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大鼠单次低剂量镉染毒后肝脏和肾脏中镉金属硫蛋白的长期周转

Long-term turnover of cadmium metallothionein in liver and kidney following a single low dose of cadmium in rats.

作者信息

Ridlington J W, Winge D R, Fowler B A

出版信息

Biochim Biophys Acta. 1981 Mar 5;673(2):177-83.

PMID:7213819
Abstract

Rats were injected subcutaneously on two consecutive days with CdCl2, and sampled animals, killed at monthly intervals from 1 to 6 months thereafter, exhibited the presence of Cd,Zn-thionein in both the liver and kidney. At 6 months, hepatic thionein was present as the two major polymorphic forms previously demonstrated in short term Cd-injection studies. [35S]cysteine incorporation studies showed that both polymorphic forms of thionein underwent continual turnover at similar rates throughout th study. The slow hepatic and renal turnover of Cd, therefore, was not due to a highly stable form of Cd-thionein, but apparently due to an inefficient mechanism for excretion of Cd from these tissues. The Cd/Zn ratio of hepatic thionein remained relatively constant, suggesting that continual thionein induction results in a long-term hepatic trapping of Zn by thionein, but the ratio of renal thionein showed a marked increase during the course of the study.

摘要

大鼠连续两天皮下注射氯化镉,此后每月间隔处死采样动物,在1至6个月内,肝脏和肾脏中均检测到镉锌硫蛋白。6个月时,肝脏硫蛋白呈现出短期镉注射研究中先前证实的两种主要多态形式。[35S]半胱氨酸掺入研究表明,在整个研究过程中,硫蛋白的两种多态形式以相似的速率持续更新。因此,镉在肝脏和肾脏中的缓慢更新并非由于镉硫蛋白的高度稳定形式,而是显然由于这些组织中镉排泄机制效率低下。肝脏硫蛋白的镉/锌比值保持相对恒定,表明持续的硫蛋白诱导导致硫蛋白对锌的长期肝脏捕获,但在研究过程中,肾脏硫蛋白的比值显著增加。

相似文献

1
Long-term turnover of cadmium metallothionein in liver and kidney following a single low dose of cadmium in rats.大鼠单次低剂量镉染毒后肝脏和肾脏中镉金属硫蛋白的长期周转
Biochim Biophys Acta. 1981 Mar 5;673(2):177-83.
2
Degradation of cadmium-thionein in rat liver and kidney.大鼠肝脏和肾脏中镉硫蛋白的降解
J Toxicol Environ Health. 1978 Sep-Nov;4(5-6):805-13. doi: 10.1080/15287397809529701.
3
Degradation of cadmium-thionein in rat liver and kidney.大鼠肝脏和肾脏中镉硫蛋白的降解
J Environ Pathol Toxicol. 1978 Nov-Dec;2(2):463-72.
4
Metabolism of 35S-labelled copper-, zinc-and cadmium-thionein in the rat.大鼠体内35S标记的铜、锌和镉硫蛋白的代谢
Chem Biol Interact. 1978 Dec;23(3):355-67. doi: 10.1016/0009-2797(78)90096-0.
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Induction of zinc-thionein in rat liver and kidneys by zinc loading as studied at isometallothionein levels.在等金属硫蛋白水平下研究锌负荷对大鼠肝脏和肾脏中锌硫蛋白的诱导作用。
Toxicol Lett. 1980 Jun;6(1):59-65. doi: 10.1016/0378-4274(80)90103-4.
6
Degradation of rat liver metallothioneins in vitro.大鼠肝脏金属硫蛋白的体外降解
Biochim Biophys Acta. 1978 Dec 18;544(3):638-46. doi: 10.1016/0304-4165(78)90338-0.
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Metal constitution of metallothionein influences inhibition of delta-aminolaevulinic acid dehydratase (porphobilinogen synthase) by lead.金属硫蛋白的金属组成影响铅对δ-氨基乙酰丙酸脱水酶(胆色素原合酶)的抑制作用。
Biochem J. 1987 Jul 15;245(2):339-45. doi: 10.1042/bj2450339.
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Postinductive actinomycin D effects on the concentrations of cadmium thionein, zinc thionein, and copper chelatin in rat liver.诱导后放线菌素D对大鼠肝脏中镉硫蛋白、锌硫蛋白和铜螯合蛋白浓度的影响。
Bioinorg Chem. 1978;8(2):93-105. doi: 10.1016/s0006-3061(00)80236-7.
9
Biological function of metallothionein-IV. Biosynthesis and degradation of liver and kidney metallothionein in rats fed diets containing zinc or cadmium.金属硫蛋白-IV的生物学功能。喂食含锌或镉日粮的大鼠肝脏和肾脏中金属硫蛋白的生物合成与降解。
Bioinorg Chem. 1978;8(3):245-54. doi: 10.1016/s0006-3061(00)80200-8.
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Induction and degradation of Zn-, Cu- and Cd-thionein in Chang liver cells.锌、铜和镉诱导的硫氧还蛋白在Chang肝细胞中的产生与降解
Chem Biol Interact. 1985 Jan;52(3):319-34. doi: 10.1016/0009-2797(85)90027-4.

引用本文的文献

1
Uptake and binding of cadmium and mercury to metallothionein in rat hepatocyte primary cultures.镉和汞在大鼠肝细胞原代培养物中对金属硫蛋白的摄取与结合
Biochem J. 1982 Nov 15;208(2):465-72. doi: 10.1042/bj2080465.
2
General aspects of cadmium: transport, uptake and metabolism by the kidney.镉的一般情况:肾脏的转运、摄取及代谢
Environ Health Perspect. 1984 Mar;54:13-20. doi: 10.1289/ehp.845413.
3
The chronic toxicity of equine cadmium metallothionein in the rat.马镉金属硫蛋白对大鼠的慢性毒性
Arch Toxicol. 1985 Aug;57(3):200-4. doi: 10.1007/BF00290888.
4
Intracellular compartmentation of metals in aquatic organisms: roles in mechanisms of cell injury.水生生物中金属的细胞内区室化:在细胞损伤机制中的作用。
Environ Health Perspect. 1987 Apr;71:121-8. doi: 10.1289/ehp.8771121.