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喂食六氯苯和铁过载对大鼠肝脏血红素生物合成酶及细胞色素P450的影响。

Effects of hexachlorobenzene feeding and iron overload on enzymes of haem biosynthesis and cytochrome P 450 in rat liver.

作者信息

Louw M, Neethling A C, Percy V A, Carstens M, Shanley B C

出版信息

Clin Sci Mol Med. 1977 Aug;53(2):111-5. doi: 10.1042/cs0530111.

Abstract
  1. The effect of hexachlorobenzene feeding on liver delta-aminolaevulinate synthase, uroporphyrinogen decarboxylase and cytochrome P 450 was studied at various time-intervals in siderotic and non-siderotic rats. 2 In the non-siderotic group hexachlorobenzene feeding led to a progress decrease in liver uroporphyrinogen decarboxylase activity, accompanied by a progressive increase in delta-aminolaevulinate synthase activity. Cytochrome P 450 concentrations were above normal throughout but fell toward the end of the experiment. 3. Similar but more marked changes were found in the siderotic animals. The fall in uroporphyrinogen decarboxylase activity occurred earlier and was significantly greater in these animals, whereas the increase in delta-aminolaevulinate synthase activity was consistently larger. Liver cytochrome P 450 concentration also rose but to a lesser extent than that in the non-siderotic rats. 4. Hexachlobenzene-induced porphyria would seem to be attributable to inhibition or inactivation of hepatic uroporphyrinogen decarboxylase. Hepatic siderosis has a synergistic effect with hexachlorobenzene on this enzyme and may exert additional effects by promoting cytochrome P 450 turnover.
摘要
  1. 在不同时间间隔,研究了给患铁沉着症和未患铁沉着症的大鼠喂食六氯苯对肝脏δ-氨基乙酰丙酸合成酶、尿卟啉原脱羧酶和细胞色素P 450的影响。2. 在未患铁沉着症的组中,喂食六氯苯导致肝脏尿卟啉原脱羧酶活性逐渐降低,同时δ-氨基乙酰丙酸合成酶活性逐渐升高。细胞色素P 450浓度始终高于正常水平,但在实验末期下降。3. 在患铁沉着症的动物中发现了类似但更明显的变化。尿卟啉原脱羧酶活性的下降出现得更早,且在这些动物中显著更大,而δ-氨基乙酰丙酸合成酶活性的增加始终更大。肝脏细胞色素P 450浓度也升高,但程度低于未患铁沉着症的大鼠。4. 六氯苯诱导的卟啉症似乎可归因于肝脏尿卟啉原脱羧酶的抑制或失活。肝脏铁沉着症与六氯苯对该酶有协同作用,并且可能通过促进细胞色素P 450周转发挥额外作用。

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