Abdel-Aziz A F, El-Sharabasy M M, El-Far M A, Yousef W M
Chemistry Department, Faculty of Science, Mansoura University, Egypt.
Cancer Lett. 1998 Aug 14;130(1-2):77-81. doi: 10.1016/s0304-3835(98)00117-7.
This study was performed on rats receiving nitrosamine precursors as potent liver carcinogens in order to investigate and follow up the porphyrin metabolism during the intake of hepatocarcinogens. As clarified from our results, progressive increases in free erythrocyte porphyrins, erythrocyte protoporphyrins, haem content and hepatic total porphyrins were observed after 2 months of intaking these carcinogens and further increases were gradually observed in parallel with the continued intake of these chemicals, which was extended to 7 months. At the same time, such elevations were also observed in the activity of hepatic delta-aminolevulinic acid (ALA)-synthetase and uroporphyrinogen-1-synthetase either in hepatic tissues or erythrocytes of these carcinogen-subjected rats. However, significant inhibition was found in the activity of erythrocyte ALA-dehydratase, which reached 40.5% of the control values after 7 months. Therefore, these observations demonstrated that the intake of hepatocarcinogens may influence the rate of hepatic porphyrin and haem biosynthesis.
本研究以接受亚硝胺前体(一种强效肝脏致癌物)的大鼠为对象,旨在研究和追踪摄入肝脏致癌物期间的卟啉代谢情况。从我们的结果可以明确看出,在摄入这些致癌物2个月后,游离红细胞卟啉、红细胞原卟啉、血红素含量和肝脏总卟啉均呈逐渐增加趋势,并且随着这些化学物质的持续摄入(持续至7个月),进一步的增加也逐渐显现。与此同时,在这些接触致癌物大鼠的肝脏组织或红细胞中,肝脏δ-氨基乙酰丙酸(ALA)合成酶和尿卟啉原-1-合成酶的活性也出现了此类升高。然而,红细胞ALA脱水酶的活性受到显著抑制,7个月后降至对照值的40.5%。因此,这些观察结果表明,摄入肝脏致癌物可能会影响肝脏卟啉和血红素的生物合成速率。