Frydman R B, Frydman B, Feinstein G
Mol Cell Biochem. 1977 Jul 5;16(2):187-92. doi: 10.1007/BF01732060.
The formation of porphyrins from porphobilinogen by a duck blood hemolysate was examined. The system was found to form mainly protoporphyrin IX and hemin, and accumulated lesser amounts of uroporphyrins, hepatacarboxylic porphyrin, and coproporphyrins. By storage at -20 degrees the accumulation of uroporphyrins and heptacarboxylic porphyrin was increased. Both porphyrins were mainly the type III isomers. By addition of dithiothreitol the porphyrin pattern reversed to the original one formed by the fresh hemolysate. Addition of a number of amines also inhibited the decarboxylating system without affecting the original isomer distribution among the porphyrins. Addition of Fe2+ (3mM) did not affect the porphyrin pattern or the isomer distribution. Addition of Pb2+ (2.5 mM) partially inhibited the decarboxylating system, whereas at higher concentrations (4 mM) it increased the decarboxylation rate of the heptacarboxylic porphyrin. The obtained results are discussed in relation to porphyrin accumulation in porphyria cutanea tarda and in acquired hepatic porphyrias.
研究了鸭血溶血产物由胆色素原形成卟啉的过程。发现该体系主要形成原卟啉IX和血红素,并积累少量的尿卟啉、七羧基卟啉和粪卟啉。通过在-20℃储存,尿卟啉和七羧基卟啉的积累增加。这两种卟啉主要是III型异构体。加入二硫苏糖醇后,卟啉模式恢复为新鲜溶血产物形成的原始模式。加入多种胺也会抑制脱羧体系,而不影响卟啉中原始异构体的分布。加入Fe2+(3mM)不影响卟啉模式或异构体分布。加入Pb2+(2.5mM)部分抑制脱羧体系,而在较高浓度(4mM)时,它会提高七羧基卟啉的脱羧速率。结合迟发性皮肤卟啉症和获得性肝卟啉症中的卟啉积累对所得结果进行了讨论。