies, the utility of urinary porphyrin profile changes as a biomarker of mercury exposure in human subjects was evaluated. Urinary porphyrin concentrations were measured in dentists participating in the Health Screening Programs conducted during the 1991 and 1992 annual meetings of the American Dental Association and compared with urinary mercury levels measured in the same subjects. Among dentists with no detectable urinary mercury, mean concentrations of urinary porphyrins were within the established normal ranges for male human subjects. In contrast, among dentists with urinary mercury in excess of 20 micrograms/L, mean urinary concentrations of four- and five-carboxyl porphyrins as well as of precoproporphyrin were elevated three to four times those of unexposed subjects. Significant differences in urinary porphyrin concentrations remained when porphyrin concentrations in spot urine samples were adjusted for creatinine levels. These findings suggest that urinary porphyrin profiles may serve as a useful biomarker of mercury exposure in clinical or epidemiologic studies of mercury-related human health risks.
卟啉作为血红素生物合成的中间体而形成。在人类和其他哺乳动物中,具有八个、七个、六个、五个和四个羧基的卟啉以一种既定模式经尿液排出。汞选择性地改变肾近端小管细胞中的卟啉代谢,导致尿液卟啉排泄模式改变。先前在大鼠中的研究表明,暴露于氢氧化甲基汞形式的汞期间,尿液卟啉谱的变化具有独特特征,即四羧基和五羧基卟啉水平高度升高(20至30倍),以及排泄一种非典型卟啉(“前粪卟啉”),其在高效液相色谱(HPLC)上的洗脱位置大约在五羧基卟啉和粪卟啉之间。尿液卟啉谱的变化与汞暴露的剂量和持续时间高度相关,并且在停止汞处理后可持续长达20周。在本研究中,评估了尿液卟啉谱变化作为人类受试者汞暴露生物标志物的效用。在参加1991年和1992年美国牙科协会年会期间进行的健康筛查项目的牙医中测量尿液卟啉浓度,并将其与同一受试者中测量的尿液汞水平进行比较。在尿液汞检测不到的牙医中,尿液卟啉的平均浓度在男性人类受试者既定的正常范围内。相比之下,在尿液汞超过20微克/升的牙医中,四羧基和五羧基卟啉以及前粪卟啉的尿液平均浓度比未暴露受试者高3至4倍。当将随机尿样中的卟啉浓度根据肌酐水平进行校正时,尿液卟啉浓度仍存在显著差异。这些发现表明,在与汞相关的人类健康风险的临床或流行病学研究中,尿液卟啉谱可能作为汞暴露的有用生物标志物。