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铁过载大鼠肝细胞血红素加氧酶的诱导作用。

Induction of liver cell haem oxygenase in iron-overloaded rats.

作者信息

Ibrahim N G, Hoffstein S T, Freedman M L

出版信息

Biochem J. 1979 May 15;180(2):257-63. doi: 10.1042/bj1800257.

Abstract

Rats were chronically iron-overloaded by intraperitonel injections of iron-dextran. Electron microscopy revealed that the excess iron was deposited in ferritin-like particles packed in lysosomes and scattered in hepatic cytoplasm. No mitochondrial iron deposition or damage was seen. Furthermore, mitochondrial preparations from chronically iron-overloaded animals were found to be contaminated with lysosomes, which could explain previously reported increases in mitochondrial iron by chemical analysis. Mitochondrial function, as measured by cytochromes a-a3, b and c concentrations as well as activity of the rate-limiting enzyme of haem synthesis, delta-aminolaevulinate synthetase, was not diminished by chronic iron-overloading. Microsomal haem was decreased by 30% at the time that haem oxygenase, the rate-limiting enzyme of haem degradation, was increased approx. 3-fold. Animals were given a single intraperitoneal injection of iron-dextran and the activities of delta-aminolaevulinate synthetase and haem oxygenase were measured over 24 h. delta-Aminolaevulinate synthetase activity increased approx. 2-fold in these acutely iron-overloaded rat livers, but at a time after the increase in haem oxygenase. These results suggest that an early consequence of excess iron in liver is acceleration of the rate of haem degradation, possible by haem oxygenase.

摘要

通过腹腔注射右旋糖酐铁使大鼠长期铁过载。电子显微镜显示,过量的铁沉积在溶酶体中包裹的铁蛋白样颗粒中,并散在于肝细胞质中。未观察到线粒体铁沉积或损伤。此外,发现来自长期铁过载动物的线粒体提取物被溶酶体污染,这可以解释先前通过化学分析报道的线粒体铁增加。通过细胞色素a-a3、b和c的浓度以及血红素合成限速酶δ-氨基乙酰丙酸合成酶的活性来衡量的线粒体功能,并未因长期铁过载而降低。在血红素降解限速酶血红素加氧酶增加约3倍时,微粒体血红素减少了30%。给动物单次腹腔注射右旋糖酐铁,并在24小时内测量δ-氨基乙酰丙酸合成酶和血红素加氧酶的活性。在这些急性铁过载的大鼠肝脏中,δ-氨基乙酰丙酸合成酶活性增加了约2倍,但在血红素加氧酶增加之后。这些结果表明,肝脏中铁过量的早期后果是血红素降解速率加快,可能是通过血红素加氧酶实现的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06a1/1161048/b8ddcde756c0/biochemj00461-0013-a.jpg

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