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镉暴露鸡胚中肝脏血红素代谢的调节改变。

Altered regulation of hepatic heme metabolism in cadmium exposed chick embryo.

作者信息

Prasad A R, Datta K

出版信息

Biochem Int. 1984 Feb;8(2):289-98.

PMID:6548141
Abstract

An investigation on the process of heme metabolism with special emphasis on ALA synthetase, heme synthetase and heme oxygenase was studied in cadmium exposed chick embryo to enlighten the mechanism of cadmium embryotoxicity. Cadmium chloride injection (2.5-10 mumole/kg) to chick embryo increases the activity of ALA synthetase by 5-7 folds, however, it inhibits the activity of heme synthetase significantly. The activity of heme oxygenase is further shown to be enhanced by cadmium chloride treatment. These changes are accompanied by a marked reduction in hepatic heme content. The induction of ALA synthetase and heme oxygenase was dependent on the initial concentration of exogenous cadmium. Pretreatment with actinomycin D completely blocks the cadmium mediated induction of both ALA synthetase and heme oxygenase. Time course studies on the stimulation of these two enzymes show that cadmium enhances the activity of heme oxygenase to its maximum level after 24 h. of injection, whereas ALA synthetase activity reaches its highest value only by 48 h. and both the enzymes remain elevated at least upto 96 h. This observation can be correlated with the hepatic heme level at different time intervals after cadmium exposure. These observations suggest the presence of regulatory process for heme metabolism which is susceptible to alteration of 'regulatory heme pool' caused by cadmium.

摘要

为了阐明镉胚胎毒性的机制,对镉暴露的鸡胚中血红素代谢过程进行了研究,特别关注了δ-氨基-γ-酮戊酸(ALA)合成酶、血红素合成酶和血红素加氧酶。给鸡胚注射氯化镉(2.5 - 10微摩尔/千克)可使ALA合成酶的活性增加5 - 7倍,然而,它会显著抑制血红素合成酶的活性。氯化镉处理还显示可增强血红素加氧酶的活性。这些变化伴随着肝脏血红素含量的显著降低。ALA合成酶和血红素加氧酶的诱导依赖于外源性镉的初始浓度。用放线菌素D预处理可完全阻断镉介导的ALA合成酶和血红素加氧酶的诱导。对这两种酶刺激的时间进程研究表明,镉注射24小时后可将血红素加氧酶的活性提高到最高水平,而ALA合成酶活性仅在48小时时达到最高值,并且这两种酶至少在96小时内都保持升高。这一观察结果可与镉暴露后不同时间间隔的肝脏血红素水平相关联。这些观察结果表明存在血红素代谢的调节过程,该过程易受镉引起的“调节性血红素池”改变的影响。

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